Genomic complexity in pediatric synovial sarcomas (Synobio study): the European pediatric soft tissue sarcoma group (EpSSG) experience

Daniel Orbach, Véronique Mosseri, Daniel Pissaloux, Gaelle Pierron, Bernadette Brennan, Andrea Ferrari, Frederic Chibon, Gianni Bisogno, Gian Luca De Salvo, Camille Chakiba, Nadège Corradini, Véronique Minard-Colin, Anna Kelsey, Dominique Ranchère-Vince

Research output: Contribution to journalArticle

Abstract

A genomic index (GI) tool using array comparative genomic hybridization (aCGH) on tumor cells has emerged as independent prognostic factor associated with the risk of metastatic relapse in synovial sarcoma (SS). The aim was to assess GI in pediatric patients with SS, to determine its value as a prognostic factor. All pediatric/adolescent/young adults' (
Original languageEnglish
Pages (from-to)1384-1393
Number of pages10
JournalCancer Medicine
Volume7
Issue number4
DOIs
Publication statusPublished - Apr 1 2018

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    Orbach, D., Mosseri, V., Pissaloux, D., Pierron, G., Brennan, B., Ferrari, A., Chibon, F., Bisogno, G., De Salvo, G. L., Chakiba, C., Corradini, N., Minard-Colin, V., Kelsey, A., & Ranchère-Vince, D. (2018). Genomic complexity in pediatric synovial sarcomas (Synobio study): the European pediatric soft tissue sarcoma group (EpSSG) experience. Cancer Medicine, 7(4), 1384-1393. https://doi.org/10.1002/cam4.1415