Pneumonitis During Durvalumab Consolidation Therapy Affects Survival in Stage III NSCLC

Yuhei Kinehara MD, PhD , Takayuki Shiroyama MD, PhD , Akihiro Tamiya MD , Motohiro Tamiya MD , Seigo Minami MD, PhD , Masaki Kanazu MD , Osamu Morimura MD, PhD , Toshie Niki MD, PhD , Satoshi Tetsumoto MD, PhD , Yoshihiko Taniguchi MD , Tomoki Kuge MD , Kazumi Nishino MD, PhD , Izumi Nagatomo MD, PhD , Atsushi Kumanogoh MD, PhD , Isao Tachibana MD, PhD
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Abstract

Introduction

Durvalumab consolidation therapy is the standard of care after concurrent chemoradiotherapy (CRT) for stage III NSCLC. Immune-related pneumonitis during durvalumab treatment is potentially fatal; however, information is lacking regarding the impact of pneumonitis on patient survival. This study investigates the effect of pulmonary and nonpulmonary immune-related adverse events (irAEs) on the efficacy of durvalumab treatment in patients with stage III NSCLC.

Methods

We retrospectively assessed 158 patients who received durvalumab after CRT at nine Japanese institutions between July 2018 and March 2020. Survival outcomes were compared between patients who developed pneumonitis with those who developed irAEs other than pneumonitis. Patients who survived for less than 3 months were excluded to reduce immortal time bias.

Results

Among 158 evaluated patients, 76 (48%) experienced grade less than or equal to one irAEs, whereas 82 (52%) experienced grade greater than or equal to two irAEs. Among the patients with grade greater than or equal to two irAEs, those with grade greater than or equal to two pneumonitis (n = 55) were compared with those with grade greater than or equal to two irAEs other than pneumonitis (n = 27). Patients with grade greater than or equal to two pneumonitis exhibited a significantly worse overall survival than those with grade greater than or equal to two irAEs that excluded pneumonitis. Multivariate analysis revealed that grade greater than or equal to two pneumonitis (hazard ratio = 3.71; 95% confidence interval, 1.85–7.45; p < 0.001) and squamous histology (hazard ratio = 2.64; 95% confidence interval, 1.29–5.42; p = 0.008) were independently associated with worse overall survival.

Conclusions

After minimizing immortal time bias, pneumonitis grade two or greater and squamous histology were poor prognostic factors in patients who received consolidation durvalumab after CRT.

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Durvalumab巩固治疗期间的肺炎影响III期NSCLC的生存
durvalumab巩固治疗是III期NSCLC同步放化疗(CRT)后的标准护理。杜伐单抗治疗期间的免疫相关性肺炎可能致命;然而,缺乏关于肺炎对患者生存影响的信息。本研究探讨肺和非肺免疫相关不良事件(irAEs)对durvalumab治疗III期NSCLC患者疗效的影响。方法回顾性评估2018年7月至2020年3月在日本9家机构接受CRT治疗的158例杜伐单抗患者。比较了发生肺炎的患者与发生非肺炎的irAEs患者的生存结果。生存时间少于3个月的患者被排除在外,以减少不朽时间偏差。结果在158例接受评估的患者中,76例(48%)经历了小于或等于1个irae的分级,82例(52%)经历了大于或等于2个irae的分级。在≥2级irAEs的患者中,将≥2级肺炎患者(n = 55)与≥2级非肺炎irAEs患者(n = 27)进行比较。大于或等于2级肺炎的患者的总生存率明显低于大于或等于2级irae(不包括肺炎)的患者。多因素分析显示,分级≥2级肺炎(风险比= 3.71;95%置信区间为1.85-7.45;p & lt;0.001)和鳞状组织学(风险比= 2.64;95%置信区间为1.29-5.42;P = 0.008)与较差的总生存期独立相关。结论:在最小化不朽时间偏差后,在CRT后接受durvalumab巩固治疗的患者中,2级或以上的肺炎和鳞状组织是不良预后因素。
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来源期刊
CiteScore
4.20
自引率
0.00%
发文量
145
审稿时长
19 weeks
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