Department of Medical Oncology/Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Department of Medical Oncology/Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Clin Lung Cancer. 2018 Sep;19(5):426-434.e1. doi: 10.1016/j.cllc.2018.04.008. Epub 2018 May 8.
Programmed death-1 (PD-1) axis inhibitors have become standard therapy in advanced non-small-cell lung cancer (NSCLC). Response might be delayed and pseudo-progression occasionally occurs in patients who eventually benefit from treatment. Additional markers beyond programmed death ligand 1 (PD-L1) expression are needed to assist in patient selection, response evaluation, and treatment decisions.
The relationship between prospectively collected clinical outcomes (response, disease control rate [DCR], treatment duration, overall survival) and hematologic parameters (neutrophil to lymphocyte ratio [NLR], absolute neutrophil count [ANC], and platelet to lymphocyte ratio [PLR]) was explored retrospectively in advanced NSCLC patients treated with PD-1 axis inhibitors at a major cancer center from May 2013 to August 2016. Hematologic parameters at baseline and during treatment (week 2 or 3 and week 8) were included.
Of 88 patients treated with PD-1 axis inhibitors, 22 (25%) experienced partial response. Baseline NLR ≤4 was associated with superior DCR (74% vs. 50%; P = .025), treatment duration (P = .037), time to progression (P = .053), and overall survival (P = .019), with no differential association according to PD-L1 tumor expression. Lower NLR and ANC during treatment were also associated with response to treatment (P = .025 and P = .017, respectively), and treatment duration (P = .036 and P = .008). No association was found between baseline PLR and DCR, response, treatment duration, nor overall survival.
Baseline NLR ≤4 and lower NLR and ANC during treatment might correlate with disease control and treatment response and should be explored further as potential predictors of treatment benefit in larger studies.
程序性死亡受体-1(PD-1)轴抑制剂已成为晚期非小细胞肺癌(NSCLC)的标准治疗方法。在最终受益于治疗的患者中,可能会出现延迟反应和假性进展。除程序性死亡配体 1(PD-L1)表达外,还需要其他标志物来协助患者选择、反应评估和治疗决策。
回顾性分析了 2013 年 5 月至 2016 年 8 月在一家主要癌症中心接受 PD-1 轴抑制剂治疗的晚期 NSCLC 患者的前瞻性收集的临床结果(反应、疾病控制率[DCR]、治疗持续时间、总生存)与血液学参数(中性粒细胞与淋巴细胞比值[NLR]、绝对中性粒细胞计数[ANC]和血小板与淋巴细胞比值[PLR])之间的关系。纳入了基线和治疗期间(第 2 或 3 周和第 8 周)的血液学参数。
88 例接受 PD-1 轴抑制剂治疗的患者中,22 例(25%)有部分缓解。基线 NLR≤4 与更好的 DCR(74% vs. 50%;P=0.025)、治疗持续时间(P=0.037)、无进展生存期(P=0.053)和总生存期(P=0.019)相关,与 PD-L1 肿瘤表达无差异相关。治疗期间 NLR 和 ANC 较低也与治疗反应(P=0.025 和 P=0.017)和治疗持续时间(P=0.036 和 P=0.008)相关。基线 PLR 与 DCR、反应、治疗持续时间或总生存均无相关性。
基线 NLR≤4 以及治疗期间 NLR 和 ANC 较低可能与疾病控制和治疗反应相关,在更大的研究中应进一步探讨其作为治疗获益的潜在预测指标。