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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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。
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。
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)。
Paediatric Strategy Forum for medicinal product development of chimeric antigen receptor T-cells in children and adolescents with cancer: ACCELERATE i
第七届多利益相关方儿科战略论坛聚焦于针对儿童和青少年癌症的嵌合抗原受体(CAR)T细胞。
Promising Immunotherapeutic Modalities for B-Cell Lymphoproliferative Disorders.
在过去几年中,许多B细胞淋巴瘤亚型和慢性淋巴细胞白血病(CLL)的治疗原则已转向更靶向的治疗。
Treatment strategies for relapse after CAR T-cell therapy in B cell lymphoma.
CART19细胞疗法已获美国食品药品监督管理局批准,用于初始治疗后12个月内复发或对一线治疗难治的患者。
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