← 返回

弥漫大 B 细胞淋巴瘤中 CAR-T 细胞治疗的预测反应标志物及 CAR-T19 失败后的治疗选择

英文原题:CAR T-Cell Therapy Predictive Response Markers in Diffuse Large B-Cell Lymphoma and Therapeutic Options After CART19 Failure.

查看英文原题

CAR T-Cell Therapy Predictive Response Markers in Diffuse Large B-Cell Lymphoma and Therapeutic Options After CART19 Failure.

PubMed 2022/07/06(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

利用经基因改造、表达嵌合抗原受体(CAR)的T细胞进行免疫治疗,已在复发/难治性B细胞淋巴瘤患者中显示显著临床疗效。然而,超过50%的治疗患者未获益,原因包括无应答或再次复发。因此,阐明预测CAR19疗效的临床和生物学特征至关重要,有望筛选更可能应答的患者。过去5年,CAR19 T细胞治疗弥漫性大B细胞淋巴瘤(DLBCL)已积累了丰富临床经验,对其疗效机制的理解也取得重大进展。本综述讨论与DLBCL患者CAR19应答相关的临床及肿瘤特征,以及输注CAR19产品的生物学特征对临床应答的影响。CAR19治疗失败的DLBCL患者预后较差,本文亦讨论新药治疗策略。

展开英文摘要原文

Immunotherapy with T cells genetically modified with chimeric antigen receptors (CARs) has shown significant clinical efficacy in patients with relapsed/refractory B-cell lymphoma. Nevertheless, more than 50% of treated patients do not benefit from such therapy due to either absence of response or further relapse. Elucidation of clinical and biological features that would predict clinical response to CART19 therapy is of paramount importance and eventually may allow for selection of those patients with greater chances of response.

In the last 5 years, significant clinical experience has been obtained in the treatment of diffuse large B-cell lymphoma (DLBCL) patients with CAR19 T cells, and major advances have been made on the understanding of CART19 efficacy mechanisms.

In this review, we discuss clinical and tumor features associated with response to CART19 in DLBCL patients as well as the impact of biological features of the infusion CART19 product on the clinical response. Prognosis of DLBCL patients that fail CART19 is poor and therapeutic approaches with new drugs are also discussed.

论文信息

作者
Caballero AC、Escribà-Garcia L、Alvarez-Fernández C、Briones J
单位
Hematology Service, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.Spain
文献类型
综述 · 非美国政府资助研究
期刊
Frontiers in immunology2022
原文标识
PubMed 35874685 · DOI 10.3389/fimmu.2022.904497