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Clinically Integrated Sequencing Alters Therapy in Children and Young Adults With High-Risk Glial Brain Tumors

Authors :
Kathryn McFadden
Arul M. Chinnaiyan
Andrew H. Zureick
Bailey Anderson
Sriram Venneti
Lili Zhao
Robert J. Lonigro
Karin M. Muraszko
Bernard L. Marini
Brendan Mullan
Patricia L. Robertson
Xuhong Cao
Pankaj Vats
Marcin Cieslik
Rajen Mody
Carl Koschmann
Jessica Everett
Paul E. McKeever
Sandra Camelo-Piragua
Yi-Mi Wu
Marcia Leonard
Hugh J. L. Garton
Cormac O. Maher
Andrew P. Lieberman
Katayoon Kasaian
Kevin Frank
John R. Prensner
Dan R. Robinson
Chandan Kumar-Sinha
Source :
JCO Precis Oncol
Publication Year :
2018
Publisher :
American Society of Clinical Oncology (ASCO), 2018.

Abstract

Purpose Brain tumors have become the leading cause of cancer-related mortality in young patients. Novel effective therapies on the basis of the unique biology of each tumor are urgently needed. The goal of this study was to evaluate the feasibility, utility, and clinical impact of integrative clinical sequencing and genetic counseling in children and young adults with high-risk brain tumors. Patients and Methods Fifty-two children and young adults with brain tumors designated by the treating neuro-oncologist to be high risk (> 25% chance for treatment failure; mean age, 10.2 years; range, 0 to 39 years) were enrolled in a prospective, observational, consecutive case series, in which participants underwent integrative clinical exome (tumor and germline DNA) and transcriptome (tumor RNA) sequencing and genetic counseling. Results were discussed in a multi-institutional brain tumor precision medicine teleconference. Results Sequencing revealed a potentially actionable germline or tumor alteration in 25 (63%) of 40 tumors with adequate tissue, of which 21 (53%) resulted in an impact on treatment or change of diagnosis. Platelet-derived growth factor receptor or fibroblast growth factor receptor pathway alterations were seen in nine of 20 (45%) glial tumors. Eight (20%) sequenced tumors harbored an oncogenic fusion isolated on RNA sequencing. Seventeen of 20 patients (85%) with glial tumors were found to have a potentially actionable result, which resulted in change of therapy in 14 (70%) patients. Patients with recurrent brain tumors receiving targeted therapy had a median progression-free survival (from time on therapy) of 4 months. Conclusion Selection of personalized agents for children and young adults with high-risk brain tumors on the basis of integrative clinical sequencing is feasible and resulted in a change in therapy in more than two thirds of children and young adults with high-risk glial tumors.

Details

ISSN :
24734284
Database :
OpenAIRE
Journal :
JCO Precision Oncology
Accession number :
edsair.doi.dedup.....97d229ffb349b0e6472e38e923065786