首页|叶酸受体阳性循环肿瘤细胞对可切除Ⅲ期鳞癌患者新辅助化疗联合免疫治疗后疗效的预测价值

叶酸受体阳性循环肿瘤细胞对可切除Ⅲ期鳞癌患者新辅助化疗联合免疫治疗后疗效的预测价值

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目的 研究治疗后叶酸受体阳性循环肿瘤细胞(folate receptor-positive circulating tumour cells,FR+-CTCs)对可切除Ⅲ期鳞癌患者新辅助化学药物治疗(以下简称化疗)联合免疫治疗疗效的预测价值.方法 收集首都医科大学附属北京胸科医院2021 年 6 月至 2023 年 6 月入院可切除Ⅲ期鳞癌患者,经过 2 周期新辅助化疗联合免疫治疗,记录患者以下指标:①一般临床资料:年龄、性别、临床分期、肿瘤位置、治疗前后白细胞计数;②治疗前后肿瘤标志物——血清癌胚抗原(carcinoembryonic antigen,CEA)、细胞角蛋白 19 片段(cytokeratin 19 fragment,CYFRA 21-1)、鳞状上皮细胞癌抗原(squamous cell carcinoma antigen,SCC)、FR+-CTCs数据;③患者术后病理结果,根据术后病理结果将患者分为两组,肿瘤病灶在病理层面上残存肿瘤细胞占比≤10%(缓解组,E组),肿瘤病灶在病理层面上残存肿瘤细胞占比>10%(NE组),比较E组和NE组患者的一般临床资料,治疗前后白细胞计数、肿瘤标志物和FR+-CTCs水平,将组间比较差异有统计学意义的变量纳入二元 Logistic 回归分析,统计分析出可切除Ⅲ期鳞癌患者新辅助化疗联合免疫治疗疗效的影响因素,采用受试者工作特征(receiver operating characteristics,ROC)曲线分析FR+-CTCs对其的预测价值.结果 最终纳入 24 例患者,E组 15 例,NE组 9 例,两组患者一般临床资料、治疗前CEA、CYFRA 21-1、SCC、FR+-CTCs比较差异均无统计学意义(P>0.05),治疗后CEA、CYFRA 21-1、SCC差异无统计学意义(P>0.05),E组治疗后FR+-CTCs显著低于NE组(P<0.05),二元Logistic回归分析显示,治疗后FR+-CTCs(OR=1.28,95%CI:1.00~1.63,P=0.047)是新辅助化疗联合免疫治疗的影响因素,ROC分析显示,治疗后FR+-CTCs截点值为 10.10,特异度 0.87,灵敏度 0.89,曲线下面积(area under the curve,AUC)0.837.结论 对可切除Ⅲ期鳞癌患者,治疗后FR+-CTCs低于 10.10 FU/3 mL是预测新辅助化疗联合免疫治疗缓解效果的可靠指标.
The predictive value of folate receptor-positive circulating tumor cells in patients with resectable stage Ⅲ squamous cell carcinoma after neoadjuvant chemotherapy combined with immunotherapy
Objective To investigate the predictive value of folate receptor-positive circulating tumor cells(FR+-CTCs)in determining the efficacy of neoadjuvant chemotherapy combined with immunotherapy in patients with resectable stage Ⅲ squamous cell carcinoma.Methods A total of patients diagnosed with resectable stage Ⅲ squamous cell carcinoma and admitted to Beijing Chest Hospital from June 2021 to June 2023 were included in this study.After receiving 2 cycles of neoadjuvant chemotherapy combined with immunotherapy,the following parameters were recorded:① general clinical data including age,gender,clinical stage,tumor location,pre-and post-treatment white blood cell count;② levels of tumor markers such as serum carcinoembryonic antigen(CEA),cytokeratin 19 fragment(CYFRA 21-1),squamous cell carcinoma antigen(SCC),and FR+-CTCs before and after treatment;③ postoperative pathological results,based on which the patients were divided into two groups:group E(<10%residual tumor cells)and NE group(>10%residual tumor cells).Binary Logistic regression analysis was performed using general clinical data,white blood cell count,tumor marker data,and FR+-CTCs data before and after treatment to statistically analyze factors influencing the efficacy of neoadjuvant chemotherapy combined with immunotherapy in patients with resectable stage Ⅲ squamous cell carcinoma.The predictive value of FR+-CTCs was assessed using receiver operating characteristics(ROC)curve analysis.Results A total of 24 patients were included in this study,with 15 patients in group E and 9 patients in the NE group.There were no significant differences observed between the two groups regarding general clinical data or pre-treatment levels of CEA,CYFRA 21-1,SCC or FR+-CTCs(P>0.05).Additionally,no statistically significant differences were found for CEA,CYFRA21-1,and SCC levels after treatment.FR+-CTCs in group E was significantly lower than that in group NE(P<0.05).Binary Logistic regression analysis showed that FR+-CTCs after treatment(OR=1.28,95%CI:1.00-1.63,P=0.047)was the influencing factor of neoadjuvant chemotherapy combined with immunotherapy.ROC analysis showed that the cut-off value of FR+-CTCs after treatment was 10.10,with a specificity of 0.87,a sensitivity of 0.89,and an area under the curve of 0.837.Conclusion For patients with resectable Ⅲ squamous cell carcinoma,FR+-CTCs after treatment lower than 10.10 FU/3 mL can predict the remission effect of neoadjuvant chemotherapy combined with immunotherapy.

squamous cell carcinomafolate receptor-positive circulating tumor cellsneoadjuvant chemotherapy combined with im-munotherapy

刘洋、杨磊、韩毅

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首都医科大学附属北京胸科医院胸外科,北京 101100

鳞癌 叶酸受体阳性循环肿瘤细胞 新辅助化疗联合免疫

北京市属医学科研院所公益发展改革试点项目

JYY2023-14

2024

首都医科大学学报
首都医科大学

首都医科大学学报

CSTPCD北大核心
影响因子:1.511
ISSN:1006-7795
年,卷(期):2024.45(4)