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Authors Luo C, Shen JY, Ying J, Fang XH, Wang XH, Fu ZX, Liu P
Received 14 July 2017
Accepted for publication 26 August 2017
Published 14 September 2017 Volume 2017:10 Pages 4553—4557
DOI https://doi.org/10.2147/OTT.S146409
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Amy Norman
Peer reviewer comments 2
Editor who approved publication: Dr Yao Dai
Abstract: Malignant melanoma is one kind of malignant disease which has high rates
of mortality, metastasis, and poor prognosis. The therapeutic landscape is
rapidly changing with the development of novel agents in recent decades, such
as anti-PD-1 agents, anti-CTLA-4 agents, and BRAF inhibitors. However, since
most of these novel agents are very expensive, not all patients can afford
them. Apatinib is a novel oral small-molecule tyrosine kinase inhibitor
targeting the intracellular domain of vascular endothelial growth factor
receptor 2 (VEGFR-2) and may also be effective on Ret, c-KIT, and c-src.
Temozolomide (TMZ) is a second-generation alkylating agent and a cytotoxic drug
for melanoma treatment. In this work, we reported a case of metastatic melanoma
with an excellent response to apatinib/TMZ combination therapy with
progression-free survival for more than one year. This patient showed high
expression of CD117, VEGFR-3, and KIT mutation
in exon 11, suggesting that apatinib may induce clinical response via inhibiting
VEGFR and c-KIT. Apatinib/TMZ combination therapy could be a new option for the
treatment of advanced melanoma with KIT mutation.
Keywords: advanced
melanoma, KIT mutation, apatinib,
temozolomide, combination therapy