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Lymphocyte to monocyte ratio is associated with response to first-line platinum-based chemotherapy and prognosis of early-stage non-small cell lung cancer patients

机译:淋巴细胞与单核细胞的比例与基于一线铂类化学疗法的反应以及早期非小细胞肺癌患者的预后相关

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Lymphocyte to monocyte ratio (LMR) has shown prognostic value in different types of cancer. This study assessed the prognostic performance of LMR in early-stage non-small cell lung cancer (NSCLC) patients and investigated the influence of LMR on the treatment response in patients receiving first-line platinum-based chemotherapy. Four hundred eighty-eight NSCLC patients and 500 healthy donors were enrolled in this study. The cutoff value for LMR was chosen by receiver operating characteristic curve analysis. The prognostic significance of markers was assessed by univariate and multivariate Cox regression models. The median overall survival was 43 months, and the median progression-free survival was 38 months. LMR was associated with disease status and the treatment response of first-line platinum-based chemotherapy. Multivariate analysis showed that LMR was an independent prognostic factor for both overall survival (hazard ratio = 1.53, 95 % confidence interval = 1.09-2.14, P = 0.015) and progression-free survival (hazard ratio = 1.20, 95 % confidence interval = 1.02-1.67, P = 0.028). Furthermore, integration of LMR into a prognostic model including TNM stage, tumor status, chemotherapy, and histological type generated a nomogram, which predicted accurately overall survival for NSCLC patients. Decreased LMR may be a potential biomarker of disease status, worse response to first-line platinum-based chemotherapy, and worse survival for NSCLC patients. A prospective study is warranted for further validation of our findings.
机译:淋巴细胞与单核细胞的比率(LMR)在不同类型的癌症中已显示出预后价值。这项研究评估了LMR在早期非小细胞肺癌(NSCLC)患者中的预后性能,并研究了LMR对接受一线铂类化学疗法的患者的治疗反应的影响。这项研究招募了488名NSCLC患者和500名健康捐献者。通过接收器工作特性曲线分析选择LMR的截止值。通过单变量和多变量Cox回归模型评估标志物的预后意义。中位总生存期为43个月,中位无进展生存期为38个月。 LMR与疾病状态和基于铂的一线化疗的治疗反应相关。多变量分析表明,LMR是总体生存(危险比= 1.53,95%置信区间= 1.09-2.14,P = 0.015)和无进展生存(危险比= 1.20,95%置信区间= 1.02)的独立预后因素-1.67,P = 0.028)。此外,将LMR整合到包括TNM分期,肿瘤状态,化学疗法和组织学类型的预后模型中产生了诺模图,该图精确预测了NSCLC患者的总体生存率。 LMR降低可能是疾病状态的潜在生物标志物,对一线铂类化学疗法的不良反应以及NSCLC患者的生存期较差。有必要进行前瞻性研究以进一步验证我们的发现。

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