Zusammenfassung
Die Behandlungsmöglichkeiten bei gastro-ösophagealen
Karzinomen reichen von der limitierten Resektion bis hin zu multimodaler
Therapie in den lokalisierten Stadien und enden bei Chemotherapie
und Symptom-orientierter Behandlung im Falle fortgeschrittener Erkrankung.
Eine akkurate klinische Festlegung des Tumorstadiums sowie darüber
hinausgehende prognostische und prädiktive Informationen
bilden idealerweise die Grundlage für die Wahl des geeigneten
Therapieverfahrens. Die Positronen-Emissions-Tomographie in Kombination
mit der Computertomographie, heutzutage vorzugsweise in Form des
Hybridbildgebungsverfahrens PET/CT, kann die Genauigkeit
des klinischen Stagings verbessern und zusätzliche prognostische Informationen
liefern. Darüber hinaus weisen die Erfahrungen spezialisierter
Zentren darauf hin, dass PET auch die Responseevaluation im Rahmen
präoperativer Chemotherapie oder Radiochemotherapie signifikant
verbessern könnte. Dieser Artikel stellt den aktuellen
Stellenwert der PET für das Staging und die multimodale Therapie
gastro-ösophagealer Karzinome dar. Zum jetzigen Zeitpunkt
bleibt allerdings unklar, ob die Prognose von Patienten tatsächlich
verbessert werden kann, wenn man die PET in die Diagnostik und Behandlung
gastro-ösophagealer Karzinome integriert. Prospektive Multicenterstudien
werden benötigt, um die Genauigkeit metabolischer Schwellenwerte
zu bestätigen und den Stellenwert PET-gesteuerter Behandlungsalgorithmen
zu erhärten.
Abstract
Treatment options for gastro-esophageal cancers reach from limited
resection to multimodality treatment in localized stages and end
with chemotherapy and symptom-oriented care in advanced disease.
Accurate clinical assessment as well as prognostic and predictive
information is needed for selecting the appropriate treatment approach.
Positron emission tomography (PET) in combination with computed
tomography (CT) in a hybrid imaging modality PET/CT may
refine the staging accuracy and add prognostic information. Moreover,
experiences from diverse centers indicate that PET also might improve
significantly the assessment of response to preoperative chemotherapy and
chemoradiotherapy. This article outlines the current value of PET
in the staging and multidisciplinary care of gastro-esophageal cancer.
However, at this stage it remains unclear if the prognosis of patients
can be improved by implementing PET in the management of these tumors.
Prospective multicenter studies have to be performed to validate
metabolic cut-off values and to proof the benefit of PET-guided
treatment decisions.
Schlüsselwörter
Positronen-Emissions-Tomographie - Staging - Therapieansprechen - Ösophaguskarzinom
- Magenkarzinom
Keywords
positron emission tomography - staging - treatment response - esophageal cancer -
gastric cancer
Literatur
1
Beyer T, Townsend D W, Brun T. et al .
A combined PET/CT scanner for
clinical oncology.
J Nucl Med.
2000;
41
1369-1379
2
Boellaard R, Krak N C, Hoekstra O S. et al .
Effects of noise, image
resolution, and ROI definition on the accuracy of standard uptake
values: a simulation study.
J Nucl Med.
2004;
45
1519-1527
3
Boellaard R, O’Doherty M J, Weber W A. et al .
FDG PET and PET/CT:
EANM procedure guidelines for tumour PET imaging: version 1.0.
Eur J Nucl Med Mol Imaging.
2010;
37
181-200
4
Boellaard R, Oyen W J, Hoekstra C J. et al .
The Netherlands protocol
for standardisation and quantification of FDG whole body PET studies
in multi-centre trials.
Eur J Nucl Med Mol Imaging.
2008;
35
2320-2333
5
Brücher B L, Weber W, Bauer M. et al .
Neoadjuvant therapy of esophageal squamous
cell carcinoma: response evaluation by positron emission tomography.
Ann Surg.
2001;
233
300-309
6
Downey R J, Akhurst T, Ilson D. et al .
Whole body 18FDG-PET and the response of
esophageal cancer to induction therapy: results of a prospective
trial.
J Clin Oncol.
2003;
21
428-432
7
Flamen P, Lerut A, Van Cutsem E. et al .
Utility of positron emission tomography
for the staging of patients with potentially operable esophageal carcinoma.
J Clin Oncol.
2000;
18
3202
8
Flamen P, Van Cutsem E, Lerut A. et al .
Positron emission tomography for assessment
of the response to induction radiochemotherapy in locally advanced
oesophageal cancer.
Ann Oncol.
2002;
13
361-368
9
Gillham C M, Lucey J A, Keogan M. et al .
(18)FDG uptake during induction chemoradiation
for oesophageal cancer fails to predict histomorphological tumour
response.
Br J Cancer.
2006;
95
1174-1179
10
Herrmann K, Ott K, Buck A K. et al .
Imaging gastric cancer with PET and the radiotracers
18F-FLT and 18F-FDG: a comparative analysis.
J Nucl Med.
2007;
48
1945-1950
11
Javeri H, Xiao L, Rohren E. et
al .
Influence of the baseline 18F-fluoro-2-deoxy-D-glucose
positron emission tomography results on survival and pathologic
response in patients with gastroesophageal cancer undergoing chemoradiation.
Cancer.
2009;
115
624-630
12
Javeri H, Xiao L, Rohren E. et
al .
The higher the decrease in the standardized uptake
value of positron emission tomography after chemoradiation, the
better the survival of patients with gastroesophageal adenocarcinoma.
Cancer.
2009;
115
5184-5192
13
Kamangar F, Dores G M, Anderson W F.
Patterns of cancer incidence, mortality,
and prevalence across five continents: defining priorities to reduce cancer
disparities in different geographic regions of the world.
J
Clin Oncol.
2006;
24
2137-2150
14
Kim M K, Ryu J S, Kim S B. et al .
Value of complete metabolic response by (18)F-fluorodeoxyglucose-positron
emission tomography in oesophageal cancer for prediction of pathologic
response and survival after preoperative chemoradiotherapy.
Eur
J Cancer.
2007;
43
1385-1391
15
Klaeser B, Nitzsche E, Schuller J C. et al .
Limited predictive value of FDG-PET for
response assessment in the preoperative treatment of esophageal cancer:
results of a prospective multi-center trial (SAKK 75/02).
Onkologie.
2009;
32
724-730
16
Levine E A, Farmer M R, Clark P. et al .
Predictive value of 18-fluoro-deoxy-glucose-positron
emission tomography (18F-FDG-PET) in the identification of responders
to chemoradiation therapy for the treatment of locally advanced
esophageal cancer.
Ann Surg.
2006;
243
472-478
17
Lordick F, Ott K, Krause B J. et al .
PET to assess early metabolic response
and to guide treatment of adenocarcinoma of the oesophagogastric
junction: the MUNICON phase II trial.
Lancet Oncol.
2007;
8
797-805
18
Lordick F, Ruers T, Aust D E, et E uropean Organisation of Research and
Treatment of Cancer(EORTC) Gastrointestinal Group.
Workshop
on the role of metabolic imaging in the neoadjuvant treatment of
gastrointestinal cancer.
Eur J Cancer.
2008;
44
1807-1819
19
Ott K, Weber W A, Lordick F. et al .
Metabolic imaging predicts response, survival,
and recurrence in adenocarcinomas of the esophagogastric junction.
J Clin Oncol.
2006;
24
4692-4698
20
Peng H Q, Halsey K, Sun C C. et al .
Clinical utility of postchemoradiation
endoscopic brush cytology and biopsy in predicting residual esophageal adenocarcinoma.
Cancer Cytopathol.
2009;
117
463-472
21
Räsänen J V, Sihvo E I, Knuuti M J. et al .
Prospective
analysis of accuracy of positron emission tomography, computed tomography,
and endoscopic ultrasonography in staging of adenocarcinoma of the
esophagus and the esophagogastric junction.
Ann Surg Oncol.
2003;
10
954-960
22
Ribi K, Koeberle D, Schuller J C. et al .
Is a change in patient-reported dysphagia
after induction chemotherapy in locally advanced esophageal cancer a
predictive factor for pathological response to neoadjuvant chemoradiation?.
Support Care Cancer.
2009 Feb 7. [Epub
ahead of print];
23
Rizk N, Downey R J, Akhurst T. et al .
Preoperative 18[F]-fluorodeoxyglucose positron
emission tomography standardized uptake values predict survival
after esophageal adenocarcinoma resection.
Ann Thorac
Surg.
2006;
81
1076-1081
24 Robert-Koch-Institut (Hrsg.)
und Gesellschaft der Epidemiologischen Krebsregister in Deutschland
e. V. (Hrsg.) .Krebs in Deutschland – Häufigkeiten und
Trends. 7. Auflage. Berlin; 2010
25
Sarkaria I S, Rizk N P, Bains M S. et al .
Post-treatment endoscopic
biopsy is a poor-predictor of pathologic response in patients undergoing
chemoradiation therapy for esophageal cancer.
Ann Surg.
2009;
249
764-767
26
Schomburg A, Bender H, Reichel C. et al .
Standardized uptake values of fluorine-18
fluorodeoxyglucose: the value of different normalization procedures.
Eur J Nucl Med.
1996;
23
571-574
27
Shields A F, Grierson J R, Dohmen B M. et al .
Imaging proliferation in
vivo with [F-18]FLT and positron emission tomography.
Nat Med.
1998;
4
1334-1336
28 Sobin L H, Gospodarowicz M K, Wittekind C. UICC: TNM classification of malignant
tumors.
7th edition. Oxford: Wiley-Blackwell; 2009
29
Stahl A, Ott K, Weber W A. et al .
FDG PET imaging of locally advanced gastric
carcinomas: correlation with endoscopic and histopathological findings.
Eur J Nucl Med Mol Imaging.
2003;
30
288-295
30
Swisher S G, Erasmus J, Maish M. et al .
2-Fluoro-2-deoxy-D-glucose positron emission
tomography imaging is predictive of pathologic response and survival
after preoperative chemoradiation in patients with esophageal carcinoma.
Cancer.
2004;
101
1776-1785
31
Vallböhmer D, Hölscher A H, Dietlein M. et al .
[18F]-Fluorodeoxyglucose-positron
emission tomography for the assessment of histopathologic response
and prognosis after completion of neoadjuvant chemoradiation in esophageal
cancer.
Ann Surg.
2009;
250
888-894
32
van Vliet E P, Heijenbrok-Kal M H, Hunink M G. et al .
Staging investigations for
oesophageal cancer: a meta-analysis.
Br J Cancer.
2008;
98
547-557
33
van Westreenen H L, Cobben D C, Jager P L. et al .
Comparison of
18F-FLT PET and 18F-FDG PET in esophageal cancer.
J Nucl
Med.
2005;
46
400-404
34
van Westreenen H L, Westerterp M, Bossuyt P M. et al .
Systematic review
of the staging performance of 18F-fluorodeoxyglucose positron emission tomography
in esophageal cancer.
J Clin Oncol.
2004;
22
3805-3812
35
Vrieze O, Haustermans K, De Wever W. et al .
Is there a role for FGD-PET in radiotherapy
planning in esophageal carcinoma?.
Radiother Oncol.
2004;
73
269-275
36
Wahl R L, Jacene H, Kasamon Y, Lodge M A.
From RECIST
to PERCIST: Evolving Considerations for PET response criteria in
solid tumors.
J Nucl Med.
2009;
50 Suppl 1
122S-150S
37
Warburg O H, Posener K, Negelein E.
Stoffwechsel der Carcinomzelle.
Biochemische Zeitschrift.
1924;
152
319-344
38
Weber W A, Ott K, Becker K. et
al .
Prediction of response to preoperative chemotherapy
in adenocarcinomas of the esophagogastric junction by metabolic
imaging.
J Clin Oncol.
2001;
19
3058-3065
39
Wieder H A, Beer A J, Lordick F. et al .
Comparison of changes in tumor metabolic
activity and tumor size during chemotherapy of adenocarcinomas of
the esophagogastric junction.
J Nucl Med.
2005;
46
2029-2034
Priv.-Doz. Dr. med. Florian Lordick
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