Z Gastroenterol 2013; 51(12): 1395-1440
DOI: 10.1055/s-0033-1356220
Leitlinie
© Georg Thieme Verlag KG Stuttgart · New York

S3-Leitlinie zum exokrinen Pankreaskarzinom

S3-Guideline Exocrine Pancreatic Cancer
T. Seufferlein
1   Klinik für Innere Medizin I, Universitätsklinikum Ulm
,
M. Porzner
1   Klinik für Innere Medizin I, Universitätsklinikum Ulm
,
T. Becker
2   Klinik für Allgemeine Chirurgie, Viszeral-, Thorax-, Transplantations- und Kinderchirurgie, Universitätsklinikum Kiel
,
V. Budach
3   Klinik für Radioonkologie und Strahlentherapie, Charité Universitätsmedizin Berlin
,
G. Ceyhan
4   Chirurgische Klinik und Poliklinik, Klinikum rechts der Isar, TU München
,
I. Esposito
5   Institut für Allgemeine Pathologie, Klinikum rechts der Isar, TU München
,
R. Fietkau
6   Strahlenklinik, Universitätsklinikum Erlangen
,
M. Follmann
7   Leitlinienprogramm Onkologie, Deutsche Krebsgesellschaft e. V., Berlin
,
H. Friess
4   Chirurgische Klinik und Poliklinik, Klinikum rechts der Isar, TU München
,
P. Galle
8   I. Medizinische Klinik und Poliklinik, Universitätsmedizin Mainz
,
M. Geißler
9   Klinik für Allgemeine Innere Medizin, Onkologie/Hämatologie, Gastroenterologie und Infektiologie, Klinikum Esslingen
,
M. Glanemann
10   Klinik für Allgemeine Chirurgie, Viszeral-, Gefäß- und Kinderchirurgie, Universitätsklinikum des Saarlandes Homburg/Saar
,
T. Gress
11   Klinik für Gastroenterologie, Endokrinologie und Stoffwechsel, Universitätsklinikum Gießen und Marburg
,
V. Heinemann
12   Medizinischen Klinik und Poliklinik III, Klinikum der Universität München LMU
,
W. Hohenberger
13   Chirurgische Klinik, Universitätsklinikum Erlangen
,
U. Hopt
14   Klinik für Allgemein- und Viszeralchirurgie, Universitätsklinikum Freiburg
,
J. Izbicki
15   Klinik für Allgemein-, Viszeral- und Thoraxchirurgie, Universitätsklinikum Hamburg-Eppendorf
,
E. Klar
16   Klinik für Allgemeine Chirurgie, Thorax-, Gefäß- und Transplantationschirurgie, Universitätsmedizin Rostock
,
J. Kleeff
4   Chirurgische Klinik und Poliklinik, Klinikum rechts der Isar, TU München
,
I. Kopp
17   AWMF-Institut für Medizinisches Wissensmanagement, Marburg
,
F. Kullmann
18   Medizinische Klinik I, Klinikum Weiden
,
T. Langer
7   Leitlinienprogramm Onkologie, Deutsche Krebsgesellschaft e. V., Berlin
,
J. Langrehr
19   Klinik für Allgemein-, Gefäß- und Viszeralchirurgie, Martin-Luther-Krankenhaus Berlin
,
M. Lerch
20   Klinik und Poliklinik für Innere Medizin A, Universitätsmedizin Greifswald
,
M. Löhr
21   Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm
,
J. Lüttges
22   Institut für Pathologie, Marienkrankenhaus Hamburg
,
M. Lutz
23   Medizinische Klinik – Schwerpunkt Gastroenterologie, Endokrinologie, Infektiologie, Caritasklinikum Saarbrücken
,
J. Mayerle
20   Klinik und Poliklinik für Innere Medizin A, Universitätsmedizin Greifswald
,
P. Michl
11   Klinik für Gastroenterologie, Endokrinologie und Stoffwechsel, Universitätsklinikum Gießen und Marburg
,
P. Möller
24   Institut für Pathologie, Universitätsklinikum Ulm
,
M. Molls
25   Klinik und Poliklinik für Strahlentherapie und Radiologische Onkologie, Klinikum rechts der Isar, TU München
,
M. Münter
26   Klinik für Strahlentherapie und Radioonkologie, Klinikum Stuttgart
,
M. Nothacker
27   AWMF-Institut für Medizinisches Wissensmanagement, Berlin
,
H. Oettle
28   Medizinische Klinik mit Schwerpunkt Hämatologie und Onkologie, Charité Universitätsmedizin Berlin
,
S. Post
29   Chirurgische Klinik, Universitätsmedizin Mannheim
,
A. Reinacher-Schick
30   Abt. für Hämatologie und Onkologie, St. Josef-Hospital, Klinikum der Ruhr-Universität Bochum
,
C. Röcken
31   Institut für Pathologie, Universitätsklinikum Kiel
,
E. Roeb
32   Medizinische Klinik II, SP Gastroenterologie, Universitätsklinikum Gießen und Marburg
,
H. Saeger
33   Klinik für Viszeral-, Thorax- und Gefäßchirurgie, Universitätsklinikum Dresden
,
R. Schmid
34   II. Medizinische Klinik und Poliklinik, Klinikum rechts der Isar, TU München
,
W. Schmiegel
35   Medizinische Klinik, Klinikum der Ruhr-Universität Bochum
,
M. Schoenberg
36   Klinik für Chirurgie, Rotkreuzklinikum München
,
J. Siveke
34   II. Medizinische Klinik und Poliklinik, Klinikum rechts der Isar, TU München
,
M. Stuschke
37   Klinik für Strahlentherapie, Universitätsklinikum Essen
,
A. Tannapfel
38   Institut für Pathologie, Ruhr-Universität Bochum
,
W. Uhl
39   Chirurgische Klinik, St. Josef-Hospital, Klinikum der Ruhr-Universität Bochum
,
S. Unverzagt
40   Institut für Medizinische Epidemiologie, Biometrie und Informatik, Martin-Luther-Universität Halle-Wittenberg
,
B. van Oorschot
41   Klinik und Poliklinik für Strahlentherapie, Universitätsklinikum Würzburg
,
Y. Vashist
15   Klinik für Allgemein-, Viszeral- und Thoraxchirurgie, Universitätsklinikum Hamburg-Eppendorf
,
J. Werner
42   Klinik für Allgemeine, Viszerale und Transplantationschirurgie, Universitätsklinikum Heidelberg
,
E. Yekebas
43   Klinik für Allgemein-, Thorax- und Viszeralchirurgie, Klinikum Darmstadt
› Institutsangaben
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
11. Dezember 2013 (online)

1. Informationen zu dieser Leitlinie

Bei diesem Dokument handelt es sich um die aktualisierte Fassung der 2006 erstmals erstellten S3-Leitlinie zum exokrinen Pankreaskarzinom.

1.1. Herausgeber

Leitlinienprogramm Onkologie der AWMF, Deutschen Krebsgesellschaft e. V. und Deutschen Krebshilfe e. V.


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1.2. Federführende Fachgesellschaft

Deutsche Gesellschaft für Verdauungs- und Stoffwechselkrankheiten


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1.3. Kontakt

Office Leitlinienprogramm Onkologie
c/o Deutsche Krebsgesellschaft e. V.
Kuno-Fischer-Straße 8
14 057 Berlin
leitlinienprogramm@krebsgesellschaft.de
www.leitlinienprogramm-onkologie.de


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1.4. Finanzierung der Leitlinie

Diese Leitlinie wurde von der Deutschen Krebshilfe im Rahmen des Leitlinienprogramms Onkologie (OL) gefördert.


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1.5. Zitierweise

Leitlinienprogramm Onkologie (Deutsche Krebsgesellschaft, Deutsche Krebshilfe, AWMF): S3-Leitlinie Exokrines Pankreaskarzinom, Langversion 1.0, 2013, AWMF Registernummer: 032 – 010OL, http://leitlinienprogramm-onkologie.de/Leitlinien.7.0.html


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1.6. Besonderer Hinweis

Die Medizin unterliegt einem fortwährenden Entwicklungsprozess, sodass alle Angaben, insbesondere zu diagnostischen und therapeutischen Verfahren, immer nur dem Wissensstand zur Zeit der Drucklegung der Leitlinie entsprechen können. Hinsichtlich der angegebenen Empfehlungen zur Therapie und der Auswahl sowie Dosierung von Medikamenten wurde die größtmögliche Sorgfalt beachtet. Gleichwohl werden die Benutzer aufgefordert, die Beipackzettel und Fachinformationen der Hersteller zur Kontrolle heranzuziehen und im Zweifelsfall einen Spezialisten zu konsultieren. Fragliche Unstimmigkeiten sollen bitte im allgemeinen Interesse der OL-Redaktion mitgeteilt werden.

Der Benutzer selbst bleibt verantwortlich für jede diagnostische und therapeutische Applikation, Medikation und Dosierung.

In dieser Leitlinie sind eingetragene Warenzeichen (geschützte Warennamen) nicht besonders kenntlich gemacht. Es kann also aus dem Fehlen eines entsprechenden Hinweises nicht geschlossen werden, dass es sich um einen freien Warennamen handelt.

Das Werk ist in allen seinen Teilen urheberrechtlich geschützt. Jede Verwertung außerhalb der Bestimmung des Urhebergesetzes ist ohne schriftliche Zustimmung des Leitlinienprogramms Onkologie (OL) unzulässig und strafbar. Kein Teil des Werkes darf in irgendeiner Form ohne schriftliche Genehmigung des OL reproduziert werden. Dies gilt insbesondere für Vervielfältigungen, Übersetzungen, Mikroverfilmungen und die Einspeicherung, Nutzung und Verwertung in elektronischen Systemen, Intranets und dem Internet.


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1.7. Ziele des Leitlinienprogramms Onkologie

Die Arbeitsgemeinschaft der Wissenschaftlichen Medizinischen Fachgesellschaften e. V., die Deutsche Krebsgesellschaft e. V. und die Deutsche Krebshilfe e. V. haben sich mit dem Leitlinienprogramm Onkologie (OL) das Ziel gesetzt, gemeinsam die Entwicklung und Fortschreibung und den Einsatz wissenschaftlich begründeter und praktikabler Leitlinien in der Onkologie zu fördern und zu unterstützen. Die Basis dieses Programms beruht auf den medizinisch-wissenschaftlichen Erkenntnissen der Fachgesellschaften und der DKG, dem Konsens der medizinischen Fachexperten, Anwender und Patienten sowie auf dem Regelwerk für die Leitlinienerstellung der AWMF [1] und der fachlichen Unterstützung und Finanzierung durch die Deutsche Krebshilfe. Um den aktuellen Stand des medizinischen Wissens abzubilden und den medizinischen Fortschritt zu berücksichtigen, müssen Leitlinien regelmäßig überprüft und fortgeschrieben werden. Die Anwendung des AWMF-Regelwerks soll hierbei Grundlage zur Entwicklung qualitativ hochwertiger onkologischer Leitlinien sein. Da Leitlinien ein wichtiges Instrument der Qualitätssicherung und des Qualitätsmanagements in der Onkologie darstellen, sollten sie gezielt und nachhaltig in den Versorgungsalltag eingebracht werden. So sind aktive Implementierungsmaßnahmen und auch Evaluationsprogramme ein wichtiger Bestandteil der Förderung des Leitlinienprogramms Onkologie. Ziel des Programms ist es, in Deutschland professionelle und mittelfristig finanziell gesicherte Voraussetzungen für die Entwicklung und Bereitstellung hochwertiger Leitlinien zu schaffen. Denn diese hochwertigen Leitlinien dienen nicht nur dem strukturierten Wissenstransfer, sondern können auch in der Gestaltung der Strukturen des Gesundheitssystems ihren Platz finden. Zu erwähnen sind hier evidenzbasierte Leitlinien als Grundlage zum Erstellen und Aktualisieren von Disease Management Programmen oder die Verwendung von aus Leitlinien extrahierten Qualitätsindikatoren im Rahmen der Zertifizierung von Organtumorzentren.


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1.8. Zusammensetzung der Leitliniengruppe

1.8.1. Koordination und Redaktion

Prof. Dr. med. Thomas Seufferlein, Universitätsklinikum Ulm

Projektmanagement

  • Dr. med. Marc Porzner, Universitätsklinikum Ulm

  • Anja Wölfer, Universitätsklinikum Halle (Saale)


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1.8.2. Beteiligte Fachgesellschaften und Organisationen

In [Tab. 1] sind die Autoren der ersten Auflage (2006) und in [Tab. 2] die beteiligten Personen an der 1. Aktualisierung (2013) aufgelistet.

Tab. 1

Beteiligte Autoren und Organisationen an der ersten Auflage (2006) der Leitlinien zum exokrinen Pankreaskarzinom.

Autoren

Organisation

Adler, Guido Prof. Dr.

DGVS

Bischoff, Stephan Prof. Dr.

DGE

Brambs, Hans-Jürgen Prof. Dr.

DRG

Feuerbach, Stefan Prof. Dr.

DRG

Grabenbauer, Gerhard Prof. Dr.

DEGRO

Hahn, Stephan Prof. Dr.

DGVS

Heinemann, Volker Prof. Dr.

DGHO/AIO

Hohenberger, Werner Prof. Dr.

DGAV/CAO-V

Kopp, Ina Prof. Dr.

AWMF

Langrehr, Jan Prof. Dr.

DGCH/CAO-V

Lutz, Manfred Prof. Dr.

DGVS

Micke, Oliver PD Dr.

DEGRO

Neuhaus, Horst Prof. Dr.

DGVS

Neuhaus, Peter Prof. Dr.

DGAV

Oettle, Helmut PD Dr.

DGHO/AIO

Schlag, Peter Prof. Dr.

DGCH

Schlottmann, Klaus PD Dr.

DGVS

Schmid, Roland Prof. Dr.

DGVS

Schmiegel, Wolff Prof. Dr.

DGVS

Seufferlein, Thomas Prof. Dr.

DGVS

Werner, Jens Prof. Dr.

DGAV/CAO-V

Wiedenmann, Bertram Prof. Dr.

DGVS

Tab. 2

Beteiligte Personen und Organisationen an der 1. Aktualisierung (2013).

Autoren

Organisation

Arnold, Dirk Prof. Dr.

DGHO

Becker, Thomas Prof. Dr.

CAO-V

Büchler, Markus Prof. Dr.

CAO-V

Budach, Volker Prof. Dr.

ARO

Ceyhan, Güralp PD Dr.

DGAV

Esposito, Irene Prof. Dr.

DGP

Fietkau, Rainer Prof. Dr.

ARO

Follmann, Markus Dr. MPH, MSc

OL

Friess, Helmut Prof. Dr.

DGAV

Galle, Peter Prof. Dr.

DGVS

Geißler, Michael Prof. Dr.

DGVS

Glanemann, Matthias Prof. Dr.

CAO-V

Gress, Thomas Prof. Dr.

DGVS

Heinemann, Volker Prof. Dr.

DGHO/AIO

Hohenberger, Werner Prof. Dr.

CAO-V

Hopt, Ulrich Prof. Dr.

DGAV

Izbicki, Jakob Prof. Dr.

CAO-V/DGAV

Klar, Ernst Prof. Dr.

CAO-V

Kleeberg, Jürgen

AdP

Kleeff, Jörg Prof. Dr.

CAO-V

Klöppel, Günter Prof. Dr.

DGP

Kopp, Ina Prof. Dr.

AWMF

Kullmann, Frank Prof. Dr.

DGVS

Langer, Thomas Dipl.-Soz.Wiss.

OL

Langrehr, Jan Prof. Dr.

CAO-V

Lerch, Markus Prof. Dr.

DGVS

Löhr, Matthias Prof. Dr.

DGVS

Lüttges, Jutta Prof. Dr.

DGP

Lutz, Manfred Prof. Dr.

DGVS

Mayerle, Julia Prof. Dr.

DGVS

Michl, Patrick Prof. Dr.

DGVS

Möller, Peter Prof. Dr.

DGP

Molls, Michael Prof. Dr.

DEGRO

Münter, Marc Prof. Dr.

DEGRO

Nothacker, Monika Dr. MPH

ÄZQ/AWMF

Oettle, Helmut PD Dr.

DGHO/AIO

Porzner, Marc Dr.

DGVS

Post, Stefan Prof. Dr.

CAO-V

Reinacher-Schick, Anke Prof. Dr.

DGVS

Röcken, Christoph Prof. Dr.

DGP

Roeb, Elke Prof. Dr.

DGVS

Saeger, Hans-Detlev Prof. Dr.

CAO-V/DGAV

Schmid, Roland Prof. Dr.

DGVS

Schmiegel, Wolff Prof. Dr.

DGVS

Schoenberg, Michael Prof. Dr.

CAO-V

Seufferlein, Thomas Prof. Dr.

DGVS

Siveke, Jens PD Dr.

DGVS

Stuschke, Martin Prof. Dr.

DEGRO

Tannapfel, Andrea Prof. Dr.

DGP

Uhl, Wolfgang Prof. Dr.

DGAV

Unverzagt, Susanne Dr.

IMEBI (als externer Auftragnehmer)

van Oorschot, Birgitt Dr.

DEGRO

Vashist, Yogesh Dr.

CAO-V

Wagener, Christoph Prof. Dr.

DGKL

Werner, Jens Prof. Dr.

CAO-V/DGAV

Wylegalla, Christian

KOK

Yekebas, Emre Prof. Dr.

CAO-V

Zimpel Tanja

AdP

Die Leitliniengruppe der 1. Aktualisierung besteht aus Vertretern aller an der histopathologischen Diagnostik und Therapie des Pankreaskarzinoms im ambulanten und stationären Bereich beteiligten Fachgruppen, einschließlich der Selbsthilfegruppen. Die jeweiligen Fachgesellschaften bzw. Verbände wurden angeschrieben und gebeten, Vertreter ihrer Gruppierung in die Leitliniengruppe zu entsenden. Darüber hinaus konnten von den einzelnen Fachgruppen weitere interessierte Vertreter in die Leitliniengruppe entsandt werden.

Außerdem waren folgende Fachgesellschaften für den Leitlinienprozess angeschrieben worden: Deutsche Röntgengesellschaft, Deutsche Gesellschaft für Ernährung, Deutsche Gesellschaft für Palliativmedizin. Diese angeschriebenen Fachgesellschaften sahen sich entweder bei der Aktualisierung der behandelten Themen (s. 2.2.1) nicht gefragt und haben daher auf die Teilnahme verzichtet oder haben nicht rückgemeldet.

Die Erarbeitung der Kapitel erfolgte in Arbeitsgruppen, deren Mitglieder in [Tab. 3] aufgeführt sind. Weitere Informationen zu den Mitgliedern der Arbeitsgruppen zu Risikofaktoren/Screening/Risikogruppen, Diagnostik sowie Supportive Therapie, können dem Leitlinienreport entnommen werden.

Tab. 3

Mitglieder der Arbeitsgruppen.

Kapitel

Koordinatoren (alphabetisch, AG-Leiter fett markiert)

Risikofaktoren/Screening/Risikogruppen (2006)

Adler G., Aschoff A., Bergheim I., Bischoff S. C., Gress T., Hahn S., Keim V., Lerch M., Lüttges J., Nagel G., Rieder H., Schmid R.

Diagnostik (2006)

Brambs H.-J., Dobritz M., Möller P., Mössner J., Post S. T., Reske S. N., Riemann J. F., Rösch T. Schäfer A.-O., Schlottmann K., Uhl W., Wagener C., Wiedenmann B.

Chirurgische Therapie (2013)

Friess H., Izbicki J., Klar E., Löhr M., Post S., Schönberg M., Uhl W.

Chirurgische Therapie/Pathologie (2013)

Esposito I., Galle P., Glanemann M., Kleeff J., Klöppel G., Lüttges J., Michl P., Möller P., Röcken C., Saeger H., Tannapfel A., Vashist Y., Werner J.

Adjuvante und neoadjuvante Therapie (2013)

Arnold D., Budach V., Fietkau R., Geißler M., Hohenberger W., Hopt U., Lerch M., Oettle H., Reinacher-Schick A., Roeb E., Siveke J., Stuschke M., Yekebas E.

Palliative Therapie (2013)

Becker T., Gress T., Heinemann V., Kullmann F., Langrehr J., Lutz M., Mayerle J., Molls M., Münter M., Schmid R., Schmiegel W., van Oorschot B.

Supportive Therapie und Nachsorge (2006)

Dietrich C. F., Feil A., Feuerbach S., Graeven U., Hege-Scheuing G., Klar E., Lordick F., Micke O., Neuhaus H., Pauls S., Scheppach W., Weitz J.


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1.8.3. Zusammensetzung der AG Qualitätsindikatoren

Die Entwicklung der Vorschläge zu Qualitätsindikatoren erfolgte durch die in [Tab. 4] aufgeführte Arbeitsgruppe.

Tab. 4

Zusammensetzung der AG Qualitätsindikatoren (2013).

Personen

Organisation

Dr. Markus Follmann MPH, MSc

Deutsche Krebsgesellschaft (DKG), Leitlinienprogramm Onkologie

Prof. Dr. Michael Geißler

Deutsche Gesellschaft für Verdauungs- und Stoffwechselkrankheiten (DGVS)

Prof. Dr. Frank Kullmann

Deutsche Gesellschaft für Verdauungs- und Stoffwechselkrankheiten (DGVS)

Dr. Monika Klinkhammer-Schalke

Arbeitsgemeinschaft Deutscher Tumorzentren (ADT)

Prof. Dr. Manfred Lutz

Deutsche Gesellschaft für Verdauungs- und Stoffwechselkrankheiten (DGVS)

Dr. Monika Nothacker, MPH

Arbeitsgemeinschaft der Wissenschaftlichen Medizinischen Fachgesellschaften e. V. (AWMF), Leitlinienprogramm Onkologie

Prof. Dr. Thomas Seufferlein

Deutsche Gesellschaft für Verdauungs- und Stoffwechselkrankheiten (DGVS)

Prof. Dr. Andrea Tannapfel

Deutsche Gesellschaft für Pathologie (DGP)

Prof. Dr. Waldemar Uhl

Deutsche Gesellschaft für Allgemein- und Viszeralchirurgie e. V. (DGAV)

Dr. Yogesh Vashist

Chirurgische Arbeitsgemeinschaft Onkologie (CAO-V)

Dr. Simone Wesselmann MBA

Deutsche Krebsgesellschaft (DKG), Bereich Zertifizierung


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1.8.4. Patientenbeteilligung

Vertreter der Selbsthilfeorganisation Arbeitskreis der Pankreatektomierten (AdP) waren sowohl an der Erstellung, als auch an der 1. Aktualisierung der Leitlinie direkt beteiligt.


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1.8.5. Methodische Begleitung bei der 1. Aktualisierung

  1. durch das Leitlinienprogramm Onkologie:

    • Prof. Dr. med. Ina Kopp (AWMF), Marburg

    • Dr. Markus Follmann, MPH, MSC (DKG), Berlin

    • Dipl.-Soz.Wiss. Thomas Langer (DKG), Berlin

  2. Dr. Susanne Unverzagt, Institut für Medizinische Epidemiologie, Biometrie und Informatik, Martin-Luther-Universität Halle (Saale)

  3. durch externe Auftragnehmer: Dr. Monika Nothacker, MPH (ehemals ÄZQ, heute AWMF), Berlin


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1.9. Weitere Dokumente zu dieser Leitlinie

Bei diesem Dokument handelt es sich um die aktualisierte Fassung der 2006 erstmals erstellten S3-Leitlinie zum exokrinen Pankreaskarzinom. Diese Leitlinie ist über die folgenden Seiten zugänglich:

  • Homepage der DGVS (www.dgvs.de)
    AWMF (www.leitlinien.net)

  • Leitlinienprogramm Onkologie (http://www.leitlinienprogramm-onkologie.de/OL/leitlinien.html)

  • Deutsche Krebsgesellschaft (http://www.krebsgesellschaft.de/wub_llevidenzbasiert,120 884.html)

  • Deutsche Krebshilfe (http://www.krebshilfe.de/)

  • Guidelines International Network (www.g-i-n.net)

Neben der Langversion gibt es folgende ergänzende Dokumente zu dieser Leitlinie:

  • Kurzfassung der Leitlinie,

  • Patientenleitlinie (Laienversion),

  • Leitlinienreport,

  • Evidenzberichte, die für die 1. Aktualisierung (2013) erstellt wurden

Alle diese Dokumente werden ebenfalls auf den o. g. Homepages abrufbar sein.


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  • Literatur

  • 1 Arbeitsgemeinschaft der Wissenschaftlichen Medizinischen Fachgesellschaften – Ständige Kommission, L. AWMF-Regelwerk „Leitlinien“. 2012 http://www.awmf.org/leitlinien/awmf-regelwerk/awmf-regelwerk.html
  • 2 Gesellschaft der epidemiologischen Krebsregister in Deutschland e, V. and K.-I. Zentrum für Krebsregisterdaten am Robert Koch-Institut. Krebs in Deutschland 2007/2008. Gesundheitsberichterstattung des Bundes, ed. R. Koch-Institut. Vol. 8. Berlin: Robert Koch-Institut; 2012
  • 3 Fernandez E, La Vecchia C, Decarli A. Attributable risks for pancreatic cancer in northern Italy. Cancer Epidemiol Biomarkers Prev 1996; 5 (01) 23-27
  • 4 Ji BT et al. Dietary factors and the risk of pancreatic cancer: a case-control study in Shanghai China. Cancer Epidemiol Biomarkers Prev 1995; 4 (08) 885-893
  • 5 Soler M et al. Diet, alcohol, coffee and pancreatic cancer: final results from an Italian study. Eur J Cancer Prev 1998; 7 (06) 455-460
  • 6 Nkondjock A et al. Dietary patterns and risk of pancreatic cancer. Int J Cancer 2005; 114 (05) 817-823
  • 7 Nothlings U et al. Meat and fat intake as risk factors for pancreatic cancer: the multiethnic cohort study. J Natl Cancer Inst 2005; 97 (19) 1458-1465
  • 8 Glade MJ. Food, nutrition, and the prevention of cancer: a global perspective. American Institute for Cancer Research/World Cancer Research Fund, American Institute for Cancer Research, 1997. Nutrition 1999; 15 (06) 523-526
  • 9 Michaud DS et al. Dietary meat, dairy products, fat, and cholesterol and pancreatic cancer risk in a prospective study. Am J Epidemiol 2003; 157 (12) 1115-1125
  • 10 Michaud DS et al. Dietary patterns and pancreatic cancer risk in men and women. J Natl Cancer Inst 2005; 97 (07) 518-524
  • 11 Hine RJ et al. Nutritional links to plausible mechanisms underlying pancreatic cancer: a conference report. Pancreas 2003; 27 (04) 356-366
  • 12 Bueno de Mesquita HB et al. Intake of foods and nutrients and cancer of the exocrine pancreas: a population-based case-control study in The Netherlands. Int J Cancer 1991; 48 (04) 540-549
  • 13 Lyon JL et al. Dietary intake as a risk factor for cancer of the exocrine pancreas. Cancer Epidemiol Biomarkers Prev 1993; 2 (06) 513-518
  • 14 Fraser GE. Associations between diet and cancer, ischemic heart disease, and all-cause mortality in non-Hispanic white California Seventh-day Adventists. Am J Clin Nutr 1999; 70 (Suppl. 03) 532S-538S
  • 15 Mills PK et al. Dietary habits and past medical history as related to fatal pancreas cancer risk among Adventists. Cancer 1988; 61 (12) 2578-2585
  • 16 Chan JM, Wang F, Holly EA. Vegetable and fruit intake and pancreatic cancer in a population-based case-control study in the San Francisco bay area. Cancer Epidemiol Biomarkers Prev 2005; 14 (09) 2093-2097
  • 17 Negri E et al. Vegetable and fruit consumption and cancer risk. Int J Cancer 1991; 48 (03) 350-354
  • 18 Larsson SC et al. Fruit and vegetable consumption in relation to pancreatic cancer risk: a prospective study. Cancer Epidemiol Biomarkers Prev 2006; 15 (02) 301-305
  • 19 Vainio H, Weiderpass E. Fruit and vegetables in cancer prevention. Nutr Cancer 2006; 54 (01) 111-142
  • 20 Lin Y et al. Nutritional factors and risk of pancreatic cancer: a population-based case-control study based on direct interview in Japan. J Gastroenterol 2005; 40 (03) 297-301
  • 21 Stolzenberg-Solomon RZ et al. Prospective study of diet and pancreatic cancer in male smokers. Am J Epidemiol 2002; 155 (09) 783-792
  • 22 Zhang J, Zhao Z, Berkel HJ. Animal fat consumption and pancreatic cancer incidence: evidence of interaction with cigarette smoking. Ann Epidemiol 2005; 15 (07) 500-508
  • 23 Anderson KE et al. Meat intake and cooking techniques: associations with pancreatic cancer. Mutat Res 2002; 506-507: 225-231
  • 24 Anderson KE et al. Dietary intake of heterocyclic amines and benzo(a)pyrene: associations with pancreatic cancer. Cancer Epidemiol Biomarkers Prev 2005; 14 (09) 2261-2265
  • 25 Ghadirian P et al. Food habits and pancreatic cancer: a case-control study of the Francophone community in Montreal, Canada. Cancer Epidemiol Biomarkers Prev 1995; 4 (08) 895-899
  • 26 Fernandez E et al. Fish consumption and cancer risk. Am J Clin Nutr 1999; 70 (01) 85-90
  • 27 Michaud DS et al. Dietary sugar, glycemic load, and pancreatic cancer risk in a prospective study. J Natl Cancer Inst 2002; 94 (17) 1293-1300
  • 28 Silvera SA et al. Glycemic index, glycemic load, and pancreatic cancer risk (Canada). Cancer Causes Control 2005; 16 (04) 431-436
  • 29 Schernhammer ES et al. Sugar-sweetened soft drink consumption and risk of pancreatic cancer in two prospective cohorts. Cancer Epidemiol Biomarkers Prev 2005; 14 (09) 2098-2105
  • 30 Lin Y et al. Risk of pancreatic cancer in relation to alcohol drinking, coffee consumption and medical history: findings from the Japan collaborative cohort study for evaluation of cancer risk. Int J Cancer 2002; 99 (05) 742-746
  • 31 Michaud DS et al. Coffee and alcohol consumption and the risk of pancreatic cancer in two prospective United States cohorts. Cancer Epidemiol Biomarkers Prev 2001; 10 (05) 429-437
  • 32 Silverman DT. Risk factors for pancreatic cancer: a case-control study based on direct interviews. Teratog Carcinog Mutagen 2001; 21 (01) 7-25
  • 33 Brown LM. Epidemiology of alcohol-associated cancers. Alcohol 2005; 35 (03) 161-168
  • 34 Ye W et al. Alcohol abuse and the risk of pancreatic cancer. Gut 2002; 51 (02) 236-239
  • 35 Talamini G et al. Alcohol and smoking as risk factors in chronic pancreatitis and pancreatic cancer. Dig Dis Sci 1999; 44 (07) 1303-1311
  • 36 MacMahon B et al. Coffee and cancer of the pancreas. N Engl J Med 1981; 304 (11) 630-633
  • 37 Gullo L, Pezzilli R, Morselli-Labate AM. Coffee and cancer of the pancreas: an Italian multicenter study. The Italian Pancreatic Cancer Study Group. Pancreas 1995; 11 (03) 223-229
  • 38 Lyon JL et al. Coffee consumption and the risk of cancer of the exocrine pancreas: a case-control study in a low-risk population. Epidemiology 1992; 3 (02) 164-170
  • 39 Harnack LJ et al. Smoking, alcohol, coffee, and tea intake and incidence of cancer of the exocrine pancreas: the Iowa Women’s Health Study. Cancer Epidemiol Biomarkers Prev 1997; 6 (12) 1081-1086
  • 40 Qiu D et al. Overview of the epidemiology of pancreatic cancer focusing on the JACC Study. J Epidemiol 2005; 15 (Suppl. 02) S157-S167
  • 41 Tavani A, La Vecchia C. Coffee and cancer: a review of epidemiological studies, 1990–1999. Eur J Cancer Prev 2000; 9 (04) 241-256
  • 42 La Vecchia C et al. Tea consumption and cancer risk. Nutr Cancer 1992; 17 (01) 27-31
  • 43 Nagano J et al. A prospective study of green tea consumption and cancer incidence, Hiroshima and Nagasaki (Japan). Cancer Causes Control 2001; 12 (06) 501-508
  • 44 Hemminki K, Dong C, Vaittinen P. Cancer risks to spouses and offspring in the Family-Cancer Database. Genet Epidemiol 2001; 20 (02) 247-257
  • 45 Hemminki K, Jiang Y. Cancer risks among long-standing spouses. Br J Cancer 2002; 86 (11) 1737-1740
  • 46 Nilsen TI, Vatten LJ. A prospective study of lifestyle factors and the risk of pancreatic cancer in Nord-Trondelag, Norway. Cancer Causes Control 2000; 11 (07) 645-652
  • 47 Berrington de Gonzalez A, Sweetland S, Spencer E. A meta-analysis of obesity and the risk of pancreatic cancer. Br J Cancer 2003; 89 (03) 519-523
  • 48 Michaud DS et al. Physical activity, obesity, height, and the risk of pancreatic cancer. Jama 2001; 286 (08) 921-929
  • 49 Patel AV et al. Obesity, recreational physical activity, and risk of pancreatic cancer in a large U. S. Cohort. Cancer Epidemiol Biomarkers Prev 2005; 14 (02) 459-466
  • 50 Rapp K et al. Obesity and incidence of cancer: a large cohort study of over 145,000 adults in Austria. Br J Cancer 2005; 93 (09) 1062-1067
  • 51 Larsson SC et al. Overall obesity, abdominal adiposity, diabetes and cigarette smoking in relation to the risk of pancreatic cancer in two Swedish population-based cohorts. Br J Cancer 2005; 93 (11) 1310-1315
  • 52 Berrington de Gonzalez A et al. Anthropometry, physical activity, and the risk of pancreatic cancer in the European prospective investigation into cancer and nutrition. Cancer Epidemiol Biomarkers Prev 2006; 15 (05) 879-885
  • 53 Silverman DT et al. Dietary and nutritional factors and pancreatic cancer: a case-control study based on direct interviews. J Natl Cancer Inst 1998; 90 (22) 1710-1719
  • 54 Stolzenberg-Solomon RZ et al. A prospective study of medical conditions, anthropometry, physical activity, and pancreatic cancer in male smokers (Finland). Cancer Causes Control 2002; 13 (05) 417-426
  • 55 Hanley AJ et al. Physical activity, anthropometric factors and risk of pancreatic cancer: results from the Canadian enhanced cancer surveillance system. Int J Cancer 2001; 94 (01) 140-147
  • 56 Coughlin SS et al. Predictors of pancreatic cancer mortality among a large cohort of United States adults. Cancer Causes Control 2000; 11 (10) 915-923
  • 57 Lin Y et al. A prospective cohort study of cigarette smoking and pancreatic cancer in Japan. Cancer Causes Control 2002; 13 (03) 249-254
  • 58 Yun YH et al. Cigarette smoking and cancer incidence risk in adult men: National Health Insurance Corporation Study. Cancer Detect Prev 2005; 29 (01) 15-24
  • 59 Chiu BC et al. Cigarette smoking and risk of bladder, pancreas, kidney, and colorectal cancers in Iowa. Ann Epidemiol 2001; 11 (01) 28-37
  • 60 Bonelli L et al. Exocrine pancreatic cancer, cigarette smoking, and diabetes mellitus: a case-control study in northern Italy. Pancreas 2003; 27 (02) 143-149
  • 61 Duell EJ et al. A population-based, case-control study of polymorphisms in carcinogen-metabolizing genes, smoking, and pancreatic adenocarcinoma risk. J Natl Cancer Inst 2002; 94 (04) 297-306
  • 62 Miyasaka K et al. Inactive aldehyde dehydrogenase-2 increased the risk of pancreatic cancer among smokers in a Japanese male population. Pancreas 2005; 30 (02) 95-98
  • 63 Wang L et al. Genetic polymorphisms in methylenetetrahydrofolate reductase and thymidylate synthase and risk of pancreatic cancer. Clin Gastroenterol Hepatol 2005; 3 (08) 743-751
  • 64 Villeneuve PJ et al. Environmental tobacco smoke and the risk of pancreatic cancer: findings from a Canadian population-based case-control study. Can J Public Health 2004; 95 (01) 32-37
  • 65 Alguacil J, Pollan M, Gustavsson P. Occupations with increased risk of pancreatic cancer in the Swedish population. Occup Environ Med 2003; 60 (08) 570-576
  • 66 Alguacil J et al. Occupation and pancreatic cancer in Spain: a case-control study based on job titles. PANKRAS II Study Group. Int J Epidemiol 2000; 29 (06) 1004-1013
  • 67 Laakkonen A, Kauppinen T, Pukkala E. Cancer risk among Finnish food industry workers. Int J Cancer 2006; 118 (10) 2567-2571
  • 68 Fryzek JP et al. A case-control study of self-reported exposures to pesticides and pancreas cancer in southeastern Michigan. Int J Cancer 1997; 72 (01) 62-67
  • 69 Ji BT et al. Occupational exposure to pesticides and pancreatic cancer. Am J Ind Med 2001; 39 (01) 92-99
  • 70 Ojajarvi IA et al. Occupational exposures and pancreatic cancer: a meta-analysis. Occup Environ Med 2000; 57 (05) 316-324
  • 71 Ojajarvi A et al. Risk of pancreatic cancer in workers exposed to chlorinated hydrocarbon solvents and related compounds: a meta-analysis. Am J Epidemiol 2001; 153 (09) 841-850
  • 72 Weiderpass E et al. Occupational exposures and gastrointestinal cancers among Finnish women. J Occup Environ Med 2003; 45 (03) 305-315
  • 73 Yassi A, Tate RB, Routledge M. Cancer incidence and mortality in workers employed at a transformer manufacturing plant: update to a cohort study. Am J Ind Med 2003; 44 (01) 58-62
  • 74 Ji J, Hemminki K. Socioeconomic and occupational risk factors for pancreatic cancer: a cohort study in Sweden. J Occup Environ Med 2006; 48 (03) 283-288
  • 75 Bjelakovic G et al. Antioxidant supplements for prevention of gastrointestinal cancers: a systematic review and meta-analysis. Lancet 2004; 364 (9441) 1219-1228
  • 76 Bjelakovic G et al. Antioxidant supplements for preventing gastrointestinal cancers. Cochrane Database Syst Rev 2004; Oct 18; (04) CD004183
  • 77 Harris RE et al. Aspirin, ibuprofen, and other non-steroidal anti-inflammatory drugs in cancer prevention: a critical review of non-selective COX-2 blockade (review). Oncol Rep 2005; 13 (04) 559-583
  • 78 Jacobs EJ et al. Aspirin use and pancreatic cancer mortality in a large United States cohort. J Natl Cancer Inst 2004; 96 (07) 524-528
  • 79 Coogan PF et al. Nonsteroidal anti-inflammatory drugs and risk of digestive cancers at sites other than the large bowel. Cancer Epidemiol Biomarkers Prev 2000; 9 (01) 119-123
  • 80 Homma T, Tsuchiya R. The study of the mass screening of persons without symptoms and of the screening of outpatients with gastrointestinal complaints or icterus for pancreatic cancer in Japan, using CA19-9 and elastase-1 or ultrasonography. Int J Pancreatol 1991; 9: 119-124
  • 81 Kim JE et al. Clinical usefulness of carbohydrate antigen 19-9 as a screening test for pancreatic cancer in an asymptomatic population. J Gastroenterol Hepatol 2004; 19 (02) 182-186
  • 82 McWilliams RR et al. Risk of malignancy in first-degree relatives of patients with pancreatic carcinoma. Cancer 2005; 104 (02) 388-394
  • 83 Klein AP et al. Prospective risk of pancreatic cancer in familial pancreatic cancer kindreds. Cancer Res 2004; 64 (07) 2634-2638
  • 84 Bartsch DK et al. CDKN2A germline mutations in familial pancreatic cancer. Ann Surg 2002; 236 (06) 730-737
  • 85 McFaul CD et al. Anticipation in familial pancreatic cancer. Gut 2006; 55 (02) 252-258
  • 86 Tersmette AC et al. Increased risk of incident pancreatic cancer among first-degree relatives of patients with familial pancreatic cancer. Clin Cancer Res 2001; 7 (03) 738-744
  • 87 Brentnall TA. Management strategies for patients with hereditary pancreatic cancer. Curr Treat Options Oncol 2005; 6 (05) 437-445
  • 88 Canto MI et al. Screening for pancreatic neoplasia in high-risk individuals: an EUS-based approach. Clin Gastroenterol Hepatol 2004; 2 (07) 606-621
  • 89 Canto MI et al. Screening for early pancreatic neoplasia in high-risk individuals: a prospective controlled study. Clin Gastroenterol Hepatol 2006; 4 (06) 766-781 ; quiz 665
  • 90 Giardiello FM et al. Very high risk of cancer in familial Peutz-Jeghers syndrome. Gastroenterology 2000; 119 (06) 1447-1453
  • 91 Lim W et al. Relative frequency and morphology of cancers in STK11 mutation carriers. Gastroenterology 2004; 126 (07) 1788-1794
  • 92 Lynch HT et al. Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: the familial atypical mole melanoma-pancreatic carcinoma syndrome. Cancer 2002; 94 (01) 84-96
  • 93 Rulyak SJ et al. Characterization of the neoplastic phenotype in the familial atypical multiple-mole melanoma-pancreatic carcinoma syndrome. Cancer 2003; 98 (04) 798-804
  • 94 Vasen HF et al. Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden). Int J Cancer 2000; 87 (06) 809-811
  • 95 Friedenson B. BRCA1 and BRCA2 pathways and the risk of cancers other than breast or ovarian. MedGenMed 2005; 7 (02) 60
  • 96 van Asperen CJ et al. Cancer risks in BRCA2 families: estimates for sites other than breast and ovary. J Med Genet 2005; 42 (09) 711-719
  • 97 Thompson D, Easton DF. Cancer Incidence in BRCA1 mutation carriers. J Natl Cancer Inst 2002; 94 (18) 1358-1365
  • 98 Lilley M, Gilchrist D. The hereditary spectrum of pancreatic cancer: the Edmonton experience. Can J Gastroenterol 2004; 18 (01) 17-21
  • 99 Aarnio M et al. Cancer risk in mutation carriers of DNA-mismatch-repair genes. Int J Cancer 1999; 81 (02) 214-218
  • 100 Geoffroy-Perez B et al. Cancer risk in heterozygotes for ataxia-telangiectasia. Int J Cancer 2001; 93 (02) 288-293
  • 101 Giardiello FM et al. Increased risk of thyroid and pancreatic carcinoma in familial adenomatous polyposis. Gut 1993; 34 (10) 1394-1396
  • 102 Couch FJ et al. Germ line Fanconi anemia complementation group C mutations and pancreatic cancer. Cancer Res 2005; 65 (02) 383-386
  • 103 Howes N et al. Clinical and genetic characteristics of hereditary pancreatitis in Europe. Clin Gastroenterol Hepatol 2004; 2 (03) 252-261
  • 104 Lowenfels AB et al. Hereditary pancreatitis and the risk of pancreatic cancer. International Hereditary Pancreatitis Study Group. J Natl Cancer Inst 1997; 89 (06) 442-446
  • 105 Kimmey MB et al. Screening and surveillance for hereditary pancreatic cancer. Gastrointest Endosc 2002; 56 (Suppl. 04) S82-S86
  • 106 Bansal P, Sonnenberg A. Pancreatitis is a risk factor for pancreatic cancer. Gastroenterology 1995; 109 (01) 247-251
  • 107 Karlson BM et al. The risk of pancreatic cancer following pancreatitis: an association due to confounding?. Gastroenterology 1997; 113 (02) 587-592
  • 108 Lowenfels AB et al. Pancreatitis and the risk of pancreatic cancer. International Pancreatitis Study Group. N Engl J Med 1993; 328 (20) 1433-1437
  • 109 Malka D et al. Risk of pancreatic adenocarcinoma in chronic pancreatitis. Gut 2002; 51 (06) 849-852
  • 110 Talamini G et al. Incidence of cancer in the course of chronic pancreatitis. Am J Gastroenterol 1999; 94 (05) 1253-1260
  • 111 Gullo L, Pezzilli R, Morselli-Labate AM. Diabetes and the risk of pancreatic cancer. Italian Pancreatic Cancer Study Group. N Engl J Med 1994; 331 (02) 81-84
  • 112 Rousseau MC et al. Diabetes mellitus and cancer risk in a population-based case-control study among men from Montreal, Canada. Int J Cancer 2006; 118 (08) 2105-2109
  • 113 Coughlin SS et al. Diabetes mellitus as a predictor of cancer mortality in a large cohort of US adults. Am J Epidemiol 2004; 159 (12) 1160-1167
  • 114 Huxley R et al. Type-II diabetes and pancreatic cancer: a meta-analysis of 36 studies. Br J Cancer 2005; 92 (11) 2076-2083
  • 115 Stolzenberg-Solomon RZ et al. Insulin, glucose, insulin resistance, and pancreatic cancer in male smokers. Jama 2005; 294 (22) 2872-2878
  • 116 Wideroff L et al. Cancer incidence in a population-based cohort of patients hospitalized with diabetes mellitus in Denmark. J Natl Cancer Inst 1997; 89 (18) 1360-1365
  • 117 Calle EE et al. Diabetes mellitus and pancreatic cancer mortality in a prospective cohort of United States adults. Cancer Causes Control 1998; 9 (04) 403-410
  • 118 Chow WH et al. Risk of pancreatic cancer following diabetes mellitus: a nationwide cohort study in Sweden. J Natl Cancer Inst 1995; 87 (12) 930-931
  • 119 Silverman DT et al. Diabetes mellitus, other medical conditions and familial history of cancer as risk factors for pancreatic cancer. Br J Cancer 1999; 80 (11) 1830-1837
  • 120 Everhart J, Wright D. Diabetes mellitus as a risk factor for pancreatic cancer. A meta-analysis. Jama 1995; 273 (20) 1605-1609
  • 121 Chari ST et al. Probability of pancreatic cancer following diabetes: a population-based study. Gastroenterology 2005; 129 (02) 504-511
  • 122 Bjornsson E, Ismael S, Nejdet S et al. Severe jaundice in Sweden in the new millennium: causes, investigations, treatment and prognosis. Scand J Gastroenterol 2003; 38 (01) 86-94
  • 123 Reisman Y et al. Clinical presentation of (subclinical) jaundice--the Euricterus project in The Netherlands. United Dutch Hospitals and Euricterus Project Management Group. Hepatogastroenterology 1996; 43 (11) 1190-1195
  • 124 Watanabe I et al. Onset symptoms and tumor locations as prognostic factors of pancreatic cancer. Pancreas 2004; 28 (02) 160-165
  • 125 Balthazar EJ. Pancreatitis associated with pancreatic carcinoma. Preoperative diagnosis: role of CT imaging in detection and evaluation. Pancreatology 2005; 5 (04) 330-344
  • 126 Mujica VR, Barkin JS, Go VL. Acute pancreatitis secondary to pancreatic carcinoma. Study Group Participants. Pancreas 2000; 21 (04) 329-332
  • 127 Adamek HE et al. Pancreatic cancer detection with magnetic resonance cholangiopancreatography and endoscopic retrograde cholangiopancreatography: a prospective controlled study. Lancet 2000; 356 (9225) 190-193
  • 128 Hanninen EL et al. Magnetic resonance cholangiopancreatography: image quality, ductal morphology, and value of additional T2- and T1-weighted sequences for the assessment of suspected pancreatic cancer. Acta Radiol 2005; 46 (02) 117-125
  • 129 Forsmark CE, Lambiase L, Vogel SB. Diagnosis of pancreatic cancer and prediction of unresectability using the tumor-associated antigen CA19-9. Pancreas 1994; 9 (06) 731-734
  • 130 Nazli O et al. The diagnostic importance of CEA and CA 19-9 for the early diagnosis of pancreatic carcinoma. Hepatogastroenterology 2000; 47 (36) 1750-1752
  • 131 Ritts Jr RE et al. Comparison of preoperative serum CA19-9 levels with results of diagnostic imaging modalities in patients undergoing laparotomy for suspected pancreatic or gallbladder disease. Pancreas 1994; 9 (06) 707-716
  • 132 Tessler DA et al. Predictors of cancer in patients with suspected pancreatic malignancy without a tissue diagnosis. Am J Surg 2006; 191 (02) 191-197
  • 133 Agarwal B et al. Endoscopic ultrasound-guided fine needle aspiration and multidetector spiral CT in the diagnosis of pancreatic cancer. Am J Gastroenterol 2004; 99 (05) 844-850
  • 134 Klapman JB et al. Negative predictive value of endoscopic ultrasound in a large series of patients with a clinical suspicion of pancreatic cancer. Am J Gastroenterol 2005; 100 (12) 2658-2661
  • 135 Varadarajulu S, Wallace MB. Applications of endoscopic ultrasonography in pancreatic cancer. Cancer Control 2004; 11 (01) 15-22
  • 136 David O et al. Pancreatic masses: a multi-institutional study of 364 fine-needle aspiration biopsies with histopathologic correlation. Diagn Cytopathol 1998; 19 (06) 423-427
  • 137 Bipat S et al. Ultrasonography, computed tomography and magnetic resonance imaging for diagnosis and determining resectability of pancreatic adenocarcinoma: a meta-analysis. J Comput Assist Tomogr 2005; 29 (04) 438-445
  • 138 Dewitt J et al. Comparison of endoscopic ultrasound and computed tomography for the preoperative evaluation of pancreatic cancer: a systematic review. Clin Gastroenterol Hepatol 2006; 4 (06) 717-725; quiz 664
  • 139 Romagnuolo J et al. Magnetic resonance cholangiopancreatography: a meta-analysis of test performance in suspected biliary disease. Ann Intern Med 2003; 139 (07) 547-557
  • 140 Pakzad F, Groves AM, Ell PJ. The role of positron emission tomography in the management of pancreatic cancer. Semin Nucl Med 2006; 36 (03) 248-256
  • 141 Schachter PP et al. The impact of laparoscopy and laparoscopic ultrasonography on the management of pancreatic cancer. Arch Surg 2000; 135 (11) 1303-1307
  • 142 Vollmer CM et al. Utility of staging laparoscopy in subsets of peripancreatic and biliary malignancies. Ann Surg 2002; 235 (01) 1-7
  • 143 van der Waaij LA, van Dullemen HM, Porte RJ. Cyst fluid analysis in the differential diagnosis of pancreatic cystic lesions: a pooled analysis. Gastrointest Endosc 2005; 62 (03) 383-389
  • 144 Doi R et al. Surgery versus radiochemotherapy for resectable locally invasive pancreatic cancer: final results of a randomized multi-institutional trial. Surg Today 2008; 38 (11) 1021-1028
  • 145 Barabino M et al. Is there still a role for laparoscopy combined with laparoscopic ultrasonography in the staging of pancreatic cancer?. Surg Endosc 2011; 25 (01) 160-165
  • 146 Contreras CM et al. Staging laparoscopy enhances the detection of occult metastases in patients with pancreatic adenocarcinoma. J Surg Oncol 2009; 100 (08) 663-669
  • 147 Doucas H et al. Assessment of pancreatic malignancy with laparoscopy and intraoperative ultrasound. Surg Endosc 2007; 21 (07) 1147-11452
  • 148 Enestvedt CK et al. Diagnostic laparoscopy for patients with potentially resectable pancreatic adenocarcinoma: is it cost-effective in the current era?. J Gastrointest Surg 2008; 12 (07) 1177-1184
  • 149 Hariharan D et al. The role of laparoscopy and laparoscopic ultrasound in the preoperative staging of pancreatico-biliary cancers – A meta-analysis. Eur J Surg Oncol 2010; 36 (10) 941-948
  • 150 Mayo SC et al. Evolving preoperative evaluation of patients with pancreatic cancer: does laparoscopy have a role in the current era?. J Am Coll Surg 2009; 208 (01) 87-95
  • 151 Muntean V et al. Staging laparoscopy in digestive cancers. J Gastrointestin Liver Dis 2009; 18 (04) 461-467
  • 152 Satoi S et al. Selective use of staging laparoscopy based on carbohydrate antigen 19-9 level and tumor size in patients with radiographically defined potentially or borderline resectable pancreatic cancer. Pancreas 2011; 40 (03) 426-432
  • 153 Shah D et al. Preoperative prediction of complete resection in pancreatic cancer. J Surg Res 2008; 147 (02) 216-220
  • 154 White R et al. Current utility of staging laparoscopy for pancreatic and peripancreatic neoplasms. J Am Coll Surg 2008; 206 (03) 445-450
  • 155 Kelly KJ et al. Prognostic impact of RT-PCR-based detection of peritoneal micrometastases in patients with pancreatic cancer undergoing curative resection. Ann Surg Oncol 2009; 16 (12) 3333-3339
  • 156 Yamada S et al. Clinical implications of peritoneal cytology in potentially resectable pancreatic cancer: positive peritoneal cytology may not confer an adverse prognosis. Ann Surg 2007; 246 (02) 254-258
  • 157 Wagner M et al. Curative resection is the single most important factor determining outcome in patients with pancreatic adenocarcinoma. Br J Surg 2004; 91 (05) 586-594
  • 158 Fusai G et al. Outcome of R1 resection in patients undergoing pancreatico-duodenectomy for pancreatic cancer. Eur J Surg Oncol 2008; 34 (12) 1309-1315
  • 159 Gaedcke J et al. The mesopancreas is the primary site for R1 resection in pancreatic head cancer: relevance for clinical trials. Langenbecks Arch Surg 2010; 395 (04) 451-458
  • 160 Hartwig W et al. Pancreatic cancer surgery in the new millennium: better prediction of outcome. Ann Surg 2011; 254 (02) 311-319
  • 161 Esposito I et al. Most pancreatic cancer resections are R1 resections. Ann Surg Oncol 2008; 15 (06) 1651-1660
  • 162 Raut CP et al. Impact of resection status on pattern of failure and survival after pancreaticoduodenectomy for pancreatic adenocarcinoma. Ann Surg 2007; 246 (01) 52-60
  • 163 Chang DK et al. Margin Clearance and Outcome in Resected Pancreatic Cancer. Journal of Clinical Oncology 2009; 27 (17) 2855-2862
  • 164 Campbell F et al. Classification of R1 resections for pancreatic cancer: the prognostic relevance of tumour involvement within 1 mm of a resection margin. Histopathology 2009; 55 (03) 277-283
  • 165 Jamieson NB et al. Positive mobilization margins alone do not influence survival following pancreatico-duodenectomy for pancreatic ductal adenocarcinoma. Ann Surg 2010; 251 (06) 1003-1010
  • 166 Diener MK, Heukaeufer C, Schwarzer G et al. Pylorus-preserving pancreaticoduodenectomy (pp Whipple) versus pancreaticoduodenectomy (classic Whipple) for surgical treatment of periampullary and pancreatic carcinoma. Cochrane Database of Systematic Reviews 2011; DOI: 10.1002/14651858.CD006053.pub4.
  • 167 Kawai M et al. Pylorus ring resection reduces delayed gastric emptying in patients undergoing pancreatoduodenectomy: a prospective, randomized, controlled trial of pylorus-resecting versus pylorus-preserving pancreatoduodenectomy. Annals of surgery 2011; 253: 495-501
  • 168 Verbeke CS. Resection margins and R1 rates in pancreatic cancer – are we there yet?. Histopathology 2008; 52 (07) 787-796
  • 169 Wittekind C et al. A uniform residual tumor (R) classification: integration of the R classification and the circumferential margin status. Cancer 2009; 115 (15) 3483-3488
  • 170 Fong Y et al. Pancreatic or liver resection for malignancy is safe and effective for the elderly. Ann Surg 1995; 222 (04) 426-434 ; discussion 434–437
  • 171 Lightner AM et al. Pancreatic resection in the elderly. J Am Coll Surg 2004; 198 (05) 697-706
  • 172 American College of Physicians. Guidelines for assessing and managing the perioperative risk from coronary artery disease associated with major noncardiac surgery. Ann Intern Med 1997; 127 (04) 309-312
  • 173 Nikfarjam M et al. Additional organ resection combined with pancreaticoduodenectomy does not increase postoperative morbidity and mortality. J Gastrointest Surg 2009; 13 (05) 915-921
  • 174 Fuhrman GM et al. Rationale for en bloc vein resection in the treatment of pancreatic adenocarcinoma adherent to the superior mesenteric-portal vein confluence. Pancreatic Tumor Study Group. Ann Surg 1996; 223 (02) 154-162
  • 175 Leach SD et al. Survival following pancreaticoduodenectomy with resection of the superior mesenteric-portal vein confluence for adenocarcinoma of the pancreatic head. Br J Surg 1998; 85 (05) 611-617
  • 176 Sasson AR et al. En bloc resection for locally advanced cancer of the pancreas: is it worthwhile?. J Gastrointest Surg 2002; 6 (02) 147-157 ; discussion 157–158
  • 177 Nakao A et al. Indications and techniques of extended resection for pancreatic cancer. World J Surg 2006; 30 (06) 976-982 ; discussion 983-984
  • 178 Shrikhande SV et al. Pancreatic resection for M1 pancreatic ductal adenocarcinoma. Ann Surg Oncol 2007; 14 (01) 118-127
  • 179 Burdelski CM et al. Multivisceral resections in pancreatic cancer: identification of risk factors. World J Surg 2011; 35 (12) 2756-2763
  • 180 Hartwig W et al. Multivisceral resection for pancreatic malignancies: risk-analysis and long-term outcome. Ann Surg 2009; 250 (01) 81-87
  • 181 Yekebas EF et al. En bloc vascular resection for locally advanced pancreatic malignancies infiltrating major blood vessels: perioperative outcome and long-term survival in 136 patients. Ann Surg 2008; 247 (02) 300-309
  • 182 Shrikhande SV et al. Superior mesenteric artery first combined with uncinate process approach versus uncinate process first approach in pancreatoduodenectomy: a comparative study evaluating perioperative outcomes. Langenbeck's Archives of Surgery 2011; 396: 1205-1212
  • 183 Ouaissi M et al. Vascular reconstruction during pancreatoduodenectomy for ductal adenocarcinoma of the pancreas improves resectability but does not achieve cure. World J Surg 2010; 34 (11) 2648-2661
  • 184 Mollberg N et al. Arterial resection during pancreatectomy for pancreatic cancer: a systematic review and meta-analysis. Ann Surg 2011; 254 (06) 882-893
  • 185 Bachellier P et al. Is the need for an arterial resection a contraindication to pancreatic resection for locally advanced pancreatic adenocarcinoma? a case-matched controlled study. Journal of Surgical Oncology 2011; 103 (01) 75-84
  • 186 Boggi U et al. Prognostic implications of tumor invasion or adhesion to peripancreatic vessels in resected pancreatic cancer. Surgery 2009; 146 (05) 869-881
  • 187 Wang C et al. Pancreaticoduodenectomy with vascular resection for local advanced pancreatic head cancer: a single center retrospective study. J Gastrointest Surg 2008; 12 (12) 2183-2190
  • 188 Varadhachary GR et al. Borderline resectable pancreatic cancer: definitions, management, and role of preoperative therapy. Ann Surg Oncol 2006; 13 (08) 1035-1046
  • 189 Li B et al. Pancreatoduodenectomy with vascular reconstruction in treating carcinoma of the pancreatic head. Hepatobiliary Pancreat Dis Int 2004; 3 (04) 612-615
  • 190 Settmacher U et al. Reconstruction of visceral arteries with homografts in excision of the pancreas]. Chirurg 2004; 75 (12) 1199-1206
  • 191 Wu YL et al. Extended Appleby's operation for pancreatic cancer involving celiac axis. J Surg Oncol 2007; 96 (05) 442-446 ; discussion 447
  • 192 Callery MP et al. Pretreatment assessment of resectable and borderline resectable pancreatic cancer: expert consensus statement. Ann Surg Oncol 2009; 16 (07) 1727-1733
  • 193 Al-Haddad M et al. Vascular resection and reconstruction for pancreatic malignancy: a single center survival study. J Gastrointest Surg 2007; 11 (09) 1168-1174
  • 194 Chakravarty KD et al. Prognosis and feasibility of en-bloc vascular resection in stage II pancreatic adenocarcinoma. World J Gastroenterol 2010; 16 (08) 997-1002
  • 195 Fukuda S et al. Significance of the depth of portal vein wall invasion after curative resection for pancreatic adenocarcinoma. Archives of Surgery 2007; 142 (02) 172-179
  • 196 Han SS et al. Clinical Significance of Portal-Superior Mesenteric Vein Resection in Pancreatoduodenectomy for Pancreatic Head Cancer. Pancreas 2012; 41: 102-106
  • 197 Kaneoka Y, Yamaguchi A, Isogai M. Portal or superior mesenteric vein resection for pancreatic head adenocarcinoma: prognostic value of the length of venous resection. Surgery 2009; 145 (04) 417-425
  • 198 Kurosaki I et al. Portal vein resection in surgery for cancer of biliary tract and pancreas: special reference to the relationship between the surgical outcome and site of primary tumor. J Gastrointest Surg 2008; 12 (05) 907-918
  • 199 Illuminati G et al. Results of a pancreatectomy with a limited venous resection for pancreatic cancer. Surg Today 2008; 38 (06) 517-523
  • 200 Toomey P et al. Resection of portovenous structures to obtain microscopically negative margins during pancreaticoduodenectomy for pancreatic adenocarcinoma is worthwhile. Am Surg 2009; 75 (09) 804-809 ; discussion 809–810
  • 201 Carrere N et al. Pancreaticoduodenectomy with mesentericoportal vein resection for adenocarcinoma of the pancreatic head. World J Surg 2006; 30 (08) 1526-1535
  • 202 Riediger H et al. Postoperative morbidity and long-term survival after pancreaticoduodenectomy with superior mesenterico-portal vein resection. J Gastrointest Surg 2006; 10 (08) 1106-1115
  • 203 Bachellier P et al. Is pancreaticoduodenectomy with mesentericoportal venous resection safe and worthwhile?. Am J Surg 2001; 182 (02) 120-129
  • 204 Yamada S et al. Pancreatic cancer with paraaortic lymph node metastasis: a contraindication for radical surgery?. Pancreas 2009; 38 (01) e13-e17
  • 205 Cordera F et al. Significance of common hepatic artery lymph node metastases during pancreaticoduodenectomy for pancreatic head adenocarcinoma. Ann Surg Oncol 2007; 14 (08) 2330-2336
  • 206 Doi R et al. Prognostic implication of para-aortic lymph node metastasis in resectable pancreatic cancer. World J Surg 2007; 31 (01) 147-154
  • 207 Kanda M et al. Pattern of lymph node metastasis spread in pancreatic cancer. Pancreas 2011; 40 (06) 951-955
  • 208 Massucco P et al. Prognostic significance of lymph node metastases in pancreatic head cancer treated with extended lymphadenectomy: not just a matter of numbers. Ann Surg Oncol 2009; 16 (12) 3323-3332
  • 209 Murakami Y et al. Prognostic impact of para-aortic lymph node metastasis in pancreatic ductal adenocarcinoma. World J Surg 2010; 34 (08) 1900-1907
  • 210 Takada T et al. Simultaneous hepatic resection with pancreato-duodenectomy for metastatic pancreatic head carcinoma: does it improve survival?. Hepatogastroenterology 1997; 44 (14) 567-573
  • 211 Schwarz RE. Technical considerations to maintain a low frequency of postoperative biliary stent-associated infections. J Hepatobiliary Pancreat Surg 2002; 9 (01) 93-97
  • 212 Gerke H et al. Complications of pancreaticoduodenectomy after neoadjuvant chemoradiation in patients with and without preoperative biliary drainage. Dig Liver Dis 2004; 36 (06) 412-418
  • 213 Jagannath P et al. Effect of preoperative biliary stenting on immediate outcome after pancreaticoduodenectomy. Br J Surg 2005; 92 (03) 356-361
  • 214 Martignoni ME et al. Effect of preoperative biliary drainage on surgical outcome after pancreatoduodenectomy. Am J Surg 2001; 181 (01) 52-59 ; discussion 87
  • 215 Sohn TA et al. Do preoperative biliary stents increase postpancreaticoduodenectomy complications?. J Gastrointest Surg 2000; 4 (03) 258-267 discussion 267–268
  • 216 van der Gaag NA et al. Preoperative biliary drainage for cancer of the head of the pancreas. N Engl J Med 2010; 362 (02) 129-137
  • 217 Schwarz M et al. Efficacy of oral ofloxacin for single-dose perioperative prophylaxis in general surgery – a controlled randomized clinical study. Langenbecks Arch Surg 2001; 386 (06) 397-401
  • 218 Targarona EM et al. Single-dose antibiotic prophylaxis in patients at high risk for infection in biliary surgery: a prospective and randomized study comparing cefonicid with mezlocillin. Surgery 1990; 107 (03) 327-334
  • 219 Kujath P et al. Current perioperative antibiotic prophylaxis. Chirurg 2006; 77 (06) 490, 492-498
  • 220 Barnett SP et al. Octreotide does not prevent postoperative pancreatic fistula or mortality following Pancreaticoduodenectomy. Am Surg 2004; 70 (03) 222-226 ; discussion 227
  • 221 Friess H, Buchler MW. Efficacy of somatostatin and its analogues in pancreatic surgery and pancreatic disorders. Digestion 1996; 57 (Suppl. 01) 97-102
  • 222 Gouillat C et al. Randomized controlled multicentre trial of somatostatin infusion after pancreaticoduodenectomy. Br J Surg 2001; 88 (11) 1456-1462
  • 223 Hesse UJ et al. Prospectively randomized trial using perioperative low-dose octreotide to prevent organ-related and general complications after pancreatic surgery and pancreatico-jejunostomy. World J Surg 2005; 29 (10) 1325-1328
  • 224 Montorsi M et al. Efficacy of octreotide in the prevention of pancreatic fistula after elective pancreatic resections: a prospective, controlled, randomized clinical trial. Surgery 1995; 117 (01) 26-31
  • 225 Pederzoli P et al. Efficacy of octreotide in the prevention of complications of elective pancreatic surgery. Italian Study Group. Br J Surg 1994; 8 (02) 265-269
  • 226 Yeo CJ et al. Does prophylactic octreotide decrease the rates of pancreatic fistula and other complications after pancreaticoduodenectomy? Results of a prospective randomized placebo-controlled trial. Ann Surg 2000; 232 (03) 419-429
  • 227 Connor S et al. Meta-analysis of the value of somatostatin and its analogues in reducing complications associated with pancreatic surgery. Br J Surg 2005; 92 (09) 1059-1067
  • 228 Warshaw AL. Implications of peritoneal cytology for staging of early pancreatic cancer. Am J Surg 1991; 161 (01) 26-29 ; discussion 29–30
  • 229 Heeckt P et al. Free intraperitoneal tumors cells in pancreatic cancer – significance for clinical course and therapy. Chirurg 1992; 63 (07) 563-567
  • 230 Kinoshita T et al. Effectiveness of intraoperative cytological examination of peritoneal washings for patients with pancreatic cancer. Nihon Geka Gakkai Zasshi 1992; 93 (11) 1410-1415
  • 231 Makary MA et al. Implications of peritoneal cytology for pancreatic cancer management. Arch Surg 1998; 133 (04) 361-365
  • 232 Konishi M et al. Prognostic value of cytologic examination of peritoneal washings in pancreatic cancer. Arch Surg 2002; 137 (04) 475-480
  • 233 Nakao A et al. Peritoneal washings cytology combined with immunocytochemical staining in pancreatic cancer. Hepatogastroenterology 1999; 46 (29) 2974-2977
  • 234 Yachida S et al. Implications of peritoneal washing cytology in patients with potentially resectable pancreatic cancer. Br J Surg 2002; 89 (05) 573-578
  • 235 Bassi C et al. Influence of surgical resection and post-operative complications on survival following adjuvant treatment for pancreatic cancer in the ESPAC-1 randomized controlled trial. Dig Surg 2005; 22 (05) 353-363
  • 236 Capussotti L et al. Extended lymphadenectomy and vein resection for pancreatic head cancer: outcomes and implications for therapy. Arch Surg 2003; 138 (12) 1316-1322
  • 237 Farnell MB et al. A prospective randomized trial comparing standard pancreatoduodenectomy with pancreatoduodenectomy with extended lymphadenectomy in resectable pancreatic head adenocarcinoma. Surgery 2005; 138 (04) 618-628 ; discussion 628–630
  • 238 Fernandez-del Castillo C, Rattner DW, Warshaw AL. Standards for pancreatic resection in the 1990s. Arch Surg 1995; 130 (03) 295-299 ; discussion 299–300
  • 239 Hartel M et al. Benefit of venous resection for ductal adenocarcinoma of the pancreatic head. Eur J Surg 2002; 168 (12) 707-712
  • 240 Ishikawa O et al. Practical grouping of positive lymph nodes in pancreatic head cancer treated by an extended pancreatectomy. Surgery 1997; 121 (03) 244-249
  • 241 Jurowich C et al. Portal vein resection in the framework of surgical therapy of pancreatic head carcinoma: clarification of indication by improved preoperative diagnostic procedures?. Chirurg 2000; 71 (07) 803-807
  • 242 Kawarada Y et al. Modified standard pancreaticoduodenectomy for the treatment of pancreatic head cancer. Digestion 1999; 60 (Suppl. 01) 120-125
  • 243 Klempnauer J et al. Extended resections of ductal pancreatic cancer--impact on operative risk and prognosis. Oncology 1996; 53 (01) 47-53
  • 244 Klinkenbijl JH et al. The advantages of pylorus-preserving pancreatoduodenectomy in malignant disease of the pancreas and periampullary region. Ann Surg 1992; 216 (02) 142-145
  • 245 Kremer B et al. Surgical possibilities for pancreatic cancer: extended resection. Ann Oncol 1999; 10 (Suppl. 04) 252-256
  • 246 Lin PW et al. Pancreaticoduodenectomy for pancreatic head cancer: PPPD versus Whipple procedure. Hepatogastroenterology 2005; 52 (65) 1601-1604
  • 247 Lygidakis NJ et al. Mono-bloc total spleno-pancreaticoduodenectomy for pancreatic head carcinoma with portal-mesenteric venous invasion. A prospective randomized study. Hepatogastroenterolog 2004; 51 (56) 427-433
  • 248 Mu DQ, Peng SY, Wang GF. Extended radical operation of pancreatic head cancer: appraisal of its clinical significance. World J Gastroenterol 2005; 11 (16) 2467-2471
  • 249 Nakao A et al. Extended radical resection versus standard resection for pancreatic cancer: the rationale for extended radical resection. Pancreas 2004; 28 (03) 289-292
  • 250 Pedrazzoli S et al. Standard versus extended lymphadenectomy associated with pancreatoduodenectomy in the surgical treatment of adenocarcinoma of the head of the pancreas: a multicenter, prospective, randomized study. Lymphadenectomy Study Group. Ann Surg 1998; 228 (04) 508-517
  • 251 Roher HD, Heise JW, Goretzki PE. Stomach saving duodenopancreatectomy. Indications and contraindications. The most important surgical steps. Zentralbl Chir 2000; 125 (12) 961-965
  • 252 Schafer M, Mullhaupt B, Clavien PA. Evidence-based pancreatic head resection for pancreatic cancer and chronic pancreatitis. Ann Surg 2002; 236 (02) 137-148
  • 253 Takada T et al. Results of a pylorus-preserving pancreatoduodenectomy for pancreatic cancer: a comparison with results of the Whipple procedure. Hepatogastroenterology 1997; 44 (18) 1536-1540
  • 254 Tran KT et al. Pylorus preserving pancreaticoduodenectomy versus standard Whipple procedure: a prospective, randomized, multicenter analysis of 170 patients with pancreatic and periampullary tumors. Ann Surg 2004; 240 (05) 738-745
  • 255 Tseng JF et al. Pancreaticoduodenectomy with vascular resection: margin status and survival duration. J Gastrointest Surg 2004; 8 (08) 935-949 discussion 949–950
  • 256 Zerbi A et al. Comparison between pylorus-preserving and Whipple pancreatoduodenectomy. Br J Surg 1995; 82 (07) 975-979
  • 257 Diener MK et al. A systematic review and meta-analysis of pylorus-preserving versus classical pancreaticoduodenectomy for surgical treatment of periampullary and pancreatic carcinoma. Ann Surg 2007; 245 (02) 187-200
  • 258 Christein JD et al. Distal pancreatectomy for resectable adenocarcinoma of the body and tail of the pancreas. J Gastrointest Surg 2005; 9 (07) 922-927
  • 259 Gebhardt C, Meyer W, Jurowich C. Is resection of left-sided ductal pancreatic carcinoma of value?. Zentralbl Chir 2000; 125 (12) 966-969
  • 260 Kayahara M et al. Distal pancreatectomy – does it have a role for pancreatic body and tail cancer. Hepatogastroenterology 1998; 45 (21) 827-832
  • 261 Mayumi T et al. Distal pancreatectomy with en bloc resection of the celiac artery for carcinoma of the body and tail of the pancreas. Int J Pancreatol 1997; 22 (01) 15-21
  • 262 Shimada K et al. Prognostic factors after distal pancreatectomy with extended lymphadenectomy for invasive pancreatic adenocarcinoma of the body and tail. Surgery 2006; 139 (03) 288-295
  • 263 Shoup M et al. Is extended resection for adenocarcinoma of the body or tail of the pancreas justified?. J Gastrointest Surg 2003; 7 (08) 946-952 discussion 952
  • 264 Kondo S et al. Results of radical distal pancreatectomy with en bloc resection of the celiac artery for locally advanced cancer of the pancreatic body. Langenbecks Arch Surg 2003; 388 (02) 101-106
  • 265 Garcea G et al. Tumour characteristics predictive of survival following resection for ductal adenocarcinoma of the head of pancreas. Eur J Surg Oncol 2007; 33 (07) 892-897
  • 266 Pai RK et al. Pattern of lymph node involvement and prognosis in pancreatic adenocarcinoma: direct lymph node invasion has similar survival to node-negative disease. Am J Surg Pathol 2011; 35 (02) 228-234
  • 267 Sahin TT et al. Prognostic Implications of Lymph Node Metastases in Carcinoma of the Body and Tail of the Pancreas. Pancreas 2011; 40: 1029-1033
  • 268 Bhatti I et al. Lymph node ratio versus number of affected lymph nodes as predictors of survival for resected pancreatic adenocarcinoma. World J Surg 2010; 34 (04) 768-775
  • 269 Hellan M et al. The impact of lymph node number on survival in patients with lymph node-negative pancreatic cancer. Pancreas 2008; 37 (01) 19-24
  • 270 House MG et al. Prognostic significance of pathologic nodal status in patients with resected pancreatic cancer. J Gastrointest Surg 2007; 11 (11) 1549-1555
  • 271 Konstantinidis IT et al. Does the mechanism of lymph node invasion affect survival in patients with pancreatic ductal adenocarcinoma?. J Gastrointest Surg 2010; 14 (02) 261-267
  • 272 La Torre M et al. Role of the Lymph node ratio in pancreatic ductal adenocarcinoma. Impact on patient stratification and prognosis. Journal of Surgical Oncology 2011; 104: 629-633
  • 273 Murakami Y et al. Number of metastatic lymph nodes, but not lymph node ratio, is an independent prognostic factor after resection of pancreatic carcinoma. J Am Coll Surg 2010; 211 (02) 196-204
  • 274 Pawlik TM et al. Prognostic relevance of lymph node ratio following pancreaticoduodenectomy for pancreatic cancer. Surgery 2007; 141 (05) 610-618
  • 275 Prenzel KL et al. Lymph node size and metastatic infiltration in adenocarcinoma of the pancreatic head. Eur J Surg Oncol 2010; 36 (10) 993-996
  • 276 Riediger H et al. The lymph node ratio is the strongest prognostic factor after resection of pancreatic cancer. J Gastrointest Surg 2009; 13 (07) 1337-1344
  • 277 Showalter TN et al. The Influence of Total Nodes Examined, Number of Positive Nodes, and Lymph Node Ratio on Survival after Surgical Resection and Adjuvant Chemoradiation for Pancreatic Cancer: A Secondary Analysis of RTOG 9704. Int J Radiat Oncol Biol Phys 2011; 81: 1328-1335
  • 278 Slidell MB et al. Impact of total lymph node count and lymph node ratio on staging and survival after pancreatectomy for pancreatic adenocarcinoma: a large, population-based analysis. Ann Surg Oncol 2008; 15 (01) 165-174
  • 279 Yeo CJ et al. Pancreaticoduodenectomy with or without distal gastrectomy and extended retroperitoneal lymphadenectomy for periampullary adenocarcinoma, part 2: randomized controlled trial evaluating survival, morbidity, and mortality. Ann Surg 2002; 236 (03) 355-366 ; discussion 366–368
  • 280 Farnell MB et al. The role of extended lymphadenectomy for adenocarcinoma of the head of the pancreas: strength of the evidence. J Gastrointest Surg 2008; 12 (04) 651-656
  • 281 Michalski CW et al. Systematic review and meta-analysis of standard and extended lymphadenectomy in pancreaticoduodenectomy for pancreatic cancer. Br J Surg 2007; 94 (03) 265-273
  • 282 De Jong MC et al. Liver-directed therapy for hepatic metastases in patients undergoing pancreaticoduodenectomy: a dual-center analysis. Ann Surg 2010; 252 (01) 142-148
  • 283 Gleisner AL et al. Is resection of periampullary or pancreatic adenocarcinoma with synchronous hepatic metastasis justified?. Cancer 2007; 110 (11) 2484-2492
  • 284 Michalski CW et al. Resection of primary pancreatic cancer and liver metastasis: a systematic review. Dig Surg 2008; 25 (06) 473-480
  • 285 Finan KR et al. Laparoscopic and open distal pancreatectomy: a comparison of outcomes. Am Surg 2009; 75 (08) 671-679 ; discussion 679–680
  • 286 Kooby DA et al. A Multicenter Analysis of Distal Pancreatectomy for Adenocarcinoma: Is Laparoscopic Resection Appropriate?. Journal of the American College of Surgeons 2010; 210 (05) 779-785
  • 287 Kooby DA et al. Left-sided pancreatectomy: a multicenter comparison of laparoscopic and open approaches. Ann Surg 2008; 248 (03) 438-446
  • 288 Cho CS et al. Laparoscopic versus open left pancreatectomy: can preoperative factors indicate the safer technique?. Ann Surg 2011; 253 (05) 975-980
  • 289 Schmidt CM et al. Total pancreatectomy (R0 resection) improves survival over subtotal pancreatectomy in isolated neck margin positive pancreatic adenocarcinoma. Surgery 2007; 142 (04) 572-578 ; discussion 578–580
  • 290 Hernandez J et al. Survival after pancreaticoduodenectomy is not improved by extending resections to achieve negative margins. Ann Surg 2009; 250 (01) 76-80
  • 291 Munding J, Uhl W, Tannapfel A. R classification and pancreatic ductal adenocarcinoma – R 0 is R 0. Z Gastroenterol 2011; 49 (10) 1423-1427
  • 292 Wittekind C, Meyer HJ (Hrsg.) TNM Klassifikation maligner Tumore. Weinheim: Wiley-Blackwell; 2010
  • 293 Fujita T et al. Evaluation of the prognostic factors and significance of lymph node status in invasive ductal carcinoma of the body or tail of the pancreas. Pancreas 2010; 39 (01) e48-e54
  • 294 Shimada K et al. Intrapancreatic nerve invasion as a predictor for recurrence after pancreaticoduodenectomy in patients with invasive ductal carcinoma of the pancreas. Pancreas 2011; 40 (03) 464-468
  • 295 Zacharias T et al. Impact of lymph node involvement on long-term survival after R0 pancreaticoduodenectomy for ductal adenocarcinoma of the pancreas. J Gastrointest Surg 2007; 11 (03) 350-356
  • 296 Wasif N et al. Impact of tumor grade on prognosis in pancreatic cancer: Should we include grade in AJCC staging?. Annals of Surgical Oncology 2010; 17 (09) 2312-2320
  • 297 Bosman FT, Carneiro F, Hruban RH, Theise ND. WHO Classification of Tumours. Vol. 3. 2010
  • 298 Kurahara H et al. Impact of lymph node micrometastasis in patients with pancreatic head cancer. World J Surg 2007; 31 (03) 483-490 ; discussion 491–492
  • 299 Menon KV et al. Impact of margin status on survival following pancreatoduodenectomy for cancer: the Leeds Pathology Protocol (LEEPP). HPB (Oxford) 2009; 11 (01) 18-24
  • 300 Fatima J et al. Pancreatoduodenectomy for ductal adenocarcinoma: implications of positive margin on survival. Arch Surg 2010; 145 (02) 167-172
  • 301 Lee SE et al. Clinical implications of immunohistochemically demonstrated lymph node micrometastasis in resectable pancreatic cancer. J Korean Med Sci 2011; 26 (07) 881-885
  • 302 Mitsunaga S et al. Detail histologic analysis of nerve plexus invasion in invasive ductal carcinoma of the pancreas and its prognostic impact. Am J Surg Pathol 2007; 31 (11) 1636-1644
  • 303 Kanda M et al. Invasion of the splenic artery is a crucial prognostic factor in carcinoma of the body and tail of the pancreas. Ann Surg 2010; 251 (03) 483-487
  • 304 Hishinuma S et al. Patterns of recurrence after curative resection of pancreatic cancer, based on autopsy findings. J Gastrointest Surg 2006; 10 (04) 511-518
  • 305 Oettle H et al. Adjuvant chemotherapy with gemcitabine vs observation in patients undergoing curative-intent resection of pancreatic cancer: a randomized controlled trial. JAMA 2007; 297 (03) 267-277
  • 306 Ueno H et al. A randomised phase III trial comparing gemcitabine with surgery-only in patients with resected pancreatic cancer: Japanese Study Group of Adjuvant Therapy for Pancreatic Cancer. Br J Cancer 2009; 101 (06) 908-915
  • 307 Neoptolemos JP et al. A randomized trial of chemoradiotherapy and chemotherapy after resection of pancreatic cancer. N Engl J Med 2004; 350 (12) 1200-1210
  • 308 Stocken DD et al. Meta-analysis of randomised adjuvant therapy trials for pancreatic cancer. Br J Cancer 2005; 92 (08) 1372-1381
  • 309 Neoptolemos JP et al. Adjuvant chemotherapy with fluorouracil plus folinic acid vs gemcitabine following pancreatic cancer resection: a randomized controlled trial. JAMA 2010; 304 (10) 1073-1081
  • 310 Yoshitomi H et al. A randomized phase II trial of adjuvant chemotherapy with uracil/tegafur and gemcitabine versus gemcitabine alone in patients with resected pancreatic cancer. Cancer 2008; 113 (09) 2448-2456
  • 311 Van Cutsem E et al. Phase III trial of bevacizumab in combination with gemcitabine and erlotinib in patients with metastatic pancreatic cancer. Journal of Clinical Oncology 2009; 27 (13) 2231-2237
  • 312 Biagi JJ et al. Association between time to initiation of adjuvant chemotherapy and survival in colorectal cancer: a systematic review and meta-analysis. JAMA 2011; 305 (22) 2335-2342
  • 313 Kalser MH, Ellenberg SS. Pancreatic cancer. Adjuvant combined radiation and chemotherapy following curative resection. Arch Surg 1985; 120 (08) 899-903
  • 314 Smeenk HG et al. Long-term survival and metastatic pattern of pancreatic and periampullary cancer after adjuvant chemoradiation or observation: long-term results of EORTC trial 40891. Ann Surg 2007; 246 (05) 734-740
  • 315 Morak MJ et al. Adjuvant intra-arterial chemotherapy and radiotherapy versus surgery alone in resectable pancreatic and periampullary cancer: a prospective randomized controlled trial. Ann Surg 2008; 248 (06) 1031-1041
  • 316 Neoptolemos JP et al. Adjuvant chemoradiotherapy and chemotherapy in resectable pancreatic cancer: a randomised controlled trial. Lancet 2001; 358 (9293) 1576-1585
  • 317 Carter R et al. Longitudinal quality of life data can provide insights on the impact of adjuvant treatment for pancreatic cancer-Subset analysis of the ESPAC-1 data. Int J Cancer 2009; 124 (12) 2960-2965
  • 318 Klinkenbijl JH et al. Adjuvant radiotherapy and 5-fluorouracil after curative resection of cancer of the pancreas and periampullary region: phase III trial of the EORTC gastrointestinal tract cancer cooperative group. Ann Surg 1999; 230 (06) 776-782 ; discussion 782–784
  • 319 Van Laethem JL et al. Adjuvant gemcitabine alone versus gemcitabine-based chemoradiotherapy after curative resection for pancreatic cancer: a randomized EORTC-40013-22012/FFCD-9203/GERCOR phase II study. J Clin Oncol 2010; 28 (29) 4450-4456
  • 320 Yeo CJ et al. Pancreaticoduodenectomy for pancreatic adenocarcinoma: postoperative adjuvant chemoradiation improves survival. A prospective, single-institution experience. Ann Surg 1997; 225 (05) 621-633 discussion 633–636
  • 321 Regine WF et al. Fluorouracil-based chemoradiation with either gemcitabine or fluorouracil chemotherapy after resection of pancreatic adenocarcinoma: 5-year analysis of the U. S. Intergroup/RTOG 9704 phase III trial. Ann Surg Oncol 2011; 18 (05) 1319-1326
  • 322 Goodman KA et al. Radiation Therapy Oncology Group consensus panel guidelines for the delineation of the clinical target volume in the postoperative treatment of pancreatic head cancer. Int J Radiat Oncol Biol Phys 2012; 83 (03) 901-908
  • 323 Brunner TB et al. Definition of elective lymphatic target volume in ductal carcinoma of the pancreatic head based on histopathologic analysis. Int J Radiat Oncol Biol Phys 2005; 62 (04) 1021-1029
  • 324 Sun W et al. Proposing the lymphatic target volume for elective radiation therapy for pancreatic cancer: a pooled analysis of clinical evidence. Radiat Oncol 2010; 5: 28
  • 325 Bosset JF et al. Conventional external irradiation alone as adjuvant treatment in resectable pancreatic cancer: results of a prospective study. Radiother Oncol 1992; 24 (03) 191-194
  • 326 Herman JM et al. Analysis of fluorouracil-based adjuvant chemotherapy and radiation after pancreaticoduodenectomy for ductal adenocarcinoma of the pancreas: results of a large, prospectively collected database at the Johns Hopkins Hospital. J Clin Oncol 2008; 26 (21) 3503-3510
  • 327 Butturini G et al. Influence of resection margins and treatment on survival in patients with pancreatic cancer: meta-analysis of randomized controlled trials. Arch Surg 2008; 143 (01) 75-83 ; discussion 83
  • 328 Assifi MM et al. Neoadjuvant therapy in pancreatic adenocarcinoma: a meta-analysis of phase II trials. Surgery 2011; 150 (03) 466-473
  • 329 Andriulli A et al. Neoadjuvant/preoperative gemcitabine for patients with localized pancreatic cancer: a meta-analysis of prospective studies. Ann Surg Oncol 2011; 19 (05) 1644-1662
  • 330 Gillen S et al. Preoperative/neoadjuvant therapy in pancreatic cancer: A systematic review and meta-analysis of response and resection percentages. PLoS Medicine 2010; 7 (04) e1000267
  • 331 Barbier L et al. Pancreatic head resectable adenocarcinoma: preoperative chemoradiation improves local control but does not affect survival. HPB (Oxford) 2011; 13 (01) 64-69
  • 332 Takahashi S et al. Borderline resectable pancreatic cancer: rationale for multidisciplinary treatment. J Hepatobiliary Pancreat Sci 2011; 18 (04) 567-574
  • 333 Haeno H et al. Computational modeling of pancreatic cancer reveals kinetics of metastasis suggesting optimum treatment strategies. Cell 2012; 148 (01) 362-375
  • 334 Chun YS et al. Significance of pathologic response to preoperative therapy in pancreatic cancer. Ann Surg Oncol 2011; 18 (13) 3601-3607
  • 335 Zhao Q et al. Pathologic complete response to neoadjuvant therapy in patients with pancreatic ductal adenocarcinoma is associated with a better prognosis. Ann Diagn Pathol 2012; 16 (01) 29-37
  • 336 Estrella JS et al. Post-therapy pathologic stage and survival in patients with pancreatic ductal adenocarcinoma treated with neoadjuvant chemoradiation. Cancer 2012; 118 (01) 268-277
  • 337 Palmer DH et al. A randomized phase 2 trial of neoadjuvant chemotherapy in resectable pancreatic cancer: gemcitabine alone versus gemcitabine combined with cisplatin. Ann Surg Oncol 2007; 14 (07) 2088-2096
  • 338 Heinrich S et al. Neoadjuvant chemotherapy generates a significant tumor response in resectable pancreatic cancer without increasing morbidity: results of a prospective phase II trial. Ann Surg 2008; 248 (06) 1014-1022
  • 339 Loehrer Sr PJ et al. Gemcitabine alone versus gemcitabine plus radiotherapy in patients with locally advanced pancreatic cancer: an Eastern Cooperative Oncology Group trial. J Clin Oncol 2011; 29 (31) 4105-4012
  • 340 Huguet F et al. Chemoradiotherapy in the management of locally advanced pancreatic carcinoma: a qualitative systematic review. J Clin Oncol 2009; 27 (13) 2269-2277
  • 341 Earle CC et al. The treatment of locally advanced pancreatic cancer: a practice guideline. Can J Gastroenterol 2003; 17 (03) 161-167
  • 342 Sultana A et al. Systematic review, including meta-analyses, on the management of locally advanced pancreatic cancer using radiation/combined modality therapy. Br J Cancer 2007; 96 (08) 1183-1190
  • 343 Chauffert B et al. Phase III trial comparing intensive induction chemoradiotherapy (60 Gy, infusional 5-FU and intermittent cisplatin) followed by maintenance gemcitabine with gemcitabine alone for locally advanced unresectable pancreatic cancer. Definitive results of the 2000–01 FFCD/SFRO study. Ann Oncol 2008; 19 (09) 1592-1599
  • 344 Huguet F et al. Impact of chemoradiotherapy after disease control with chemotherapy in locally advanced pancreatic adenocarcinoma in GERCOR Phase II and III studies. J Clin Oncol 2007; 20: 326-331
  • 345 Krishnan S et al. Induction chemotherapy selects patients with locally advanced, unresectable pancreatic cancer for optimal benefit from consolidative chemoradiation therapy. Cancer 2007; 110 (01) 47-55
  • 346 Huguet F et al. Radiotherapy technical considerations in the management of locally advanced pancreatic cancer: American-French consensus recommendations. Int J Radiat Oncol Biol Phys 2012; 83 (05) 1355-1364
  • 347 Katz MH et al. Standardization of surgical and pathologic variables is needed in multicenter trials of adjuvant therapy for pancreatic cancer: results from the ACOSOG Z5031 trial. Ann Surg Oncol 2011; 18 (02) 337-344
  • 348 Tempero MA et al. Pancreatic Adenocarcinoma, version 2. 2012: featured updates to the NCCN Guidelines. J Natl Compr Canc Netw 2012; 10 (06) 703-713
  • 349 Yovino S et al. Analysis of local control in patients receiving IMRT for resected pancreatic cancers. Int J Radiat Oncol Biol Phys 2012; 83 (03) 916-920
  • 350 Murphy JD et al. Full-dose gemcitabine and concurrent radiotherapy for unresectable pancreatic cancer. Int J Radiat Oncol Biol Phys 2007; 68 (03) 801-808
  • 351 Ben-Josef E et al. Intensity-modulated radiotherapy (IMRT) and concurrent capecitabine for pancreatic cancer. Int J Radiat Oncol Biol Phys 2004; 59 (02) 454-459
  • 352 Wilkowski R et al. Chemoradiotherapy with concurrent gemcitabine and cisplatin with or without sequential chemotherapy with gemcitabine/cisplatin vs chemoradiotherapy with concurrent 5-fluorouracil in patients with locally advanced pancreatic cancer– a multi-centre randomised phase II study. Br J Cancer 2009; 101 (11) 1853-1859
  • 353 Regine WF et al. Fluorouracil vs gemcitabine chemotherapy before and after fluorouracil-based chemoradiation following resection of pancreatic adenocarcinoma: a randomized controlled trial. JAMA 2008; 299 (09) 1019-1026
  • 354 Epelbaum R et al. Phase II study of gemcitabine combined with radiation therapy in patients with localized, unresectable pancreatic cancer. J Surg Oncol 2002; 81 (03) 138-143
  • 355 Zhu CP et al. Gemcitabine in the chemoradiotherapy for locally advanced pancreatic cancer: a meta-analysis. Radiother Oncol 2011; 99 (02) 108-113
  • 356 Goldstein D et al. Gemcitabine with a specific conformal 3D 5FU radiochemotherapy technique is safe and effective in the definitive management of locally advanced pancreatic cancer. Br J Cancer 2007; 97 (04) 464-471
  • 357 Hammel P et al. Randomized multicenter phase III study in patients with locally advanced adenocarcinoma of the pancreas: Gemcitabine with or without chemoradiotherapy and with or without erlotinib – LAP 07 study. ASCO Meeting Abstracts 2011; 29 (Suppl. 15) e14619
  • 358 Wilkowski R et al. Combined chemoradiotherapy for isolated local recurrence after primary resection of pancreatic cancer. JOP 2006; 7 (01) 34-40
  • 359 Rwigema JC et al. Stereotactic body radiotherapy in the treatment of advanced adenocarcinoma of the pancreas. Am J Clin Oncol 2011; 34 (01) 63-69
  • 360 Didolkar MS et al. Image-guided stereotactic radiosurgery for locally advanced pancreatic adenocarcinoma results of first 85 patients. J Gastrointest Surg 2010; 14 (10) 1547-1559
  • 361 Kasperk R et al. Intraoperative radiotherapy for pancreatic carcinoma. Br J Surg 1995; 82 (09) 1259-1261
  • 362 Reni M et al. Effect on local control and survival of electron beam intraoperative irradiation for resectable pancreatic adenocarcinoma. Int J Radiat Oncol Biol Phys 2001; 50 (03) 651-658
  • 363 Yamaguchi K et al. ERT following IORT improves survival of patients with resectable pancreatic cancer. Hepatogastroenterology 2005; 52 (64) 1244-1249
  • 364 Messick C et al. Early experience with intraoperative radiotherapy in patients with resected pancreatic adenocarcinoma. Am J Surg 2008; 195 (03) 308-311 ; discussion 312
  • 365 Showalter TN et al. Does intraoperative radiation therapy improve local tumor control in patients undergoing pancreaticoduodenectomy for pancreatic adenocarcinoma? A propensity score analysis. Ann Surg Oncol 2009; 16 (08) 2116-2122
  • 366 Ruano-Ravina A, Almazan Ortega R, Guedea F. Intraoperative radiotherapy in pancreatic cancer: a systematic review. Radiother Oncol 2008; 87 (03) 318-325
  • 367 Zygogianni GA et al. Intraoperative radiation therapy on pancreatic cancer patients: a review of the literature. Minerva Chir 2011; 66 (04) 361-369
  • 368 Nagai S et al. Prognostic implications of intraoperative radiotherapy for unresectable pancreatic cancer. Pancreatology 2011; 11 (01) 68-75
  • 369 Karasawa K et al. Efficacy of novel hypoxic cell sensitiser doranidazole in the treatment of locally advanced pancreatic cancer: long-term results of a placebo-controlled randomised study. Radiother Oncol 2008; 87 (03) 326-330
  • 370 Mallinson CN et al. Chemotherapy in pancreatic cancer: results of a controlled, prospective, randomised, multicentre trial. Br Med J 1980; 281 (6255) 1589-1591
  • 371 Palmer KR et al. Chemotherapy prolongs survival in inoperable pancreatic carcinoma. Br J Surg 1994; 81 (06) 882-885
  • 372 Glimelius B et al. Chemotherapy improves survival and quality of life in advanced pancreatic and biliary cancer. Ann Oncol 1996; 7 (06) 593-600
  • 373 Yip D et al. Chemotherapy and radiotherapy for inoperable advanced pancreatic cancer. Cochrane Database Syst Rev 2006; 3 CD002093
  • 374 Burris 3rd HA et al. Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trial. J Clin Oncol 1997; 15 (06) 2403-2413
  • 375 Sultana A et al. Meta-analyses of chemotherapy for locally advanced and metastatic pancreatic cancer. Journal of Clinical Oncology 2007; 25 (18) 2607-2615
  • 376 Conroy T et al. FOLFIRINOX versus gemcitabine for metastatic pancreatic cancer. N Engl J Med 2011; 364 (19) 1817-1825
  • 377 Louvet C et al. Gemcitabine in combination with oxaliplatin compared with gemcitabine alone in locally advanced or metastatic pancreatic cancer: results of a GERCOR and GISCAD phase III trial. J Clin Oncol 2005; 23 (15) 3509-3516
  • 378 Heinemann V et al. Randomized phase III trial of gemcitabine plus cisplatin compared with gemcitabine alone in advanced pancreatic cancer. J Clin Oncol 2006; 24 (24) 3946-3952
  • 379 Berlin JD et al. Phase III study of gemcitabine in combination with fluorouracil versus gemcitabine alone in patients with advanced pancreatic carcinoma: Eastern Cooperative Oncology Group Trial E2297. J Clin Oncol 2002; 20 (15) 3270-3275
  • 380 Van Cutsem E et al. Phase III trial of gemcitabine plus tipifarnib compared with gemcitabine plus placebo in advanced pancreatic cancer. J Clin Oncol 2004; 22 (08) 1430-1438
  • 381 Storniolo AM et al. An investigational new drug treatment program for patients with gemcitabine: results for over 3000 patients with pancreatic carcinoma. Cancer 1999; 85 (06) 1261-1268
  • 382 Herrmann R et al. Gemcitabine (G) plus capecitabine (C) versus G alone in locally advanced or metastatic pancreatic cancer: a randomized phase III study of the Swiss Group for Clinical Cancer Research (SAKK) and the Central European Cooperative Oncology Group (CECOG). J Clin Oncol 2005; 23 (Suppl. 16) A4010
  • 383 Colucci G et al. Randomized phase III trial of gemcitabine plus cisplatin compared with single-agent gemcitabine as first-line treatment of patients with advanced pancreatic cancer: the GIP-1 study. J Clin Oncol 2010; 28 (10) 1645-1651
  • 384 Cunningham D et al. Phase III randomized comparison of gemcitabine versus gemcitabine plus capecitabine in patients with advanced pancreatic cancer. Journal of clinical oncology: official journal of the American Society of Clinical Oncology 2009; 27: 5513-5518
  • 385 Moore MJ et al. Erlotinib plus gemcitabine compared with gemcitabine alone in patients with advanced pancreatic cancer: A phase III trial of the National Cancer Institute of Canada Clinical Trials Group. Journal of Clinical Oncology 2007; 25 (15) 1960-1966
  • 386 Philip PA et al. Phase III study comparing gemcitabine plus cetuximab versus gemcitabine in patients with advanced pancreatic adenocarcinoma: Southwest oncology group-directed intergroup trial S0205. Journal of Clinical Oncology 2010; 28 (22) 3605-3610
  • 387 Poplin E et al. Phase III, randomized study of gemcitabine and oxaliplatin versus gemcitabine (fixed-dose rate infusion) compared with gemcitabine (30-minute infusion) in patients with pancreatic carcinoma E6201: a trial of the Eastern Cooperative Oncology Group. Journal of clinical oncology: official journal of the American Society of Clinical Oncology 2009; 3778-3785
  • 388 Herrmann R et al. Gemcitabine plus capecitabine compared with gemcitabine alone in advanced pancreatic cancer: a randomized, multicenter, phase III trial of the Swiss Group for Clinical Cancer Research and the Central European Cooperative Oncology Group. Journal of clinical oncology: official journal of the American Society of Clinical Oncology 2007; 25: 2212-2217
  • 389 Kindler HL et al. Axitinib plus gemcitabine versus placebo plus gemcitabine in patients with advanced pancreatic adenocarcinoma: A double-blind randomised phase 3 study. The Lancet Oncology 2011; 12 (03) 256-262
  • 390 Kindler HL et al. Gemcitabine plus bevacizumab compared with gemcitabine plus placebo in patients with advanced pancreatic cancer: phase III trial of the Cancer and Leukemia Group B (CALGB 80303). J Clin Oncol 2010; 28 (22) 3617-3622
  • 391 Heinemann V et al. Meta-analysis of randomized trials: evaluation of benefit from gemcitabine-based combination chemotherapy applied in advanced pancreatic cancer. BMC Cancer 2008; 8: 82
  • 392 Hu J et al. A meta-analysis of gemcitabine containing chemotherapy for locally advanced and metastatic pancreatic adenocarcinoma. Journal of Hematology and Oncology 2011; 4: 11
  • 393 von Hoff D. Randomized phase 3 study of weekly nab-paclitaxel plus gemcitabine versus gemcitabine alone in patients with metastatic adenocarcinoma of the pancreas (MPACT). Phase 3 metastatic pancreatic cancer. in ASCO GI, Abstract LBA148. San Francisco, CA: 2012
  • 394 Von Hoff DD et al. Increased Survival in Pancreatic Cancer with nab-Paclitaxel plus Gemcitabine. N Engl J Med 2013; 369: 1691-1703
  • 395 Pelzer U et al. Best supportive care (BSC) versus oxaliplatin, folinic acid and 5-fluorouracil (OFF) plus BSC in patients for second-line advanced pancreatic cancer: a phase III-study from the German CONKO-study group. Eur J Cancer 2011; 47 (11) 1676-1681
  • 396 Mercadante S. Pain treatment and outcomes for patients with advanced cancer who receive follow-up care at home. Cancer 1999; 85 (08) 1849-1858
  • 397 Zech DF et al. Validation of World Health Organization Guidelines for cancer pain relief: a 10-year prospective study. Pain 1995; 63 (01) 65-76
  • 398 Marinangeli F et al. Use of strong opioids in advanced cancer pain: a randomized trial. J Pain Symptom Manage 2004; 27 (05) 409-416
  • 399 Grahm AL, Andren-Sandberg A. Prospective evaluation of pain in exocrine pancreatic cancer. Digestion 1997; 58 (06) 542-549
  • 400 Caraceni A, Portenoy RK. Pain management in patients with pancreatic carcinoma. Cancer 1996; 78 (Suppl. 03) 639-653
  • 401 Ross GJ et al. Sonographically guided paracentesis for palliation of symptomatic malignant ascites. Am J Roentgenol Am J Roentgenol 1989; 153 (06) 1309-1311
  • 402 McNicol E et al. Nonsteroidal anti-inflammatory drugs, alone or combined with opioids, for cancer pain: a systematic review. J Clin Oncol 2004; 22 (10) 1975-1992
  • 403 Carr DB et al. Evidence report on the treatment of pain in cancer patients. J Natl Cancer Inst Monogr 2004; 32: 23-31
  • 404 Payne R et al. Quality of life and cancer pain: satisfaction and side effects with transdermal fentanyl versus oral morphine. J Clin Oncol 1998; 16 (04) 1588-1593
  • 405 De Conno F et al. Role of rectal route in treating cancer pain: a randomized crossover clinical trial of oral versus rectal morphine administration in opioid-naive cancer patients with pain. J Clin Oncol 1995; 13 (04) 1004-1008
  • 406 Cherny NI. The management of cancer pain. CA Cancer J Clin 2000; 50 (02) 70-116 ; quiz 117–120
  • 407 Gilmer-Hill HS et al. Intrathecal morphine delivered via subcutaneous pump for intractable pain in pancreatic cancer. Surg Neurol 1999; 51 (01) 6-11
  • 408 Staats PS et al. The effects of alcohol celiac plexus block, pain, and mood on longevity in patients with unresectable pancreatic cancer: a double-blind, randomized, placebo-controlled study. Pain Med 2001; 2 (01) 28-34
  • 409 Eisenberg E, Carr DB, Chalmers TC. Neurolytic celiac plexus block for treatment of cancer pain: a meta-analysis. Anesth Analg 1995; 80 (02) 290-295
  • 410 Wong GY et al. Effect of neurolytic celiac plexus block on pain relief, quality of life, and survival in patients with unresectable pancreatic cancer: a randomized controlled trial. Jama 2004; 291 (09) 1092-1099
  • 411 Stefaniak T et al. A comparison of two invasive techniques in the management of intractable pain due to inoperable pancreatic cancer: neurolytic celiac plexus block and videothoracoscopic splanchnicectomy. Eur J Surg Oncol 2005; 31 (07) 768-773
  • 412 Arends J et al. ESPEN Guidelines on Enteral Nutrition: Non-surgical oncology. Clin Nutr 2006; 25 (02) 245-259
  • 413 Arends J et al. DGEM Leitlinie Enterale Ernährung: Onkologie. Akt Ernähr Med 2003; 28: 61-68
  • 414 Bjelakovic G et al. Mortality in randomized trials of antioxidant supplements for primary and secondary prevention: systematic review and meta-analysis. Jama 2007; 297 (08) 842-857
  • 415 Wigmore SJ et al. Ibuprofen reduces energy expenditure and acute-phase protein production compared with placebo in pancreatic cancer patients. Br J Cancer 1995; 72 (01) 185-188
  • 416 Gordon JN et al. Thalidomide in the treatment of cancer cachexia: a randomised placebo controlled trial. Gut 2005; 54 (04) 540-545
  • 417 Jatoi A et al. Dronabinol versus megestrol acetate versus combination therapy for cancer-associated anorexia: a North Central Cancer Treatment Group study. J Clin Oncol 2002; 20 (02) 567-573
  • 418 Loprinzi CL et al. Randomized comparison of megestrol acetate versus dexamethasone versus fluoxymesterone for the treatment of cancer anorexia/cachexia. J Clin Oncol 1999; 17 (10) 3299-3306
  • 419 Moss AC, Morris E, Mac MathunaP. Palliative biliary stents for obstructing pancreatic carcinoma. Cochrane Database Syst Rev 2006; (01) CD004200
  • 420 Hausegger KA et al. Treatment of malignant biliary obstruction with polyurethane-covered Wallstents. Am J Roentgenol Am J Roentgenol 1998; 170 (02) 403-408
  • 421 Isayama H et al. A prospective randomised study of „covered“ versus „uncovered“ diamond stents for the management of distal malignant biliary obstruction. Gut 2004; 53 (05) 729-734
  • 422 Speer AG et al. Randomised trial of endoscopic versus percutaneous stent insertion in malignant obstructive jaundice. Lancet 1987; 2 (8550) 57-62
  • 423 Urbach DR et al. Cohort study of surgical bypass to the gallbladder or bile duct for the palliation of jaundice due to pancreatic cancer. Ann Surg 2003; 237 (01) 86-93
  • 424 DiFronzo LA, Egrari S, O'Connell TX. Choledochoduodenostomy for palliation in unresectable pancreatic cancer. Arch Surg 1998; 133 (08) 820-825
  • 425 Aranha GV, Prinz RA, Greenlee HB. Biliary enteric bypass for benign and malignant disease. Am Surg 1987; 53 (07) 403-406
  • 426 Song HY et al. A dual expandable nitinol stent: experience in 102 patients with malignant gastroduodenal strictures. J Vasc Interv Radiol 2004; 15 (12) 1443-1449
  • 427 Kaw M et al. Role of self-expandable metal stents in the palliation of malignant duodenal obstruction. Surg Endosc 2003; 17 (04) 646-650
  • 428 Lillemoe KD et al. Is prophylactic gastrojejunostomy indicated for unresectable periampullary cancer? A prospective randomized trial. Ann Surg 1999; 230 (03) 322-328 ; discussion 328–330
  • 429 Smith TJ et al. 2006 update of recommendations for the use of white blood cell growth factors: an evidence-based clinical practice guideline. J Clin Oncol 2006; 24 (19) 3187-3205
  • 430 Rizzo JD et al. Use of epoetin in patients with cancer: evidence-based clinical practice guidelines of the American Society of Clinical Oncology and the American Society of Hematology. J Clin Oncol 2002; 20 (19) 4083-4107
  • 431 Bokemeyer C et al. EORTC guidelines for the use of erythropoietic proteins in anaemic patients with cancer: 2006 update. Eur J Cancer 2007; 43 (02) 258-270
  • 432 Schuchter LM et al. 2002 update of recommendations for the use of chemotherapy and radiotherapy protectants: clinical practice guidelines of the American Society of Clinical Oncology. J Clin Oncol 2002; 20 (12) 2895-2903
  • 433 Altenhofen L et al. (ÄZQ), Ä.Z. f. Q. i.d.M. Kompendium Q-M-A. Qualitätsmanagement in der ambulanten Versorgung. 3. ed. Dt. Ärzte-Verl; 2008
  • 434 Altenhofen L et al. (ÄZQ), Ä.Z. f. Q. i.d.M. Manual Qualitätsindikatoren. Manual für Autoren. 2009. [cited äzq Schriftenreihe: 36; Available from: http://www.aezq.de/mdb/edocs/pdf/schriftenreihe/schriftenreihe36.pdf