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Cobimetinib Plus Vemurafenib: A Review in BRAF(V600) Mutation-Positive Unresectable or Metastatic Melanoma

机译:Cobimetinib加Vemurafenib:BRAF(V600)突变阳性不可切除或转移性黑色素瘤的综述

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摘要

The MEK inhibitor cobimetinib (Cotellic (R)) is indicated for the treatment of patients with BRAF(V600) mutation-positive unresectable or metastatic melanoma, in combination with the BRAF inhibitor vemurafenib (Zelboraf (R)). In the pivotal coBRIM trial, previously untreated patients with BRAF(V600) mutation-positive unresectable, stage IIIC or stage IV melanoma received cobimetinib 60 mg once daily for the first 21 days of each 28-day cycle plus vemurafenib 960 mg twice daily or vemurafenib alone. Compared with vemurafenib alone, cobimetinib plus vemurafenib significantly prolonged progression-free survival (primary endpoint) and was associated with a significantly higher overall response rate and significantly prolonged overall survival. Cobimetinib plus vemurafenib had a manageable tolerability profile. In conclusion, cobimetinib plus vemurafenib is a valuable option for use in BRAF(V600) mutation-positive unresectable or metastatic melanoma.
机译:MEK抑制剂cobimetinib(Cotellic(R))与BRAF抑制剂vemurafenib(Zelboraf(R))结合用于治疗患有BRAF(V600)突变阳性,不可切除或转移性黑色素瘤的患者。在关键性coBRIM试验中,先前未经治疗的BRAF(V600)突变阳性,不可切除,IIIC期或IV期黑色素瘤患者在每个28天周期的前21天中每天一次接受Cobimetinib 60 mg联合维拉非尼960 mg每天两次或维拉非尼单独。与单独的vemurafenib相比,cobimetinib加上vemurafenib显着延长了无进展生存期(主要终点),并且显着提高了总缓解率并显着延长了总生存期。 Cobimetinib加vemurafenib具有可控的耐受性。总之,cobimetinib加vemurafenib是用于BRAF(V600)突变阳性,不可切除或转移性黑色素瘤的宝贵选择。

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