Published online Oct 15, 2020. doi: 10.4251/wjgo.v12.i10.1080
Peer-review started: June 17, 2020
First decision: July 4, 2020
Revised: July 7, 2020
Accepted: September 22, 2020
Article in press: September 22, 2020
Published online: October 15, 2020
Processing time: 119 Days and 4.9 Hours
The treatment of metastatic colorectal cancer (mCRC) harboring BRAF V600 mutations is challenging. These tumors are often refractory to standard treatment. Therefore, the patients may exhibit rapid clinical deterioration, depriving them of the chance to receive salvage therapy. In newly diagnosed patients with good performance status, the administration of an intensive chemotherapy regimen like FOLFOXIRI (5-fluorouracil, leucovorin, oxaliplatin, and irinotecan) along with the antiangiogenic agent bevacizumab can modify this aggressive behavior of the disease and improve patient clinical outcomes. The recently published results of the BEACON (Binimetinib, Encorafenib, and Cetuximab Combined to Treat BRAF-Mutant Colorectal Cancer) study demonstrated that a combination therapy consisting of BRAF, epidermal growth factor receptor, and mitogen-activated protein kinase kinase inhibitors could be a useful second-or third-line alternative. This review summarizes the current treatment strategies for BRAF-mutant mCRC.
Core Tip: The treatment of BRAF-mutant metastatic colorectal cancer (mCRC) is particularly challenging. This review discusses the current treatment options for BRAF-mutant mCRC and the expanding role of targeted therapy in its management.