4.2 Review

Chimeric Antigen Receptor Therapy: How Are We Driving in Solid Tumors?

期刊

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
卷 26, 期 10, 页码 1759-1769

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2020.06.020

关键词

Immune effector cell therapy; Solid tumor; Cancer immunotherapy; Chimeric antigen receptor T cells; T cell receptor

资金

  1. American Physicians Fellowship for Medicine in Israel

向作者/读者索取更多资源

Immune effector cell (IEC) therapy is emerging as a promising approach in the field of cancer immunotherapy. Clinical IEC trials, predominantly using chimeric antigen receptor (CAR) T cells, have shown excellent responses in CD19+ B cell malignancies and multiple myeloma. In solid tumors, preclinical data are encouraging, but clinical data are in their infancy, and there are challenges in using CAR T therapy in this setting, including (1) on-target off-tumor toxicity, (2) optimal target identification, (3) effective trafficking into bulky tumor tissue, and (4) resistance to tumor immune evasion mechanisms. Novel techniques and modifications are being explored in both the preclinical and clinical settings, aiming to improve treatment efficacy and address the aforementioned obstacles to successful CAR T therapy in solid tumors. Here we review these challenges in a clinically oriented approach and summarize published clinical trials using CAR T therapy in a variety of solid tumors. (c) 2020 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据