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突破试验排除标准:接受 BCMA 靶向 CAR-T 治疗的血透多发性骨髓瘤患者的多中心分析

英文原题:Overcoming Trial Exclusion: A Multicenter Analysis of Hemodialysis Multiple Myeloma Patients Who Underwent BCMA-Directed CAR-T Therapy.

查看英文原题

Overcoming Trial Exclusion: A Multicenter Analysis of Hemodialysis Multiple Myeloma Patients Who Underwent BCMA-Directed CAR-T Therapy.

PubMed 2026/08/13(内容时间) Curr Oncol Q2 · IF 3.6(JCR 2025)

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中文摘要

多发性骨髓瘤(MM)合并终末期肾病(ESRD)需要血液透析(HD)的患者,其中黑人比例过高,被所有 BCMA 靶向CAR-T 细胞疗法的关键性试验排除,从而在这一人群中留下了关键性的证据空白。

我们开展了一项多中心回顾性分析,纳入 2021 年 6 月至 2025 年 12 月期间在美国两个中心接受 CAR-T 治疗时正在接受 HD 的所有 MM 患者。在 284 例 CAR-T 接受者中,8 例(2.8%)依赖 HD。中位年龄为 63 岁;62.5% 为女性,75% 为黑人;患者既往接受过中位 6 线治疗。5 例接受 ciltacabtagene autoleucel,3 例接受 idecabtagene vicleucel;淋巴细胞清除采用苯达莫司汀(n = 4)或减剂量的氟达拉滨/环磷酰胺(n = 4)。细胞因子释放综合征发生于 37.5%(均为 1 级),无 3 级事件——显著低于关键性试验(76-95%)。所有 7 例可评估患者均在 30 天前实现中性粒细胞恢复。1 例在 CAR-T 治疗前即存在长期血细胞减少的患者发生了 4 级 ICAN,并死于真菌性肺炎。中位无进展生存期为 17.5 个月,中位总生存期未达到。治疗相关死亡率为 12.5%。CAR-T 疗法在精心筛选的 HD 依赖 MM 患者中可行、相对安全且有效,支持在适当调整剂量的情况下扩大其适用资格。

展开英文摘要原文

Multiple myeloma (MM) patients with end-stage renal disease (ESRD) requiring hemodialysis (HD), who are disproportionately Black, have been excluded from all pivotal trials of BCMA-directed chimeric antigen receptor T-cell (CAR-T) therapy, leaving a critical evidence gap in a population.

We conducted a multicenter retrospective analysis of all MM patients who received CAR-T therapy while on HD at two U. S. centers between June 2021 and December 2025. Of 284 CAR-T recipients, 8 (2. 8%) were HD-dependent. Median age was 63 years; 62. 5% were female and 75% were Black; patients had received a median of 6 prior lines. Five received ciltacabtagene autoleucel and three received idecabtagene vicleucel; lymphodepletion was bendamustine ( n = 4) or dose-reduced fludarabine/cyclophosphamide ( n = 4). Cytokine release syndrome occurred in 37.

5% (all Grade 1), with no grade 3 events-substantially lower than pivotal trials (76-95%). All 7 evaluable patients achieved neutrophil recovery by Day 30. One patient with prolonged pre-existing cytopenia pre-CAR-T therapy developed ICAN grade 4 and died from fungal pneumonia.

Median progression-free survival was 17. 5 months and median overall survival was not reached. Treatment-related mortality was 12. 5%. CAR-T therapy is feasible, relatively safe, and effective in carefully selected HD-dependent MM patients, supporting expanded eligibility with appropriate dose modification.

论文信息

作者
Zolotov E、Mody R、Doucette K、Chappell A、Accolatse-Mati C、Parmar H、Di Palma-Grisi J、Biran N
单位
Division of Myeloma, John Theurer Cancer Center (JTCC), Hackensack University Medical Center, Hackensack, NJ 07601, USA.United States
文献类型
多中心研究
期刊
Current oncology (Toronto, Ont.)2026 Aug 13
原文标识
PubMed 42645380 · DOI 10.3390/curroncol33080475