Dabrafenib plus Trametinib in Pediatric Glioma with BRAF V600 Mutations

曲美替尼 达布拉芬尼 医学 肿瘤科 内科学 化疗 无进展生存期 胶质瘤 MEK抑制剂 临床试验 长春新碱 外科 威罗菲尼 癌症研究 癌症 环磷酰胺 生物 MAPK/ERK通路 激酶 细胞生物学 转移性黑色素瘤
作者
Éric Bouffet,Jordan R. Hansford,Maria Luisa Garré,Junichi Hara,Ashley Plant,Isabelle Aerts,Franco Locatelli,Jasper van der Lugt,L. I. Papusha,Felix Sahm,Uri Tabori,Kenneth J. Cohen,Roger J. Packer,Olaf Witt,Larissa Sandalic,Ana Bento Pereira da Silva,Mark W. Russo,Darren Hargrave
出处
期刊:The New England Journal of Medicine [New England Journal of Medicine]
卷期号:389 (12): 1108-1120 被引量:69
标识
DOI:10.1056/nejmoa2303815
摘要

Detection of the BRAF V600E mutation in pediatric low-grade glioma has been associated with a lower response to standard chemotherapy. In previous trials, dabrafenib (both as monotherapy and in combination with trametinib) has shown efficacy in recurrent pediatric low-grade glioma with BRAF V600 mutations, findings that warrant further evaluation of this combination as first-line therapy. Download a PDF of the Research Summary. In this phase 2 trial, patients with pediatric low-grade glioma with BRAF V600 mutations who were scheduled to receive first-line therapy were randomly assigned in a 2:1 ratio to receive dabrafenib plus trametinib or standard chemotherapy (carboplatin plus vincristine). The primary outcome was the independently assessed overall response (complete or partial response) according to the Response Assessment in Neuro-Oncology criteria. Also assessed were the clinical benefit (complete or partial response or stable disease for ≥24 weeks) and progression-free survival. A total of 110 patients underwent randomization (73 to receive dabrafenib plus trametinib and 37 to receive standard chemotherapy). At a median follow-up of 18.9 months, an overall response occurred in 47% of the patients treated with dabrafenib plus trametinib and in 11% of those treated with chemotherapy (risk ratio, 4.31; 95% confidence interval [CI], 1.7 to 11.2; P<0.001). Clinical benefit was observed in 86% of the patients receiving dabrafenib plus trametinib and in 46% receiving chemotherapy (risk ratio, 1.88; 95% CI, 1.3 to 2.7). The median progression-free survival was significantly longer with dabrafenib plus trametinib than with chemotherapy (20.1 months vs. 7.4 months; hazard ratio, 0.31; 95% CI, 0.17 to 0.55; P<0.001). Grade 3 or higher adverse events occurred in 47% of the patients receiving dabrafenib plus trametinib and in 94% of those receiving chemotherapy. Among pediatric patients with low-grade glioma with BRAF V600 mutations, dabrafenib plus trametinib resulted in significantly more responses, longer progression-free survival, and a better safety profile than standard chemotherapy as first-line therapy. (Funded by Novartis; ClinicalTrials.gov number, NCT02684058.) QUICK TAKE VIDEO SUMMARYDabrafenib plus Trametinib in Pediatric Glioma 02:11
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