ATRT-40. IMPACT OF MOLECULAR SUBTYPES ON TREATMENT OUTCOMES IN RHABDOID TUMORS - A REPORT FROM THE RARE TUMOR CONSORTIUM

Abstract BACKGROUND Rhabdoid Tumors (RTs) are rare heritable cancers with bi-allelic SMARCB1/A4 alterations, arising in the brain (Atypical Teratoid/Rhabdoid Tumors/ATRTs) and in various extra-cranial locations (Malignant Rhabdoid Tumors/MRTs). Recent studies uncovered molecular sub-types of ATRTs a...

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Veröffentlicht in:	Neuro-oncology (Charlottesville, Va.) Va.), 2018-06, Vol.20 (suppl_2), p.i36-i36
Hauptverfasser:	Ho, Ben, Fonseca, Adriana, Al-Karmi, Salma, Margol, Ashley, Yao, Fupan, Cheng, Sylvia, Grant, Ronald, Handsford, Jordan, Gupta, Abha, Vasiljevic, Alexandre, Pawel, Bruce, Jabado, Nada, Hawkins, Cynthia, Lafay-Cousin, Lucie, Judkins, Alexander, Bouffet, Eric, Huang, Annie
Format:	Artikel
Sprache:	eng
Schlagworte:	Abstracts
Online-Zugang:	Volltext
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