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:Key predictors of long-term outcomes in BCMA-targeted CAR-T therapy for relapsed/refractory multiple myeloma.
Key predictors of long-term outcomes in BCMA-targeted CAR-T therapy for relapsed/refractory multiple myeloma.
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BCMA CAR-T 治疗在部分 r/r MM 患者中可提供持久缓解。早期干预可能通过促进持续 MRD 阴性来改善患者预后,从而改善整体治疗结局。
B细胞成熟抗原(BCMA)靶向CAR-T 细胞疗法在复发/难治性多发性骨髓瘤(r/r MM)患者中表现出高缓解率。然而,影响缓解持续时间的具体因素仍知之甚少。
这项单中心、回顾性观察性研究纳入了56例在中国同济医院接受BCMA CAR-T 疗法(equecabtagene autoleucel)治疗的r/r MM患者。我们分析了缓解率和长期临床结局,并确定了影响BCMA CAR-T 疗法长期疗效的关键因素。
中位随访39.6个月时,ORR为96.4%。在患者中,96.4%(56例中的54例)达到MRD阴性,而80.4%(56例中的45例)达到CR或sCR。在三重暴露、高细胞遗传学风险或未达到CR的患者中观察到较差的结局。较好的结局与CAR-T 细胞持续存在至少六个月和持续MRD阴性相关。延长的MRD阴性与更长的PFS强烈相关,对于维持MRD阴性12、24和36个月的患者,中位PFS持续时间分别为58个月、64个月和未达到(NR)。保持MRD阴性和无进展的患者表现出更高的CAR-T 细胞扩增峰值。此外,CAR-T 细胞持续存在与MRD阴性持续时间、PFS和OS呈正相关。
B-cell maturation antigen (BCMA)-directed chimeric antigen receptor T-cell (CAR-T) therapy exhibits high response rates in patients with relapsed/refractory multiple myeloma (r/r MM). However, the specific factors that influence the response duration remain poorly understood.
This single-centre, retrospective observational study included 56 patients with r/r MM who received BCMA CAR-T therapy (equecabtagene autoleucel) at Tongji Hospital, China. We analysed response rates and long-term clinical outcomes and identified key factors contributing to the long-term efficacy of BCMA CAR-T therapy.
At a median follow-up of 39.6 months, the overall response rate (ORR) was 96.4%. Among the patients, 96.4% (54 of 56) achieved minimal residual disease (MRD) negativity, whereas 80.4% (45 of 56) achieved complete response (CR) or stringent complete response (sCR). Poorer outcomes were observed in patients with triple exposure, high cytogenetic risk, or failure to achieve CR. Better outcomes were associated with a CAR-T cell persistence of at least six months and sustained MRD negativity. Prolonged MRD negativity was strongly correlated with longer progression-free survival (PFS), with median PFS durations of 58 months, 64 months, and not reached (NR) for patients who maintained MRD negativity for 12, 24, and 36 months, respectively. Patients who remained MRD-negative and progression-free exhibited higher CAR-T cell expansion peaks. Additionally, CAR-T cell persistence was positively correlated with the duration of MRD negativity duration, PFS, and overall survival (OS).
BCMA CAR-T therapy provides durable responses in a subset of patients with r/r MM. Early intervention may improve patient prognosis by promoting sustained MRD negativity, thus improving overall treatment outcomes. TRIAL REGISTRATION: Trial registration Chinese Clinical Trial Registry, ChiCTR2000033946 ( https://www.chictr.org.cn/showproj.html?proj=53503 ), Registered June 18, 2020. Trial registration Chinese Clinical Trial Registry, ChiCTR1800018137 ( https://www.chictr.org.cn/showproj.html?proj=30653 ), Registered August 31, 2018.
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