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BCMA CAR-T 治疗联合泊马度胺治疗复发/难治性多发性骨髓瘤的安全性与有效性

英文原题:BCMA CAR-T therapy combined with pomalidomide is a safe and effective treatment for relapsed/refractory multiple myeloma.

查看英文原题

BCMA CAR-T therapy combined with pomalidomide is a safe and effective treatment for relapsed/refractory multiple myeloma.

PubMed 2024/11/29(内容时间) J Transl Med Q1 · IF 9.7(JCR 2025)

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研究概要

我们的结果证实,BCMA CAR-T 细胞治疗联合长期泊马度胺复发率低、治疗相关副作用可控,为治疗 R/R MM 提供了一个有前景的选择。

中文摘要

靶向B细胞成熟抗原(BCMA)的嵌合抗原受体(CAR)T细胞疗法治疗复发/难治性多发性骨髓瘤(R/R MM)显示显著疗效,但仍有患者在治疗后短期内复发或疾病快速进展。长期使用泊马度胺可增强T细胞功能,可能提高BCMA CAR-T 细胞疗效。

研究开展了一项单中心回顾性临床研究。纳入接受BCMA CAR-T 细胞输注的复发/难治性MM患者,并比较输注1个月后开始长期泊马度胺治疗(4 mg/日)或未接受泊马度胺治疗的患者。评估输注后应答和不良事件,并在体外评估泊马度胺对BCMA CAR-T 细胞的作用。

BCMA CAR-T 总体客观缓解率(ORR)为100%。CAR-T 细胞输注3个月后,8例接受泊马度胺的患者中,除2例停止维持治疗并失访外,其余6例(6/6)均达到非常好的部分缓解(VGPR)或完全缓解(CR);未接受泊马度胺治疗的患者中仅5/8达到VGPR或更好。中位随访27个月时,未接受泊马度胺的8例患者中位疾病进展时间(TTP)为5.85个月(范围1–14个月),总生存期(OS)为10.7个月(范围1.2–16个月)。CAR-T 输注后接受泊马度胺治疗的8例患者中位TTP为13个月(范围7–13个月),OS尚未达到。随访期间未观察到长期血液学毒性或药物诱导的肝损伤。从机制上看,泊马度胺通过抑制细胞凋亡并增强细胞毒性,提高BCMA CAR-T 细胞的抗骨髓瘤效力。

结果证实BCMA CAR-T 细胞疗法联合长期泊马度胺具有较低复发率,且治疗相关副作用可控,为R/R MM治疗提供了一种有前景的选择。

展开英文摘要原文

B-cell maturation antigen (BCMA)-targeted chimeric antigen receptor T-cell (CAR T-cell) therapy has exhibited remarkable efficacy in refractory or relapsed multiple myeloma (R/R MM), but recurrence and rapid progression of disease are still observed within a short time after treatment. Long-term pomalidomide therapy, which potentiates T-cell functionality, might enhance the efficacy of BCMA CAR T-cell therapy.

We performed a single-center retrospective clinical study. Patients with relapsed or refractory multiple myeloma who received BCMA CAR T-cell infusion were enrolled in our study, and were followed by long-term pomalidomide treatment (4 mg/day) or not one month after infusion. The response and adverse events were assessed after infusion. The effect of pomalidomide on BCMA CAR T-cells was assessed in vitro.

The objective response rate (ORR) of BCMA-CART was 100%. Three months following CAR T-cell infusion, of the 8 patients receiving pomalidomide, except for 2 patients who stopped maintenance therapy and were lost to follow-up, all patients (6/6) achieved VGPR (very good partial response) or CR (complete response), while only 5 patients (5/8) who did not receive pomalidomide treatment achieved VGPR or better. At a median follow-up of 27 months, for the 8 patients who did not receive pomalidomide administration, the median TTP (time to progression) was 5.85 (1-14) months, while the OS (overall survival) was 10.7 (1.2-16) months. Of the 8 patients who received pomalidomide therapy after CAR T-cell infusion, the median TTP was 13 (7-13) months, while the OS was not reached. Moreover, neither long-term hematological toxicity nor drug-induced liver damage was observed during the follow-up period. Mechanistically, pomalidomide promotes antimyeloma efficacy of BCMA CAR T-cells by inhibiting cell apoptosis and enhancing cytoxicity.

Our results confirmed that BCMA CAR T-cell therapy combined with long-term pomalidomide had a low recurrence rate and manageable therapy-related side effects, providing a promising option for treating R/R MM.

论文信息

作者
Yan Y、Tu Y、Cheng Q、Zhang J、Wang E、Deng Z、Yu Y、Wang L
第一作者单位
Department of Hematology, The Third Xiangya Hospital, Central South University, Changsha, 410013, Hunan, China.China
通讯作者单位
Department of Hematology, The Third Xiangya Hospital, Central South University, Changsha, 410013, Hunan, China. lixiner1975@163.com.China
文献类型
非美国政府资助研究
期刊
Journal of translational medicine2024 Nov 29
原文标识
PubMed 39614361 · DOI 10.1186/s12967-024-05772-w