KEYNOTE-604中患者报告的健康相关生活质量:将派姆单抗或安慰剂添加到依托泊苷和铂中作为广泛期SCLC的一线治疗

IF 3 Q2 ONCOLOGY
Hye Ryun Kim MD, PhD , Mark M. Awad MD, PhD , Alejandro Navarro MD , Maya Gottfried MD , Solange Peters MD, PhD , Tibor Csőszi MD , Parneet K. Cheema MD , Delvys Rodriguez-Abreu MD, PhD , Mirjana Wollner MD , James Chih-Hsin Yang MD, PhD , Julien Mazieres MD, PhD , Francisco J. Orlandi MD , Alexander Luft MD, PhD , Mahmut Gümüş MD , Terufumi Kato MD , Gregory P. Kalemkerian MD , Yiwen Luo PhD , Melissa L. Santorelli PhD, MPH , M. Catherine Pietanza MD , Charles M. Rudin MD, PhD
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引用次数: 0

摘要

在KEYNOTE-604 iii期研究(NCT03066778)中,派姆单抗加依托泊苷和铂化疗(EP)显著(p = 0.0023)改善了先前未治疗的大范围SCLC (ES-SCLC)的无进展生存期。我们报告KEYNOTE-604中与健康相关的生活质量(HRQoL)结果。方法:IV期SCLC患者以1:1的比例随机化,每3周使用派姆单抗200 mg或安慰剂,共35个周期加上4个周期的EP。次要终点包括欧洲癌症研究与治疗组织生活质量问卷核心30 (QLQ-C30)全球健康状况/生活质量(GHS/QoL)量表从基线到第18周的平均变化,以及QLQ-C30和qlq -肺癌模块13中咳嗽、胸痛或呼吸困难复合结局恶化的时间。报告了双侧标称p值。结果:共有439例患者完成了至少一项QLQ-C30和QLQ-Lung Cancer Module 13评估(pembrolizumab + EP, n = 221;安慰剂+ EP, n = 218)。GHS/QoL评分从基线到第18周有所改善:派姆单抗加EP组的最小二乘平均值(95%置信区间[CI])变化为8.7(5.3-12.1),安慰剂加EP组为4.2(0.9-7.5)。pembrolizumab联合EP组最小二乘平均评分的组间差异得到改善(4.4 [95% CI: 0.2-8.7], p = 0.040])。复合终点到恶化的中位时间分别为未达到和8.7个月(95% CI: 5.9-未达到)(风险比= 0.80 [95% CI: 0.56-1.14], p = 0.208)。结论:一线派姆单抗加EP治疗可维持ES-SCLC患者的HRQoL,并且可能比安慰剂加EP有更大的改善。结合KEYNOTE-604的疗效和安全性发现,HRQoL数据支持派姆单抗治疗ES-SCLC的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patient-Reported Health-Related Quality of Life in KEYNOTE-604: Pembrolizumab or Placebo Added to Etoposide and Platinum as First-Line Therapy for Extensive-Stage SCLC

Introduction

In the phase 3 KEYNOTE-604 study (NCT03066778), pembrolizumab plus etoposide and platinum chemotherapy (EP) significantly (p = 0.0023) improved progression-free survival versus placebo plus EP in previously untreated extensive-stage SCLC (ES-SCLC). We present health-related quality of life (HRQoL) results from KEYNOTE-604.

Methods

Patients with stage IV SCLC were randomized 1:1 to pembrolizumab 200 mg or placebo every 3 weeks for 35 cycles plus four cycles of EP. Secondary end points included mean change from baseline to week 18 in the European Organisation for Research and Treatment of Cancer Quality-of-Life Questionnaire—Core 30 (QLQ-C30) global health status/quality of life (GHS/QoL) scale and time to deterioration in the composite outcome of cough, chest pain, or dyspnea from QLQ-C30 and QLQ—Lung Cancer Module 13. Two-sided, nominal p values are reported.

Results

A total of 439 patients completed at least one QLQ-C30 and QLQ—Lung Cancer Module 13 assessment (pembrolizumab + EP, n = 221; placebo + EP, n = 218). GHS/QoL scores improved from baseline to week 18: least squares mean (95% confidence interval [CI]) changes were 8.7 (5.3–12.1) for pembrolizumab plus EP and 4.2 (0.9–7.5) for placebo plus EP. Between-group differences in least squares mean scores were improved for pembrolizumab plus EP (4.4 [95% CI: 0.2–8.7], p = 0.040]). Median time to deterioration for the composite end point was not reached and 8.7 (95% CI: 5.9–not reached) months, respectively (hazard ratio = 0.80 [95% CI: 0.56–1.14], p = 0.208).

Conclusions

First-line pembrolizumab plus EP therapy maintained HRQoL in patients with ES-SCLC and may be associated with greater improvement than placebo plus EP. Together with the efficacy and safety findings in KEYNOTE-604, HRQoL data support the benefit of pembrolizumab in ES-SCLC.

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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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