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The Clinical Significance of Mutations in Metastatic Oral Mucosal Melanoma in China

Overview
Journal Oncotarget
Specialty Oncology
Date 2017 Nov 16
PMID 29137292
Citations 4
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Abstract

mutations are frequently detected in mucosal melanomas, but their clinical significance in metastatic oral mucosal melanomas (OMM) remains unclear. The main purpose of this study was to investigate the clinical and pathological features of metastatic OMMs with mutations and the efficiency of the tyrosine kinase inhibitor imatinib in treating metastatic OMMs. We found thatresidual primary lesion and neck lymph nodes could act as independent prognostic factors in metastatic OMM patients. mutations were detected in 22 out of 139 (15.8%) metastatic OMM patients. Under chemotherapy, the overall survival (OS) of mutant patients was significantly shorter than that of wild-type patients. The Ki67 expression was significantly higher in mutant patients than in wild-type patients. In distant metastatic OMM patients with mutations, the treatment with c-Kit inhibitor resulted in a better OS. In conclusion, residual primary lesion, cervical lymph nodes and mutations act as adverse prognostic factors of metastatic OMMs. The Kit inhibitor imatinib could benefit metastatic OMM patients with mutations.

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References
1.
Omholt K, Grafstrom E, Kanter-Lewensohn L, Hansson J, Ragnarsson-Olding B . KIT pathway alterations in mucosal melanomas of the vulva and other sites. Clin Cancer Res. 2011; 17(12):3933-42. DOI: 10.1158/1078-0432.CCR-10-2917. View

2.
Haiducu M, Hinek A, Astanehe A, Lee T, Kalia S . Extracutaneous melanoma epidemiology in British Columbia. Melanoma Res. 2014; 24(4):377-80. DOI: 10.1097/CMR.0000000000000075. View

3.
Keller D, Thomay A, Gaughan J, Olszanski A, Wu H, Berger A . Outcomes in patients with mucosal melanomas. J Surg Oncol. 2013; 108(8):516-20. DOI: 10.1002/jso.23445. View

4.
Woodman S, Davies M . Targeting KIT in melanoma: a paradigm of molecular medicine and targeted therapeutics. Biochem Pharmacol. 2010; 80(5):568-74. PMC: 3935736. DOI: 10.1016/j.bcp.2010.04.032. View

5.
Todd J, Scurr L, Becker T, Kefford R, Rizos H . The MAPK pathway functions as a redundant survival signal that reinforces the PI3K cascade in c-Kit mutant melanoma. Oncogene. 2012; 33(2):236-45. DOI: 10.1038/onc.2012.562. View