"The End of the Golden Weather": therapeutic strategies for mantle cell lymphoma relapsed or refractory to covalent BTK inhibitors.

Haematologica

Department of Haematology, Sir Charles Gairdner Hospital, Nedlands, WA, Australia; Linear Clinical Research, Nedlands, WA, Australia; Medical School, University of Western Australia, Nedlands, WA.

Published: November 2024

AI Article Synopsis

  • Mantle cell lymphoma (MCL) is a type of non-Hodgkin lymphoma that frequently relapses after initial treatment, leading to an ongoing need for improved management strategies.
  • Patients often respond to covalent Bruton's tyrosine kinase inhibitors (cBTKi) during the first relapse, but these responses are not long-lasting, highlighting the need to understand why some patients develop resistance.
  • The review suggests focusing on advanced treatment options, such as CAR T-cell therapy and other innovative therapies like non-covalent BTK inhibitors and antibody-drug conjugates, while encouraging participation in clinical trials.

Article Abstract

Mantle cell lymphoma (MCL) is a subtype of non-Hodgkin lymphoma which is often characterised by a pattern of continued relapse after frontline chemoimmunotherapy. Although patients are usually able to regain durable disease control with covalent Bruton's tyrosine kinase inhibitors (cBTKi) at first relapse, it is now appreciated that such responses are often not sustained and the management of such patients represents a significant area of unmet need. There is an imperative to better understand resistance mechanisms and identify high-risk subsets of patients for whom cBTKi responses may be particularly short. Allogeneic stem cell transplant has an established role in appropriate candidates, however contemporary consensus is to preferentially offer chimeric antigen receptor (CAR) T-cell therapy. In this Review, we consider the available data on both existing and emerging treatment options, including non-covalent BTK inhibitors, bispecific antibodies, antibody-drug conjugates and Bcl-2 inhibitors and propose a treatment strategy prioritising clinical trials where available.

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Source
http://dx.doi.org/10.3324/haematol.2024.286205DOI Listing

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