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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Main Authors: Krantz BA, Dave N, Komatsubara KM, Marr BP, Carvajal RD
Format: Article
Language:English
Published: Dove Medical Press 2017-01-01
Series:Clinical Ophthalmology
Subjects:
MEK
Online Access:https://www.dovepress.com/uveal-melanoma-epidemiology-etiology-and-treatment-of-primary-disease-peer-reviewed-article-OPTH
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spelling 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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