免疫性血小板减少症的新兴治疗进展:2025 ASH 年会精选早期与关键性试验亮点
Emerging therapeutic advances for immune thrombocytopenia: highlights from selected early‑phase and pivotal trials at the 2025 ASH annual meeting.
本通讯重点介绍了 2025 ASH 年会上报告的免疫性血小板减少症 (ITP) 新兴免疫靶向疗法。
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Emerging therapeutic advances for immune thrombocytopenia: highlights from selected early‑phase and pivotal trials at the 2025 ASH annual meeting.
本通讯重点介绍了 2025 ASH 年会上报告的免疫性血小板减少症 (ITP) 新兴免疫靶向疗法。
Multiple Myeloma and Mimicry: Gastrointestinal Tract Histologic Findings in Patients Following Chimeric Antigen Receptor T-cell Therapy and Anti-CD38
我们的研究结果提示,CAR-T 治疗可引起胃肠道损伤,其特征为上皮细胞凋亡和上皮内淋巴细胞增多,并且主要累及深部黏膜的隐窝和腺体。
Non-ICANS neurotoxicities CD19-directed CAR T-cell therapy and the emergence of movement and neurocognitive treatment-emergent adverse events: a case
我们报告一例63岁男性弥漫性大B细胞淋巴瘤(DLBCL)患者,在接受靶向CD19的CAR T细胞疗法axicabtagene ciloleucel(axi-cel)治疗后第+22天,于初始发生CRS和ICANS之后,出现迟发性神经毒性。
Combining a CAR and a chimeric costimulatory receptor enhances T cell sensitivity to low antigen density and promotes persistence.
尽管使用针对血液系统恶性肿瘤的CAR-T细胞取得了高缓解率,仍有相当比例的患者最终出现肿瘤复发。
Trends in Nephrology: From nihilism to targeted treatment of antibody-mediated rejection.
抗CD38抗体目前构成了治疗AMR证据最强的药物类别。
Monospecific and Bispecific Chimeric Antigen Receptor (CAR) T-cell Therapy in Multiple Myeloma: A Systematic Review, Meta-analysis and Meta-regression
分析了 44 个队列(2 个一线队列和 42 个复发/难治性队列)的 52 篇报告,共纳入 1833 例患者。
Translating B-Cell and Plasma-Cell Targeting from Oncology to Autoimmunity: Modalities, Quantitative Bridging, and a Development Roadmap.
B 细胞通过自身抗体产生、抗原提呈和细胞因子失调,以及致病性 B 细胞或浆细胞区室的持续存在,驱动 B 细胞恶性肿瘤和多种自身免疫性疾病。
Targets for CAR Therapy in Multiple Myeloma.
多发性骨髓瘤(MM或浆细胞骨髓瘤)是一种异质性B细胞恶性肿瘤,通常表现出高复发率、耐药性以及肿瘤亚克隆的分子多样性。
Comparative efficacy and safety of BCMA-targeted CAR T cells and BiTEs in relapsed/refractory multiple myeloma: a meta-analysis of interventional and
共纳入 26 项研究,包含 2,246 例患者。
Unveiling causal immune cell-gene associations in multiple myeloma: insights from systematic reviews and Mendelian randomization analyses.
我们的研究支持CAR-T细胞疗法在rrMM患者中的疗效和安全性,ORR为82.2%,严重CRS(6.3%)和神经毒性(0.9%)发生率低。这一发现还提示BCMA/CD19双特异性CAR-T细胞具有更优的ORR,尚待临床确认。MR分析揭示了免疫细胞、VDR和VHL等基因与MM之间的关联,增进了我们对其病理生理学的理解。
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