Evolving therapeutic strategies in mantle cell lymphoma: advancements and future directions
Mantle cell lymphoma (MCL) is a biologically and clinically heterogeneous B-cell malignancy with a historically poor prognosis. Recent advances have substantially expanded treatment options, particularly through the integration of targeted therapies, chemotherapy-free regimens, and cellular approaches. Frontline treatment now incorporates Bruton's tyrosine kinase inhibitors (BTKi) in combination with chemotherapy and in chemotherapy-free regimens. For patients with relapsed or refractory disease, particularly those previously exposed to BTKi, chimeric antigen receptor T-cell (CAR T) therapies and third-generation BTKi like pirtobrutinib provide highly effective options while several novel agents, including bispecific antibodies (bsAbs), are under investigation. Nevertheless, achieving long-lasting remissions is still a major challenge, especially among high-risk patients. Future directions include optimizing sequencing, refining rational combination therapies, expanding the application of bsAbs, and integrating small molecules and novel immunoconjugates to enhance therapeutic efficacy and long-term outcomes. This review provides an overview of the current and emerging therapies for MCL, highlighting how the integration of biological agents, strategic combinations, and patient-centered approaches are driving the next phase of MCL treatment.
Authors
- Rita Tavarozzi (ORCID: https://orcid.org/0000-0003-3696-7806)
- Nawar Maher (ORCID: https://orcid.org/0009-0007-9307-1965)
- M Ladetto
- Giulia Zacchi
- Antonella Sofia
- Gioacchino Catania
- Francesca D’Andrea
- Manuela Zanni
Institutions
- Università degli Studi del Piemonte Orientale “Amedeo Avogadro” (IT)
- Piedmont University (US)
- Azienda Ospedaliera Nazionale SS. Antonio e Biagio e Cesare Arrigo (IT)
Publication Details
- Journal
- Leukemia
- Published
- 2026-04-15
- DOI
- https://doi.org/10.1038/s41375-026-02942-1
- Primary Topic
- Lymphoma Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Leukemia and Lymphoma Society
- Università degli Studi del Piemonte Orientale