| Literature DB >> 31866478 |
Nathan Singh1, Elena Orlando2, Jun Xu3, Jie Xu3, Zev Binder4, McKensie A Collins3, Donald M O'Rourke4, J Joseph Melenhorst5.
Abstract
Chimeric antigen receptor (CAR)-engineered T cells have demonstrated remarkable success in the treatment of B cell malignancies. FDA approval of these therapies represents a watershed moment in the development of therapies for cancer. Despite the successes of the last decade, many patients will unfortunately not experience durable responses to CAR therapy. Emerging research has shed light on the biology responsible for these failures, and further highlighted the hurdles to broader success. Here, we review the recent research identifying how interactions between cancer cells and engineered immune cells result in resistance to CAR therapies.Entities:
Keywords: Chimeric antigen receptor; Resistance
Mesh:
Substances:
Year: 2019 PMID: 31866478 PMCID: PMC7684646 DOI: 10.1016/j.semcancer.2019.12.002
Source DB: PubMed Journal: Semin Cancer Biol ISSN: 1044-579X Impact factor: 15.707