FGFR2b表达过高的晚期胃癌或胃食管交界癌患者使用贝马单抗加mFOLFOX6治疗后的健康相关生活质量

Z.A. Wainberg , P.C. Enzinger , S. Qin , K. Yamaguchi , J. Wang , X. Zhou , A. Gnanasakthy , K. Taylor , A. Yusuf , I. Majer , A. Jamotte , Y.-K. Kang
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引用次数: 0

摘要

背景在II期随机双盲FIGHT试验(NCT03694522)中,相对于单独使用mFOLFOX6,贝马利珠单抗联合mFOLFOX6治疗既往未经治疗的纤维母细胞生长因子受体2b过表达的局部晚期或转移性胃癌或胃食管交界癌患者的无进展生存期和总生存期均有所改善。利用最终分析的数据,我们分析了患者报告的结果(PROs),以评估在mFOLFOX6基础上加用贝马单抗对健康相关生活质量(HRQoL)的影响。材料与方法患者按1:1随机分配至贝马单抗加mFOLFOX6(n = 77)或安慰剂加mFOLFOX(n = 78)。在基线、第6周、之后的每8周和治疗结束时,对欧洲癌症研究和治疗组织核心30项生活质量(EORTC QLQ-C30)和EuroQol EQ-5D-5L进行问卷调查。使用重复测量混合模型估算PRO评分与基线相比的最小二乘法平均变化;使用Cox比例危险模型评估恶化和改善的时间。结果贝马单抗治疗组和安慰剂治疗组的基线PRO评分和随时间变化的PRO评估达标率相似。各治疗组的主要EORTC QLQ-C30量表(总体健康状况/QoL、身体功能、疲劳、恶心呕吐和食欲不振)和EQ-5D-5L视觉模拟量表与基线相比的最小二乘法平均变化随着时间的推移相似。对恶化时间、持续恶化和改善情况的分析表明,各治疗组之间的 HRQoL 相似。
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Health-related quality of life with bemarituzumab plus mFOLFOX6 in patients with FGFR2b-overexpressing, advanced gastric or gastroesophageal junction cancer

Background

In the phase II, randomized, double-blind FIGHT trial (NCT03694522), treatment with bemarituzumab plus mFOLFOX6 resulted in improvements in progression-free survival and overall survival relative to mFOLFOX6 alone in previously untreated locally advanced or metastatic gastric or gastroesophageal junction cancer with fibroblast growth factor receptor 2b overexpression. Using data from the final analysis, we analyzed patient-reported outcomes (PROs) to evaluate the impact of adding bemarituzumab to mFOLFOX6 on health-related quality of life (HRQoL).

Materials and methods

Patients were randomized 1 : 1 to bemarituzumab plus mFOLFOX6 (n = 77) or placebo plus mFOLFOX (n = 78). European Organisation for Research and Treatment of Cancer Core 30-item Quality of Life (EORTC QLQ-C30) and the EuroQol EQ-5D-5L questionnaires were administered at baseline, week 6, every 8 weeks thereafter, and at end-of-treatment visit. Least-squares mean changes from baseline in PRO scale scores were estimated using mixed models for repeated measures; time to deterioration and improvement were assessed using Cox proportional hazards models. Analyses were exploratory post hoc.

Results

PRO scale scores at baseline and compliance rates across PRO assessments over time were similar between the bemarituzumab and placebo arms. Least-squares mean changes from baseline on key EORTC QLQ-C30 scales (global health status/QoL, physical functioning, fatigue, nausea and vomiting, and appetite loss) and the EQ-5D-5L visual analog scale were similar over time between treatment arms. Analyses of time to deterioration, sustained deterioration, and improvement suggested similar HRQoL between treatment arms.

Conclusions

Treatment with bemarituzumab plus mFOLFOX6 was associated with sustained HRQoL relative to mFOLFOX6 alone.
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