下一代基于抗体的癌症治疗:抗体-药物偶联物和双特异性抗体在血液系统恶性肿瘤和实体瘤中的应用
Next-generation antibody-based therapeutics in cancer: antibody-drug conjugates bispecific antibodies across hematologic malignancies and solid tumors
肿瘤学的治疗范式正在经历由抗体药物偶联物(ADC)和双特异性抗体(bsAb)驱动的深刻变革。
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Next-generation antibody-based therapeutics in cancer: antibody-drug conjugates bispecific antibodies across hematologic malignancies and solid tumors
肿瘤学的治疗范式正在经历由抗体药物偶联物(ADC)和双特异性抗体(bsAb)驱动的深刻变革。
Hattrick against Lymphoma with Trispecific CAR T Cells.
Vasu 及其同事报告了靶向 CD19、CD20 和 CD22 的快速制备三特异性CAR-T 细胞的首批临床评估之一。
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%。
Short ramp-up glofitamab halves mortality risk after anti-CD19 CAR T-cell therapy failure in patients with diffuse large B-cell lymphoma: final result
在这项稳健的疗效比较研究中,CAR-T 细胞治疗失败后首次复发或进展时给予短爬坡 glofitamab,与同期非双特异性挽救治疗相比显著提高了生存机会。
Clinical outcomes and spatial transcriptomic profiles of CD19/20 CAR-T therapy in relapsed or refractory B-cell non-Hodgkin's lymphoma.
双特异性 CD19/20 CAR-T 疗法产生了持久的临床活性,且毒性可控。
Study of Allo-QuadCAR01-T, an Allogeneic CAR-T Targeting CD19/CD20, in Patients With Relapsed or Refractory B-Cell Malignancies
这是一项 I/II 期注册临床试验,评估细胞治疗用于淋巴瘤、白血病的安全性、可行性及初步疗效。当前状态:招募中。计划入组 178 例。试验地点:美国 · 芝加哥、埃文斯顿、普罗维登斯、纳什维尔(共 13 个中心)。登记号:NCT07284433。
Demethylation-primed tandem CD19/CD20 CAR T cells in relapsed/refractory B-cell lymphoma: a phase I/II trial.
在此,我们报告一项开放标签非随机I/II期试验(NCT04697940),评估经DAC预处理的CD19/CD20双靶向CAR T细胞(dCAR T)在23例复发或难治性NHL患者中的应用。
Influence of B cell-lineage targeted CAR-T cell therapy on humoral immunity and vaccine-induced antibody response.
72 名参与者的一个亚组接受了 CARTx 后疫苗反应的评估。
AI-guided CAR designs and targeted pathway modulation to enhance multi-antigen CAR T cell durability and overcome antigen escape.
综合起来,我们的研究提出了一种新一代 AI 引导的 CAR-T 策略,该策略整合基于结构的优化与细胞内调控,以改善持久性、拓宽抗原覆盖并确保持久的治疗疗效。
Development of tandem canine CAR T cells to enable comparative studies of aggressive B-cell lymphoma.
抗CD19CAR-T(CAR T)细胞对弥漫大B细胞淋巴瘤(DLBCL)具有令人期待的治疗潜力,但许多接受治疗的患者因CD19阴性克隆驱动的疾病进展而复发。
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