RNA fusion transcript panel identifies diverse repertoire of fusions in adult glioma patients with therapeutic implications

Author:

Kothari Shawn1,Dusenbery Anna C2,Doucette Abigail1,Zhang Daniel Y3,Ballinger Dominique2,Desai Arati4,Morrissette Jennifer J D2,Bagley Stephen J1,Nasrallah MacLean P2ORCID

Affiliation:

1. Division of Hematology/Oncology, Perelman School of Medicine at the University of Pennsylvania , Philadelphia, Pennsylvania , USA

2. Department of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania , Philadelphia, Pennsylvania , USA

3. Biochemistry and Molecular Biophysics Graduate Group, Perelman School of Medicine at the University of Pennsylvania , Philadelphia, Pennsylvania , USA

4. Electronic Phenotyping Core, Abramson Cancer Center, University of Pennsylvania , Philadelphia, Pennsylvania , USA

Abstract

Abstract Background Recurrent gliomas are therapeutically challenging diseases with few treatment options available. One area of potential therapeutic vulnerability is the presence of targetable oncogenic fusion proteins. Methods To better understand the clinical benefit of routinely testing for fusion proteins in adult glioma patients, we performed a retrospective review of 647 adult patients with glioma who underwent surgical resection at our center between August 2017 and May 2021 and whose tumors were analyzed with an in-house fusion transcript panel. Results Fifty-two patients (8%) were found to harbor a potentially targetable fusion with 11 (21%) of these patients receiving treatment with a fusion-targeted inhibitor. The targetable genes found to be involved in a fusion included FGFR3, MET, EGFR, NTRK1, NTRK2, BRAF, ROS1, and PIK3CA. Conclusions This analysis demonstrates that routine clinical testing for gene fusions identifies a diverse repertoire of potential therapeutic targets in adult patients with glioma and can offer rational therapeutic options for patients with recurrent disease.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Medicine (miscellaneous)

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