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实体瘤的 CAR-T 细胞治疗:过去与未来

英文原题:Chimeric Antigen Receptor T-Cell Therapy for Solid Tumors: The Past and the Future.

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Chimeric Antigen Receptor T-Cell Therapy for Solid Tumors: The Past and the Future.

PubMed 2022/12/28(内容时间) J Immunother Precis Oncol Q2 · IF 3.1(JCR 2025)

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中文摘要

嵌合抗原受体(CAR)T细胞疗法已成为晚期血液系统恶性肿瘤多种适应证的新标准治疗。尽管开展了多项临床前和早期临床试验,这一创新疗法用于实体瘤的总体临床经验仍令人失望。CAR-T 细胞疗法失败且实体瘤抗肿瘤活性有限,归因于多种机制,包括肿瘤抗原异质性、恶劣的肿瘤微环境、CAR-T 细胞难以迁移至肿瘤部位,以及某些情境下不可接受的毒性等。然而,人们对这些失败机制的认识已取得显著进步,并开始采用多种新兴方法克服挑战。本综述在简述实体瘤免疫疗法历史背景后,重点介绍CAR-T 细胞设计的最新进展,总结已完成的临床试验,并讨论CAR-T 细胞疗法当前面临的挑战及建议的应对策略。

展开英文摘要原文

Chimeric antigen receptor (CAR) T-cell therapy is the new standard treatment for various indications in patients with advanced hematologic malignancies. Despite the several preclinical and early phase clinical trials, the overall clinical experience has been disappointing when applying this innovative therapy in solid tumors.

The failure of CAR T-cell therapy and its limited antitumor activity in solid tumors have been attributed to several mechanisms, including tumor antigen heterogeneity, the hostile tumor microenvironment and poor trafficking of CAR T cells into tumor sites, and the unacceptable toxicities in some settings, among others.

However, remarkable improvements have been made in understanding many of these failure mechanisms for which several emerging novel approaches are being applied to overcome these challenges. In this review, after a brief historic background for immunotherapy in solid tumors, we highlight the recent developments achieved in CAR T-cell designs, summarize completed clinical trials, and discuss current challenges facing CAR T-cell therapy and the suggested strategies to overcome these barriers.

论文信息

作者
Srour SA、Akin S
第一作者单位
Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.United States
通讯作者单位
Department of Medical Oncology, Hacettepe University Cancer Institute, Hacettepe University, Ankara, Turkey.Turkey
文献类型
综述
期刊
Journal of immunotherapy and precision oncology2023 Feb
原文标识
PubMed 36751657 · DOI 10.36401/JIPO-22-7