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信迪利单抗联合化疗作为一线治疗对晚期食管鳞状细胞癌患者健康相关生活质量的影响:3期随机ORIENT-15研究结果

Effects of sintilimab plus chemotherapy as first-line treatment on health-related quality of life in patients with advanced esophageal squamous cell carcinoma: results from the randomized phase 3 ORIENT-15 study.

作者信息

Lu Zhihao, Kong Li, Wang Buhai, Wang Junye, Liu Lianke, Shu Yongqian, Yang Lei, Sun Guogui, Cao Guochun, Ji Yinghua, Cui Tongjian, Liu Hu, Qiu Wensheng, Li Na, Li Gaofeng, Luo Hui, Hou Xinfang, Zhang Yanqiao, Yue Wenbin, Xue Liying, Liu Zheng, Pan Yueyin, Gao Shegan, Wang Xiuwen, Pan Zhanyu, Zhang Shuqun, Lin Gen, Xie Yanru, Gu Kangsheng, Ren Tiejun, Li Weidong, Li Tao, Wang Shoufeng, He Wei, Fan Yun, Liang Jun, Xia Bing, Zhao Li, Wang Shuxuan, Shen Lin

机构信息

Beijing University Cancer Hospital and Institute, Beijing, China.

Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China.

出版信息

EClinicalMedicine. 2024 May 17;72:102623. doi: 10.1016/j.eclinm.2024.102623. eCollection 2024 Jun.

Abstract

BACKGROUND

In ORIENT-15 study, sintilimab plus chemotherapy demonstrated significant improvement on overall survival (OS) versus placebo plus chemotherapy in first-line treatment of advanced esophageal squamous cell carcinoma (ESCC). Here, we report effect of sintilimab plus chemotherapy on health-related quality of life (HRQoL) in patients with advanced ESCC.

METHODS

From December 14, 2018 to August 28, 2022, HRQoL was evaluated in all randomized patients using European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire Core 30 items (QLQ-C30), EORTC Quality of Life Questionnaire Oesophageal Cancer Module 18 items (QLQ-OES18), and visual analogue scale (VAS) of the EuroQol five-dimensional five-level questionnaire (EQ-5D-5L). Mean scores of each scale were described by treatment group through week 60. Least-squares mean (LSM) score change from baseline through week 24 were analyzed using the mixed-model repeated-measures method. Time to the first onset of deterioration (TTD) and OS for each scale were estimated. Clinical Trials Registration: NCT03748134.

FINDINGS

As of August 28, 2022, 689 of 690 enrolled patients were assessed for HRQoL analysis (sintilimab group: 340, placebo group: 349). Median follow-up was 32.2 months. Differences in LSM favored sintilimab over placebo for QLQ-C30 social functioning (LSM difference: 3.06, 95% CI: 0.55 to 5.57; P = 0.0170), pain (-2.24, 95% CI: -4.30 to -0.17; P = 0.0337), fatigue (-2.24, 95% CI: -4.46 to -0.02; P = 0.0479), constipation (-3.27, 95% CI -5.49 to -1.05; P = 0.0039), QLQ-OES18 pain (-1.77, 95% CI -3.11 to -0.43; P = 0.0097), trouble swallowing saliva (-2.09, 95% CI: -3.77 to -0.42; P = 0.0146), and choked when swallowing (-3.23, 95% CI: -5.60 to -0.86; P = 0.0076). TTD favored sintilimab over placebo for QLQ-OES18 dysphagia (Hazard ratio [HR]: 0.76, 95% CI: 0.61-0.94, P = 0.0104), and trouble swallowing saliva (HR: 0.48, 95% CI: 0.35-0.67, P < 0.0001). Improved OS were observed in patients with better performance in several functioning and symptom scales of QLQ-C30 and QLQ-QES18.

INTERPRETATION

The statistically significant differences of several HRQoL scales and improvements in delayed deterioration observed in our study further support the use of sintilimab plus chemotherapy as first-line treatment for advanced ESCC.

FUNDING

This study was funded by Innovent Biologics and was co-funded by Eli Lilly.

摘要

背景

在ORIENT-15研究中,与安慰剂联合化疗相比,信迪利单抗联合化疗在晚期食管鳞状细胞癌(ESCC)一线治疗中显著改善了总生存期(OS)。在此,我们报告信迪利单抗联合化疗对晚期ESCC患者健康相关生活质量(HRQoL)的影响。

方法

从2018年12月14日至2022年8月28日,使用欧洲癌症研究与治疗组织(EORTC)生活质量问卷核心30项(QLQ-C30)、EORTC生活质量问卷食管癌模块18项(QLQ-OES18)以及欧洲五维健康量表(EQ-5D-5L)的视觉模拟量表(VAS)对所有随机分组患者的HRQoL进行评估。各量表的平均得分按治疗组描述至第60周。使用混合模型重复测量方法分析从基线到第24周的最小二乘均值(LSM)得分变化。估计各量表首次出现恶化的时间(TTD)和OS。临床试验注册号:NCT03748134。

结果

截至2022年8月28日,690例入组患者中的689例接受了HRQoL分析(信迪利单抗组:共340例,安慰剂组:共349例)。中位随访时间为32.2个月。在QLQ-C30社会功能方面,LSM差异显示信迪利单抗优于安慰剂(LSM差异:3.06,95%置信区间:0.55至5.57;P = 0.0170)、疼痛(-2.24,95%置信区间:-4.30至-0.17;P = 0.0337)、疲劳(-2.24,95%置信区间:-4.46至-0.02;P = 0.0479)、便秘(-3.27,95%置信区间-5.49至-1.05;P = 0.0039)、QLQ-OES18疼痛(-1.77,95%置信区间-3.11至-0.43;P = 0.0097)、吞咽唾液困难(-2.09,95%置信区间:-3.77至-0.42;P = 0.0146)以及吞咽时哽咽(-3.23,95%置信区间:-5.60至-0.86;P = 0.0076)。在QLQ-OES18吞咽困难方面,TTD显示信迪利单抗优于安慰剂(风险比[HR]:0.76,95%置信区间:0.61 - 0.94,P = 0.0104),以及吞咽唾液困难(HR:0.48,95%置信区间:0.35 - 0.67,P < 0.0001)。在QLQ-C30和QLQ-QES18的几个功能和症状量表中表现较好的患者观察到OS改善。

解读

我们的研究中观察到的几个HRQoL量表具有统计学显著差异以及延迟恶化的改善,进一步支持信迪利单抗联合化疗作为晚期ESCC的一线治疗方法。

资助

本研究由信达生物制药资助,并由礼来公司共同资助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9c5/11127225/2932646bda3e/gr1.jpg

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