FDA Approval Summary: Vorasidenib for <i>IDH</i> -Mutant Grade 2 Astrocytoma or Oligodendroglioma Following Surgery

On August 6, 2024, the FDA granted traditional approval to vorasidenib (Voranigo, Servier Pharmaceuticals, LLC) for the treatment of adult and pediatric patients 12 years and older with grade 2 astrocytoma or oligodendroglioma with a susceptible isocitrate dehydrogenase 1 or 2 mutation following surgery, including biopsy, subtotal resection, or gross total resection. The approval was based on data from a randomized, multicenter, double-blind trial of vorasidenib compared with placebo. The primary objective was to demonstrate the efficacy of vorasidenib based on radiographic progression-free survival (PFS) per blinded independent central review according to the modified Response Assessment for Neuro-oncology for Low-Grade Gliomas criteria. PFS was assessed in 331 patients, and the HR was 0.39 (95% confidence interval, 0.27-0.56; P value < 0.0001). The most common (≥15%) adverse reactions included fatigue, headache, COVID-19, musculoskeletal pain, diarrhea, nausea, and seizure. PFS was considered an appropriate endpoint for this disease, considering the long natural history and the randomized design allowed for the interpretation of the treatment effect in this rare malignancy. This was the first FDA approval for a targeted therapy for isocitrate dehydrogenase-mutant grade 2 gliomas.

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Publication Details

Journal
Clinical Cancer Research
Published
2025-09-05
DOI
https://doi.org/10.1158/1078-0432.ccr-25-1333
Citations
5
Primary Topic
Glioma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
8.13
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article

FDA Approval Summary: Vorasidenib for IDH -Mutant Grade 2 Astrocytoma or Oligodendroglioma Following Surgery

Nam Atiqur Rahman, Michael I. Barbato, Yuching Yang, Amy Barone et al.
5 citations
Clinical Cancer Research
Glioma Diagnosis and Treatment
8.13
article

FDA Approval Summary: Vorasidenib for IDH -Mutant Grade 2 Astrocytoma or Oligodendroglioma Following Surgery

Nam Atiqur Rahman, Michael I. Barbato, Yuching Yang, Amy Barone, Jianghong Fan, Sarah E. Dorff, Barbara Scepura, A. K. Sinha, Shan Pradhan, Maritsa Stephenson, Xiaoxue Li, Shenghui Tang, Hong Zhao, Stephanie Aungst, Richard Pazdur, Paul G. Kluetz, Nicole Drezner, Erin Larkins, Claudia P. Miller, Vishal Bhatnagar, Ye Xiong, Youwei Bi, Hua Zhou, Haleh Saber, Suryatheja Ananthula
article en
5 citations

Abstract

On August 6, 2024, the FDA granted traditional approval to vorasidenib (Voranigo, Servier Pharmaceuticals, LLC) for the treatment of adult and pediatric patients 12 years and older with grade 2 astrocytoma or oligodendroglioma with a susceptible isocitrate dehydrogenase 1 or 2 mutation following surgery, including biopsy, subtotal resection, or gross total resection. The approval was based on data from a randomized, multicenter, double-blind trial of vorasidenib compared with placebo. The primary objective was to demonstrate the efficacy of vorasidenib based on radiographic progression-free survival (PFS) per blinded independent central review according to the modified Response Assessment for Neuro-oncology for Low-Grade Gliomas criteria. PFS was assessed in 331 patients, and the HR was 0.39 (95% confidence interval, 0.27-0.56; P value < 0.0001). The most common (≥15%) adverse reactions included fatigue, headache, COVID-19, musculoskeletal pain, diarrhea, nausea, and seizure. PFS was considered an appropriate endpoint for this disease, considering the long natural history and the randomized design allowed for the interpretation of the treatment effect in this rare malignancy. This was the first FDA approval for a targeted therapy for isocitrate dehydrogenase-mutant grade 2 gliomas.

Clinical Cancer ResearchVol. 31(21)
United States Food and Drug Administration (US), Center for Drug Evaluation and Research (US)
Openalex Percentile: Top 2%
Glioma Diagnosis and Treatment
8.13
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