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:Phase II Study of BCMA Chimeric Antigen Receptor T-Cell Therapy in Patients With Newly Diagnosed Multiple Myeloma Ineligible for or Not Proceeding to Autologous Stem-Cell Transplantation (CAREMM-001).
Phase II Study of BCMA Chimeric Antigen Receptor T-Cell Therapy in Patients With Newly Diagnosed Multiple Myeloma Ineligible for or Not Proceeding to Autologous Stem-Cell Transplantation (CAREMM-001).
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一线 BCMA CAR-T 治疗在不适合或未进行 ASCT 的 NDMM 人群中诱导深度、快速且持久的缓解,且安全性可控。这些发现支持将其作为一种可能改变实践的策略在该人群中进一步开展研究。
新诊断多发性骨髓瘤(NDMM)患者若不适合或未进行自体干细胞移植(ASCT)——通常是由于年龄或虚弱——接受多线有效治疗的机会有限,这凸显了对新型一线治疗策略的需求。
在这项II期、开放标签、单臂试验(ClinicalTrials.gov标识符:NCT05860036)中,患者接受3-4个周期方案允许的诱导治疗,随后接受B细胞成熟抗原(BCMA)CAR-T 输注,以及后续巩固治疗和来那度胺维持治疗。主要终点为输注后第3个月时微小残留病(MRD)阴性(10 -5)率。
2023年4月4日至2024年12月26日期间,共筛选43例患者,入组40例,36例接受输注(中位年龄68岁[46-75])。在输注队列中,输注后第3个月的MRD阴性率为100%(36/36;95% CI,90.3至100.0)。中位随访时间为输注后15.8个月(范围,4.3-26.0),未观察到MRD复发。完全缓解率(CRR)从输注前的33.3%(12/36;95% CI,18.6至51.0)升高至第3个月的69.4%(25/36;95% CI,51.9至83.7),并在末次随访时达到94.4%(34/36;95% CI,81.3至99.3)。最常见的3至4级不良事件为一过性血细胞减少,包括淋巴细胞减少(100%)、中性粒细胞减少(88.9%)、白细胞减少(80.6%)、血小板减少(19.4%)和贫血(8.3%)。细胞因子释放综合征发生于52.8%的患者(均为1至2级),免疫效应细胞相关神经毒性发生于5.6%(均为1级),感染发生于30.6%(3级为19.4%)。截至数据截止时,未发生死亡或疾病进展。
Patients with newly diagnosed multiple myeloma (NDMM) who are ineligible for or not proceeding to autologous stem-cell transplantation (ASCT)-often because of age or frailty-have limited opportunities to receive multiple effective lines of therapy, underscoring the need for novel frontline strategies.
In this phase II, open-label, single-arm trial (ClinicalTrials.gov identifier: NCT05860036), patients received 3-4 cycles of protocol-allowed induction, followed by B-cell maturation antigen (BCMA) CAR-T infusion, and subsequent consolidation and lenalidomide maintenance. The primary end point was the rate of minimal residual disease (MRD) negativity (10 -5 ) at Month three postinfusion.
Between April 4, 2023, and December 26, 2024, 43 patients were screened, 40 were enrolled, and 36 received infusion (median age, 68 years [46-75]). In the infused cohort, the MRD negativity rate at Month three postinfusion was 100% (36 of 36; 95% CI, 90.3 to 100.0). With a median follow-up of 15.8 months postinfusion (range, 4.3-26.0), no MRD recurrence was observed. The complete response rate (CRR) increased from 33.3% (12 of 36; 95% CI, 18.6 to 51.0) preinfusion to 69.4% (25 of 36; 95% CI, 51.9 to 83.7) at Month 3% and 94.4% (34 of 36; 95% CI, 81.3 to 99.3) at last follow-up. The most common grade 3 to 4 adverse events were transient cytopenia, including lymphopenia (100%), neutropenia (88.9%), leukopenia (80.6%), thrombocytopenia (19.4%), and anemia (8.3%). Cytokine release syndrome occurred in 52.8% of patients (all grade 1 to 2), immune effector cell-associated neurotoxicity in 5.6% (all grade 1), and infections in 30.6% (grade 3 in 19.4%). No deaths or disease progressions occurred by cutoff.
Frontline BCMA CAR-T therapy induces deep, rapid, and durable remissions with a manageable safety profile in the NDMM population ineligible for or not proceeding to ASCT. These findings support its investigation as a potentially practice-changing strategy for this population.
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