作者
Bernd Kasper,Elizabeth H. Baldini,Sylvie Bonvalot,Dario Callegaro,Kenneth Cardona,Chiara Colombo,Nadège Corradini,Aimeé M. Crago,Angelo Paolo Dei Tos,Palma Dileo,Eldad Elnekave,Joseph P. Erinjeri,Fariba Navid,Jeffrey M. Farma,Andrea Ferrari,Marco Fiore,Rebecca A. Gladdy,Mrinal M. Gounder,Rick L. Haas,Olga Husson,Jean‐Emmanuel Kurtz,Alex J. Lazar,Daniel Orbach,Nicolas Penel,R. Ratan,Chandrajit P. Raut,Christina L. Roland,Ann-Rose W. Schut,Monika Sparber‐Sauer,D. Strauß,Winette T.A. van der Graaf,Marco Vitellaro,Aaron R. Weiss,Alessandro Gronchi,Benjamin A. Alman,Steven Attia,Jyoti Bajpai,Giacomo Giulio Baldi,Livia Barbieri,Christina Baumgarten,Charlotte Benson,Jean‐Yves Blay,Kjetil Boye,Bernadette Brennan,Andre Domenico Campanacci,Paolo G. Casali,Michela Casanova,Tom Wie-Wu Chen,Lorenzo D’Ambrosio,Cláudia Callegaro de Menezes,Armelle Dufresne,Hans Roland Dürr,Anna Maria Frezza,David Gyorki,Sam Hackett,Florian Haller,Audrey Hélaine,Peter Hohenberger,Toni Ibrahim,Shintaro Iwata,Robin L. Jones,Akira Kawai,Mohamed Kelany,David G. Kirsch,Andreas Leithner,Andrea MacNeill,Christina Messiou,Robert G. Maki,Carlo Morosi,Andrea Napolitano,Yoshihiro Nishida,Elena Palassini,Shreyaskumar Patel,Giulia Personeni,Raphael E. Pollock,Emanuele Rausa,Evelyne Roets,Enrica Rossi,Piotr Rutkowski,D. Salvatore,Claudia Sangalli,Marta Sbaraglia,Paul D. Smith,Silvia Stacchiotti,William D. Tap,Gabriel Tinoco,Dimitri Tzanis,Michiel A. J. van de Sande,Kim van der Zande,Winan J. van Houdt,Cornelis Verhoef,Andrew J. Wagner,Eva Wardelmann,Jeanne Whiting
摘要
Importance Desmoid tumor (DT) is a rare and locally aggressive monoclonal, fibroblastic proliferation characterized by a variable and often unpredictable clinical course. Previously, surgery was the standard primary treatment modality; however, within the past decade, a paradigm shift toward less-invasive management has been introduced and an effort to harmonize the strategy among clinicians has been made. To update the 2020 global evidence-based consensus guideline on the management of patients with DT, the Desmoid Tumor Working Group convened a 1-day consensus meeting in Milan, Italy, on June 30, 2023, under the auspices of the European Reference Network on Rare Adult Solid Cancers and Sarcoma Patient Advocacy Global Network, the Desmoid Foundation Italy, and the Desmoid Tumor Research Foundation. The meeting brought together over 90 adult and pediatric sarcoma experts from different disciplines as well as patients and patient advocates from around the world. Observations The 2023 update of the global evidence-based consensus guideline focused on the positioning of local therapies alongside surgery and radiotherapy in the treatment algorithm as well as the positioning of the newest class of medical agents, such as γ-secretase inhibitors. Literature searches of MEDLINE and Embase databases were performed for English-language randomized clinical trials (RCTs) of systemic therapies to obtain data to support the consensus recommendations. Of the 18 full-text articles retrieved, only 4 articles met the inclusion criteria. The 2023 consensus guideline is informed by a number of new aspects, including data for local ablative therapies such as cryotherapy; other indications for surgery; and the γ-secretase inhibitor nirogacestat, the first representative of the newest class of medical agents and first approved drug for DT. Management of DT is complex and should be carried out exclusively in designated DT referral centers equipped with a multidisciplinary tumor board. Selection of the appropriate strategy should consider DT-related symptoms, associated risks, tumor location, disease morbidities, available treatment options, and preferences of individual patients. Conclusions and Relevance The therapeutic armamentarium of DT therapy is continually expanding. It is imperative to carefully select the management strategy for each patient with DT to optimize tumor control and enhance quality of life.