Zusammenfassung
Ziel: Zur Evaluation der Wertigkeit der externen Radiotherapie (RT) bei der Behandlung
der pigmentierten villonodulären Synovitis (PVNS) wurde von der Arbeitsgruppe „Strahlentherapie
nicht-maligner Erkrankungen“ der Deutschen Gesellschaft für Radioonkologie (DEGRO)
eine nationale Patterns-of-Care-Studie (PCS) durchgeführt. Material und Methode: Ein strukturierter Fragebogen zur Erhebung von Informationen zur Vorbehandlung, der
RT-Indikation und -Technik sowie der Effektivität hinsichtlich der Progressionsfreiheit
und funktionellen Ergebnisse sowie möglicher Nebenwirkungen der RT wurde an alle 227
Strahlentherapieinstitutionen in Deutschland versandt. Ergebnisse: Mit einer Rücklaufrate von 83,2 % ist PCS national repräsentativ. Klinische Erfahrungen
zur Behandlung der PVNS lagen in 10 % der Einrichtungen vor. Auswertbar waren 41 Fälle
aus 14 Institutionen, über die ausreichende Angaben vorlagen. Alle 41 Fälle waren
primär mit 1 bis > 4 Eingriffen chirurgisch vorbehandelt worden. Die RT wurde bei
nicht komplett resektablen Fällen oder präventiv in der Rezidivsituation indiziert.
Die applizierten Gesamtdosen variierten zwischen 30–50 Gy (median 36 Gy). In 39 Fällen
(95,1 %) wurde eine Progression der PVNS verhindert, davon wurde in 34 Fällen (82,9 %)
ein sehr gutes oder gutes funktionelles Ergebnis erzielt. Gravierende Früh- oder Spätnebenwirkungen
der RT wurden nicht beobachtet. Schlussfolgerungen: Die postoperative RT ist eine nebenwirkungsarme Therapieoption, durch die bei nicht
komplett resektablen Läsionen oder adjuvant nach Resektion von Rezidiven der PVNS
eine Optimierung der lokalen Kontrolle erzielt werden kann. Die empfohlenen Gesamtdosen
liegen bei mindestens 30 bis 36 Gy.
Abstract
Aim: Pigmented villonodular synovitis (PVNS) is a rare proliferative disorder arising
from synovial cells of the tendon sheets and joint capsules. The potential value of
external beam radiation therapy in the interdisciplinary management of PVNS is demonstrated
by a comprehensive literature review on the clinical use of radiotherapy and the results
of national patterns of care study (PCS) which was conducted by the German Cooperative
Group on Radiotherapy in Benign Diseases (GCG-BD) in 2008–2009. Material and Method: A structured questionnaire was mailed to all 227 RT institutions in Germany to assess
all previous treatments, the RT indication and techniques, the rate of local control,
the functional outcome and the possible adverse effects related to the use of external
beam radiation therapy (RT). For comparison of the clinical outcome data, a systematic
literature research in several international electronic databases and a conventional
library search were performed to identify publications addressing the use of RT for
PVNS. Results: Based on an overall response rate of 83.2 %, the PCS was nationally representative.
Ten percent of institutions presented clinical experience with the use of RT for PVNS;
from this database a total of 41 treated sites from 14 institutions were evaluable
for long-term analysis. The primary therapeutic approach was cytoreductive surgery
in all cases. In cases of residual tissue or complete resection of extensive local
recurrences, RT was applied in 39 cases (95.1 %). An excellent or good functional
outcome was noted in 34 cases (82.9 %). The use of RT was not associated with early
or late toxicity larger than RTOG grade II. The literature review identified 19 published
studies (1940–2009) which represented a total of 140 cases or patients, respectively.
After follow-up periods ranging from 1–250 months and administration of total doses
in the range of 16–50 Gy the overall rate of local control was 84.5 %. Conclusion: Both the results of the national PCS and the literature review demonstrate that RT
is a very safe and effective treatment option for the prevention of disease progression
or recurrence in PVNS after primary surgical interventions. The planned treatment
volume should include the whole synovial space and eventually all invasive components
of the disease. Currently, total doses in the range of 30–36 Gy are recommended.
Schlüsselwörter
pigmentierte villonoduläre Synovitis - nicht maligne Erkrankungen/Tumoren - Patterns-of-Care-Studie
(PCS) - Gelenkprobleme - Radiotherapie
Key words
pigmented villonodular synovitis - benign disease/tumours - patterns of care study
- joint disorders - radiotherapy
Literatur
- 1
O'Connell J X, Fanburg J C, Rosenberg A E.
Giant cell tumor of tendon sheath and pigmented villonodular synovitis: immunophenotype
suggests a synovial cell origin.
Hum Pathol.
1995;
26
771-775
- 2
Choong P F, Willén H, Nilbert M et al.
Pigmented villonodular synovitis. Monoclonality and metastasis – case for neoplastic
origin.
Acta Orthop Scand.
1995;
66
64-68
- 3
Chassaignac M.
Cancer de la gaine des tendons.
Gaz Hop Civ Milit.
1852;
47
185-186
- 4
Jaffé H L, Lichtenstein L, Sutro C J.
Pigmented villonodular synovitis, bursitis, and tenosynovitis. A discussion of the
synovial and bursal equivalents of the tenosynovial lesion commonly noted as xanthoma,
xanthoranuloma, giant cell tumor or myeloplaxoma of the tendon sheath lesion itself.
Arch Pathol.
1941;
31
731-765
- 5
Flandry F, McCann S B, Hughston J C et al.
Current concepts review: pigmented villonodular synovitis.
J Bone Joint Surg [Am].
1987;
69
942-949
- 6
Myers B W, Masi A T, Feigenbaum S L.
Pigmented villonodular synovitis and tendosynovitis: a clinical and epidemiologic
study of 166 cases and literature review.
Medicine.
1980;
59
223-228
- 7
Mohr W.
Pigmentierte villonoduläre Synovitis – eine Übersicht unter Berücksichtigung von 166
Beobachtungen.
Pathologe.
1992;
13
314-321
- 8
Bruns J, Yazigee O, Habermann C R.
Pigmentierte villonoduläre Synovialitis und tenosynovialer Riesenzelltumor.
Z Orthop Unfall.
2008;
146
663-675
- 9
Klompmaker J, Veith R P, Robinson P H et al.
Pigmented villonodular synovitis.
Arch Orthop Trauma Surg.
1990;
109
205-210
- 10
Chiari C, Pirich C, Brannath W et al.
What affects the recurrence and clinical outcome of pigmented villonodular synovitis?.
Clin Orthop Relat Res.
2006;
450
172-178
- 11
Vastel L, Lambert P, De Pinieux G et al.
Surgical treatment of pigmented villonodular synovitis of the hip.
J Bone Joint Surg [Am].
2005;
87
1019-1024
- 12
De Ponti A, Sansone V, da Gama Malchèr M.
Result of arthroscopic treatment of pigmented villonodular synovitis of the knee.
Arthroscopy.
2003;
19
602-607
- 13
Ogilvie-Harris D J, McLean J, Zarnett M E.
Pigmented villonodular synovitis of the knee. The results of total arthroscopic synovectomy,
partial, arthroscopic synovectomy, and arthroscopic local excision.
J Bone Joint Surg [Am].
1992;
74
119-123
- 14
Neuß W, Herrmann B, Wirtz D C.
Rezidiv einer pigmentierten villo-nodulären Synovialitis (PVNS).
Z Orthop.
2001;
139
366-369
- 15
Dines J S, DeBerardino T M, Wells J L et al.
Long-term follow-up of surgically treated localized pigmented villonodular synovitis
of the knee.
Arthroscopy.
2007;
23
930-937
- 16
Kroot E J, Kraan M C, Smeets T J et al.
Tumor necrosis factor alpha blockage in treatment resisting pigmented villonodular
synovitis.
Ann Rheum Dis.
2005;
64
497-499
- 17
Fiocco U, Oliviero F, Sovran F et al.
[Intra-articular treatment with the TNF-alpha antagonist, etanercept, in severe diffuse
pigmented villonodular synovitis of the knee].
Reumatismo.
2006;
58
268-274
- 18
Blay J Y, El Sayadi H, Thiesse P et al.
Complete response to imatinib in relapsing pigmented villonodular synovitis/tenosynovial
giant cell tumor (PVNS/TGCT).
Ann Oncol.
2008;
19
821-822
- 19
Friedman M, Ginzler A.
Xanthogranuloma of the knee joint.
Bull Hosp Joint Dis.
1940;
1
17-22
- 20
Greenfield M M, Wallace K M.
Pigmented villonodular synovitis.
Radiology.
1950;
54
350-356
- 21
Shafer S J, Larmon W A.
Pigmented villonodular synovitis.
Surg Gynecol Obstet.
1951;
92
574-580
- 22
Ghormley R K, Romness J O.
Pigmented villonodular synovitis (xanthomatosis) of the hip joint.
Staff Meetings of the Mayo Clinic.
1954;
29
171-180
- 23
Friedman M, Schwartz E E.
Irradiation therapy of pigmented villonodular synovitis.
Bull Hosp Joint Dis.
1957;
18
19-32
- 24
Ustinova V F, Podliashuk E L, Rodionova S S.
Combined treatment of diffuse form of pigmented villonodular synovitis.
Med Radiol (Mosk).
1986;
31
27-31
- 25
O'Sullivan B, Cummings B, Catton C et al.
Outcome following radiation treatment for high-risk pigmented villonodular synovitis.
Int J Radiat Oncol Biol Phys.
1995;
32
777-786
- 26
Remy S, Lafenêtre O, Huchet A et al.
Radiothérapie postoperative d'une tumeur bénigne de la cheiveille.
Cancer Radiother.
1999;
3
242-244
- 27
Kotwal P P, Gupta V, Malhorta R.
Recurrence of pigmented villonodular synovitis (PVNS) after previous surgery.
J Bone Joint Surg [Br].
2000;
82
571-573
- 28
Blanco C E, Leon H O, Guthrie T B.
Combined partial arthroscopic synovectomy and radiation therapy for diffuse pigmented
villonodular synovitis of the knee.
Arthroscopy.
2001;
17
527-531
- 29
Chin K R, Barr S J, Winalski C et al.
Treatment of advanced primary and recurrent diffuse pigmented villonodular synovitis
of the knee.
J Bone Joint Surg [Am].
2002;
84
2192-2202
- 30
Brien E W, Sacoman D M, Mira J M.
Pigmented villonodular synovitis of the foot and ankle.
Foot Ankle Int.
2004;
15
908-913
- 31
Bisbinas I, De Silva U, Grimer R J.
Pigmented villonodular synovitis of the foot and ankle: a 12-year experience from
a tertiary orthopedic oncology unit.
J Foot Ankle Surg.
2004;
43
407-411
- 32
Lee M, Mahroof S, Pringle J et al.
Diffuse pigmented villonodular synovitis of the foot and ankle treated with surgery
and radiotherapy.
Int Orthop.
2005;
29
403-405
- 33
Tselis N, Heyd R, Zamboglou N.
Pigmented villonodular synovitis of the distal radioulnar joint.
Strahlenther Onkol.
2006;
182
247-251
- 34
Berger B, Ganswindt U, Bamberg M et al.
External beam radiotherapy as postoperative treatment of the diffuse pigmented villonodular
synovitis.
Int J Radiat Oncol Biol Phys.
2007;
67
130-134
- 35
Vavrik P, Jarosova K, Popelka S.
Polyarticular form of pigmented villonodular synovitis. Radiation and surgical therapy:
long term follow up.
Acta Chir Orthop Traumatol Cech.
2008;
75
392-395
- 36
Horoschak M, Tran P T, Bachireddy P et al.
External beam radiation therapy enhances local control in pigmented villonodular synovitis.
Int J Radiat Oncol Biol Phys.
2009;
75
183-187
- 37
Nassar W A, Bassiony A A, Eighazaly H A.
Treatment of diffuse pigmented villonodular synovitis of the knee with combined surgical
and radiosynovectomy.
HSS J.
2009;
5
19-23
- 38
Ward Sr. W G, Boles C A, Ball J D et al.
Diffuse pigmented villonodular synovitis: preliminary results with intralesional resection
and p 32 synoviorthesis.
Clin Orthop Relat Res.
2007;
454
186-191
- 39
Shabat S, Kollender Y, Merimsky O et al.
The use of surgery and yttrium 90 in the management of extensive and diffuse pigmented
villonodular synovitis of large joints.
Rheumatology (Oxford).
2002;
41
1113-1118
- 40
Kat S, Kutz R, Elbracht T et al.
Radiosynovectomy in pigmented villonodular synovitis.
Nuklearmedizin.
2000;
39
209-213
- 41
Micke O, Seegenschmiedt M H.
Radiotherapy in painful heel spurs (plantar fasciitis) – results of a national patterns
of care study.
Int J Radiat Oncol Biol Phys.
2004;
58
828-843
- 42
Micke O, Seegenschmiedt M H.
Radiation therapy for aggressive fibromatosis (desmoids tumors): results of a national
Patterns of Care Study.
Int J Radiat Oncol Biol Phys.
2005;
61
882-891
- 43
Olschewski T, Seegenschmiedt M H.
Radiotherapy of Langerhans cell histiocytosis: results and implications of a National
Patterns-of-Care Study.
Strahlenther Onkol.
2006;
182
629-634
- 44
Mann H, Whitney D.
On a test of whether one of two random variables is stochastically larger than the
other.
Ann Math Stat.
1947;
18
50-60
- 45
Kruskal W H, Wallis W A.
Use of ranks in one-criterion variance analysis.
J Am Stat Ass.
1952;
47
583-621
- 46
Feldman S E, Klinger E.
Short cut calculation of the Fisher-Yates exact test.
Psychomet.
1963;
28
289-291
- 47
Behrend S W, Coia L R.
Patterns of care in radiation oncology.
Semin Oncol Nurs.
1999;
15
303-315
- 48 Seegenschmiedt M H, Micke O. Patterns-of-Care Study for non-malignant Diseases
in Germany.. In: Seegenschmiedt M H, Makoski H B, Trott K R, et al., eds. Radiotherapy
for non-malignant Disorders. Contemporary Concepts and clinical Results.. Berlin,
Heidelberg: Springer; 2008: 459-466
- 49
Kling D H, Sashin D.
Hemorrhagic villous synovitis of the knee joint due to xanthoma.
Arch Surg.
1935;
30
52-61
- 50
Kampen W U, Voth M, Pinkert J et al.
Therapeutic status of radiosynovirtesis of the knee with yttrium-90 [90Y] colloid
in rheumatoid arthritis and related indications.
Rheumatology (Oxford).
2007;
48
16-24
- 51
Bickels J, Isaakov J, Kollender Y et al.
Unacceptable complications following intra-articular injection of yttrium 90 in an
ankle joint for diffuse pigmented villonoduloar synovitis.
J Bone Joint Surg [Am].
2008;
90
326-328
- 52
Sojan S, Bartholomeusz D.
Cutaneous radiation necrosis as a complication of yttrium-90 synovectomy.
Hell J Nucl Med.
2005;
8
58-59
- 53
Peters W, Lee P.
Radiation necrosis overlying the ankle joint after injection with yttrium-90.
Ann Plast Surg.
1994;
32
542-543
- 54
Kampen W U, Matis E, Czech N et al.
Komplikationen nach Radiosynovirtese: erste Ergebnisse einer Umfrage zu Häufigkeit
und therapeutischen Optionen.
Nuklearmedizin.
2004;
43 (Suppl.)
A21
1 Die Software BiAS® wurde im Institut für Biomathematik an der Frankfurter Universitätsklinik
von Herrn Dr. Hanns Ackermann entwickelt, die Version 8.05 stammt aus dem Jahr 2004.
Dr. Reinhard Heyd
Strahlenklinik
Klinikum Offenbach
Starkenburgring 66
63069 Offenbach
Telefon: 0 69/84 05-33 35
Fax: 0 69/84 05-33 34
eMail: reiniheyd@aol.com