首页|NLR、PILE评分与PD-1抑制剂治疗晚期非小细胞肺癌的疗效及预后的相关性

NLR、PILE评分与PD-1抑制剂治疗晚期非小细胞肺癌的疗效及预后的相关性

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目的 探讨中性粒细胞-淋巴细胞比值(neutrophil to lymphocyte ratio,NLR)、PILE评分与程序性细胞死亡蛋白-1(programmed cell death protein 1,PD-1)抑制剂治疗的晚期非小细胞肺癌(non-small cell lung cancer,NSCLC)患者疗效及预后的关系.方法 回顾性分析邵阳市中心医院在2020年6月至2021年12月收治的使用PD-1抑制剂治疗的109例晚期NSCLC患者的资料,计算患者治疗前的NLR、PILE评分,分析其与疗效及预后的相关性.结果 低NLR组比高NLR组有更高的疾病控制率(disease control rate,DCR)(P<0.05),PILE评分低分组较PILE评分高分组有更高的客观缓解率(objective response rate,ORR)和DCR(均P<0.05).在多因素分析中,NLR、PILE评分是影响PFS的独立危险因素(均P<0.05).结论 高NLR、高PILE评分与PD-1抑制剂治疗的晚期NSCLC患者的疗效更差有关,且高NLR、高PILE评分是患者预后不良的独立危险因素.
Correlation between NLR and PILE scores and the efficacy and prognosis in advanced non-small cell lung cancer treated with PD-1 inhibitors
Objective To investigate the relationship between neutrophil to lymphocyte ratio(NLR)and PILE scores and the efficacy and prognosis of patients with advanced non-small cell lung cancer(NSCLC)treated with PD-1 inhibitors.Methods The data of 109 patients with advanced NSCLC treated with PD-1 inhibitors admitted to Shaoyang Central Hospital from June 2020 to December 2021 were retrospectively analyzed.The calculate the patients'pre-treatment NLR and PILE scores were calculated,and their correlation with the efficacy and prognosis were analyzed.Results The low NLR group had a higher disease control rate(DCR)than the high NLR group(P<0.05),and the low PILE score group had a higher objective response rate(ORR)and DCR than the high PILE score group(all P<0.05).In multivariate analysis,NLR and PILE scores were independent risk factors affecting patients'PFS(all P<0.05).Conclusion High NLR and high PILE scores are associated with worse outcomes in patients with advanced NSCLC receiving PD-1 inhibitors and are independent risk factors for poor prognosis in patients.

advanced non-small cell lung cancerPD-1 inhibitorsNLRPILE scores

尹华婕、曾腾达、吴旭、伍妮、周玲、刘新福

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南华大学 附属邵阳医院 血液肿瘤科,湖南邵阳,422000

晚期非小细胞肺癌 PD-1抑制剂 NLR PILE评分

邵阳市科技局科研项目

2020NS40

2024

邵阳学院学报(自然科学版)
邵阳学院

邵阳学院学报(自然科学版)

影响因子:0.286
ISSN:1672-7010
年,卷(期):2024.21(2)
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