Egami Saeka, Kawazoe Hitoshi, Hashimoto Hironobu, Uozumi Ryuji, Arami Toko, Sakiyama Naomi, Ohe Yuichiro, Nakada Hideo, Aomori Tohru, Ikemura Shinnosuke, Fukunaga Koichi, Yamaguchi Masakazu, Nakamura Tomonori
Division of Pharmaceutical Care Sciences, Center for Social Pharmacy and Pharmaceutical Care Sciences, Keio University Faculty of Pharmacy, Tokyo, Japan.
Division of Pharmaceutical Care Sciences, Keio University Graduate School of Pharmaceutical Sciences, Tokyo, Japan.
Front Oncol. 2021 May 27;11:618570. doi: 10.3389/fonc.2021.618570. eCollection 2021.
Among patients with advanced non-small-cell lung cancer who were treated with nivolumab monotherapy, the association of peripheral blood count data (at baseline and 2 weeks after treatment initiation) with the early onset of immune-related adverse events (irAEs) and treatment efficacy has not been clearly established. This study aimed to identify peripheral blood count data that may be predictive of the development of nivolumab-induced irAEs in a real-world clinical setting.
This multicenter observational study retrospectively evaluated consecutive patients with advanced non-small-cell lung cancer undergoing nivolumab monotherapy in the second- or later-line setting between December 2015 and November 2018 at the National Cancer Center Hospital and Keio University Hospital in Japan. The primary endpoint was the association between peripheral blood count data and irAEs during the 6-week study period. Receiver operating characteristic curve and multivariable logistic regression analyses were performed.
Of the 171 patients evaluated, 73 (42.7%) had ≥1 irAE during the first 6 weeks following treatment initiation. The median time to irAEs from the initiation of nivolumab was 15 (interquartile range: 13-28) days. Receiver operating characteristic curve analyses revealed that the optimal cut-off values of the absolute lymphocyte count, neutrophil-to-lymphocyte ratio, and lymphocyte-to-monocyte ratio 2 weeks after treatment initiation for early irAE onset were 820, 4.3, and 2.2, respectively. In multivariable logistic regression analyses, absolute lymphocyte count >820 at 2 weeks after treatment initiation was significantly associated with an increased risk of early onset of any irAE. In contrast, no significant association was observed for the neutrophil-to-lymphocyte ratio (>4.3) or the lymphocyte-to-monocyte ratio (>2.2) at 2 weeks following treatment initiation.
The absolute lymphocyte count >820 at 2 weeks following nivolumab initiation predicts early onset of irAEs during a 6-week study period. Routinely available absolute lymphocyte count, which is measured after the initiation of nivolumab, may be useful for identifying patients at risk of early onset of irAEs.
在接受纳武利尤单抗单药治疗的晚期非小细胞肺癌患者中,外周血细胞计数数据(基线时及治疗开始后2周)与免疫相关不良事件(irAEs)的早期发生及治疗疗效之间的关联尚未明确确立。本研究旨在确定在真实临床环境中可能预测纳武利尤单抗诱导的irAEs发生的外周血细胞计数数据。
这项多中心观察性研究回顾性评估了2015年12月至2018年11月期间在日本国立癌症中心医院和庆应义塾大学医院接受二线或后续治疗的晚期非小细胞肺癌患者,这些患者接受纳武利尤单抗单药治疗。主要终点是6周研究期间外周血细胞计数数据与irAEs之间的关联。进行了受试者操作特征曲线和多变量逻辑回归分析。
在评估的171例患者中,73例(42.7%)在治疗开始后的前6周内发生了≥1次irAE。从纳武利尤单抗开始治疗到发生irAEs的中位时间为15天(四分位间距:13 - 28天)。受试者操作特征曲线分析显示,治疗开始后2周时绝对淋巴细胞计数、中性粒细胞与淋巴细胞比值以及淋巴细胞与单核细胞比值预测早期irAE发生的最佳截断值分别为820、4.3和2.2。在多变量逻辑回归分析中,治疗开始后2周时绝对淋巴细胞计数>820与任何irAE早期发生风险增加显著相关。相比之下,治疗开始后2周时中性粒细胞与淋巴细胞比值(>4.3)或淋巴细胞与单核细胞比值(>2.2)未观察到显著关联。
纳武利尤单抗开始治疗后2周时绝对淋巴细胞计数>820可预测6周研究期间irAEs的早期发生。纳武利尤单抗开始治疗后常规检测的绝对淋巴细胞计数可能有助于识别有irAEs早期发生风险的患者。