Clinical features and outcomes of young patients with epithelioid sarcoma: an analysis from the Children's Oncology Group and the European paediatric soft tissue Sarcoma Study Group prospective clinical trials-Reference-Cited by-同舟云学术

Clinical features and outcomes of young patients with epithelioid sarcoma: an analysis from the Children's Oncology Group and the European paediatric soft tissue Sarcoma Study Group prospective clinical trials

Published:2019-05 Issue: Volume:112 Page:98-106
ISSN:0959-8049
Container-title:European Journal of Cancer
language:en
Short-container-title:European Journal of Cancer

Author:

Spunt Sheri L.,Francotte Nadine,De Salvo Gian Luca^ORCID,Chi Yueh-Yun,Zanetti Ilaria,Hayes–Jordan Andrea,Kao Simon C.,Orbach Daniel^ORCID,Brennan Bernadette,Weiss Aaron R.,van Noesel Max M.,Million Lynn,Alaggio Rita,Parham David M.,Kelsey Anna,Randall R. Lor,McCarville M. Beth,Bisogno Gianni,Hawkins Douglas S.,Ferrari Andrea^ORCID

Funder

Children’s Oncology Group

St. Baldrick's Foundation

Fondazione Città della Speranza

Publisher

Elsevier BV

Subject

Cancer Research,Oncology

Reference29 articles.

1. Loss of INI1 expression is characteristic of both conventional and proximal-type epithelioid sarcoma;Hornick;Am J Surg Pathol,2009

2. SMARCB1/INI1 tumor suppressor gene is frequently inactivated in epithelioid sarcomas;Modena;Cancer Res,2005

3. Childhood nonrhabdomyosarcoma soft tissue sarcomas are not adult-type tumors;Spunt;J Clin Oncol,2006