曲美替尼
威罗菲尼
医学
黑色素瘤
达布拉芬尼
MEK抑制剂
转移性黑色素瘤
肿瘤科
癌症研究
临床试验
内科学
MAPK/ERK通路
激酶
生物
细胞生物学
作者
Judy W. King,Paul Nathan
出处
期刊:Future Oncology
[Future Medicine]
日期:2014-07-01
卷期号:10 (9): 1559-1570
被引量:18
摘要
Approximately 50% of patients with cutaneous metastatic melanoma harbor a somatic BRAF mutation. BRAF inhibitors are now established in the treatment paradigm of BRAF mutant melanoma, following the approval of vemurafenib by the US FDA in 2011. The vast majority of patients obtain some degree of tumor shrinkage with oral BRAF inhibitors, and responses are often rapid. However, resistance inevitably develops, with a median progression-free survival of 5–7 months. The oral MEK inhibitor trametinib has also shown activity in BRAF mutant melanoma in Phase III trials. We review the rationale for treating BRAF mutant melanoma with trametinib, as single-agent therapy and in combination with BRAF inhibitors, as well as the clinical data to date.
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