Prognostic Significance of Excision Repair Cross-Complementation Group 1 on Circulating Tumor Cells for Nasopharyngeal Carcinoma

被引:1
|
作者
Liu, Ting [1 ]
Li, Yuanqing [1 ]
Song, Junmei [1 ]
Li, Bo [1 ]
Wang, Rensheng [1 ,2 ]
Huang, Tingting [1 ,2 ]
Qin, Yutao [1 ]
机构
[1] Guangxi Med Univ, Dept Radiat Oncol, Affiliated Hosp 1, Shuangyong Rd, Nanning 530021, Peoples R China
[2] Guangxi Med Univ, Guangxi Key Lab High Incidence Tumor Prevent & Tre, Minist Educ, Nanning, Peoples R China
关键词
circulating tumor cells(1); excision repair cross-complementation group 1(2); epithelial-mesenchymal transition(3); nasopharyngeal carcinoma(4); prognosis(5); CLINICAL-SIGNIFICANCE; EXPRESSION; DIAGNOSIS; MARKER;
D O I
10.1177/10732748241251562
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Liquid biopsy, including the detection of circulating tumor cells (CTCs), has emerged as a promising tool for cancer diagnosis and monitoring. However, the prognostic value of CTCs in nasopharyngeal carcinoma (NPC) remains unclear due to the lack of phenotypic characterization. The expression of Excision Repair Cross-Complementation Group 1 (ERCC1) and CTCs epithelial-mesenchymal transition (EMT) have been associated with treatment efficacy. In this study, we aimed to evaluate the prognostic significance of ERCC1 expression on CTCs and their EMT subtypes before treatment in NPC. Methods: We retrospectively analyzed 108 newly diagnosed locally advanced NPC patients who underwent CanPatrol (TM) CTC testing between November 2018 and November 2021. CTCs were counted and classified into epithelial, epithelial-mesenchymal hybrid, and mesenchymal subtypes. ERCC1 expression was divided into negative and positive groups. Clinical features and survival outcomes were analyzed. Results: The positive rate of CTCs was 92.6% (100/108), with an ERCC1 positivity rate of 74% (74/100). Further analysis of the subtypes showed that positive ERCC1 on mesenchymal CTCs was associated with a later N stage (P = .01). Positive ERCC1 expression was associated with poor overall survival (OS; P = .039) and disease-free survival (DFS; P = .035). Further analysis of subtypes showed that the positive ERCC1 on mesenchymal-type CTCs was associated with poor OS (P = .012) and metastasis-free survival (MFS; P = .001). Conclusion: Our findings suggest that ERCC1 expression on CTCs may serve as a new prognostic marker for NPC patients. Evaluating CTCs subtypes may become an auxiliary tool for personalized and precise treatment.
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页数:14
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