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过继性T细胞疗法:障碍与机遇概述

Adoptive T cell therapy: An overview of obstacles and opportunities.

作者信息

Baruch Erez Nissim, Berg Amy Lauren, Besser Michal Judith, Schachter Jacob, Markel Gal

机构信息

The Ella Lemelbaum Institute of Immuno-oncology, Institute of Oncology, Sheba Medical Center, Tel Hashomer, Israel.

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

Cancer. 2017 Jun 1;123(S11):2154-2162. doi: 10.1002/cncr.30491.


DOI:10.1002/cncr.30491
PMID:28543698
Abstract

The therapeutic potential of adoptive cell therapy (ACT) in cancer patients was first acknowledged 3 decades ago, but it was an esoteric approach at the time. In recent years, technological advancements have transformed ACT into a viable therapeutic option that can be curative in some patients. In fact, current ACT response rates are 80% to 90% for hematological malignancies and 30% for metastatic melanoma refractory to multiple lines of therapy. Although these results are encouraging, there is still much to be done to fulfill ACT's potential, specifically with regard to improving clinical efficacy, expanding clinical indications, reducing toxicity, and increasing production and cost-effectiveness. This review addresses the current major obstacles to ACT and presents potential solutions. Cancer 2017;123:2154-62. © 2017 American Cancer Society.

摘要

30年前人们首次认识到过继性细胞疗法(ACT)对癌症患者的治疗潜力,但在当时这是一种深奥的方法。近年来,技术进步已将ACT转变为一种可行的治疗选择,在某些患者中可能具有治愈效果。事实上,目前ACT对血液系统恶性肿瘤的缓解率为80%至90%,对多线治疗难治的转移性黑色素瘤的缓解率为30%。尽管这些结果令人鼓舞,但要充分发挥ACT的潜力仍有许多工作要做,特别是在提高临床疗效、扩大临床适应症、降低毒性以及提高产量和成本效益方面。本文综述了ACT目前面临的主要障碍并提出了潜在的解决方案。《癌症》2017年;123:2154 - 62。© 2017美国癌症协会。

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