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Updated: Aug 5, 2026

08:31
Bioprinting of Hydrogel Tumor Slices as a 3D Model for Mantle Cell Lymphoma
Published on: September 12, 2025
First-Line Bruton's Tyrosine Kinase Inhibitor-Based Regimens for Mantle Cell Lymphoma
Robert Puckrin1, Diego Villa2,3, Isabelle Fleury4
1Arthur J.E. Child Comprehensive Cancer Centre, University of Calgary, Calgary, AB T2N 5G2, Canada.
Current Oncology (Toronto, Ont.)
|July 27, 2026
Summary
Novel covalent Bruton's tyrosine kinase inhibitor (cBTKi) combinations are evolving first-line (1L) therapy for mantle cell lymphoma (MCL). Patient-specific factors beyond traditional criteria guide optimal selection of these advanced cBTKi regimens.
Area of Science:
- Oncology
- Hematology
- Clinical Trials
Background:
- First-line (1L) therapy for mantle cell lymphoma (MCL) is rapidly advancing.
- Novel covalent Bruton's tyrosine kinase inhibitor (cBTKi) combinations demonstrate significant activity in recent trials.
Purpose of the Study:
- To explore the selection of 1L therapy for MCL considering emerging cBTKi options.
- To analyze the benefits, limitations, and challenges of novel cBTKi regimens in MCL treatment.
Main Methods:
- Review of recent phase II and phase III clinical trials involving cBTKi combinations.
- Presentation and discussion of three illustrative patient cases for 1L therapy selection.
- Analysis of factors influencing treatment decisions, including MCL biology and patient risk tolerance.
Main Results:
- cBTKi combinations show consistent activity in MCL treatment.
- Traditional selection criteria may not fully apply to novel cBTKi regimens.
- Additional factors like MCL biology and patient risk are crucial for therapy selection.
Conclusions:
- The evolving landscape of MCL therapy requires a multifaceted approach to selecting 1L treatment.
- Patient-specific factors and emerging cBTKi options necessitate careful consideration for optimal outcomes.
- Further research is needed to address evidence gaps for these novel regimens.
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