Literature DB >> 33910263

Ultra-rare sarcomas: A consensus paper from the Connective Tissue Oncology Society community of experts on the incidence threshold and the list of entities.

Silvia Stacchiotti1, Anna Maria Frezza1, Jean-Yves Blay2, Elizabeth H Baldini3, Sylvie Bonvalot4, Judith V M G Bovée5, Dario Callegaro6, Paolo G Casali1, RuRu Chun-Ju Chiang7,8, George D Demetri9, Elisabeth G Demicco10, Jayesh Desai11, Mikael Eriksson12, Hans Gelderblom13, Suzanne George9, Mrinal M Gounder14,15, Alessandro Gronchi6, Abha Gupta16,17, Rick L Haas18,19, Andrea Hayes-Jardon20, Peter Hohenberger21, Kevin B Jones22, Robin L Jones23, Bernd Kasper21, Akira Kawai24, David G Kirsch25, Eugene S Kleinerman26, Axel Le Cesne27, Jiwon Lim28, María Dolores Chirlaque López29, Roberta Maestro30, Rafael Marcos-Gragera31, Javier Martin Broto32, Tomohiro Matsuda33, Olivier Mir27, Shreyaskumar R Patel34, Chandrajit P Raut35,36, Albiruni R A Razak17, Damon R Reed37, Piotr Rutkowski38, Roberta G Sanfilippo1, Marta Sbaraglia39, Inga-Marie Schaefer40, Dirk C Strauss23, Kirsten Sundby Hall41, William D Tap14,15, David M Thomas42, Winette T A van der Graaf43, Winan J van Houdt44, Otto Visser45, Margaret von Mehren46, Andrew J Wagner9, Breelyn A Wilky47, Young-Joo Won28, Christopher D M Fletcher40, Angelo P Dei Tos39, Annalisa Trama48.   

Abstract

BACKGROUND: Among sarcomas, which are rare cancers, many types are exceedingly rare; however, a definition of ultra-rare cancers has not been established. The problem of ultra-rare sarcomas is particularly relevant because they represent unique diseases, and their rarity poses major challenges for diagnosis, understanding disease biology, generating clinical evidence to support new drug development, and achieving formal authorization for novel therapies.
METHODS: The Connective Tissue Oncology Society promoted a consensus effort in November 2019 to establish how to define ultra-rare sarcomas through expert consensus and epidemiologic data and to work out a comprehensive list of these diseases. The list of ultra-rare sarcomas was based on the 2020 World Health Organization classification, The incidence rates were estimated using the Information Network on Rare Cancers (RARECARENet) database and NETSARC (the French Sarcoma Network's clinical-pathologic registry). Incidence rates were further validated in collaboration with the Asian cancer registries of Japan, Korea, and Taiwan.
RESULTS: It was agreed that the best criterion for a definition of ultra-rare sarcomas would be incidence. Ultra-rare sarcomas were defined as those with an incidence of approximately ≤1 per 1,000,000, to include those entities whose rarity renders them extremely difficult to conduct well powered, prospective clinical studies. On the basis of this threshold, a list of ultra-rare sarcomas was defined, which comprised 56 soft tissue sarcoma types and 21 bone sarcoma types.
CONCLUSIONS: Altogether, the incidence of ultra-rare sarcomas accounts for roughly 20% of all soft tissue and bone sarcomas. This confirms that the challenges inherent in ultra-rare sarcomas affect large numbers of patients.
© 2021 American Cancer Society.

Entities:  

Keywords:  drug development; incidence; rarity; registry; sarcoma; ultra-rare

Mesh:

Year:  2021        PMID: 33910263      PMCID: PMC8319065          DOI: 10.1002/cncr.33618

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  15 in total

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9.  Rare cancers are not rare in Asia as well: The rare cancer burden in East Asia.

Authors:  Tomohiro Matsuda; Young-Joo Won; RuRu Chun-Ju Chiang; Jiwon Lim; Kumiko Saika; Keisuke Fukui; Wen-Chung Lee; Laura Botta; Alice Bernasconi; Annalisa Trama
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10.  The cost-saving effect of centralized histological reviews with soft tissue and visceral sarcomas, GIST, and desmoid tumors: The experiences of the pathologists of the French Sarcoma Group.

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