靶向 CD19、CD20 和 CD22 的床旁制备三特异性 CAR T 细胞首次人体试验的安全性与临床结局
Safety and Clinical Outcomes of a First-in-Human Trial of Point-of-Care Manufactured Trispecific CAR T Cells Targeting CD19, CD20, and CD22.
总体缓解率为50%,其中淋巴瘤患者的完全缓解率为83%。
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按「中国试验优先 → 正在招募 → 更新更近」排序。信息来自 ClinicalTrials.gov 与 CDE 公开登记。能否入组、费用与可及性,以登记原文和主治医生判断为准。
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Safety and Clinical Outcomes of a First-in-Human Trial of Point-of-Care Manufactured Trispecific CAR T Cells Targeting CD19, CD20, and CD22.
总体缓解率为50%,其中淋巴瘤患者的完全缓解率为83%。
DLBCL Cells Emerge after CD19 CAR T Cells with Cross-Antigen Resistance and a Gene Signature Predictive of Clinical CAR T-cell Response.
我们的研究结果表明,前期双抗原靶向和联合治疗可能改善临床结局。
ARI0003: Co-transduced CD19/BCMA dual-targeting CAR-T cells for the treatment of non-Hodgkin lymphoma.
CD19 CAR-T 疗法在复发/难治性非霍奇金淋巴瘤(NHL)中已取得显著缓解。
Efficacy and safety analysis of CAR-T cell salvage therapy in relapsed/refractory diffuse large B-cell lymphoma after failure of bispecific antibody t
CAR-T 挽救治疗在 BsAb R/R DLBCL 患者中显示出高缓解率和可控的安全性。早期生存数据表明,在这一 BsAb 耐药的高危人群中具有令人鼓舞的临床获益,尽管需要延长随访以确认持久性。本研究为 CAR-T 作为该情境下的一种潜在挽救策略提供了支持性证据。
Alternative splicing of its 5'-UTR limits CD20 mRNA translation and enables resistance to CD20-directed immunotherapies.
CD19和CD22中编码外显子的异常跳跃损害了B细胞恶性肿瘤对免疫治疗的反应。
Dual-targeting CAR T cells for B-cell acute lymphoblastic leukemia and B-cell non-Hodgkin lymphoma.
涵盖所有生产策略的 1 期和 2 期试验显示,这是一种安全的方法,具有相当的缓解率和初始产品扩增。
Preclinical Evidence of an Allogeneic Dual CD20xCD22 CAR to Target a Broad Spectrum of Patients with B-cell Malignancies.
尽管自体嵌合抗原受体(CAR)T 细胞取得了显著成功,但部分患者仍因肿瘤抗原逃逸以及抗原表达低或不均等机制而复发。
Guided by target selection, inotuzumab ozogamicin successfully salvaged a patient with refractory follicular lymphoma after anti-CD19 and anti-CD22 CA
一名 69 岁男性患者被诊断为难治性滤泡性淋巴瘤(FL),其胸腔积液中 43.6% 的异常 B 淋巴细胞表达 CD20-、CD19+、CD22+。
Efficacy and safety of CD19-specific CAR-T cell-based therapy in secondary central nervous system lymphoma.
在此,我们回顾性分析了15例接受CD19特异性CAR-T细胞治疗的R/R继发性CNSL患者。
Sequential different B-cell antigen-targeted CAR T-cell therapy for pediatric refractory/relapsed Burkitt lymphoma.
从末次输注至数据截止日期的中位时间为 17 个月(范围 15-23 个月)。
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