TY - JOUR
T1 - EHA–EU MCL network guidelines for diagnosis and treatment of mantle cell lymphoma
AU - the EHA Guidelines Committee and the European MCL Network
AU - Jerkeman, Mats
AU - Aurer, Igor
AU - Campo, Elias
AU - Cheah, Chan Y.
AU - Clark, Jonathan
AU - Doorduijn, Jeanette
AU - Eyre, Toby A.
AU - Fehr, Martin
AU - Giné, Eva
AU - Gomes da Silva, Maria
AU - Klener, Pavel
AU - Ladetto, Marco
AU - Ribrag, Vincent
AU - Shpilberg, Ofer
AU - Walewski, Jan
AU - Dreyling, Martin
N1 - Publisher Copyright:
© 2025 The Author(s). HemaSphere published by John Wiley & Sons Ltd on behalf of European Hematology Association.
PY - 2025/10
Y1 - 2025/10
N2 - Mantle cell lymphoma (MCL) is a relatively rare B-cell lymphoma subtype, with a higher incidence among males and a median age of 70 years at diagnosis. MCL is characterized by clinically diverse behavior, from indolent disease to extremely aggressive, related to the presence of biological risk factors such as proliferation rate and TP53 mutations. Most often, patients present with disseminated disease, necessitating systemic treatment. Immunochemotherapy has historically been the mainstay of treatment, but recent data indicate that addition of novel agents, especially covalent Bruton tyrosine kinase inhibitors (cBTKi), may substantially improve outcome in younger and older patients, although a curative approach remains to be shown. In elderly patients, the standard of care is still immuno-chemotherapy such as rituximab-bendamustine, although this may be challenged by non-chemotherapeutic options, such as rituximab plus cBTKi. For patients with relapsed or refractory disease, treatment options are developing rapidly, including CAR-T cell therapy, novel BTK targeting agents, BCL2 inhibitors, and T-cell engagers. In this clinical practice guideline, we present current evidence-based recommendations for diagnosis, staging, treatment, and follow-up of MCL.
AB - Mantle cell lymphoma (MCL) is a relatively rare B-cell lymphoma subtype, with a higher incidence among males and a median age of 70 years at diagnosis. MCL is characterized by clinically diverse behavior, from indolent disease to extremely aggressive, related to the presence of biological risk factors such as proliferation rate and TP53 mutations. Most often, patients present with disseminated disease, necessitating systemic treatment. Immunochemotherapy has historically been the mainstay of treatment, but recent data indicate that addition of novel agents, especially covalent Bruton tyrosine kinase inhibitors (cBTKi), may substantially improve outcome in younger and older patients, although a curative approach remains to be shown. In elderly patients, the standard of care is still immuno-chemotherapy such as rituximab-bendamustine, although this may be challenged by non-chemotherapeutic options, such as rituximab plus cBTKi. For patients with relapsed or refractory disease, treatment options are developing rapidly, including CAR-T cell therapy, novel BTK targeting agents, BCL2 inhibitors, and T-cell engagers. In this clinical practice guideline, we present current evidence-based recommendations for diagnosis, staging, treatment, and follow-up of MCL.
UR - https://www.scopus.com/pages/publications/105021030165
U2 - 10.1002/hem3.70233
DO - 10.1002/hem3.70233
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AN - SCOPUS:105021030165
SN - 2572-9241
VL - 9
JO - HemaSphere
JF - HemaSphere
IS - 10
M1 - e70233
ER -