Despite many recent therapeutic advances, mantle cell lymphoma (MCL) remains a largely incurable disease. Treatments for patients with relapsed/refractory (R/R) disease are limited in number and in response durability. Therefore, improving the efficacy of frontline (1L) treatment, and specifically maximizing the duration of first remission, remains of critical importance to obtain favorable long-term outcomes. As 1L treatments become more effective, improving tolerability is also becoming an increasingly realistic goal. Targeted agents, which are now mainstays of treatment in R/R MCL, are establishing new, paradigm-changing roles in frontline treatment. Here, we review data supporting current standard-of-care approaches and explore 6 main areas of possible focus for advancement of 1L management: optimizing the chemoimmunotherapy (CIT) backbone, adding targeted agents to CIT, redefining the role of autologous stem cell transplantation, improving maintenance therapy, using targeted agent combinations with omission of CIT, and using measurable residual disease–guided therapy. We highlight several ongoing phase 3 trials that may soon impact frontline MCL management, and outline some areas of necessary investigation as the field continues to strive toward a cure for this disease.
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Mantle Cell Lymphoma|
February 13, 2025
Frontline management of mantle cell lymphoma
Christine E. Ryan,
Christine E. Ryan
Division of Lymphoma, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA
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Philippe Armand,
Philippe Armand
Division of Lymphoma, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA
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Ann S. LaCasce
Ann S. LaCasce
Division of Lymphoma, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA
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Blood (2025) 145 (7): 663–672.
Article history
Submitted:
January 8, 2024
Accepted:
February 29, 2024
First Edition:
March 18, 2024
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Citation
Christine E. Ryan, Philippe Armand, Ann S. LaCasce; Frontline management of mantle cell lymphoma. Blood 2025; 145 (7): 663–672. doi: https://doi.org/10.1182/blood.2023022352
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