首页|微RNA对非小细胞肺癌程序性死亡蛋白1抑制剂联合同步化疗疗效的预测价值

微RNA对非小细胞肺癌程序性死亡蛋白1抑制剂联合同步化疗疗效的预测价值

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目的 分析血清微RNA(miR-218、miR-329、miR-567)对非小细胞肺癌(non-small cell lung cancer,NSCLC)患者程序性死亡蛋白1(programmed death-1,PD-1)抑制剂联合同步化疗临床疗效的预测价值.方法 采用便利抽样法前瞻性选取2021年1月—2023年1月北京大学第一医院太原医院收治的160例行PD-1抑制剂联合同步化疗治疗的NSCLC患者为研究对象,收集患者血清miR-218、miR-329、miR-567水平以及临床疗效等相关资料,并根据临床疗效将患者分为缓解组(部分缓解与完全缓解)与未缓解组(疾病稳定与疾病进展),采用受试者操作特征曲线分析血清miR-218、miR-329、miR-567水平对NSCLC患者PD-1抑制剂联合同步化疗临床疗效的预测价值.结果 160例患者中疾病进展34例(21.2%)、疾病稳定85例(53.1%)、部分缓解39例(24.4%)、完全缓解2例(1.2%),分为缓解组41例、未缓解组119例.多因素logistic回归分析结果显示,血清miR-218、miR-329、miR-567高水平对提高NSCLC患者PD-1抑制剂联合同步化疗临床疗效具有促进作用(P<0.05).受试者操作特征曲线分析结果显示,根据联合检测血清miR-218、miR-329、miR-567的预测概率截断值预测NSCLC患者PD-1抑制剂联合同步化疗临床疗效的曲线下面积及其95%置信区间为0.938(0.855,0.964),灵敏度为82.9%,特异度为92.4%,阳性预测值为79.1%,阴性预测值为94.0%.结论 联合检测血清miR-218、miR-329、miR-567水平,对NSCLC患者PD-1抑制剂联合同步化疗的治疗效果具有较高的预测价值.
Value of microRNAs in predicting the efficacy of programmed death-1 inhibitor combined with synchronous chemotherapy in non-small cell lung cancer
Objective To analyze the value of serum microRNAs(miR-218,miR-329,and miR-567)in predicting the clinical efficacy of programmed death-1(PD-1)inhibitor combined with synchronous chemotherapy in patients with non-small cell lung cancer(NSCLC).Methods A total of 160 patients with NSCLC treated with PD-1 inhibitor combined with synchronous chemotherapy in Taiyuan Hospital,Peking University First Hospital between January 2021 and January 2023 were prospectively selected as the study objects by convenience sampling,and the serum levels of miR-218,miR-329,and miR-567 and the clinical efficacy of the patients were collected.According to the clinical efficacy,the patients were divided into remission group(partial remission and complete remission)and non-remission group(stable disease and disease progression).Receiver operating characteristic(ROC)curve was used to analyze the predictive value of serum miR-218,miR-329 and miR-567 levels in the clinical efficacy of PD-1 inhibitor combined with synchronous chemotherapy in patients with NSCLC.Results Of the 160 patients,34(21.2%)had disease progression,85(53.1%)had stable disease,39(24.4%)had partial remission,and 2(1.2%)had complete remission.They were divided into remission group(41 cases)and non-remission group(119 cases).Multiple logistic regression analysis showed that high levels of serum miR-218,miR-329,and miR-567 could promote the clinical efficacy of PD-1 inhibitor combined with synchronous chemotherapy in patients with NSCLC(all P<0.05).ROC curve analysis showed that,for predicting the clinical efficacy of PD-1 inhibitor combined with synchronous chemotherapy in patients with NSCLC according to the cut-off value of the joint prediction probability of serum miR-218,miR-329,and miR-567,the area under the ROC curve was 0.938[95%confidence interval(0.855,0.964)],and the sensitivity,specificity,positive predictive value,and negative predictive value were 82.9%,92.4%,79.1%,and 94.0%,respectively.Conclusion The combined detection of serum miR-218,miR-329 and miR-567 levels has a high predictive value for the therapeutic effect of PD-1 inhibitor combined with synchronous chemotherapy in patients with NSCLC.

Serum microRNAsmiR-218miR-329miR-567non-small cell lung cancerprogrammed death-1 inhibitorsynchronous chemotherapyclinical efficacy

董立慧、张之君、侯翠芳

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北京大学第一医院太原医院肿瘤科(太原 030009)

血清微RNA miR-218 miR-329 miR-567 非小细胞肺癌 程序性死亡蛋白1抑制剂 同步化学治疗 临床疗效

2024

华西医学
四川大学华西医院

华西医学

CSTPCD
影响因子:0.744
ISSN:1002-0179
年,卷(期):2024.39(1)
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