Department of Pathology, University of Virginia, Charlottesville, VA.
Department of Epidemiology, University of Washington, Seattle, WA.
Am J Surg Pathol. 2024 Oct 1;48(10):1270-1276. doi: 10.1097/PAS.0000000000002288. Epub 2024 Jul 12.
Merkel cell carcinoma (MCC) is a rare and aggressive neuroendocrine tumor of the skin. Risk factors include extensive sun damage, infection with Merkel cell polyomavirus, and an immunocompromised state. PRAME, also known as preferentially expressed antigen in melanoma, is a cancer-testis antigen recently found to be a useful diagnostic tool in the workup of melanocytic neoplasms. However, the expression pattern of PRAME in Merkel cell carcinoma is unknown. In this study, we examine PRAME expression in Merkel cell carcinoma and explore its prognostic implications. The institutional archives at the University of Virginia were used to search for tumors classified as Merkel cell carcinoma from 2004 to 2022. All potential cases were reviewed to confirm the diagnosis, and electronic medical records were searched for clinical and demographic data. Tumors were subsequently immunostained for PRAME and Merkel cell polyomavirus. Cox proportional hazards regression models were used to estimate relative (all-cause) survival of PRAME positivity and MCPyV positivity in our study as well as MCC-specific survival of PRAME positivity. Univariate and multivariable models were created for each outcome related to all-cause survival. A total of 39 cases were included in the study. Twenty-eight percent (11 cases) demonstrated strong PRAME expression, and 27% of cases were positive for Merkel cell polyomavirus. There was no statistically significant correlation between PRAME expression and virus positivity. With respect to PRAME, the adjusted all-cause mortality hazard ratio was 11.4 (95% CI: 1.8, 70.8). The unadjusted MCC-specific hazard ratio was 4.6 (95% CI: 0.8, 27.5). The adjusted hazard ratio pertaining to Merkel cell polyomavirus infection was 0.25 (95% CI: 0.02, 2.96). In this limited cohort, PRAME expression appears to correlate with worse outcomes in Merkel cell carcinoma.
默克尔细胞癌(Merkel cell carcinoma,MCC)是一种罕见且侵袭性的皮肤神经内分泌肿瘤。危险因素包括广泛的太阳损伤、感染 Merkel 细胞多瘤病毒以及免疫功能低下状态。PRAME,也称为黑色素瘤中优先表达的抗原,是一种最近在黑色素细胞肿瘤的检查中被发现是有用的诊断工具的癌-睾丸抗原。然而,PRAME 在默克尔细胞癌中的表达模式尚不清楚。在这项研究中,我们研究了 PRAME 在默克尔细胞癌中的表达,并探讨了其预后意义。弗吉尼亚大学的机构档案被用于搜索 2004 年至 2022 年分类为默克尔细胞癌的肿瘤。所有潜在病例均经审查以确认诊断,并搜索电子病历以获取临床和人口统计学数据。随后对肿瘤进行 PRAME 和 Merkel 细胞多瘤病毒免疫染色。Cox 比例风险回归模型用于估计我们研究中 PRAME 阳性和 MCPyV 阳性的相对(全因)生存率以及 PRAME 阳性的 MCC 特异性生存率。为每个与全因生存率相关的结果创建了单变量和多变量模型。研究共纳入 39 例病例。28%(11 例)表现出强烈的 PRAME 表达,27%的病例 Merkel 细胞多瘤病毒阳性。PRAME 表达与病毒阳性之间没有统计学上的显著相关性。就 PRAME 而言,全因死亡率的调整后危险比为 11.4(95%CI:1.8,70.8)。未经调整的 MCC 特异性危险比为 4.6(95%CI:0.8,27.5)。Merkel 细胞多瘤病毒感染的调整后危险比为 0.25(95%CI:0.02,2.96)。在这个有限的队列中,PRAME 表达似乎与默克尔细胞癌的不良预后相关。