Changes in Merkel cell oncoprotein antibodies after radiation therapy in curatively treated Merkel cell carcinoma and association with recurrence

被引:0
作者
Liu, Kevin X. [1 ]
Shin, Kee-Young [2 ]
Thakuria, Manisha [3 ,4 ]
Schoenfeld, Jonathan D. [1 ,3 ]
Tishler, Roy B. [1 ,3 ]
Silk, Ann W. [3 ,5 ]
Yoon, Charles H. [3 ,6 ]
Fite, Elliott [1 ]
Margalit, Danielle N. [1 ,3 ]
机构
[1] Brigham & Womens Hosp, Dana Farber Canc Inst, Dept Radiat Oncol, 450 Brookline Ave, Boston, MA 02215 USA
[2] Dana Farber Canc Inst, Dept Data Sci, Boston, MA USA
[3] Dana Farber Brigham & Womens Canc Ctr, Merkel Cell Carcinoma Ctr Excellence, Boston, MA USA
[4] Brigham & Womens Hosp, Dept Dermatol, Boston, MA 02215 USA
[5] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA USA
[6] Dana Farber Brigham & Womens Canc Ctr, Dept Surg, Div Surg Oncol, Boston, MA USA
基金
美国国家卫生研究院;
关键词
antibody; Merkel cell carcinoma (MCC); Merkel cell oncoprotein antibodies (AMERK); radiation therapy; recurrence; OUTCOMES; TUMOR; POLYOMAVIRUS; RADIOTHERAPY; SURVIVAL;
D O I
10.1002/cncr.35507
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundSerum 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.MethodsThis 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.ResultsThe 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).ConclusionsPositive 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. Merkel cell oncoprotein antibodies (AMERK) positivity was correlated with other known features of Merkel cell polyomavirus-associated Merkel cell carcinoma, including nonhead and neck site, younger age, and more favorable cancer outcomes. Among patients who had AMERK-positive disease, male sex was associated with recurrence, but no specific decrease in AMERK levels after radiation therapy was associated with event-free survival.
引用
收藏
页码:4267 / 4275
页数:9
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