Allogeneic hematopoietic cell transplantation for therapy-related myeloid neoplasms arising following treatment for multiple myeloma: a retrospective study on behalf of the Chronic Malignancies Working Party of the EBMT

Therapy-related myeloid neoplasms (t-MN) are a complication of multiple myeloma (MM) treatment. Our retrospective, EBMT registry study included 157 such patients allografted (allo-HCT) between 2006 and 2018. Most patients (130) had a prior autologous HCT. Fifty-seven (36.4%) were transplanted for t-...

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Veröffentlicht in:Bone marrow transplantation (Basingstoke) 2024-11
Hauptverfasser: Raj, Kavita, Eikema, Diderik-Jan, Lawless, Sarah, Koster, Linda, Kunadt, Desiree, Kröger, Nicolaus, Platzbecker, Uwe, Stelljes, Matthias, Bethge, Wolfgang, Holderried, Tobias, Fanin, Renato, Zeiser, Robert, Kuball, Jürgen, Leblond, Véronique, Nicholson, Emma, Passweg, Jakob, Potter, Victoria, Bay, Jacques-Olivier, Bazarbachi, Ali, Corral, Lucía López, Gurnari, Carmelo, Scheid, Christof, Drozd-Sokolowska, Joanna, Morris, Treen Curly, Hayden, Patrick, Yakoub-Agha, Ibrahim, Robin, Marie, McLornan, Donal P
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Sprache:eng
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Zusammenfassung:Therapy-related myeloid neoplasms (t-MN) are a complication of multiple myeloma (MM) treatment. Our retrospective, EBMT registry study included 157 such patients allografted (allo-HCT) between 2006 and 2018. Most patients (130) had a prior autologous HCT. Fifty-seven (36.4%) were transplanted for t-AML and 100 (63.6%) for t-MDS. Median times from MM and t-MN diagnoses to allo-HCT were 72.6 (interquartile range (IQR), 46.1-102.9) and 6.4 (IQR, 3.9-9.4) months. Fifty-eight (38.4%) t-MN patients were in complete remission (CR) at allo-HCT predominantly conditioned with reduced intensity (70.3%). With a median follow-up of 64.9 (95% CI: 39-76) months, relapse incidence (RI) from MM at 1 and 5 years was 4% (0-10%) and 12% (2-22%), respectively, with few deaths (n = 3) only due to MM disease progression, whereas t-MN RI and non-relapse mortality (NRM) at 1 and 5 years were 35% (95% CI 28-43%) and 45% (95% CI: 36-53%) and 20% (95% CI 13-26%) and 31% (95% CI: 23-39%). Overall survival (OS) and progression-free survival (PFS) estimates at 1 and 5 years were 55% (95% CI: 47-63%) and 27% (95% CI: 19-35%) and 45% (95% CI 36-53%) and 24% (95% CI 16-32%). Older (>65 years) t-MN patients with high-risk cytogenetics do not benefit from allo-HCT.
ISSN:0268-3369
1476-5365
1476-5365
DOI:10.1038/s41409-024-02462-5