决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Immunotherapies for Childhood Cancer.
过去 50 年间,儿童癌症治疗取得了实质性进展,5 年生存率达到 85%。
儿童癌症生存人数创历史新高。过去50年治疗进步使5年生存率达到约85%,但仍有10%至15%患者复发或难治,生存率显著较低。进一步强化细胞毒性化疗因严重毒性或疗效不足而失败,凸显新策略需求。免疫疗法正拓展至多种儿童癌症:靶向GD2的单抗已使神经母细胞瘤出现持久影像学和组织学应答;CD19双特异性抗体和CAR-T则改变了儿童难治性急性淋巴细胞白血病的治疗前景。本文综述儿童癌症免疫疗法的临床开发,聚焦急性淋巴细胞白血病和神经母细胞瘤这两类已被免疫治疗改变的主要癌症,介绍最新进展并讨论未来方向。
Children are surviving cancer in greater numbers than ever. Over the last 50 years, substantial advancements in pediatric cancer treatment have resulted in an 85% 5-year survival rate. Nonetheless, a notable 10%-15% of patients encounter relapse or develop refractory disease, leading to significantly lower survival. Recent attempts to further intensify cytotoxic chemotherapy have failed due to either severe toxicities or ineffectiveness, highlighting the need for new treatment strategies. Immunotherapies are emerging and expanding their clinical application to a wide array of cancers, including those affecting children. In pediatric cancers, monoclonal antibodies targeting GD2 have demonstrated durable radiographic and histologic responses in neuroblastoma (NB), and CD19-targeted bispecific antibodies (BsAbs) and chimeric antigen receptor (CAR) T cells have likewise changed the outlook for refractory acute lymphoblastic leukemia (ALL) in children. This review discusses the clinical development of immunotherapies for pediatric cancers, focusing on pediatric ALL and NB, two major pediatric cancers transformed by immunotherapy, updates on the recent advancements in immunotherapies, and further discusses the future directions of immunotherapy for pediatric cancers.
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