D
Dominique Ranchère-Vince
Researcher at University of Lyon
Publications - 121
Citations - 5886
Dominique Ranchère-Vince is an academic researcher from University of Lyon. The author has contributed to research in topics: Sarcoma & Soft tissue sarcoma. The author has an hindex of 37, co-authored 117 publications receiving 4786 citations. Previous affiliations of Dominique Ranchère-Vince include Institut Gustave Roussy & Claude Bernard University Lyon 1.
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Journal Article
Fonctionnement et impact d’un comité pluridisciplinaire en cancérologie
Patrick Castel,Jean-Yves Blay,Pierre Meeus,Marie-Pierre Sunyach,Dominique Ranchère-Vince,Philippe Thiesse,Christophe Bergeron,Perrine Marec-Berard,A. Lurkin,Isabelle Ray-Coquard +9 more
TL;DR: The functioning of a multidisciplinary specialized committee in a rare tumor shows that the quality of decisions does not only rely on the collective deliberation, but also on the individual and specific competencies of some members of the committee that other members admit.
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Genetic analyses of undifferentiated small round cell sarcoma identifies a novel sarcoma subtype with a recurrent CRTC1-SS18 gene fusion.
Abdullah Alholle,Marie Karanian,Anna T. Brini,Mark R. Morris,Vinodh Kannappan,Stefania Niada,Angela Niblett,Dominique Ranchère-Vince,Daniel Pissaloux,Christophe Delfour,Aurelie Maran-Gonzalez,Cristina R. Antonescu,Vaiyapuri Sumathi,Franck Tirode,Farida Latif +14 more
TL;DR: It is concluded that the novel gene fusion identified in this study adds a new subtype to the USRCSs with unique gene signatures, and may be of therapeutic relevance.
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Clear Cell Myomelanocytic Tumor (PEComa) of the Duodenum in a Child With a History of Neuroblastoma
Tony Mhanna,Dominique Ranchère-Vince,Valérie Hervieu,Dominique Tardieu,Jean-Yves Scoazec,Christian Partensky +5 more
TL;DR: A case of digestive clear cell myomelanocytic tumor (PEComa) that is unique in its location and presentation is reported, which suggests a possible association between PEComa and neuroblastoma, 2 unusual tumors that belong to the spectrum of lesions known to occur in patients with tuberous sclerosis and that may share a possible common pathogenetic mechanism.
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Incidence, épidémiologie des sarcomes et biologie moléculaire. Résultats préliminaires de l’étude EMS en Rhône-Alpes
Françoise Ducimetière,A. Lurkin,Dominique Ranchère-Vince,Anne-Valérie Decouvelaere,Isaac S,Claret-Tournier C,Suignard Y,D Salameire,Dominic Cellier,Laurent Alberti,Pierre-Paul Bringuier,J-Y. Blay,I.L. Ray-Coquard +12 more
TL;DR: Sarcomas comprise a heterogeneous group of mesenchymal neoplasms, which can be grouped into three general categories: soft tissue, visceral and primary bone sarcoma as discussed by the authors.
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Pazopanib for the treatment of soft-tissue sarcoma
Pierre Heudel,Philippe Cassier,Olfa Derbel,Armelle Dufresne,Pierre Meeus,Philippe Thiesse,Dominique Ranchère-Vince,Jean-Yves Blay,Isabelle Ray-Coquard +8 more
TL;DR: This review details the development of this new therapeutic class in the treatment of metastatic soft-tissue sarcomas and in comparison with sunitinib or sorafenib, pazopanib has a similar toxicity profile and is generally well tolerated.