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A clinicopathological review of 33 patients with vulvar melanoma identifies c-KIT as a prognostic marker
JournalItem (Reviews, Editorials, Rezensionen, Urteilsanmerkungen etc. in einer wissenschaftlichen Zeitschrift)
 
ID 4390831
Author(s) Heinzelmann-Schwarz, Viola A.; Nixdorf, Sheri; Valadan, Mehrnaz; Diczbalis, Monica; Olivier, Jake; Otton, Geoff; Fedier, André; Hacker, Neville F.; Scurry, James P.
Author(s) at UniBasel Heinzelmann, Viola
Year 2014
Title A clinicopathological review of 33 patients with vulvar melanoma identifies c-KIT as a prognostic marker
Journal International journal of molecular medicine
Volume 33
Number 4
Pages 784-794
Keywords Adult; Aged; Aged, 80 and over; Biomarkers, Tumor/metabolism; Cell Proliferation; Cohort Studies; Female; Humans; Immunohistochemistry; Kaplan-Meier Estimate; Melanocytes/metabolism/pathology; Melanoma/immunology/*metabolism/*pathology; Middle Aged; Molecular Targeted Therapy; Multivariate Analysis; Prognosis; Proto-Oncogene Proteins c-kit/*metabolism; Risk Factors; Treatment Outcome; Vulvar Neoplasms/immunology/*metabolism/*pathology
Abstract Vulvar melanoma is the second most common vulvar cancer. Patients with vulvar melanoma usually present with the disease at a late stage and have a poor prognosis. The prognostic predictors reported in the literature are not unequivocal and the role of lichen sclerosus and c-KIT mutations in the aetiology of vulvar melanoma is unclear. Breslow staging currently seems to be the most adequate predictor of prognosis. We thus performed a clinicopathological and literature review to identify suitable predictors of prognosis and survival and investigated the expression of c-KIT (by immunohistochemistry) in patients with vulvar melanoma (n=33) from the Gynaecological Cancer Centres of the Royal Hospital for Women (Sydney, Australia) and John Hunter Hospital (Newcastle, Australia). Our series of 33 patients fitted the expected clinical profile of older women: delayed presentation, high stage, limited response to treatment and poor prognosis. We identified 3 patients (9.1%) with lichen sclerosus associated with melanoma in situ, although no lichen sclerosus was found in the areas of invasive melanoma. No patient had vulvar nevi. We identified a) Breslow's depth, b) an absence of any of the pathological risk factors, such as satellitosis, in-transit metastasis, lymphovascular space invasion (LVSI) and dermal mitosis, c) removal of inguino-femoral lymph nodes, d) lateral margin of <1 cm, and e) c-KIT expression as valuable prognostic predictors for disease-free survival. We conclude that c-KIT expression is, apart from Breslow's depth, another valuable predictor of prognosis and survival. Lichen sclerosus may be associated with vulvar melanoma.
Publisher D.A. Spandidos
ISSN/ISBN 1107-3756 ; 1791-244X
URL https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3976128
edoc-URL https://edoc.unibas.ch/61863/
Full Text on edoc No
Digital Object Identifier DOI 10.3892/ijmm.2014.1659
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/24535703
ISI-Number WOS:000334313000005
Document type (ISI) Article
 
   

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