威罗菲尼
阿替唑单抗
医学
无容量
易普利姆玛
彭布罗利珠单抗
癌症研究
黑色素瘤
肿瘤科
免疫检查点
MEK抑制剂
内科学
曲美替尼
转移性黑色素瘤
免疫疗法
MAPK/ERK通路
癌症
生物
激酶
细胞生物学
作者
Andreas M. Schmitt,Lucy Dumas,James Larkin
标识
DOI:10.1080/14737140.2022.2017286
摘要
The treatment of metastatic melanoma has been revolutionized by the introduction of immune checkpoint inhibitors and BRAF/MEK inhibition. Nevertheless, almost half of patients will progress or show primary resistance to treatment. The combination of BRAF/MEK and immune checkpoint inhibition might achieve higher response rates and improve long-term disease control. The IMspire150 trial investigated the combination of atezolizumab, cobimetinib and vemurafenib versus cobimetinib and vemurafenib alone.This review covers the efficacy and safety of atezolizumab, cobimetinib and vemurafenib for patients with advanced or metastatic BRAF mutant melanoma. The combination is compared with the current standard of care including BRAF/MEK inhibition and treatment with immune checkpoint inhibitors.Atezolizumab plus cobimetinib and vemurafenib showed superior progression-free survival in metastatic melanoma compared to cobimetinib and vemurafenib alone. Triplet therapy might be an option in situations of urgent need for disease control, when oncologists choose BRAF/MEK inhibition over immune checkpoint inhibition as first line treatment. At this time results are not mature yet, and longer follow-up including overall survival data is needed. The future role of this combination will also be determined by a comparison with the combination of ipilimumab and nivolumab.
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