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idecabtagene vicleucel(ide-cel)CAR-T 细胞治疗三类药物暴露的复发/难治性多发性骨髓瘤患者的真实世界经验

英文原题:Real-life experiences with CAR T-cell therapy with idecabtagene vicleucel (ide-cel) for triple-class exposed relapsed/refractory multiple myeloma patients.

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Real-life experiences with CAR T-cell therapy with idecabtagene vicleucel (ide-cel) for triple-class exposed relapsed/refractory multiple myeloma patients.

PubMed 2023/04/15(内容时间) BMC Cancer Q2 · IF 4.1(JCR 2025)

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研究概要

我们报告了首批接受商业化 ide-cel 治疗的复发/难治性多发性骨髓瘤队列之一。

中文摘要

CAR-T 改变了复发/难治性多发性骨髓瘤(RRMM)治疗格局,带来前所未有缓解。伊德卡布塔基因-维克鲁赛(ide-cel)近期获批用于三类药物暴露后的RRMM。本文报告商业化ide-cel真实世界应用经验。

单一学术中心回顾首批16例三类药物暴露RRMM患者,评估毒性、疗效、CAR-T 扩增和可溶性BCMA(sBCMA)。

2022年6至10月连续治疗16例,中位年龄69岁;38%高危细胞遗传学,19%为R-ISS III期,31%髓外病变;既往治疗中位6线。制备成功率88%,6%需再次单采,6%接受超规格产品。3个月总体缓解率69%(严格完全缓解44%、完全缓解6%、非常好部分缓解19%)。15例(94%)发生CRS,88%为1级、6%为2级;1例(6%)发生1级ICANS;发热性中性粒细胞减少69%,感染31%;持续血液学毒性25%。其他毒性包括肝酶升高38%、结肠炎6%(3级)和DIC 6%(2级)。CAR-T 扩增较高者应答更多(100%比38%);无应答者常见sBCMA未下降或趋于平台。

该首批商业ide-cel队列ORR为69%,安全性可管理,但持续血液学毒性仍是重要挑战。疗效与体内CAR-T 扩增相关,需进一步研究优化扩增。

展开英文摘要原文

Chimeric antigen receptor (CAR) T-cell therapy has revolutionized the treatment landscape of relapsed/refractory multiple myeloma (RRMM), leading to unprecedented responses in this patient population. Idecabtagene vicleucel (ide-cel) has been recently approved for treatment of triple-class exposed RRMM. We report real-life experiences with the commercial use of ide-cel in RRMM patients.

We performed a retrospective analysis of the first 16 triple-class exposed RRMM patients treated with ide-cel at a single academic center. We assessed toxicities, response to treatment, CAR T expansion and soluble BCMA (sBCMA) levels.

We identified 16 consecutive RRMM patients treated with ide-cel between 06-10/2022. Median age was 69 years, 6 (38%) patients had high-risk cytogenetics, 3 (19%) R-ISS stage III, and 5 (31%) extramedullary disease. Median number of previous treatment lines was 6 (3-12). Manufacturing success rate was 88% (6% required second lymphapheresis, 6% received an out-of-specification product). At 3 months, the overall response rate (ORR) was 69% (44% sCR, 6% CR, 19% VGPR). Cytokine release syndrome (CRS) occurred in 15 (94%) patients (88% G1, 6% G2), immune effector-cell associated neurotoxicity syndrome (ICANS) in 1 (6% G1), febrile neutropenia in 11 (69%), and infections in 5 (31%). Prolonged hematologic toxicity occurred in 4/16 (25%) patients. Other non-hematological toxicities were elevated hepatic enzymes (38%), colitis (6%, G3) and DIC (6%, G2). Responses were more frequent in patients with higher CAR T expansion (100% vs 38%), and lack of decrease or plateau of sBCMA levels was typically observed in non-responders.

We report one of the first cohorts of RRMM treated with commercial ide-cel. The ORR was 69% and safety profile was manageable, but prolonged hematologic toxicity still represents a major challenge. Responses correlated with in vivo CAR T cell expansion, underlining the need of further research to optimize CAR T expansion.

论文信息

作者
Sanoyan DA、Seipel K、Bacher U、Kronig MN、Porret N、Wiedemann G、Daskalakis M、Pabst T
第一作者单位
Department of Medical Oncology, Inselspital, University Hospital of Bern, Center for Hemato-Oncology; University Cancer Center, Bern, 3010, Switzerland.Switzerland
通讯作者单位
Department of Medical Oncology, Inselspital, University Hospital of Bern, Center for Hemato-Oncology; University Cancer Center, Bern, 3010, Switzerland. Thomas.pabst@insel.ch.Switzerland
期刊
BMC cancer2023 Apr 15
原文标识
PubMed 37061680 · DOI 10.1186/s12885-023-10824-3