CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Overcoming Trial Exclusion: A Multicenter Analysis of Hemodialysis Multiple Myeloma Patients Who Underwent BCMA-Directed CAR-T Therapy.
Overcoming Trial Exclusion: A Multicenter Analysis of Hemodialysis Multiple Myeloma Patients Who Underwent BCMA-Directed CAR-T Therapy.
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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。
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.
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