首页|血清CXCL12水平预测非小细胞肺癌免疫检查点抑制剂治疗反应的临床意义

血清CXCL12水平预测非小细胞肺癌免疫检查点抑制剂治疗反应的临床意义

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目的 探讨基质细胞衍生因子1(CXCL12)对接受免疫检查点抑制剂(ICIs)治疗的非小细胞肺癌(NSCLC)患者治疗反应的预测价值.方法 回顾性分析2022年1月至2022年12月间大庆市人民医院收治的70例ⅢB/Ⅳ期不可手术切除的NSCLC患者,均接受ICIs治疗,每8周评价ICIs治疗反应.采用实体瘤疗效评价标准(RECIST)1.1版评价疗效,分为完全缓解(CR)、部分缓解(PR)、疾病稳定(SD)和疾病进展(PD),以CR+PR+SD计算客观缓解率.临床获益定义为CR、PR或SD≥12周;无临床获益定义为PD或SD<12周.采用酶联免疫吸附法(ELISA)法检测血清CXCL12水平,分析其与治疗反应的关系.Logistic回归模型分析影响客观缓解和临床获益的因素.采用受试者特征工作(ROC)曲线分析基线血清CXCL12水平预测客观缓解和临床获益的效能.结果 根据ICIs治疗反应分为:客观缓解组(46例)和进展组(24例);临床获益组(35例)和临床未获益组(35例).客观缓解组和临床获益组的基线血清CXCL12水平分别为1.38(1.16,2.17)ng/ml和1.37(1.14,1.83)ng/ml,低于进展组和临床未获益组的2.71(1.94,3.06)ng/ml和2.69(1.70,3.42)ng/ml,差异均有统计学意义(P<0.05).基线血清CXCL12水平仅与TNM分期有关(P<0.05),而与其他临床病理参数均无关(P>0.05).Logistic回归分析显示,基线血清CXCL12水平是影响NSCLC患者客观缓解和临床获益的独立因素(P<0.05).基线血清CXCL12水平预测客观缓解和临床获益的效能较好,其灵敏度分别为0.792、0.714,特异度分别为0.717、0.800,截断值均为1.880 ng/ml.结论 血清CXCL12水平是预测晚期NSCLC患者ICIs治疗获益的潜在生物标志物.
Clinical significance of serum CXCL12 level in predicting immune checkpoint inhibitor response in patients with non-small cell lung cancer
Objective To investigate the predictive value of stromal cell derived factor 1(CXCL12)in treatment response of non-small cell lung cancer(NSCLC)patients treated with immune checkpoint inhibitors(ICIs).Methods A retrospective analysis was performed on 70 patients with stage Ⅲ B/Ⅳ unresectable NSCLC treated with ICIs in Daqing People's Hospital from January 2022 to December 2022,and ICIs response was assessed every 8 weeks.The efficacy was evaluated by Response Evaluationn Criteria in Solid Tumors(RECIST version,1.1)including complete response(CR),partial response(PR),stable disease(SD)and progressive disease(PD),and the objective response rate was calculated by CR+PR+SD.Clinical benefit was defined as CR,PR,or SD≥12 weeks;No clinical benefit was defined as PD or SD<12 weeks.The serum CXCL12 levels were detected by enzyme-linked immunosorbent assay(ELISA)and the relationship between CXCL12 and treatment response was analyzed.The factors affecting objective mitigation and clinical benefit were analyzed by Logistics regression model.Baseline serum CXCL12 levels were analyzed using subject characteristic work curves to predict objective response and clinical benefit.Results According to ICIs treatment response,the patients were divided into objective remission group(46 cases),progress group(24 cases),clinical benefit group(35 cases)and clinical no benefit group(35 cases).The baseline serum CXCL12 levels in the objective response group and clinical benefit group were 1.38(1.16,2.17)ng/ml and 1.37(1.14,1.83)ng/ml,respectively,which were lower than the 2.71(1.94,3.06)ng/ml and 2.69(1.70,3.42)ng/ml in the progressive and clinical no benefit groups,the differences were statistically significant(P<0.05).The serum CXCL12 level at baseline was only correlated with the stage(P<0.05),but not with other clinicopathological parameters.Logistic regression model analysis showed that baseline serum CXCL12 was an independent factor affecting objective remission and clinical benefit in NSCLC patients(P<0.05).Baseline serum CXCL12 had a good ability to predict objective response and clinical benefit,with sensitivity of 0.792,0.714,specificity of 0.717,0.800,and cutoff values of 1.880 ng/ml.Conclusion Serum CXCL12 level is a potential biomarker for predicting the benefit of ICIs treatment in patients with advanced NSCLC.

Non-small cell lung cancer(NSCLC)Stromal cell-derived factor 1(CXCL12)Immune checkpoint inhibitors(ICIs)Treatment response

宋春莲、杨立伟、马维艳

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163000 黑龙江大庆 大庆市人民医院肿瘤二科

非小细胞肺癌 基质细胞衍生因子1 免疫检查点抑制剂 治疗反应

2024

临床肿瘤学杂志
解放军第八一医院

临床肿瘤学杂志

CSTPCD
影响因子:1.583
ISSN:1009-0460
年,卷(期):2024.29(10)