靶向 CD79b 的三种新型 CAR 用于非霍奇金淋巴瘤治疗的临床前开发及靶抗原丢失特征分析
Preclinical development of three novel CARs targeting CD79b for the treatment of non-Hodgkin's lymphoma and characterization of the loss of the target
基于特异性、疗效和靶抗原丢失,CARLY3 代表了一种针对非霍奇金淋巴瘤的潜在新型 CAR 治疗。
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Preclinical development of three novel CARs targeting CD79b for the treatment of non-Hodgkin's lymphoma and characterization of the loss of the target
基于特异性、疗效和靶抗原丢失,CARLY3 代表了一种针对非霍奇金淋巴瘤的潜在新型 CAR 治疗。
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。
Unlocking T cell exhaustion: Insights and implications for CAR-T cell therapy.
然而,尽管取得了这些进展,CAR-T疗法的疗效往往受到T细胞耗竭的影响,这一现象阻碍了CAR-T细胞的持久性和效应功能,导致接受CD19或CD22 CAR-T细胞治疗血液系统恶性肿瘤的患者复发率高达75%。
Dual-targeted CAR T-cell immunotherapies for hematological malignancies: latest updates from the 2023 ASH annual meeting.
在过去几年中,双靶点嵌合抗原受体(CAR)T细胞疗法已被用于血液系统恶性肿瘤的治疗,以减少治疗失败,特别是在抗原逃逸的情况下。
Early intrathecal dexamethasone and methotrexate as an effective approach for immune effector cell-associated neurotoxicity syndrome after CAR-T cell
我们的数据提示,早期给予 IDM 可能有助于快速缓解 CAR-T 细胞治疗后的重度或类固醇难治性 ICANS,这可能为这些患者的后续治疗创造机会。
Infectious complications of CAR T-cell therapy across novel antigen targets in the first 30 days.
我们提供了输注后30天内多种靶点和疾病感染风险的广泛概述,阐明了独特特征和共性,突出了对改善患者预后重要的方面。
Identifying Modifiers of CAR T-Cell Therapeutic Efficacy and Safety: A Systematic Review and Individual Patient Data Meta-Analysis.
我们为 IPDMA 确定了 89 项试验,共纳入 2,331 例患者。
Quantitative pharmacology of dual-targeted bicistronic CAR-T-cell therapy using multiscale mechanistic modeling.
尽管单靶点嵌合抗原受体(CAR)T 细胞疗法在血液系统恶性肿瘤中取得初步成功,其长期疗效常受抗原异质性和抗原逃逸的阻碍。
Mutations in immunodeficiency-related genes may increase the risk of infection after CAR-T-cell therapy: a report of two cases.
对于 CAR-T 细胞治疗后出现持续性或复发性感染的患者,建议筛查免疫缺陷相关基因突变,其结果可能有助于 CAR-T 治疗后感染的管理。
Updated Clinical Perspectives and Challenges of Chimeric Antigen Receptor-T Cell Therapy in Colorectal Cancer and Invasive Breast Cancer.
近年来,结直肠癌(CRC)和乳腺癌(BC)的发病率在全球范围内上升,并因缺乏选择性抗肿瘤疗法而导致更高的死亡率。
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