Miller David M, Shalhout Sophia Z, Wright Kayla M, Miller Matt A, Kaufman Howard L, Emerick Kevin S, Reeder Harrison T, Silk Ann W, Thakuria Manisha
Department of Medicine, Division of Hematology/Oncology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Department of Dermatology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Cancer. 2024 Aug 1;130(15):2670-2682. doi: 10.1002/cncr.35314. Epub 2024 May 2.
Merkel cell carcinoma (MCC) is an aggressive cancer with often poor outcomes. Limited biomarkers exist for predicting clinical outcomes. The Merkel cell polyomavirus (MCPyV) serum antibody test (AMERK) has shown potential for indicating better recurrence-free survival in a single-institution study. The study aimed to evaluate the link between initial AMERK serostatus and survival. Secondary objectives included examining the relationship between initial AMERK titer levels and tumor burden.
A retrospective cohort study across two institutions analyzed patients tested with AMERK within 90 days of MCC diagnosis. Regression models assessed the association of survival outcomes with serostatus, considering various factors. The relationship between AMERK titer and tumor burden indicators was evaluated using ANOVA. Significance testing was exploratory, without a fixed significance level.
Of 261 MCC patients tested, 49.4% were initially seropositive (titer ≥75). Multivariable analysis showed that seropositivity improved recurrence, event-free, overall, and MCC-specific survival rates. Strong associations were found between initial AMERK titer and clinical, tumor, and nodal stages, tumor size, and disease extent. Notably, improved survival with seropositivity was observed only in patients with localized disease at initial presentation.
Circulating antibodies to MCPyV oncoproteins, as indicated by the AMERK test, are linked with better survival in MCC patients with localized disease at presentation. This could enhance patient risk profiling and treatment personalization. The study's retrospective nature and exploratory analysis are key limitations.
Merkel cell carcinoma (MCC) is a potentially aggressive skin cancer, and tools to predict patient outcomes are limited. A blood test called anti-Merkel cell panel (AMERK), which checks for specific antibodies related to this cancer, might give us some clues. In this study, we looked at 261 MCC patients who took the AMERK test within 90 days of diagnosis. We found that patients with an initial positive AMERK result tended to have better outcomes, especially if their cancer was in the early stages. However, it is important to note that this study has limitations, including using retrospective data and exploratory analyses.
默克尔细胞癌(MCC)是一种侵袭性癌症,预后往往较差。用于预测临床结果的生物标志物有限。默克尔细胞多瘤病毒(MCPyV)血清抗体检测(AMERK)在一项单机构研究中显示出提示更好无复发生存率的潜力。该研究旨在评估初始AMERK血清状态与生存之间的联系。次要目标包括检查初始AMERK滴度水平与肿瘤负荷之间的关系。
一项跨两个机构的回顾性队列研究分析了在MCC诊断后90天内接受AMERK检测的患者。回归模型评估了生存结果与血清状态的关联,同时考虑了各种因素。使用方差分析评估AMERK滴度与肿瘤负荷指标之间的关系。显著性检验是探索性的,没有固定的显著性水平。
在261例接受检测的MCC患者中,49.4%最初血清呈阳性(滴度≥75)。多变量分析表明,血清阳性改善了复发、无事件、总体和MCC特异性生存率。在初始AMERK滴度与临床、肿瘤和淋巴结分期、肿瘤大小及疾病范围之间发现了强关联。值得注意的是,仅在初始表现为局限性疾病的患者中观察到血清阳性与生存率提高有关。
如AMERK检测所示,针对MCPyV癌蛋白的循环抗体与初诊时为局限性疾病的MCC患者更好的生存率相关。这可能会加强患者风险评估和治疗个性化。该研究的回顾性性质和探索性分析是关键局限性。
默克尔细胞癌(MCC)是一种潜在侵袭性皮肤癌,预测患者预后的工具有限。一种名为抗默克尔细胞检测板(AMERK)的血液检测,用于检查与这种癌症相关的特定抗体,可能会给我们一些线索。在这项研究中,我们观察了261例在诊断后90天内接受AMERK检测的MCC患者。我们发现,初始AMERK结果为阳性的患者往往预后更好,尤其是如果他们的癌症处于早期阶段。然而,需要注意的是,这项研究存在局限性,包括使用回顾性数据和探索性分析。