西妥昔单抗
医学
结直肠癌
肿瘤科
内科学
养生
V600E型
临床试验
MEK抑制剂
癌症研究
MAPK/ERK通路
癌症
激酶
突变体
基因
细胞生物学
化学
生物
生物化学
作者
Faisal Shahjehan,Saivaishnavi Kamatham,Chandrikha Chandrasekharan,Pashtoon Murtaza Kasi
出处
期刊:Drugs of Today
[Prous Science]
日期:2019-11-01
卷期号:55 (11): 683-683
被引量:10
标识
DOI:10.1358/dot.2019.55.11.3035584
摘要
BRAF V600E mutations are associated with 8-10% of metastatic colorectal cancers (mCRC) and carry a poor prognosis with limited therapeutic options. In contrast to metastatic melanoma, BRAF inhibition alone or in combination with mitogen-activated protein kinase kinase (MEK) inhibitors has shown little utility in the treatment of BRAF V600E-mutant mCRC. This is secondary to upstream activation of the epidermal growth factor receptor (EGFR) pathway and other escape mechanisms. Combining RAF and MEK inhibitors with inhibition of the EGFR pathway through an anti-EGFR receptor antibody (cetuximab) led to the BEACON clinical trial (binimetinib, encorafenib and cetuximab). Trial patients had undergone at least one prior line of chemotherapy. The trial met all its endpoints and is now included in NCCN (National Comprehensive Cancer Network) guidelines. Herein we provide updates in treatment options for patients with BRAF V600E-mutant mCRC, focusing on the practice-changing BEACON-triplet regimen, the first chemotherapy-free combination regimen for mCRC. This combination is being explored frontline in the ANCHOR clinical trial.
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