Significance of BRAF Kinase Inhibitors for Melanoma Treatment: From Bench to Bedside.
Taku FujimuraYasuhiro FujisawaYumi KambayashiSetsuya AibaPublished in: Cancers (2019)
According to clinical trials, BRAF kinase inhibitors in combination with MEK kinase inhibitors are among the most promising chemotherapy regimens for the treatment of advanced BRAF-mutant melanoma, though the rate of BRAF mutation gene-bearing cutaneous melanoma is limited, especially in the Asian population. In addition, drug resistance sometimes abrogates the persistent efficacy of combined therapy with BRAF and MEK inhibitors. Therefore, recent pre-clinical study-based clinical trials have attempted to identify optimal drugs (e.g., immune checkpoint inhibitors or histone deacetylase (HDAC) inhibitors) that improve the anti-melanoma effects of BRAF and MEK inhibitors. In addition, the development of novel protocols to avoid resistance of BRAF inhibitors is another purpose of recent pre-clinical and early clinical trials. This review focuses on pre-clinical studies and early to phase III clinical trials to discuss the development of combined therapy based on BRAF inhibitors for BRAF-mutant advanced melanoma, as well as mechanisms of resistance to BRAF inhibitors.
Keyphrases
- clinical trial
- wild type
- metastatic colorectal cancer
- phase iii
- histone deacetylase
- open label
- phase ii
- randomized controlled trial
- skin cancer
- gene expression
- double blind
- stem cells
- squamous cell carcinoma
- mesenchymal stem cells
- genome wide
- signaling pathway
- bone marrow
- basal cell carcinoma
- placebo controlled
- genome wide identification