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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:BCMA CAR-T therapy combined with pomalidomide is a safe and effective treatment for relapsed/refractory multiple myeloma.
BCMA CAR-T therapy combined with pomalidomide is a safe and effective treatment for relapsed/refractory multiple myeloma.
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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。
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。
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.
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