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Primary bilateral uveal melanoma: a population‐based study and systematic review
Author(s) -
Scott Jeffrey F,
Vyas Ritva,
Galvin Jessica,
Gotow Erica,
Fiessinger Lori,
Gerstenblith Adam T,
Gerstenblith Meg R
Publication year - 2018
Publication title -
clinical and experimental ophthalmology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.3
H-Index - 74
eISSN - 1442-9071
pISSN - 1442-6404
DOI - 10.1111/ceo.13129
Subject(s) - medicine , epidemiology , demographics , disease , melanoma , population , retrospective cohort study , rare disease , surgery , database , demography , environmental health , cancer research , sociology , computer science
Importance Primary bilateral uveal melanoma (UM) is a rare and incompletely described entity. It is not known how these patients compare to those with unilateral UM. Background We sought to comprehensively characterize and compare patients with primary bilateral and unilateral UM. Design Retrospective, population‐based and systematic review. Participants Patients with bilateral ( n = 52) and unilateral UM ( n = 8915). Methods We analysed cases of primary bilateral UM from three data sources: (i) the University Hospitals Cleveland Medical Center pathology database from 1996 to 2016 ( n = 1); (ii) the Surveillance, Epidemiology and End‐Results (SEER)‐18 database from 1973 to 2013 ( n = 5) and (iii) a systematic review of the English language literature ( n = 46). Cases of unilateral UM were obtained from the SEER‐18 database from 1973 to 2013 for comparison ( n = 8915). Main Outcome Measures Demographics, clinicopathological characteristics, treatments and survival. Results There were no differences in sex, race, mean age at diagnosis, site of uveal involvement, metastases at diagnosis, or treatment among patients with bilateral as compared to unilateral UM. Additionally, there were no clinicopathological differences between the two UMs in each patient with bilateral disease. Overall survival did not differ between unilateral and bilateral UM patients, or between bilateral UM patients who presented with, or subsequently developed, bilateral disease. Conclusions and Relevance Bilateral and unilateral UM patients share similar demographics, clinicopathological characteristics, treatments and prognoses. Moreover, the development of bilateral disease does not portend a poorer prognosis and patients should be treated similarly to those with unilateral disease.