在全国范围内接受化疗的 III 期 NSCLC 患者中,PD-L1 评分与杜伐单抗巩固治疗效果之间的关系

IF 3.3 3区 医学 Q2 ONCOLOGY
Ronald Damhuis , Idris Bahce , Suresh Senan
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引用次数: 0

摘要

背景太平洋试验报告称,III期NSCLC患者在同时接受化放疗(CRT)后使用durvalumab可改善疗效。事后亚组分析显示,PD-L1阴性病例的疗效并不理想。我们将全国范围内的生存数据与试验结果进行了比较,并评估了 PD-L1 的影响。患者和方法我们从荷兰癌症登记处查询了临床 III 期患者的数据,这些患者接受了 CRT(同步或连续给药)。通过制表和逻辑回归分析评估了使用杜伐单抗进行巩固治疗的预测因素。总生存期(OS)从开始放疗或开始使用杜瓦鲁单抗起计算,并按PD-L1评分进行分层。结果2017年至2021年间,使用杜瓦鲁单抗巩固治疗的比例分别从2%增至21%、40%、57%和62%。在2020-2021年期间,年龄较小、同时接受CRT治疗、表现评分较好和接受质子辐射的患者更常使用durvalumab,但与PD-L1评分无关。对于接受durvalumab治疗的患者(n = 1639),总体4年OS为53%(95%CI 50-57),同时接受CRT治疗后的4年OS为56%(95%CI 52-60)。PD-L1≧50%亚组的4年OS要好得多,为67%(95%CI 59-73),PD-L1 0和1-49亚组的情况相似,分别为51%(95%CI 42-58)和46%(95%CI 39-54)。PD-L1阴性患者的总生存率与PD-L1 1-49患者的生存率相似,这对欧洲药品管理局施加的限制提出了质疑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association Between PD-L1 Score and the Outcomes of Consolidation Durvalumab in a Large Nationwide Series of Patients With Stage III NSCLC Treated With Chemoradiotherapy

Background

The Pacific trial reported improved outcomes when durvalumab was administered following concurrent chemoradiotherapy (CRT) for stage III NSCLC. Post-hoc subgroup analysis did not show favorable results for PD-L1 negative cases. We compared nationwide survival data with the trial outcomes, and evaluated the influence of PD-L1.

Patients and methods

Data from the Netherlands Cancer Registry were queried regarding patients with clinical stage III who underwent CRT, either by concurrent or sequential administration. Predictors for the use of consolidation treatment with durvalumab were evaluated by tabulations and logistic regression analysis. Overall survival (OS) was calculated from start of radiation or start of durvalumab and was stratified by PD-L1 score.

Results

Between 2017 and 2021, application of consolidation durvalumab increased from 2% to 21%, 40%, 57%, 62%, respectively. In the period 2020-2021, durvalumab use was more frequent among patients with younger age, concurrent CRT, better performance score and proton radiation, but was irrespective of PD-L1 score.
For patients receiving durvalumab (n = 1639), the 4-year OS was 53% overall (95%CI 50-57), and it was 56% (95%CI 52-60) after concurrent CRT. Four-year OS was considerably better for the PD-L1 subgroup ≧50% at 67% (95%CI 59-73), and it was similar for PD-L1 subgroups 0 and 1-49, at 51% (95%CI 42-58) and 46% (95%CI 39-54), respectively.

Conclusion

In real-world clinical practice, survival outcomes were equivalent to results from trial series. Overall survival in patients with negative PD-L1 was similar to the survival in patients with PD-L1 1-49, questioning the restrictions imposed by the European Medicines Agency.
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来源期刊
Clinical lung cancer
Clinical lung cancer 医学-肿瘤学
CiteScore
7.00
自引率
2.80%
发文量
159
审稿时长
24 days
期刊介绍: Clinical Lung Cancer is a peer-reviewed bimonthly journal that publishes original articles describing various aspects of clinical and translational research of lung cancer. Clinical Lung Cancer is devoted to articles on detection, diagnosis, prevention, and treatment of lung cancer. The main emphasis is on recent scientific developments in all areas related to lung cancer. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
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