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A Nonviral Approach to Generate Transient Chimeric Antigen Receptor T Cells Using mRNA for Cancer Immunotherapy
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BTK Inhibitors and CAR T-Cell Therapy in Treating Mantle Cell Lymphoma-Finding a Dancing Partner
Javier L Munoz1, Yucai Wang2, Preetesh Jain3
1Mayo Clinic, Phoenix, AZ, USA.
Current Oncology Reports
|May 21, 2022
Summary
Combining Bruton
Area of Science:
- Hematology
- Oncology
- Immunotherapy
Background:
- Relapsed or refractory mantle cell lymphoma (R/R MCL) treatment has been transformed by Bruton's tyrosine kinase (BTK) inhibitors and chimeric antigen receptor (CAR) T-cell therapy.
- Approved BTK inhibitors for R/R MCL include ibrutinib, acalabrutinib, and zanubrutinib.
- Brexucabtagene autoleucel is an approved CAR T-cell therapy for R/R MCL, demonstrating efficacy in the ZUMA-2 trial.
Purpose of the Study:
- To review the feasibility of combining BTK inhibitors (BTKis) with CAR T-cell therapy for R/R MCL.
- To explore potential combination treatment scenarios for R/R MCL.
- To evaluate the potential benefits of combination strategies as these therapies become standard.
Main Methods:
- Review of current literature on BTK inhibitors and CAR T-cell therapy in R/R MCL.
- Analysis of existing evidence for combined treatment efficacy.
- Presentation of potential combination treatment scenarios.
Main Results:
- BTKis and CAR T-cell therapy represent significant advancements in R/R MCL treatment.
- Evidence suggests that combining BTKis with CAR T-cell therapy may enhance CAR T-cell efficacy.
- Combination strategies warrant evaluation for improved outcomes in R/R MCL.
Conclusions:
- Combination of BTK inhibitors and CAR T-cell therapy is a feasible strategy for R/R MCL.
- Further evaluation of combination treatment is crucial as these therapies become standard care.
- Optimizing combination strategies may improve patient outcomes in R/R MCL.
Keywords:
Bruton’s tyrosine kinaseChimeric antigen receptor T-cell therapyCombination therapyRelapsed/refractory mantle cell lymphomaMore Related Videos
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