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复发/难治性多发性骨髓瘤患者接受 idecabtagene vicleucel(ide-cel,bb2121)后长达 2 年的患者报告体验分析:2 期 KarMMa 试验的纵向结果

英文原题:Analysis of patient-reported experiences up to 2 years after receiving idecabtagene vicleucel (ide-cel, bb2121) for relapsed or refractory multiple myeloma: Longitudinal findings from the phase 2 KarMMa trial.

查看英文原题

Analysis of patient-reported experiences up to 2 years after receiving idecabtagene vicleucel (ide-cel, bb2121) for relapsed or refractory multiple myeloma: Longitudinal findings from the phase 2 KarMMa trial.

PubMed 2023/04/03(内容时间) Leuk Res Q2 · IF 2.4(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

对患者体验的纵向分析显示,治疗后长达 24 个月内 ide-cel 持续带来获益且更受偏好。

中文摘要

了解关键II期KarMMa试验中,复发/难治性多发性骨髓瘤患者接受ide-cel CAR-T 后的长期体验。

定性研究分析输注后6至24个月进行的半结构式访谈,结合主题、定量和纵向分析,探讨患者对治疗体验、优缺点及长期健康相关生活质量的看法,并根据患者叙述获益和已知缓解持续时间构建治疗历程。

分析45名输注后6至24个月患者访谈。所有人至少报告一项治疗优势,最常见为疗效(42/45,93%)、副作用少或无(35/45,78%)及避免其他治疗(34/45,76%)。患者普遍报告治疗6个月后躯体健康、功能、情绪、社交生活和未来展望改善;多数改善在18和24个月仍保持稳定。最常见历程为躯体、功能或情绪获益,同时缓解不足2年。

纵向患者体验分析显示ide-cel治疗后获益持续,患者偏好可维持至24个月。试验注册号NCT03361748(2017年12月5日)。

展开英文摘要原文

To understand the long-term experience of patients receiving ide-cel chimeric antigen receptor T (CAR T) cell therapy for relapsed or refractory multiple myeloma in the pivotal phase 2 KarMMa trial.

This qualitative study analyzed semi-structured patient interviews 6-24 months after ide-cel infusion. Thematic analysis with quantitative and longitudinal analyses explored patient perceptions of ide-cel treatment experience, advantages and disadvantages, and long-term health-related quality of life impact. Patient journeys were developed from narrative analysis of perceived treatment benefits with known remission length.

Interviews with 45 patients 6-24 months postinfusion were analyzed; all reported 1 ide-cel treatment advantage, most often related to efficacy (n = 42/45, 93%), few or no side effects (n = 35/45, 78%), and avoidance of other treatments (n = 34/45, 76%). Patients generally reported 6-month improvements in physical health, functioning, emotional well-being, social life, and outlook on the future; these improvements mostly remained "stable" through 18 and 24 months. The most common patient journeys comprised physical, functioning, or emotional benefit with remission < 2 years.

Longitudinal analysis of patient experiences showed sustained benefits and preference for ide-cel up to 24 months after treatment. Trial Registration Number and Date: NCT03361748. December 5, 2017.

论文信息

作者
Delforge M、Otero PR、Shah N、Moshkovich O、Braverman J、Dhanda DS、Lanar S、Devlen J
单位
University Hospital Leuven, Leuven, Belgium. Electronic address: michel.delforge@uzleuven.de.Belgium
文献类型
II 期临床试验 · 非美国政府资助研究
期刊
Leukemia research2023 Jun
原文标识
PubMed 37087950 · DOI 10.1016/j.leukres.2023.107074