Second allogeneic transplants for multiple myeloma: a report from the EBMT Chronic Malignancies Working Party
dc.contributor.author | Hayden, P. J. | |
dc.contributor.author | Eikema, D. J. | |
dc.contributor.author | de Wreede, L. C. | |
dc.contributor.author | Koster, L. | |
dc.contributor.author | Kröger, N. | |
dc.contributor.author | Einsele, H. | |
dc.contributor.author | Minnema, M. | |
dc.contributor.author | Dominietto, A. | |
dc.contributor.author | Potter, M. | |
dc.contributor.author | Passweg, J. | |
dc.contributor.author | Bermúdez, A. | |
dc.contributor.author | Nguyen-Quoc, S. | |
dc.contributor.author | Platzbecker, U. | |
dc.contributor.author | Tischer, J. | |
dc.contributor.author | Ciceri, F. | |
dc.contributor.author | Veelken, J. H. | |
dc.contributor.author | Ljungman, P. | |
dc.contributor.author | Schaap, N. | |
dc.contributor.author | Forcade, E. | |
dc.contributor.author | Carella, A. M. | |
dc.contributor.author | Gandemer, V. | |
dc.contributor.author | Arcese, W. | |
dc.contributor.author | Bloor, Adrian | |
dc.contributor.author | Olivieri, A. | |
dc.contributor.author | Vincent, L. | |
dc.contributor.author | Beksac, M. | |
dc.contributor.author | Schönland, S | |
dc.contributor.author | Yakoub-Agha, I. | |
dc.date.accessioned | 2021-07-19T10:28:43Z | |
dc.date.available | 2021-07-19T10:28:43Z | |
dc.date.issued | 2021 | en |
dc.identifier.citation | Hayden PJ, Eikema D-J, de Wreede LC, Koster L, Kröger N, Einsele H, et al. Second allogeneic transplants for multiple myeloma: a report from the EBMT Chronic Malignancies Working Party. Bone Marrow Transplant. 2021 May 11. | en |
dc.identifier.pmid | 33976382 | en |
dc.identifier.doi | 10.1038/s41409-021-01286-x | en |
dc.identifier.uri | http://hdl.handle.net/10541/624083 | |
dc.description.abstract | The EBMT Chronic Malignancies Working Party performed a retrospective analysis of 215 patients who underwent a second allo-HCT for myeloma between 1994 and 2017, 159 for relapse and 56 for graft failure. In the relapse group, overall survival (OS) was 38% (30-46%) at 2 years and 25% (17-32%) at 5 years. Patients who had a HLA-identical sibling (HLAid-Sib) donor for their first and second transplants had superior OS (5 year OS: HLAid-Sib/HLAid-Sib: 35% (24-46%); Others 9% (0-17%), p < 0.001). There was a significantly higher incidence of acute grade II-IV GvHD in those patients who had also developed GvHD following their initial HLA-identical sibling allo-HCT (HLAid-Sib/HLAid-Sib: 50% (33-67%); Other 22% (8-36%), p = 0.03). More as opposed to fewer than 2 years between transplants was associated with superior 5-yr OS (31% (21-40%) vs. 10% (1-20%), P = 0.005). On multivariate analysis, consecutive HLA-identical sibling donor transplants conferred a significant OS advantage (0.4 (0.24-0.67), p < 0.001). In the graft failure group, OS was 41% at 2 years. In summary, a second allo-HCT using a HLA-identical sibling donor, if available, provides the best transplant outcomes for relapsed myeloma in this setting. | en |
dc.language.iso | en | en |
dc.relation.url | https://dx.doi.org/10.1038/s41409-021-01286-x | en |
dc.title | Second allogeneic transplants for multiple myeloma: a report from the EBMT Chronic Malignancies Working Party | en |
dc.type | Article | en |
dc.contributor.department | Department of Haematology, Trinity College Dublin, St. James's Hospital, Dublin, Ireland. | en |
dc.identifier.journal | Bone Marrow Transplantation | en |
dc.description.note | en] | |
refterms.dateFOA | 2021-07-26T10:14:23Z |