CAR T-Cell therapy for the management of mantle cell lymphoma.
Zoufang HuangVivek P ChavdaRajashri BezbaruahHemant DhamneDong-Hua YangHong-Bing ZhaoPublished in: Molecular cancer (2023)
Mantle cell lymphoma (MCL) is a subtype of Non-Hodgkin lymphoma (NHL) of mature B-cells characterized by translocation, which is typically due to excess expression of Cyclin D1. Although with the progress in our knowledge of the causes for MCL and available treatments for MCL, this cancer is still incurable. Age, male gender, rapid advancement, significant nodal involvement, elevated serum lactate dehydrogenase level, and prognostic indications including increased expression of Ki-67 and presence of TP53 mutation, are symbols of poor outcome. Advanced immunotherapy using chimeric antigen receptor (CAR)-T cells is advantageous for patients suffering from B-cell malignancies and MCL. Targeting B-cell antigens on the cell surface is a feasible approach in re-occurring (R/R) MCL because of significant responses obtained in other B-cell cancers. USFDA has approved brexucabtagene autoleucel (Tecartus, KTE-X19), a novel CAR T-cell therapy to be used in patients with MCL who have not responded to previous treatments or have relapsed. The FDA approved this new treatment depending on the outcomes of the ZUMA-2 clinical trial. Serious adverse reactions, moderate anti-tumor activity, allergen withdrawal, antigen escape, limited tumor infiltration, and trafficking are major barriers to successful CAR T-cell therapy. This review is a brief synopsis of the development of CAR T-cell therapy for MCL.
Keyphrases
- cell therapy
- stem cells
- mesenchymal stem cells
- end stage renal disease
- clinical trial
- poor prognosis
- cell surface
- chronic kidney disease
- healthcare
- study protocol
- randomized controlled trial
- acute myeloid leukemia
- type diabetes
- acute lymphoblastic leukemia
- ejection fraction
- high intensity
- peritoneal dialysis
- drug administration
- cancer therapy
- drug delivery
- mental health
- patient reported outcomes
- adipose tissue
- papillary thyroid
- drug induced