Non-BRAF targeted therapies for melanoma: protein kinase inhibitors in Phase II clinical trials

被引:2
作者
Bhatia, Shilpa [1 ]
Emdad, Luni [1 ,2 ,3 ]
Das, Swadesh K. [1 ,2 ]
Hamed, Hossein [4 ]
Dent, Paul [2 ,3 ,4 ,5 ]
Sarkar, Devanand [1 ,2 ,3 ]
Fisher, Paul B. [1 ,2 ,3 ]
机构
[1] Virginia Commonwealth Univ, Sch Med, Dept Human & Mol Genet, Richmond, VA 23284 USA
[2] Virginia Commonwealth Univ, VCU Inst Mol Med, Sch Med, Richmond, VA 23284 USA
[3] Virginia Commonwealth Univ, Sch Med, VCU Massey Canc Ctr, Richmond, VA 23284 USA
[4] Virginia Commonwealth Univ, Sch Med, Dept Neurosurg, Richmond, VA 23284 USA
[5] Virginia Commonwealth Univ, Sch Med, Dept Biochem & Mol Biol, Richmond, VA 23284 USA
基金
美国国家卫生研究院;
关键词
clinical trials; melanoma; non-BRAF mutations; protein kinase inhibitors; targeted therapies; ENDOTHELIAL GROWTH-FACTOR; OPEN-LABEL; PROMOTE ANGIOGENESIS; METASTATIC MELANOMA; SELECTIVE INHIBITOR; TUMOR-SUPPRESSOR; MAPK PATHWAY; MUTATIONS; EXPRESSION; KIT;
D O I
10.1517/13543784.2014.884558
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Melanoma is one of the most aggressive forms of cutaneous malignancies displaying a substantial mortality rate among the various forms of skin cancers. The management of patients with advanced melanoma poses a significant challenge considering that the disease is refractory to most conventional therapies. Areas covered: This review highlights some of the genes and signaling molecules that are mutated in melanoma patients. The authors also discuss protein kinase inhibitors targeting non-BRAF mutations that are now being evaluated in Phase II clinical trials. Expert opinion: In light of several preclinical and clinical studies, it is clear that targeting single-gene mutations may not provide a desired therapeutic gain in the context of melanoma. Consequently, research will need to focus on rational combinations of novel therapeutic agents targeting multiple genetic aberrations or deregulated pathways to achieve a desired maximum clinical benefit. There is certainly a need for a better understanding of the complex and redundant molecular signatures associated with melanoma development; this would open up new avenues for creating the next generation of targeted and effective therapeutics.
引用
收藏
页码:489 / 500
页数:12
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