Ruiz-Bañobre Juan, Areses-Manrique María C, Mosquera-Martínez Joaquín, Cortegoso Alexandra, Afonso-Afonso Francisco J, de Dios-Álvarez Noemí, Fernández-Núñez Natalia, Azpitarte-Raposeiras Cristina, Amenedo Margarita, Santomé Lucía, Fírvida-Pérez José Luis, García-Campelo Rosario, García-González Jorge, Casal-Rubio Joaquín, Vázquez Sergio
Medical Oncology Department, Complejo Hospitalario Universitario de Ferrol, Ferrol, Spain.
Translational Medical Oncology Group (Oncomet), Health Research Institute of Santiago (IDIS), University Clinical Hospital of Santiago de Compostela, CIBERONC, Santiago de Compostela, Spain.
Transl Lung Cancer Res. 2019 Dec;8(6):1078-1085. doi: 10.21037/tlcr.2019.11.07.
The lung immune prognostic index (LIPI) has been proposed as a new categorical blood-based biomarker to select advanced non-small cell lung cancer (NSCLC) patients for anti-programmed cell death-1 (PD-1) or programmed death ligand 1 (PD-L1) therapy. In this study, we investigate for the first time to the best of our knowledge the prognostic and predictive utility of the LIPI in a multicenter nivolumab monotherapy-based cohort. We retrospectively analyzed the influence of the baseline LIPI on overall survival (OS), progression-free survival (PFS), disease control rate (DCR), and overall response rate (ORR) among 153 patients of a cohort of 188 advanced NSCLC patients treated with nivolumab in the second line of therapy or beyond. Worse LIPI was significantly associated with shorter OS in univariate [hazard ratio (HR) =3.12, 95% confidence interval (CI), 2.12-4.60; P<0.0001] and multivariate (HR =3.67, 95% CI, 1.96-6.86; P<0.0001) analyses. Worse LIPI was associated with shorter PFS (HR =1.45, 95% CI, 1.05-2.03; P=0.03), but this correlation did not reach statistical significance in multivariate analysis (HR =1.49, 95% CI, 0.94-2.38; P=0.09). Worse LIPI was associated with lower DCR in univariate [odds ratio (OR) =0.41, 95% CI, 0.24-0.70; P=0.001] and multivariate (OR =0.44, 95% CI, 0.25-0.78; P=0.005) analyses. This study confirms the utility of the LIPI in prognostication and disease control prediction in advanced NSCLC patients treated with nivolumab in the second line of therapy or beyond.
肺免疫预后指数(LIPI)已被提议作为一种新的基于血液的分类生物标志物,用于选择晚期非小细胞肺癌(NSCLC)患者进行抗程序性细胞死亡蛋白1(PD-1)或程序性死亡配体1(PD-L1)治疗。在本研究中,据我们所知,我们首次在一个基于纳武单抗单药治疗的多中心队列中研究了LIPI的预后和预测效用。我们回顾性分析了188例接受二线及以上纳武单抗治疗的晚期NSCLC患者队列中153例患者的基线LIPI对总生存期(OS)、无进展生存期(PFS)、疾病控制率(DCR)和总缓解率(ORR)的影响。在单因素分析中[风险比(HR)=3.12,95%置信区间(CI),2.12 - 4.60;P<0.0001]和多因素分析中(HR =3.67,95%CI,1.96 - 6.86;P<0.0001),较差的LIPI与较短的OS显著相关。较差的LIPI与较短的PFS相关(HR =1.45,95%CI,1.05 - 2.03;P =0.03),但这种相关性在多因素分析中未达到统计学意义(HR =1.49,95%CI,0.94 - 2.38;P =0.09)。在单因素分析[比值比(OR)=0.41,95%CI,0.24 - 0.70;P =0.001]和多因素分析中(OR =0.44,95%CI,0.25 - 0.78;P =0.005),较差的LIPI与较低的DCR相关。本研究证实了LIPI在二线及以上接受纳武单抗治疗的晚期NSCLC患者的预后评估和疾病控制预测中的效用。