Efficacy and Safety of Anti-B-Cell Maturation Antigen Chimeric Antigen Receptor T-Cell for the Treatment of Relapsed and Refractory AL Amyloidosis.

IF 42.1 1区 医学 Q1 ONCOLOGY
Journal of Clinical Oncology Pub Date : 2025-06-10 Epub Date: 2024-12-09 DOI:10.1200/JCO-24-02252
Eyal Lebel, Nathalie Asherie, Shlomit Kfir-Erenfeld, Sigal Grisariu, Batia Avni, Shlomo Elias, Miri Assayag, Tali Dubnikov-Sharon, Marjorie Pick, Rivka Alexander-Shani, Nomi Bessig, Shlomit Herr, Alaa Shehadeh, Aseel Ishtay, Shelly Pimienta, Vladimir Vainstein, Eran Zimran, Yael Cohen, Irit Avivi, Cyrille Cohen, Polina Stepensky, Moshe E Gatt
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引用次数: 0

Abstract

Purpose: The use of anti-B-cell maturation antigen (BCMA) chimeric antigen receptor T-cell (CART) therapy for AL amyloidosis (AL) is limited owing to patient frailty. HBI0101 anti-BCMA CART was the first proof of concept for its applicability to AL. This report addresses the AL patient cohort treated to date within the phase Ia/Ib clinical trial (ClinicalTrials.gov identifier: NCT04720313).

Methods: After lymphodepletion, most AL patients were infused with 800 × 106 CARTs.

Results: Sixteen patients were treated, with a median of four previous lines of therapy (range, 3-10), 14/16 were triple class refractory, and 6/16 were refractory to belantamab. Most patients (13/16) had cardiac involvement, including five with MAYO stage IIIa/IIIb at study entry. Cytokine release syndrome was frequent (14/16) but mostly low grade (grade 3: 3/16, no grade 4/5). No neurologic toxicity or treatment-related deaths were observed. There were five grade 3 AL-related organ deteriorations resolved quickly with supportive care. The overall hematologic response rate was 15/16 (94%) and complete response (CR) was 12/16 (75%). Minimal residual disease negativity was achieved in 9/14 evaluable patients. Most patients (8/13 evaluable) achieved an objective organ response. Seven patients died during long-term follow-up, three while in CR/very good partial response, and the median overall survival was 10.1 months (95% CI, 5.8 to not reached).

Conclusion: This largest clinical trial of AL patients treated with anti-BCMA CART demonstrates acceptable and manageable toxicity in a highly frail and resistant population with remarkable efficacy, leading to fast organ responses. Among patients with baseline advanced cardiac disease, deaths in the first year were frequent, suggesting that this effective therapy should be considered earlier in the course of therapy. Anti-BCMA CART may become a powerful tool for improving organ function and survival in patients with AL.

抗b细胞成熟抗原嵌合抗原受体t细胞治疗复发和难治性AL淀粉样变性的疗效和安全性。
目的:抗b细胞成熟抗原(BCMA)嵌合抗原受体t细胞(CART)治疗AL淀粉样变性(AL)由于患者虚弱而受到限制。HBI0101抗bcma CART是其适用于AL的首个概念证明。该报告涉及迄今为止在Ia/Ib期临床试验(ClinicalTrials.gov标识符:NCT04720313)中治疗的AL患者队列。方法:大多数AL患者在淋巴细胞清除后给予800 × 106的cart。结果:16例患者接受治疗,中位数为4个既往治疗线(范围3-10),14/16为三级难治,6/16对贝兰他单抗难治。大多数患者(13/16)有心脏受累,包括5例在研究开始时为MAYO IIIa/IIIb期。细胞因子释放综合征发生率高(14/16),但多为低级别(3级:3/16,无4/5级)。未观察到神经毒性或治疗相关死亡。有5例3级al相关器官恶化在支持治疗下迅速消退。总血液学缓解率为15/16(94%),完全缓解(CR)为12/16(75%)。在9/14可评估的患者中达到最小残留疾病阴性。大多数患者(8/13可评估)达到客观器官反应。7例患者在长期随访中死亡,3例在CR/非常好的部分缓解中死亡,中位总生存期为10.1个月(95% CI, 5.8至未达到)。结论:这项规模最大的AL患者抗bcma CART临床试验在高度虚弱和耐药人群中显示出可接受和可控的毒性,疗效显著,导致器官反应快速。在基线为晚期心脏病的患者中,第一年的死亡是常见的,这表明在治疗过程中应尽早考虑这种有效的治疗方法。抗bcma CART可能成为改善AL患者器官功能和生存的有力工具。
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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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