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Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography
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Relapsed/Refractory Mantle Cell Lymphoma: Beyond BTK Inhibitors
Madelyn Burkart1,2, Reem Karmali2
1Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Journal of Personalized Medicine
|March 25, 2022
Summary
Mantle cell lymphoma (MCL) treatment remains challenging due to relapsed or refractory disease. Bruton's tyrosine kinase inhibitors (BTKi) improved outcomes, but resistance necessitates further therapeutic strategies.
Area of Science:
- Hematology
- Oncology
- Immunology
Background:
- Mantle cell lymphoma (MCL) is an aggressive B-cell non-Hodgkin lymphoma (B-NHL) with poor prognoses in relapsed or refractory (R/R) stages.
- Conventional therapies for R/R MCL offer palliation rather than cure, highlighting the need for novel treatment approaches.
Purpose of the Study:
- To review current evidence on treatments for R/R MCL following progression on Bruton's tyrosine kinase inhibitors (BTKi).
- To discuss emerging therapies and sequencing strategies for R/R MCL post-BTKi failure.
Main Methods:
- Literature review of studies evaluating treatments for R/R MCL.
- Analysis of clinical trial data and real-world evidence for therapies used after BTKi failure.
Main Results:
- Bruton's tyrosine kinase inhibitors (BTKi) have improved progression-free survival (PFS) in R/R MCL compared to the pre-BTKi era.
- Despite BTKi efficacy, resistance develops, leading to poor outcomes with a median overall survival (OS) of 6-10 months.
- Chimeric antigen receptor (CAR) T-cell therapy shows promise in patients progressing after BTKi treatment.
Conclusions:
- Treatment of R/R MCL after BTKi failure remains a significant clinical challenge.
- Optimal sequencing and combination of therapies beyond BTKi are under investigation.
- Further research is crucial to establish effective, curative strategies for R/R MCL.
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