The Antibody Drug Conjugate, Belantamab-Mafodotin, in the Treatment of Multiple Myeloma: A Comprehensive Review.

Autor: Almodovar Diaz AA; Division of Hematology, Mayo Clinic, Rochester, MN, USA., Alouch SS; Division of Hematology, Mayo Clinic, Rochester, MN, USA., Chawla Y; Division of Hematology, Mayo Clinic, Rochester, MN, USA., Gonsalves WI; Division of Hematology, Mayo Clinic, Rochester, MN, USA.
Jazyk: angličtina
Zdroj: Blood and lymphatic cancer : targets and therapy [Blood Lymphat Cancer] 2024 Dec 06; Vol. 14, pp. 71-87. Date of Electronic Publication: 2024 Dec 06 (Print Publication: 2024).
DOI: 10.2147/BLCTT.S490021
Abstrakt: Despite recent advancements in treatments, including proteasome inhibitors, immunomodulators, and anti-CD38 monoclonal antibodies, multiple myeloma (MM) remains mostly incurable with patients frequently experiencing disease relapses due to therapy resistance. Hence there is an urgent need for innovative treatments for patients with relapsed and/or refractory MM (RRMM). This review examines Belantamab mafodotin, the first antibody-drug conjugate (ADC) targeting B-cell maturation antigen (BCMA), which has shown efficacy in pre-clinical and clinical settings for RRMM. BCMA, a type III transmembrane glycoprotein critical for B cell functions, is predominantly expressed in malignant plasma cells making it a promising therapeutic target. ADCs, comprising a monoclonal antibody, a cytotoxic payload, and a linker, offer a targeted and potent therapeutic approach to cancer treatment. Belantamab mafodotin integrates an afucosylated monoclonal antibody and monomethyl auristatin F (MMAF) as its cytotoxic agent. It induces apoptosis in MM cells by disrupting microtubule formation and interfering with important signaling pathways. The series of DREAMM (Driving Excellence in Approaches to MM) studies have extensively evaluated Belantamab mafodotin in various clinical settings. This review provides a comprehensive overview of pre-clinical and clinical data supporting Belantamab mafodotin as a future therapeutic option for RRMM.
Competing Interests: These authors declare no competing financial interests.
(© 2024 Almodovar Diaz et al.)
Databáze: MEDLINE