Bagley Stephen J, Kothari Shawn, Aggarwal Charu, Bauml Joshua M, Alley Evan W, Evans Tracey L, Kosteva John A, Ciunci Christine A, Gabriel Peter E, Thompson Jeffrey C, Stonehouse-Lee Susan, Sherry Victoria E, Gilbert Elizabeth, Eaby-Sandy Beth, Mutale Faith, DiLullo Gloria, Cohen Roger B, Vachani Anil, Langer Corey J
Division of Hematology/Oncology, Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Division of Hematology/Oncology, Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Lung Cancer. 2017 Apr;106:1-7. doi: 10.1016/j.lungcan.2017.01.013. Epub 2017 Jan 25.
Efficient use of nivolumab in non-small-cell lung cancer (NSCLC) has been limited by the lack of a definitive predictive biomarker. In patients with metastatic melanoma treated with ipilimumab, a pretreatment neutrophil-to-lymphocyte ratio (NLR)<5 has been associated with improved survival. This retrospective cohort study aimed to determine whether the pretreatment NLR was associated with outcomes in NSCLC patients treated with nivolumab.
We reviewed the medical records of all patients with previously treated advanced NSCLC who received nivolumab between March 2015 and March 2016 outside of a clinical trial at the University of Pennsylvania. Patients were dichotomized according to pretreatment NLR<5 vs. ≥5. Multivariable logistic regression and Cox proportional hazards models were used to assess the impact of pretreatment NLR on overall survival (OS), progression-free survival (PFS), and overall response rate (ORR).
175 patients were treated. Median age was 68 (range, 33-88); 54% were female. Twenty-five percent of patients had an Eastern Cooperative Oncology Group Performance Status (ECOG PS) ≥2; 46% had received ≥2 prior systemic therapies. In multivariate analyses, pretreatment neutrophil-to-lymphocyte ratio (NLR) ≥5 was independently associated with inferior OS (median 5.5 vs. 8.4 months; HR 2.07, 95% CI 1.3-3.3; p=0.002) and inferior PFS (median 1.9 vs. 2.8 months; HR 1.43, 95% CI 1.02-2.0; p=0.04).
In a cohort of patients with NSCLC treated with nivolumab in routine practice, pretreatment NLR≥5 was associated with inferior outcomes. It is unclear whether this marker is predictive or prognostic. Prospective studies are warranted to determine the utility of NLR in the context of other biomarkers of programmed death-1 (PD-1) therapy.
由于缺乏明确的预测生物标志物,纳武单抗在非小细胞肺癌(NSCLC)中的有效应用受到限制。在接受伊匹单抗治疗的转移性黑色素瘤患者中,治疗前中性粒细胞与淋巴细胞比值(NLR)<5与生存期改善相关。这项回顾性队列研究旨在确定治疗前NLR是否与接受纳武单抗治疗的NSCLC患者的预后相关。
我们回顾了2015年3月至2016年3月在宾夕法尼亚大学非临床试验中接受纳武单抗治疗的所有先前治疗过的晚期NSCLC患者的病历。根据治疗前NLR<5与≥5将患者分为两组。采用多变量逻辑回归和Cox比例风险模型评估治疗前NLR对总生存期(OS)、无进展生存期(PFS)和总缓解率(ORR)的影响。
175例患者接受了治疗。中位年龄为68岁(范围33 - 88岁);54%为女性。25%的患者东部肿瘤协作组体能状态(ECOG PS)≥2;46%的患者先前接受过≥2种全身治疗。在多变量分析中,治疗前中性粒细胞与淋巴细胞比值(NLR)≥5与较差的OS(中位生存期5.5个月对8.4个月;风险比2.07,95%置信区间1.3 - 3.3;p = 0.002)和较差的PFS(中位生存期1.9个月对2.8个月;风险比1.43,95%置信区间1.02 - 2.0;p = 0.04)独立相关。
在常规实践中接受纳武单抗治疗的NSCLC患者队列中,治疗前NLR≥5与较差的预后相关。尚不清楚该标志物是预测性的还是预后性的。有必要进行前瞻性研究以确定NLR在程序性死亡-1(PD-1)治疗的其他生物标志物背景下的效用。