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Uveal melanoma prognostication: from lesion size and cell type to molecular class

Abstract Objective To review the evidence for molecular genetic testing of uveal melanoma in the context of prognostic indicators of metastasis and tumour-related mortality. Design Review of the literature and personal experiences of the authors. Methods We conducted a MEDLINE, Embase, and PubMed li...

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Published in:Canadian journal of ophthalmology 2012-06, Vol.47 (3), p.246-253
Main Authors: Gill, Harmeet S., MD, FRCSC, Char, Devron H., MD, FACS
Format: Article
Language:English
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Summary:Abstract Objective To review the evidence for molecular genetic testing of uveal melanoma in the context of prognostic indicators of metastasis and tumour-related mortality. Design Review of the literature and personal experiences of the authors. Methods We conducted a MEDLINE, Embase, and PubMed literature search (1980–2011) for English-language abstracts and full-text references regarding molecular genetic testing of uveal melanoma. Search terms included uveal , melanoma , cytogenetic , gene , and molecular . All studies in which patients with primary uveal melanoma underwent molecular genetic testing with survival data for disease-related metastasis and mortality were reviewed. Results From 176 identified articles, 40 were scientific studies of uveal melanomas that included histologic and molecular genetic analysis. Of those, 24 included survival data, correlation of molecular genetic features with other prognostic indicators, or both. Cytogenetic and microarray gene expression analysis allows uveal melanoma lesions to be classified as high risk or low risk for metastasis and disease-related mortality. Gene expression profiling supersedes clinical, histologic, and cytogenetic prognosticators. Conclusions Uveal melanoma comprises a heterogeneous group of malignancies based on its molecular biology. Molecular class by gene expression profiling has the most strongly predictive value for uveal melanoma metastasis and mortality.
ISSN:0008-4182
1715-3360
DOI:10.1016/j.jcjo.2012.03.038