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Emerging novel agents for patients with advanced Ewing sarcoma: a report from the Children’s Oncology Group (COG) New Agents for Ewing Sarcoma Task Force [version 1; peer review: 3 approved]

Authors :
Kelly Bailey
Carrye Cost
Ian Davis
Julia Glade-Bender
Patrick Grohar
Peter Houghton
Michael Isakoff
Elizabeth Stewart
Nadia Laack
Jason Yustein
Damon Reed
Katherine Janeway
Richard Gorlick
Stephen Lessnick
Steven DuBois
Pooja Hingorani
Source :
F1000Research, Vol 8 (2019)
Publication Year :
2019
Publisher :
F1000 Research Ltd, 2019.

Abstract

Ewing sarcoma is a small round blue cell malignancy arising from bone or soft tissue and most commonly affects adolescents and young adults. Metastatic and relapsed Ewing sarcoma have poor outcomes and recurrences remain common. Owing to the poor outcomes associated with advanced disease and the need for a clear research strategy, the Children’s Oncology Group Bone Tumor Committee formed the New Agents for Ewing Sarcoma Task Force to bring together experts in the field to evaluate and prioritize new agents for incorporation into clinical trials. This group’s mission was to evaluate scientific and clinical challenges in moving new agents forward and to recommend agents and trial designs to the Bone Tumor Committee. The task force generated a framework for vetting prospective agents that included critical evaluation of each drug by using both clinical and non-clinical parameters. Representative appraisal of agents of highest priority, including eribulin, dinutuximab, cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors, anti-angiogenic tyrosine kinase inhibitors, and poly-ADP-ribose polymerase (PARP) inhibitors, is described. The task force continues to analyze new compounds by using the paradigm established.

Subjects

Subjects :
Medicine
Science

Details

Language :
English
ISSN :
20461402
Volume :
8
Database :
Directory of Open Access Journals
Journal :
F1000Research
Publication Type :
Academic Journal
Accession number :
edsdoj.443fdb2786094b91af779ecb997a6867
Document Type :
article
Full Text :
https://doi.org/10.12688/f1000research.18139.1