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我如何利用 CD19 CAR-T 细胞成功或失败的风险因素指导 B 细胞 ALL 儿童和青少年及年轻成人患者的管理

英文原题:How I use risk factors for success or failure of CD19 CAR T cells to guide management of children and AYA with B-cell ALL.

查看英文原题

How I use risk factors for success or failure of CD19 CAR T cells to guide management of children and AYA with B-cell ALL.

PubMed 2023/03/16(内容时间) Blood Q1 · IF 23.9(JCR 2025)

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中文摘要

通过克服化疗耐药,嵌合抗原受体(CAR)T细胞促进深度、完全缓解,并为相当一部分化疗难治性疾病患者提供长期治愈的可能。然而,这一成功也伴随着10%至30%的患者未能达到缓解,以及超过半数接受治疗的患者最终出现复发。随着在儿童、青少年和年轻成人(AYA)中使用CAR-T 细胞治疗复发/难治性B细胞急性淋巴细胞白血病(B-ALL)已积累十余年经验,且距美国食品药品监督管理局首次批准已过去5年,界定患者特异性风险因素细微差别的数据正在不断涌现。随着2种独特的CD19 CAR-T 细胞构建体在B-ALL中实现商业化可及,本文中,我们回顾当前文献,概述我们对患者的处理方法,并讨论个体因素如何为优化接受CD19 CAR-T 细胞的儿童和AYA患者的结局提供策略信息。

我们纳入了来自前瞻性研究和近期大型回顾性研究的数据,这些数据为理解CAR-T 细胞治疗失败风险何时较高提供了见解,并提供了关于何时应考虑巩固性造血细胞移植或实验性CAR-T 细胞和/或替代免疫治疗的视角。

我们还提出了需要开展前瞻性试验以解决CAR-T 细胞治疗最佳使用问题的领域。

展开英文摘要原文

By overcoming chemotherapeutic resistance, chimeric antigen receptor (CAR) T cells facilitate deep, complete remissions and offer the potential for long-term cure in a substantial fraction of patients with chemotherapy refractory disease.

However, that success is tempered with 10% to 30% of patients not achieving remission and over half of patients treated eventually experiencing relapse. With over a decade of experience using CAR T cells in children, adolescents, and young adults (AYA) to treat relapsed/refractory B-cell acute lymphoblastic leukemia (B-ALL) and 5 years since the first US Food and Drug Administration approval, data defining the nuances of patient-specific risk factors are emerging.

With the commercial availability of 2 unique CD19 CAR T-cell constructs for B-ALL, in this article, we review the current literature, outline our approach to patients, and discuss how individual factors inform strategies to optimize outcomes in children and AYA receiving CD19 CAR T cells.

We include data from both prospective and recent large retrospective studies that offer insight into understanding when the risks of CAR T-cell therapy failure are high and offer perspectives suggesting when consolidative hematopoietic cell transplantation or experimental CAR T-cell and/or alternative immunotherapy should be considered.

We also propose areas where prospective trials addressing the optimal use of CAR T-cell therapy are needed.

论文信息

作者
Myers RM、Shah NN、Pulsipher MA
第一作者单位
Division of Oncology, Cell Therapy and Transplant Section, Children's Hospital of Philadelphia, Philadelphia, PA.United States
通讯作者单位
Division of Hematology and Oncology, Intermountain Primary Children's Hospital, Huntsman Cancer Institute, Spencer Fox Eccles School of Medicine at the University of Utah, Salt Lake City, UT.
文献类型
综述
期刊
Blood2023 Mar 16
原文标识
PubMed 36416729 · DOI 10.1182/blood.2022016937