Desmoid tumors located in the abdomen or associated with adenomatous polyposis: French intergroup clinical practice guidelines for diagnosis, treatment, and follow-up (SNFGE, FFCD, GERCOR, UNICANCER, SFCD, SFED, SFRO, ACHBT, SFR)

被引:9
作者
Benech, Nicolas [1 ]
Bonvalot, Sylvie [2 ]
Dufresne, Armelle [3 ]
Gangi, Afshin [4 ]
Le Pechoux, Cecile [5 ]
Lopez-Trabada-Ataz, Daniel [6 ]
Meurgey, Alexandra [7 ]
Nicolas, Nayla [8 ]
Orbach, Daniel [9 ]
Penel, Nicolas [10 ,11 ]
Salas, Sebastien [12 ]
Saurin, Jean-Christophe [1 ]
Walter, Thomas [13 ]
Lecomte, Thierry [14 ]
Bouche, Olivier [15 ]
机构
[1] Hosp Civils Lyon, Serv Hepatogastroenterol, Hop Edouard Herriot, F-69003 Lyon, France
[2] Inst Curie, Dept Surg, Paris, France
[3] Leon Berard Canc Ctr, Dept Oncol Med, 28 Rue Laennec, F-69373 Lyon 08, France
[4] Strasbourg Univ, Univ Hosp Strasbourg, Ntervent Radiol, F-67200 Strasbourg, France
[5] Gustave Roussy Canc Campus, Dept Oncol Radiotherapie, 114 Rue Edouard Vaillant, F-94800 Villejuif, France
[6] Hop St Antoine, Serv Oncol Med, 184 Rue Faubourg St Antoine, F-75012 Paris, France
[7] Leon Berard Canc Ctr, Dept Biopathol, 28 Rue Laennec, F-69373 Lyon 08, France
[8] Inst Curie, Dept Radiol, Paris, France
[9] Inst Curie, SIREDO Oncol Ctr Care Innovat & Res Children Adol, Paris, France
[10] Ctr Oscar Lambret, Lille, France
[11] Lille Univ, Lille, France
[12] Aix Marseille Univ, Oncol Unit, AP HM, Marseille, France
[13] Hosp Civils Lyon, Serv Oncol, Hop Edouard Herriot, F-69003 Lyon, France
[14] CHU Tours, Dept Hepatogastroenterol & Digest Oncol, Tours, France
[15] CHU Reims, Dept Digest Oncol, Reims, France
关键词
Desmoid tumors; Desmoid-type fibromatosis; French clinical practice guidelines; Familial adenomatous polyposis; Mesenchymal tumors; Soft tissue sarcoma; SARCOMA PATIENTS EURONET; PHASE-II; EUROPEAN ORGANIZATION; FIBROMATOSIS; MANAGEMENT; CONSENSUS; CTNNB1; TISSUE; RISK; METHOTREXATE;
D O I
10.1016/j.dld.2022.03.004
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Introduction: Desmoid tumor (DT) of the abdomen is a challenging and rare disease. The level of evidence available to document their treatment is relatively low, however, recent publications of prospective studies have allowed to precise their management.Methods: This document is a summary of the French intergroup guidelines realized by all French medical and surgical societies involved in the management of DT located in the abdomen or associated with adenomatous polyposis. Recommendations are graded in four categories (A, B, C and D), according to the level of evidence found in the literature until January 2021.Results: When the diagnosis of DT is suspected a percutaneous biopsy should be performed when possible. A molecular analysis looking for pathogenic mutations of the CTNNB1 and APC genes should be systematically performed. When a somatic pathogenic variant of the APC gene is present, an intestinal polyposis should be searched. Due to a high rate of spontaneous regression, non-complicated DT should first benefit from an active surveillance with MRI within 2 months after diagnosis to assess the dynamic of tumor growth. The treatment decision must be discussed in an expert center, favoring the less toxic treatments which can include broad spectrum tyrosine kinase inhibitor or conventional chemotherapy (methotrexate-vinblastine). Surgery, outside the context of emergency, should only be considered for favorable location in an expert center.Conclusion: French guidelines for DT management were elaborated to help offering the best personalized therapeutic strategy in daily clinical practice as the DT therapeutic landscape is complexifying. Each individual case must be discussed within a multidisciplinary expert team.(c) 2022 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:737 / 746
页数:10
相关论文
共 58 条
  • [1] The management of desmoid tumours: A joint global consensus-based guideline approach for adult and paediatric patients
    Alman, Ben
    Attia, Steven
    Baumgarten, Christina
    Benson, Charlotte
    Blay, Jean-Yves
    Bonvalot, Sylvie
    Breuing, Jessica
    Cardona, Ken
    Casali, Paolo G.
    van Coevorden, Frits
    Colombo, Chiara
    Tos, Angelo P. Dei
    Dileo, Palma
    Ferrari, Andrea
    Fiore, Marco
    Frezza, Anna M.
    Garcia, Jesica
    Gladdy, Rebecca
    Gounder, Mrinal
    Gronchi, Alessandro
    Haas, Rick
    Hackett, Sam
    Haller, Florian
    Hohenberger, Peter
    Husson, Olga
    Jones, Robin L.
    Judson, Ian
    Kasper, Bernd
    Kawai, Akira
    Kogosov, Vlada
    Lazar, Alex J.
    Maki, Robert
    Mathes, Tim
    Messiou, Christina
    Navid, Fariba
    Nishida, Yoshihiro
    Palassini, Elena
    Penel, Nicolas
    Pollock, Robert
    Pieper, Dawid
    Portnoy, Marlene
    Raut, Chandrajit P.
    Roets, Evelyne
    Sandrucci, Sergio
    Sbaraglia, Marta
    Stacchiotti, Silvia
    Thornton, Katherine A.
    van der Graaf, Winette
    van der Zande, Kim
    van Houdt, Winan J.
    [J]. EUROPEAN JOURNAL OF CANCER, 2020, 127 : 96 - 107
  • [2] Azzarelli A, 2001, CANCER, V92, P1259, DOI 10.1002/1097-0142(20010901)92:5<1259::AID-CNCR1446>3.0.CO
  • [3] 2-Y
  • [4] Desmoid Tumors and Celecoxib with Sorafenib
    Benech, Nicolas
    Walter, Thomas
    Saurin, Jean-Christophe
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2017, 376 (26) : 2595 - 2597
  • [5] Extra-abdominal primary fibromatosis:: Aggressive management could be avoided in a subgroup of patients
    Bonvalot, S.
    Eldweny, H.
    Haddad, V.
    Rimareix, F.
    Missenard, G.
    Oberlin, O.
    Vanel, D.
    Terrier, P.
    Blay, J. Y.
    Le Cesne, A.
    Le Pechoux, C.
    [J]. EJSO, 2008, 34 (04): : 462 - 468
  • [6] Spontaneous Regression of Primary Abdominal Wall Desmoid Tumors: More Common than Previously Thought
    Bonvalot, Sylvie
    Ternes, Nils
    Fiore, Marco
    Bitsakou, Georgina
    Colombo, Chiara
    Honore, Charles
    Marrari, Andrea
    Le Cesne, Axel
    Perrone, Federica
    Dunant, Ariane
    Gronchi, Alessandro
    [J]. ANNALS OF SURGICAL ONCOLOGY, 2013, 20 (13) : 4096 - 4102
  • [7] Role of Imaging in Management of Desmoid-type Fibromatosis: A Primer for Radiologists
    Braschi-Amirfarzan, Marta
    Keraliya, Abhishek R.
    Krajewski, Katherine M.
    Tirumani, Sree Harsha
    Shinagare, Atul B.
    Hornick, Jason L.
    Baldini, Elizabeth H.
    George, Suzanne
    Ramaiya, Nikhil H.
    Jagannathan, Jyothi P.
    [J]. RADIOGRAPHICS, 2016, 36 (03) : 767 - 782
  • [8] Toward Observation as First-line Management in Abdominal Desmoid Tumors
    Burtenshaw, Sally M.
    Cannell, Amanda J.
    McAlister, Edward D.
    Siddique, Saquib
    Kandel, Rita
    Blackstein, Martin E.
    Swallow, Carol J.
    Gladdy, Rebecca A.
    [J]. ANNALS OF SURGICAL ONCOLOGY, 2016, 23 (07) : 2212 - 2219
  • [9] Soft tissue and visceral sarcomas: ESMO-EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up (vol 29, pg 51, 2018)
    Casali, P. G.
    Abecassis, N.
    Aro, H. T.
    Bauer, S.
    Biagini, R.
    Bielack, S.
    Bonvalot, S.
    Boukovinas, I.
    Bovee, J. V. M. G.
    Brodovvicz, T.
    Broto, J. M.
    Buonadonna, A.
    De Alava, E.
    Tos, A. P. Dei
    Del Muro, X. G.
    Dileo, P.
    Eriksson, M.
    Fedenko, A.
    Ferraresi, V.
    Ferrari, A.
    Ferrari, S.
    Frezza, A. M.
    Gasperoni, S.
    Gelderblom, H.
    Gil, T.
    Grignani, G.
    Gronchi, A.
    Haas, R. L.
    Hassan, B.
    Hohenberger, P.
    Lssels, R.
    Joensuu, H.
    Jones, R. L.
    Judson, I.
    Jutte, P.
    Kaal, S.
    Kasper, B.
    Kopeckova, K.
    Krakorova, D. A.
    Le Cesne, A.
    Lugowska, I.
    Merimsky, O.
    Montemurro, M.
    Pantaleo, M. A.
    Piana, R.
    Picci, P.
    Piperno-Neumann, S.
    Pousa, A. L.
    Reichardt, P.
    Robinson, M. H.
    [J]. ANNALS OF ONCOLOGY, 2018, 29 : 268 - 269
  • [10] FAMILIAL ADENOMATOUS POLYPOSIS - DESMOID TUMORS AND LACK OF OPHTHALMIC LESIONS (CHRPE) ASSOCIATED WITH APC MUTATIONS BEYOND CODON-1444
    CASPARI, R
    OLSCHWANG, S
    FRIEDL, W
    MANDL, M
    BOISSON, C
    BOKER, T
    AUGUSTIN, A
    KADMON, M
    MOSLEIN, G
    THOMAS, G
    PROPPING, P
    [J]. HUMAN MOLECULAR GENETICS, 1995, 4 (03) : 337 - 340