Health-related quality of life and quality-adjusted progression free survival for carfilzomib and dexamethasone maintenance following salvage autologous stem-cell transplantation in patients with multiple myeloma: a randomized phase 2 trial by the Nordic Myeloma Study Group.

IF 2.4 Q2 HEALTH CARE SCIENCES & SERVICES
Lene Kongsgaard Nielsen, Fredrik Schjesvold, Sören Möller, Nina Guldbrandsen, Markus Hansson, Kari Remes, Valdas Peceliunas, Niels Abildgaard, Henrik Gregersen, Madeleine T King
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引用次数: 0

Abstract

Background: Decisions regarding maintenance therapy in patients with multiple myeloma should be based on both treatment efficacy and health-related quality of life (HRQL) consequences. In the CARFI trial, patients with first relapse of multiple myeloma underwent salvage autologous stem cell transplantation (salvage ASCT) before randomization to carfilzomib-dexamethasone maintenance therapy (Kd) or observation. The primary clinical endpoint was time to progression, which was extended by 8 months by Kd. The aim of this paper is to present the all HRQL endpoints of the CARFI trial including the HRQL effect of Kd maintenance therapy relative to observation. The primary HRQL endpoint was assessed by EORTC QLQ-C30 Summary score (QLQ-C30-sum) at 8 months follow-up. A key secondary HRQL endpoint was quality-adjusted progression-free-survival (QAPFS).

Methods: HRQL was assessed with EORTC QLQ-C30, EORTC QLQ-MY20 and FACT/GOG-Ntx at randomization and every second month during follow-up. HRQL data were analyzed with linear mixed effect models until 8 months follow-up. QAPFS per individual was calculated by multiplying progression-free survival (PFS) by two quality-adjustment metrics, the QLQ-C30-sum and EORTC Quality of Life Utility Measure-Core 10 dimensions (QLU-C10D). The QAPFS per treatment group was estimated with the Kaplan-Meier method. P < 0.05 was used for statistical significance, and a between-group minimal important difference of 10 points was interpreted as clinically relevant for the QLQ-C30-sum.

Results: 168 patients were randomized. HRQL questionnaire compliance was 93%. For the QLQ-C30-sum, the difference of 4.62 points (95% confidence interval (CI) -8.9: -0.4, p = 0.032) was not clinically relevant. PFS was 19.3 months for the Kd maintenance group and 16.8 months for the observation group; difference = 2.5 months (95% CI 0.5; 4.5). QAPFS based on the QLQ-C30-sum for the Kd maintenance group was 18.0 months (95% CI 16.4; 19.6) and for the observation group 15.0 months (95% CI 13.5; 16.5); difference = 3.0 months (95% CI 0.8-5.3). QAPFS based on the QLU-C10D for the Kd maintenance group was 17.5 months (95% CI 15.9; 19.2) and 14.0 months (95% CI 12.4; 15.5) for the observation group; difference = 3.5 months (95% CI 1.1-5.9).

Conclusions: Kd maintenance therapy after salvage ASCT did not adversely affect overall HRQL, but adjustment for HRQL reduced the PFS compared to unadjusted PFS. PFS of maintenance therapy should be quality-adjusted to balance the benefits and HRQL impact.

多发性骨髓瘤患者自体干细胞移植挽救治疗后,卡非佐米和地塞米松维持治疗的健康相关生活质量和质量调整后无进展生存期:北欧骨髓瘤研究小组的一项随机二期试验。
背景:决定对多发性骨髓瘤患者进行维持治疗时,应同时考虑治疗效果和与健康相关的生活质量(HRQL)。在CARFI试验中,首次复发的多发性骨髓瘤患者在随机接受卡非佐米-地塞米松维持治疗(Kd)或观察前接受了挽救性自体干细胞移植(挽救性ASCT)。主要临床终点是进展时间,Kd将进展时间延长了8个月。本文旨在介绍CARFI试验的所有HRQL终点,包括Kd维持治疗相对于观察治疗的HRQL效果。主要的 HRQL 终点由随访 8 个月时的 EORTC QLQ-C30 总分(QLQ-C30-sum)进行评估。方法:随机化时和随访期间每隔一个月用 EORTC QLQ-C30、EORTC QLQ-MY20 和 FACT/GOG-Ntx 评估 HRQL。在随访 8 个月前,采用线性混合效应模型对 HRQL 数据进行分析。将无进展生存期(PFS)乘以两个质量调整指标(QLQ-C30-sum 和 EORTC 生活质量效用测量-核心 10 维度 (QLU-C10D)),计算出每个人的 QAPFS。每个治疗组的 QAPFS 采用 Kaplan-Meier 法估算。P 结果:168名患者接受了随机治疗。HRQL问卷符合率为93%。在 QLQ-C30 总分方面,4.62 分的差异(95% 置信区间 (CI) -8.9: -0.4,P = 0.032)与临床无关。Kd维持组的PFS为19.3个月,观察组为16.8个月;差异=2.5个月(95% CI 0.5; 4.5)。根据 QLQ-C30-sum 计算,Kd 维持组的 QAPFS 为 18.0 个月(95% CI 16.4; 19.6),观察组为 15.0 个月(95% CI 13.5; 16.5);差异 = 3.0 个月(95% CI 0.8-5.3)。根据QLU-C10D,Kd维持治疗组的QAPFS为17.5个月(95% CI 15.9; 19.2),观察组为14.0个月(95% CI 12.4; 15.5);差异=3.5个月(95% CI 1.1-5.9):结论:抢救性ASCT后的Kd维持治疗不会对总体HRQL产生不利影响,但与未调整的PFS相比,调整HRQL会降低PFS。维持治疗的 PFS 应进行质量调整,以平衡获益和 HRQL 影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Patient-Reported Outcomes
Journal of Patient-Reported Outcomes Health Professions-Health Information Management
CiteScore
3.80
自引率
7.40%
发文量
120
审稿时长
20 weeks
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