核心概念
Oral drug vorasidenib shows significant efficacy in delaying disease progression and improving quality of life for patients with certain brain tumors.
要約
The article discusses the potential treatment landscape change for patients with a specific type of brain tumor using the oral targeted drug vorasidenib. Key highlights include:
- Vorasidenib awaiting approval for gliomas with IDH1 and IDH2 mutations.
- Phase 3 INDIGO trial results show significant delay in disease progression with vorasidenib.
- Median progression-free survival of 27.7 months with vorasidenib compared to 11.1 months with placebo.
- Vorasidenib associated with longer time to next treatment and well-tolerated by patients.
- Potential to delay toxic chemotherapies and radiation, improving long-term survival and quality of life.
- Vorasidenib is an oral inhibitor of IDH1 and IDH2 enzymes, crossing the blood-brain barrier.
- Study details of the INDIGO trial involving 331 patients with grade 2 gliomas with IDH mutations.
- Adverse events and fast-track status from the US FDA for vorasidenib.
統計
The median progression-free survival (PFS) was 27.7 months for patients on vorasidenib, compared with 11.1 months for patients assigned to placebo (hazard ratio (HR) for progression or death with vorasidenib of 0.39 (P < .0001)).
The time to next therapy was significantly longer with vorasidenib, with a median not yet reached, compared to 17.4 months for placebo (hazard ratio, 0.26, P < .001).
Grade 3 or 4 alanine aminotransferase elevations occurred in 9.6% of patients assigned to vorasidenib, but not in the placebo group.
引用
"The results of this study really suggest that in selected patients with IDH mutant low-grade gliomas we can potentially delay the use of these toxic chemotherapies and radiation, maybe for years if not many years, and as a result delay the long-term toxicities of those therapies in a group of patients who typically are experiencing long-term survival." - Glenn Lesser, MD