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
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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