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Peripheral Blood Markers Identify Risk of Immune-Related Toxicity in Advanced Non-Small Cell Lung Cancer Treated with Immune-Checkpoint Inhibitors

机译:外周血标记识别用免疫检查点抑制剂治疗的晚期非小细胞肺癌中免疫相关毒性风险

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Background Immune-checkpoint inhibitors (ICIs) are now standard of care for advanced non-small cell lung cancer (NSCLC). Unfortunately, many patients experience immune-related adverse events (irAEs), which are usually mild and reversible, but they require timely management and may be life threatening. No predictive markers of irAEs are available. Materials and Methods The neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) were evaluated in patients with NSCLC consecutively treated with ICIs. Prespecified cutoff values of NLR and PLR were used and related to outcome and onset of irAEs. A control group of patients with advanced NSCLC not receiving ICIs was included. Results The study included 184 patients: 26 (14.1%) received pembrolizumab upfront, and 142 (77%) received ICIs (pembrolizumab, nivolumab or atezolizumab) after one or more lines of chemotherapy. The median number of ICIs cycles was six (range, 1–61). The median progression-free survival and overall survival were 4.8 (95% CI, 3.4–6.3) and 20.6 (95% CI, 14.7–26.5) months, respectively. Sixty patients (32.6%) developed irAEs, mainly grade 1–2 (65.0%), causing ICI interruption in 46 cases (25.0%). Low NLR and low PLR at baseline were significantly associated with the development of irAEs (odds ratio [OR], 2.2; p = .018 and OR, 2.8; p = .003, respectively). Multivariate analyses confirmed PLR as independent predictive marker of irAEs (OR, 2.3; p = .020). Conclusion NLR and PLR may predict the appearance of irAEs in non-oncogene-addicted aNSCLC, although this conclusion warrants prospective validation. Implications for Practice This study was designed to investigate the role of blood biomarkers in predicting the occurrence of immune-related adverse events (irAEs) in patients with advanced non-small cell lung cancer receiving immunotherapy. The results of the study suggest a potential predictive role of neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio as markers for irAE development in this category of patients. These data provide rationale for an easy and feasible application to be validated in clinical practice.
机译:背景技术免疫检查点抑制剂(ICIS)现在是先进的非小细胞肺癌(NSCLC)的护理标准。不幸的是,许多患者经历免疫相关不良事件(IRAE),通常是轻度和可逆的,但它们需要及时管理,可能是危及生命。没有可获得伊拉斯的预测标记。用ICIS连续治疗的NSCLC患者评估了材料和方法中性粒细胞对淋巴细胞比(NLR)和血小板到淋巴细胞比(PLR)。使用NLR和PLR的预先确定的截止值,与伊拉克的结果和发作相关。包括未接受ICIS的高级NSCLC患者的对照组。结果该研究包括184名患者:26例(14.1%)接受Pembrolizumab前期,142(77%)接受icis(Pembrolizumab,Nivolumab或atezolizumab)后,在一种或多种化疗的化疗后。 ICIS循环的中位数是六(范围,1-61)。中位进展的存活和总生存率分别为4.8(95%CI,3.4-6.3)和20.6(95%CI,14.7-26.5)个月。六十名患者(32.6%)开发了伊拉克,主要是1-2级(65.0%),导致ICI中断46例(25.0%)。基线的低NLR和低PLR与IRAE的发育显着相关(差距比[或],2.2; P = .018和或,2.8; P = .003)。多变量分析证实PLR作为IRAES的独立预测标记(或2.3; P = .020)。结论NLR和PLR可以预测非癌基因上瘾的ANSCLC中伊拉克斯的外观,尽管该结论认证了前瞻性验证。对实践的影响本研究旨在探讨血液生物标志物在预测高级非小细胞肺癌接受免疫疗法的患者中预测免疫相关不良事件(IRAES)的发生。该研究的结果表明中性粒细胞对淋巴细胞比和血小板到淋巴细胞比例的潜在预测作用,作为这类患者IRAE发育的标志物。这些数据提供了在临床实践中验证的简单可行应用的理由。

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