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替沙格赛定用于治疗复发/难治性B细胞急性淋巴细胞白血病的儿童和年轻成人。

Tisagenlecleucel for treatment of children and young adults with relapsed/refractory B-cell acute lymphoblastic leukemia.

作者信息

Si Lim Stephanie J, Grupp Stephen A, DiNofia Amanda M

机构信息

Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.

Division of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.

出版信息

Pediatr Blood Cancer. 2021 Sep;68(9):e29123. doi: 10.1002/pbc.29123. Epub 2021 Jun 1.

Abstract

The treatment landscape for cancer therapy has changed drastically over the past decade. Tisagenlecleucel, the first genetically engineered adoptive cellular therapy approved by the United States Food and Drug Administration, has revolutionized this field by demonstrating impressive clinical success in children and young adults with relapsed/refractory B-cell acute lymphoblastic leukemia (r/r B-ALL). Now 3 years since its approval, we have gained a deeper understanding on the basic immunobiology and clinical efficacy of this drug. This review will provide an updated summary of tisagenlecleucel in childhood and young adults with r/r B-ALL, common side effects and their associated management strategies, as well as barriers that remain to be addressed in order to realize the maximum potential of this drug.

摘要

在过去十年中,癌症治疗领域发生了巨大变化。替沙格赛定(Tisagenlecleucel)是美国食品药品监督管理局批准的首个基因工程过继性细胞疗法,它在复发/难治性B细胞急性淋巴细胞白血病(r/r B-ALL)的儿童和年轻成人患者中取得了令人瞩目的临床成功,从而彻底改变了这一领域。自其获批至今已有3年,我们对这种药物的基础免疫生物学和临床疗效有了更深入的了解。本综述将提供关于替沙格赛定在r/r B-ALL儿童和年轻成人患者中的最新总结、常见副作用及其相关管理策略,以及为实现该药物的最大潜力仍有待解决的障碍。

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