Conjunctival Melanoma: A Clinical Review and Update

被引:2
|
作者
Butt, Karam [1 ]
Hussain, Rumana [2 ,3 ]
Coupland, Sarah E. [1 ,3 ]
Krishna, Yamini [1 ,3 ]
机构
[1] Liverpool Univ Hosp NHS Fdn Trust, Natl Specialist Ophthalm Pathol Serv, Liverpool Clin Labs, Liverpool L7 8YE, England
[2] Liverpool Univ Hosp NHS Fdn Trust, St Pauls Eye Unit, Liverpool L7 8YE, England
[3] Univ Liverpool, Inst Life Course & Med Sci, Dept Eye & Vis Sci, Liverpool L7 8TX, England
关键词
conjunctival melanocytic intraepithelial lesions; C-MIL; conjunctival melanoma; ocular oncology; targeted therapy; immunotherapy; PRIMARY ACQUIRED MELANOSIS; MELANOCYTIC INTRAEPITHELIAL LESIONS; AMERICAN JOINT COMMITTEE; SQUAMOUS-CELL CARCINOMA; MALIGNANT-MELANOMA; BRAF MUTATIONS; COPY NUMBER; NRAS MUTATIONS; GENE MUTATION; HARBOR BRAF;
D O I
10.3390/cancers16183121
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Conjunctival melanoma (Co-M) is a rare and aggressive eye surface cancer. It is often misdiagnosed or overlooked, leading to late diagnosis. Co-M can cause sight loss and even eye loss, impacting quality-of-life. The numbers of new cases globally are rising at alarming rates. There is no standard treatment for Co-M and management varies between eye cancer centres. In similar to 25% of cases the cancer spreads elsewhere in the body, which can lead to death. The aim of this review is to concisely present what is currently known about Co-M presentation, its development and progression, clinical management and outcomes, and finally summarise future directions for research into novel therapies. Conjunctival melanoma (Co-M) is an aggressive, invasive eye and eyelid cancer. Its global incidence of similar to 1 in a million is increasing at a rate ratio of similar to 1.4, but this rises sharply in over 65-year-olds. Although rare, Co-M has a devastating impact on the lives of those who develop it. Co-M is often misdiagnosed or overlooked, leading to vision loss either from the destructive effects of the tumour or side effects of therapy, facial disfigurement from radical surgery, and death from metastases. Due to its rarity, there is limited evidence for diagnosis and management; hence, there is no standardised treatment and not all cases are referred to a specialised ocular oncology centre. Recent progress in cancer immunology and genetics have revolutionised the treatment of cutaneous melanomas, which share some similarities to Co-M. Importantly, a better understanding of Co-M and its precursor lesions is urgently needed to lead to the development of novel targeted and immunotherapies both for local tumour control and disseminated disease. This review aims to provide a comprehensive clinical overview of the current knowledge regarding Co-M, its epidemiology, pathogenesis, presentation, diagnosis and recent changes in the classification of its precursor lesions, management, and recent advances in novel biological therapies for personalised treatment of this disease.
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页数:17
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