默克尔细胞癌放射治疗后默克尔细胞癌蛋白抗体的变化及其与复发的关系。
Changes in Merkel cell oncoprotein antibodies after radiation therapy in curatively treated Merkel cell carcinoma and association with recurrence.
发表日期:2024 Aug 05
作者:
Kevin X Liu, Kee-Young Shin, Manisha Thakuria, Jonathan D Schoenfeld, Roy B Tishler, Ann W Silk, Charles H Yoon, Elliott Fite, Danielle N Margalit
来源:
CANCER
摘要:
大约 50% 的默克尔细胞癌 (MCC) 患者可检测到默克尔癌蛋白 (AMERK) 血清抗体,可用于监测复发情况。本研究的目的是表征接受 MCC 治疗性放射治疗 (RT) 的患者的 AMERK 水平,并确定 AMERK 与复发之间的关联。这是一项针对 MCC 患者的回顾性研究,这些患者在接受治疗前进行了基线 AMERK 测量。 2010 年至 2020 年的意向 RT。使用 Kaplan-Meier 方法和 Cox 回归计算无事件生存期 (EFS)。通过死亡作为竞争风险和格雷检验来分析 MCC 相关复发 (CIMR) 的累积发生率。作者确定了 88 名进行基线 AMERK 测量的患者,其中 52 名 (59%) 具有可检测水平。 AMERK 阳性与较年轻的中位年龄(67.8 岁对比 72.0 岁;p = 0.02)和肿瘤部位(p = 0.02)相关,头颈部患病者的阳性率较低(17.3% 对比 44.4%) )。 EFS(71.3% vs. 60.4%;p = .30)和 CIMR(24.4% vs. 39.6%;p = .23)在 AMERK 阳性患者中更为有利。两名患者在放疗野出现复发,且基线时均为 AMERK 阴性。 RT 后达到 AMERK 最低点的中位时间为 11.2 个月;并且,在 RT 后 6 个月的标志性分析中,AMERK 阳性患者转为阴性或水平下降 ≥ 50% 的患者比例与 EFS 无关(87.1% 对比 85.0%;p = .90) 或 CIMR (12.9% vs. 15.0%; p = .62)。阳性 AMERK 基线水平与 MCC 诊断时的年轻年龄和非头颈肿瘤位置相关,可能与病毒病原学的分布有关。无法确定与 EFS 相关的特定 RT 后 AMERK 下降。© 2024 美国癌症协会。
Serum antibodies to the Merkel oncoprotein (AMERK) are detectable in approximately 50% of patients with Merkel cell carcinoma (MCC) and can be used to monitor for recurrence. The objective of this study was to characterize AMERK levels in patients receiving curative-intent radiation therapy (RT) for MCC and identify associations between AMERK and recurrence.This was a retrospective study of patients with MCC who had baseline AMERK measurements before they received curative-intent RT from 2010 to 2020. Event-free survival (EFS) was calculated using the Kaplan-Meier method and Cox regression. The cumulative incidence of MCC-related recurrence (CIMR) was analyzed with death as a competing risk and the Gray test.The authors identified 88 patients who had baseline AMERK measurements, including 52 (59%) with detectable levels. AMERK positivity was associated with younger median age (67.8 vs. 72.0 years; p = .02) and tumor site (p = 0.02), with lower rates for those who had disease in the head/neck region (17.3% vs. 44.4%). EFS (71.3% vs. 60.4%; p = .30) and CIMR (24.4% vs. 39.6%; p = .23) were more favorable in AMERK-positive patients. Two patients had recurrences in the RT field, and both were AMERK-negative at baseline. The median time to AMERK nadir after RT was 11.2 months; and, in a 6-month post-RT landmark analysis, the proportion of patients who were AMERK-positive who became negative or who had levels that decreased by ≥50% were not associated with EFS (87.1% vs. 85.0%; p = .90) or CIMR (12.9% vs. 15.0%; p = .62).Positive AMERK baseline levels were correlated with younger age at MCC diagnosis and nonhead and neck tumor location, possibly related to the distribution of viral etiology. A specific post-RT AMERK decline correlating with EFS could not be identified.© 2024 American Cancer Society.