Back to Search Start Over

Role of the tumor board when prescribing mutant isocitrate dehydrogenase inhibitors to patients with isocitrate dehydrogenase-mutant glioma.

Authors :
Roth, Patrick
Capper, David
Calabrese, Evan
Halasz, Lia M
Jakola, Asgeir S
Source :
Neuro-Oncology Practice. 2025 Supplement, Vol. 12, pi29-i37. 9p.
Publication Year :
2025

Abstract

Isocitrate dehydrogenase (IDH)-mutant gliomas, comprising both astrocytomas and oligodendrogliomas, represent a distinct group of tumors that pose an interdisciplinary challenge. Addressing the needs of affected patients requires close collaboration among various disciplines, including neuropathology, neuroradiology, neurosurgery, radiation oncology, neurology, medical oncology, and other relevant specialties when necessary. Interdisciplinary tumor boards are central in determining the ideal diagnostic and therapeutic strategies for these patients. The key tasks of a tumor board include the evaluation of imaging findings, selecting the appropriate surgical approach, discussing additional treatment options, and identification/determination of tumor recurrence and progression. In addition to established treatments such as radiotherapy and alkylating chemotherapy, patients with an isocitrate dehydrogenase (IDH)-mutant glioma for whom additional treatment is indicated may now also have the option of receiving treatment with an mutant isocitrate dehydrogenase inhibitor such as vorasidenib or ivosidenib. In this regard, the collaborative nature of tumor boards becomes even more crucial for evaluating comprehensively the needs of these patients. Through interdisciplinary discussions, tumor boards aim to develop personalized treatment strategies that maximize therapeutic efficacy while minimizing potential side effects and preserving patients' quality of life. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20542577
Volume :
12
Database :
Academic Search Index
Journal :
Neuro-Oncology Practice
Publication Type :
Academic Journal
Accession number :
182369596
Full Text :
https://doi.org/10.1093/nop/npae100