Uveal melanoma: epidemiology, etiology, and treatment of primary disease
Benjamin A Krantz,1 Nikita Dave,2 Kimberly M Komatsubara,2 Brian P Marr,3,4 Richard D Carvajal5 1Division of Hospital Medicine, 2Division of Hematology/Oncology, Columbia University Medical Center, 3Ophthalmic Oncology Service, Memorial Sloan Kettering Cancer Center, 4Department of Ophthalmology, W...
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doaj-d477b246766a4bcdab97755a872512382020-11-24T22:14:45ZengDove Medical PressClinical Ophthalmology1177-54832017-01-01Volume 1127928931067Uveal melanoma: epidemiology, etiology, and treatment of primary diseaseKrantz BADave NKomatsubara KMMarr BPCarvajal RDBenjamin A Krantz,1 Nikita Dave,2 Kimberly M Komatsubara,2 Brian P Marr,3,4 Richard D Carvajal5 1Division of Hospital Medicine, 2Division of Hematology/Oncology, Columbia University Medical Center, 3Ophthalmic Oncology Service, Memorial Sloan Kettering Cancer Center, 4Department of Ophthalmology, Weill Cornell Medical College, 5Division of Hematology/Oncology, Columbia University Medical Center, New York, NY, USA Abstract: Uveal melanoma (UM) is the most common intraocular malignancy and arises from melanocytes in the iris, ciliary body, or choroid. Early diagnosis and local treatment is crucial, as survival correlates with primary tumor size. However, approximately 50% of patients will develop metastatic disease with 6–12 months’ survival from metastatic diagnosis. Genomic analyses have led to the development of gene-expression profiles that effectively predict metastatic progression; unfortunately, no adjuvant therapy has been shown to prolong survival to date. New insights into the molecular biology of UM have found frequent activating mutations in genes encoding for the G-protein α-subunit, GNAQ and GNA11, and improved understanding of the downstream signaling pathways MAPK, PI3K/Akt, and Hippo have afforded an array of new targets for treatment of this disease. Studies are under way with rationally developed regimens targeting these pathways, and novel agents are under development. We review the diagnosis, management, and surveillance of primary UM and the adjuvant therapy trials under way. Keywords: uveal melanoma, ocular melanoma, GNAQ, GNA11, MAP kinase, MEKhttps://www.dovepress.com/uveal-melanoma-epidemiology-etiology-and-treatment-of-primary-disease-peer-reviewed-article-OPTHUveal MelanomaOcular MelanomaGNAQGNA11MAP KinaseMEK |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Krantz BA Dave N Komatsubara KM Marr BP Carvajal RD |
spellingShingle |
Krantz BA Dave N Komatsubara KM Marr BP Carvajal RD Uveal melanoma: epidemiology, etiology, and treatment of primary disease Clinical Ophthalmology Uveal Melanoma Ocular Melanoma GNAQ GNA11 MAP Kinase MEK |
author_facet |
Krantz BA Dave N Komatsubara KM Marr BP Carvajal RD |
author_sort |
Krantz BA |
title |
Uveal melanoma: epidemiology, etiology, and treatment of primary disease |
title_short |
Uveal melanoma: epidemiology, etiology, and treatment of primary disease |
title_full |
Uveal melanoma: epidemiology, etiology, and treatment of primary disease |
title_fullStr |
Uveal melanoma: epidemiology, etiology, and treatment of primary disease |
title_full_unstemmed |
Uveal melanoma: epidemiology, etiology, and treatment of primary disease |
title_sort |
uveal melanoma: epidemiology, etiology, and treatment of primary disease |
publisher |
Dove Medical Press |
series |
Clinical Ophthalmology |
issn |
1177-5483 |
publishDate |
2017-01-01 |
description |
Benjamin A Krantz,1 Nikita Dave,2 Kimberly M Komatsubara,2 Brian P Marr,3,4 Richard D Carvajal5 1Division of Hospital Medicine, 2Division of Hematology/Oncology, Columbia University Medical Center, 3Ophthalmic Oncology Service, Memorial Sloan Kettering Cancer Center, 4Department of Ophthalmology, Weill Cornell Medical College, 5Division of Hematology/Oncology, Columbia University Medical Center, New York, NY, USA Abstract: Uveal melanoma (UM) is the most common intraocular malignancy and arises from melanocytes in the iris, ciliary body, or choroid. Early diagnosis and local treatment is crucial, as survival correlates with primary tumor size. However, approximately 50% of patients will develop metastatic disease with 6–12 months’ survival from metastatic diagnosis. Genomic analyses have led to the development of gene-expression profiles that effectively predict metastatic progression; unfortunately, no adjuvant therapy has been shown to prolong survival to date. New insights into the molecular biology of UM have found frequent activating mutations in genes encoding for the G-protein α-subunit, GNAQ and GNA11, and improved understanding of the downstream signaling pathways MAPK, PI3K/Akt, and Hippo have afforded an array of new targets for treatment of this disease. Studies are under way with rationally developed regimens targeting these pathways, and novel agents are under development. We review the diagnosis, management, and surveillance of primary UM and the adjuvant therapy trials under way. Keywords: uveal melanoma, ocular melanoma, GNAQ, GNA11, MAP kinase, MEK |
topic |
Uveal Melanoma Ocular Melanoma GNAQ GNA11 MAP Kinase MEK |
url |
https://www.dovepress.com/uveal-melanoma-epidemiology-etiology-and-treatment-of-primary-disease-peer-reviewed-article-OPTH |
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