Real-world efficacy of single-agent belantamab mafodotin in relapsed systemic AL amyloidosis
Garg, Mamta
Garg, Mamta
Abstract
Systemic light chain (AL) amyloidosis is a relapsing plasma cell disorder. Therapy is limited, particularly for triple-class refractory disease. We report the use of belantamab mafodotin, a BCMA-directed drug-antibody conjugate, for relapsed AL amyloidosis, including patients traditionally excluded from clinical trials. Thirty-one patients were reviewed, with a median of three prior lines of therapy. The median follow-up was 12 months (95% CI 4-19), and a median of five doses were delivered. The best haematological overall response rate was 71%, and the complete/very good partial response was 58%. Sixty-eight percent had keratopathy and improved in all. Belantamab mafodotin has high efficacy and good tolerability in patients with relapsed AL amyloidosis.
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Date
2024-01-03
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Khwaja, J., Bomsztyk, J., Atta, M., Bygrave, C., Forbes, A., Durairaj, S., Fernandes, S., Taylor, J., Paterson, P., Brearton, G., Crawley, C., Sheehy, O., Brown, R., Soutar, R., Garg, M., Rydzewski, A., Jamroziak, K., Mahmood, S., & Wechalekar, A. D. (2024). Real-world efficacy of single-agent belantamab mafodotin in relapsed systemic AL amyloidosis. British journal of haematology, 10.1111/bjh.19286. Advance online publication. https://doi.org/10.1111/bjh.19286
