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:Clinical Outcomes of BCMA CAR-T Cells in a Multiple Myeloma Patient With Central Nervous System Invasion.
Clinical Outcomes of BCMA CAR-T Cells in a Multiple Myeloma Patient With Central Nervous System Invasion.
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本病例报告表明,BCMA CAR-T 能够以较低的不良事件有效清除中枢神经系统受累的多发性骨髓瘤,提示 CAR-T 细胞治疗可能成为此类难治性疾病的可行治疗选择。
多发性骨髓瘤(MM)是第二常见的血液系统恶性肿瘤,目前仍缺乏有效临床治疗。累及中枢神经系统(CNS)的 MM 尤为罕见。靶向 B 细胞成熟抗原(BCMA)的CAR-T 细胞疗法在治疗复发/难治性 MM 方面前景良好,但鲜有研究报告其能否抑制累及 CNS 的 MM。 病例介绍:本文报告一例特殊病例:一名 63 岁男性患有 CNS 受累的 MM,并迅速出现多器官髓外疾病(EMD)进展。CAR-T 输注前,患者一线接受 5 个周期硼替佐米、多柔比星和地塞米松(PAD)治疗及自体移植;随后二线接受 2 个周期硼替佐米、来那度胺和地塞米松(VRD),三线接受达雷妥尤单抗、硼替佐米和地塞米松(DVD)。由于疾病仍快速进展,患者接受 BCMA CAR-T 输注;1 个月后达到严格完全缓解(sCR),缓解持续 4 个月。同时仅观察到 1 级细胞因子释放综合征(CRS)。
本病例显示 BCMA CAR-T 可有效清除累及 CNS 的 MM,且不良事件较轻,提示 CAR-T 细胞疗法可作为此类难治性疾病的可行治疗选择。 临床试验注册:ClinicalTrials.gov,注册号 NCT04537442.a。
Multiple myeloma (MM) is the second most common hematological malignancy that still lacks effective clinical treatments. In particular, MM with central nervous system (CNS) invasion occurs rarely. Although B-cell maturation antigen (BCMA)-targeted chimeric antigen receptor-T (CAR-T) cell therapy has shown great promise for the treatment of relapsed/refractory MM, few studies have reported whether BCMA CAR-T could inhibit MM with CNS invasion. CASE PRESENTATION: In this study, we report a special case of a 63-year-old male patient who suffered MM with CNS invasion and presented rapid extramedullary disease (EMD) progression into multiple organs. Before CAR-T cell infusion, this patient received five cycles of bortezomib, Adriamycin, and dexamethasone (PAD) and an autologous transplant as the front-line treatment, followed by two cycles of bortezomib, lenalidomide, and dexamethasone (VRD) as the second-line regimen, and daratumumab, bortezomib, dexamethasone (DVD) as the third-line regimen. Since the patient still showed rapid progressive disease (PD), BCMA CAR-T cells were infused, and 1 month later, a stringent complete response (sCR) was achieved, and the response lasted for 4 months. Meanwhile, only grade 1 cytokine release syndrome (CRS) was observed.
This case report demonstrated that BCMA CAR-T could effectively eradicate CNS-involved MM with low adverse events, suggesting that CAR-T cell therapy could be a feasible therapeutic option for this kind of refractory disease. CLINICAL TRIAL REGISTRATION: https://ClinicalTrials.gov, identifier: NCT04537442.a.
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