曲美替尼
达布拉芬尼
威罗菲尼
医学
达卡巴嗪
易普利姆玛
肿瘤科
内科学
无容量
人口
黑色素瘤
彭布罗利珠单抗
无进展生存期
癌症研究
转移性黑色素瘤
化疗
生物
癌症
免疫疗法
MAPK/ERK通路
激酶
遗传学
环境卫生
作者
Nathaly Garzón‐Orjuela,Laura Prieto‐Pinto,Pieralessandro Lasalvia,Daniel Herrera,Johanna Castrillón,Diana C. González-Bravo,Camilo Castañeda‐Cardona,Diego Rosselli
摘要
The current systematic review aimed to evaluate and compare the efficacy and safety of dabrafenib-trametinib with those of other therapeutic alternatives in the treatment of patients with unresectable advanced/metastatic melanoma with BRAF-V600 mutation. The search was carried out on four databases up to July 2018. Two separate network meta-analyses (NMA) were performed using the frequentist method (random effects): one with an exclusive population with BRAF-V600 mutation (NMA-pBRAFV600) and another with mixed population (with or without the mutation: NMA-pMixed). An evidence profile was included using the GRADE method for NMA. The validity of the final estimator in the NMA-pMixed was assessed via a sensitivity analysis. Nine clinical trials were included in the NMA-pBRAFV600. Dabrafenib-trametinib was found to have a favorable effect on overall survival (OS) and progression-free survival (PFS) compared with dabrafenib, vemurafenib, and dacarbazine and on partial response rate (PRR) and overall response rate compared with dacarbazine and vemurafenib. In the NMA-pMixed, dabrafenib-trametinib was found to have a positive effect on OS versus ipilimumab 3 mg/kg and on PFS and PRR versus ipilimumab, nivolumab, and pembrolizumab. However, dabrafenib-trametinib and vemurafenib-cobimetinib significantly differed in terms of efficacy. In addition, dabrafenib-trametinib has a favorable effect on Grades 3 and 4 adverse events.
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