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:Feasibility of post-induction consolidation with BCMA CAR-T cell therapy in newly diagnosed multiple myeloma not proceeding to ASCT: A preliminary case series.
Feasibility of post-induction consolidation with BCMA CAR-T cell therapy in newly diagnosed multiple myeloma not proceeding to ASCT: A preliminary case series.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
B细胞成熟抗原(BCMA)嵌合抗原受体(CAR)T细胞疗法在复发/难治性多发性骨髓瘤(MM)中显示出有前景的疗效。然而,支持其用于更早治疗阶段的证据仍有限。
本研究报告一组初步病例,评估BCMA CAR-T 细胞疗法作为诱导治疗后巩固治疗,用于未接受自体干细胞移植(ASCT)的新诊断多发性骨髓瘤(NDMM)患者的可行性。分析纳入4例患者。诱导治疗后,所有患者均达到非常好的部分缓解或更佳疗效;因不符合移植条件或个人意愿,未接受ASCT。随后均接受BCMA CAR-T 细胞巩固治疗。所有患者均良好耐受BCMA CAR-T 细胞输注。所有病例均发生细胞因子释放综合征,但仅为1–2级,且未观察到免疫效应细胞相关神经毒性综合征。治疗后,患者维持或进一步加深缓解,最终均达到严格完全缓解(sCR)和微小残留病(MRD)阴性。中位随访17.8个月期间,所有患者均维持sCR和MRD阴性,无需追加抗肿瘤治疗,且均未复发或进展。这些初步结果提示,对于未接受ASCT的NDMM患者,BCMA CAR-T 作为诱导后巩固治疗具有可行性且毒性可管理,值得在更大规模前瞻性研究中进一步评估。
B-cell maturation antigen (BCMA) chimeric antigen receptor (CAR) T cell therapy has demonstrated promising efficacy in relapsed/refractory multiple myeloma (MM).
However, evidence supporting its use in earlier treatment settings remains limited.
This study presents a preliminary case series evaluating the feasibility of BCMA CAR-T cell therapy as post-induction consolidation in newly diagnosed multiple myeloma (NDMM) patients who did not proceed to autologous stem cell transplantation (ASCT). Four patients were included in this analysis. After induction therapy, all patients achieved very good partial response or better and did not proceed to ASCT due to ineligibility or personal preference. They subsequently received BCMA CAR-T cell therapy as consolidation treatment. All patients tolerated the BCMA CAR-T cell infusion well. Cytokine release syndrome occurred in all cases, but was limited to grades 1-2, and no immune effector cell-associated neurotoxicity syndrome was observed.
Following therapy, patients maintained or further deepened responses and ultimately reached stringent complete response (sCR) and minimal residual disease (MRD) negativity. During a median follow-up period of 17. 8 months, all patients remained in sCR status and MRD negativity without the need for additional anti-tumor therapy, and none experienced relapse or disease progression.
These preliminary results suggest that BCMA CAR-T cell therapy as post-induction consolidation is feasible and associated with manageable toxicity in NDMM patients not proceeding to ASCT, warranting further evaluation in larger prospective studies.
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