International Myeloma Working Group immunotherapy committee consensus guidelines and recommendations for optimal use of T-cell-engaging bispecific antibodies in multiple myeloma

Publication date

2024-05

Authors

International Myeloma Working Group

Editors

Advisors

Supervisors

Document Type

Article

Collections

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License

taverne

Abstract

Multiple myeloma remains an incurable disease, despite the development of numerous drug classes and combinations that have contributed to improved overall survival. Immunotherapies directed against cancer cell-surface antigens, such as chimeric antigen receptor (CAR) T-cell therapy and T-cell-redirecting bispecific antibodies, have recently received regulatory approvals and shown unprecedented efficacy. However, these immunotherapies have unique mechanisms of action and toxicities that are different to previous treatments for myeloma, so experiences from clinical trials and early access programmes are essential for providing specific recommendations for management of patients, especially as these agents become available across many parts of the world. Here, we provide expert consensus clinical practice guidelines for the use of bispecific antibodies for the treatment of myeloma. The International Myeloma Working Group is also involved in the collection of prospective real-time data of patients treated with such immunotherapies, with the aim of learning continuously and adapting clinical practices to optimise the management of patients receiving immunotherapies.

Keywords

Antibodies, Bispecific/therapeutic use, Antineoplastic Agents, Immunological/therapeutic use, Consensus, Humans, Immunotherapy/methods, Multiple Myeloma/immunology, T-Lymphocytes/immunology, Taverne, Oncology, Journal Article, Review, Research Support, Non-U.S. Gov't, Practice Guideline

Citation

International Myeloma Working Group 2024, 'International Myeloma Working Group immunotherapy committee consensus guidelines and recommendations for optimal use of T-cell-engaging bispecific antibodies in multiple myeloma', LANCET ONCOLOGY, vol. 25, no. 5, pp. e205-e216. https://doi.org/10.1016/S1470-2045(24)00043-3