Efficacy, Safety, and Challenges of CAR T-Cells in the Treatment of Solid Tumors.
Qiuqiang ChenChangquan LingWenxue MaPublished in: Cancers (2022)
Immunotherapy has been the fifth pillar of cancer treatment in the past decade. Chimeric antigen receptor (CAR) T-cell therapy is a newly designed adoptive immunotherapy that is able to target and further eliminate cancer cells by engaging with MHC-independent tumor-antigens. CAR T-cell therapy has exhibited conspicuous clinical efficacy in hematological malignancies, but more than half of patients will relapse. Of note, the efficacy of CAR T-cell therapy has been even more disappointing in solid tumors. These challenges mainly include (1) the failures of CAR T-cells to treat highly heterogeneous solid tumors due to the difficulty in identifying unique tumor antigen targets, (2) the expression of target antigens in non-cancer cells, (3) the inability of CAR T-cells to effectively infiltrate solid tumors, (4) the short lifespan and lack of persistence of CAR T-cells, and (5) cytokine release syndrome and neurotoxicity. In combination with these characteristics, the ideal CAR T-cell therapy for solid tumors should maintain adequate T-cell response over a long term while sparing healthy tissues. This article reviewed the status, clinical application, efficacy, safety, and challenges of CAR T-cell therapies, as well as the latest progress of CAR T-cell therapies for solid tumors. In addition, the potential strategies to improve the efficacy of CAR T-cells and prevent side effects in solid tumors were also explored.
Keyphrases
- cell therapy
- stem cells
- mesenchymal stem cells
- end stage renal disease
- poor prognosis
- induced apoptosis
- dendritic cells
- newly diagnosed
- gene expression
- chronic kidney disease
- ejection fraction
- oxidative stress
- bone marrow
- risk assessment
- cell death
- cell cycle arrest
- case report
- long non coding rna
- robot assisted
- free survival
- minimally invasive
- smoking cessation
- patient reported