Clinical Strategies for Enhancing the Efficacy of CAR T-Cell Therapy for Hematological Malignancies.
Qianzhen LiuZengping LiuRongxue WanWenhua HuangPublished in: Cancers (2022)
Chimeric antigen receptor (CAR) T cells have been successfully used for hematological malignancies, especially for relapsed/refractory B-cell acute lymphoblastic leukemia and non-Hodgkin's lymphoma. Patients who have undergone conventional chemo-immunotherapy and have relapsed can achieve complete remission for several months with the infusion of CAR T-cells. However, side effects and short duration of response are still major barriers to further CAR T-cell therapy. To improve the efficacy, multiple targets, the discovery of new target antigens, and CAR T-cell optimization have been extensively studied. Nevertheless, the fact that the determination of the efficacy of CAR T-cell therapy is inseparable from the discussion of clinical application strategies has rarely been discussed. In this review, we will discuss some clinical application strategies, including lymphodepletion regimens, dosing strategies, combination treatment, and side effect management, which are closely related to augmenting and maximizing the efficacy of CAR T-cell therapy.
Keyphrases
- cell therapy
- acute lymphoblastic leukemia
- stem cells
- mesenchymal stem cells
- diffuse large b cell lymphoma
- hodgkin lymphoma
- end stage renal disease
- acute myeloid leukemia
- ejection fraction
- small molecule
- low dose
- chronic kidney disease
- newly diagnosed
- photodynamic therapy
- squamous cell carcinoma
- immune response
- multidrug resistant
- cell proliferation
- peritoneal dialysis
- systemic lupus erythematosus
- bone marrow
- cell cycle arrest
- mass spectrometry
- patient reported outcomes
- disease activity
- single cell
- rectal cancer