Belantamab mafodotin in Relapsed/Refractory AL Amyloidosis- real-world multi-center experience and review of the literature.
Journal
Acta haematologica
ISSN: 1421-9662
Titre abrégé: Acta Haematol
Pays: Switzerland
ID NLM: 0141053
Informations de publication
Date de publication:
02 Oct 2024
02 Oct 2024
Historique:
received:
26
06
2024
accepted:
14
09
2024
medline:
3
10
2024
pubmed:
3
10
2024
entrez:
2
10
2024
Statut:
aheadofprint
Résumé
Treatment for relapsed/refractory AL amyloidosis (AL) is an unmet need. The safety and efficacy of belantamab mafodotin (BLM) in multiple myeloma (MM) are known, whereas in AL data are limited. We report a multicenter cohort of AL patients receiving BLM, and review all previous data on BLM therapy in AL. Twelve patients with a median of 3 (range 2-9) prior lines of therapy were included. The overall hematological response rate (ORR) was 75% (9/12), including 5 complete responses. Six of the 10 evaluable patients had organ responses. The median event-free survival/overall survival were 22.3 and 28.8 months, respectively. Grade 3 toxicities were mostly infections and keratopathy, occurring in 7/12 (58%). Hematological toxicities were rare. No grade 4/5 toxicities occurred. Review of previous series reveals BLM provides an ORR of 60-83% with similar rates of corneal toxicity. BLM, being an off-the shelf therapy, with acceptable toxicity even in frail patients, may be a valuable option in AL, with a high ORR, and a signal for durable responses and high-quality organ responses.
Identifiants
pubmed: 39357511
pii: 000541594
doi: 10.1159/000541594
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1-16Informations de copyright
The Author(s). Published by S. Karger AG, Basel.