Nisanova Arina, Park Susanna S, Amin Aana, Zako Carly, Wilson Machelle D, Scholey Jessica, Afshar Armin R, Tsai Tony, Char Devron H, Mishra Kavita K
Department of Radiation Oncology, University of California San Francisco, San Francisco, California.
Department of Ophthalmology and Vision Science, University of California Davis, Sacramento, California.
Ophthalmol Sci. 2024 Dec 24;5(4):100687. doi: 10.1016/j.xops.2024.100687. eCollection 2025 Jul-Aug.
To identify risk factors associated with uveal melanoma (UM) in adolescents and young adults (AYAs).
A retrospective case-control study.
Two hundred forty-seven UM patients aged 13 to 45 treated with proton beam radiation therapy and 401 age- and sex-matched controls at a tertiary academic center.
We obtained demographic and genetic data, environmental exposures, and social, medical, and ocular history via retrospective chart review and phone follow-up.
The main outcome measures included the prevalence and odds ratios (ORs) of the investigated risk factors in UM patients compared with controls.
The median age of UM diagnosis was 38 years (range: 13-45 years); the median follow-up was 102 months (range: 3-329 months). Identified novel risk factors for UM included family history of cutaneous melanoma (OR = 3.06, = 0.002), Ashkenazi Jewish ancestry (2.98, = 0.02), prior eye trauma (2.94, = 0.01), secondhand cigarette smoke exposure (2.39, < 0.001), and previous head and neck surgery (1.81, = 0.007). Some known risk factors identified include choroidal nevi (11.39, < 0.001), light eye color (4.69, < 0.001), White race (4.63, < 0.001), outdoor sunlight exposure (4.20, < 0.001), recent pregnancy (4.0, = 0.002), occupational (2.39, = 0.003) and toxic chemical (2.27, = 0.03) exposures, family history of any cancer (2.16, < 0.001), lack of ultraviolet-blocking eyewear use (2.13, = 0.01), indoor tanning (2.10, = 0.03), and propensity to sunburn (1.89, < 0.05). The prevalence of oculodermal melanocytosis ( = 0.03) and family history of UM ( < 0.001) were significantly greater in UM patients than in controls. Uveal melanoma T-categories were as follows: 39% T1, 37% T2, 19% T3, and 5% T4. Gene expression profiling was available in 64 patients and showed 59% class 1A, 19% class 1B, and 22% class 2 tumors. Thirteen patients underwent genetic screening; identified germline mutations included and The estimated 10-year metastasis-free progression rate and overall survival were 80% and 81%, respectively.
This study identified several novel risk factors for UM in AYAs and confirmed select established risk factors seen in UM patients of all ages. To the best of our knowledge, this is the first explicit and comprehensive investigation of risk factors among a younger cohort and may help further elucidate UM pathogenesis.
Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
确定青少年及青年(AYA)葡萄膜黑色素瘤(UM)的相关危险因素。
一项回顾性病例对照研究。
在一家三级学术中心接受质子束放射治疗的247例年龄在13至45岁的UM患者以及401例年龄和性别匹配的对照者。
通过回顾性病历审查和电话随访获取人口统计学和基因数据、环境暴露情况以及社会、医疗和眼部病史。
主要观察指标包括UM患者与对照者中所调查危险因素的患病率和比值比(OR)。
UM诊断的中位年龄为38岁(范围:13 - 45岁);中位随访时间为102个月(范围:3 - 329个月)。确定的UM新危险因素包括皮肤黑色素瘤家族史(OR = 3.06,P = 0.002)、阿什肯纳兹犹太裔血统(2.98,P = 0.02)、既往眼外伤(2.94,P = 0.01)、二手烟暴露(2.39,P < 0.001)以及既往头颈部手术(1.81,P = 0.007)。确定的一些已知危险因素包括脉络膜痣(11.39,P < 0.001)、浅色眼睛(4.69,P < 0.001)、白种人(4.63,P < 0.001)、户外阳光暴露(4.20,P < 0.001)、近期妊娠(4.0,P = 0.002)、职业(2.39,P = 0.003)和有毒化学物质(2.27,P = 0.03)暴露、任何癌症家族史(2.16,P < 0.001)、缺乏使用防紫外线眼镜(2.13,P = 0.01)、室内晒黑(2.10,P = 0.03)以及易晒伤(1.89,P < 0.05)。UM患者中眼皮肤黑素细胞增多症(P = 0.03)和UM家族史(P < 0.001)的患病率显著高于对照者。葡萄膜黑色素瘤T分类如下:39%为T1,37%为T2,19%为T3,5%为T4。64例患者有基因表达谱分析结果,显示59%为1A类,19%为1B类,22%为2类肿瘤。13例患者接受了基因筛查;鉴定出的种系突变包括 和 估计的10年无转移进展率和总生存率分别为80%和81%。
本研究确定了AYA中UM的几个新危险因素,并证实了在各年龄段UM患者中观察到的部分既定危险因素。据我们所知,这是首次对较年轻队列中的危险因素进行明确且全面的调查,可能有助于进一步阐明UM的发病机制。
专有或商业披露信息可在本文末尾的脚注和披露部分中找到。