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Allo-SCT for multiple myeloma: a review of outcomes at a single transplant center
Allogeneic stem cell transplant for multiple myeloma (MM) is one treatment associated with long-term disease-free survival. The high incidence of treatment-related mortality and relapses, however, are important reasons for controversy about the role of allografting in the management of MM. We review...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376198/ https://www.ncbi.nlm.nih.gov/pubmed/22327126 http://dx.doi.org/10.1038/bmt.2012.1 |
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author | Bensinger, W Rotta, M Storer, B Chauncey, T Holmberg, L Becker, P Sandmaier, B M Storb, R Maloney, D |
author_facet | Bensinger, W Rotta, M Storer, B Chauncey, T Holmberg, L Becker, P Sandmaier, B M Storb, R Maloney, D |
author_sort | Bensinger, W |
collection | PubMed |
description | Allogeneic stem cell transplant for multiple myeloma (MM) is one treatment associated with long-term disease-free survival. The high incidence of treatment-related mortality and relapses, however, are important reasons for controversy about the role of allografting in the management of MM. We reviewed our results of allografting for MM spanning a period of 34 years in order to better define long-term outcomes and identify areas of progress as well as areas requiring improvement. A total of 278 patients received allogeneic marrow or PBSCs after high-dose myeloablative (N=144) or reduced intensity, non-myeloablative (N=134) regimens. In multivariable analysis, adjusting for differences in patient groups, reduced intensity/non-myeloablative transplants were associated with significantly less acute GVHD, lower transplant mortality, better PFS and overall survival. There were no significant differences in relapse, progression or chronic GVHD, when adjusted. In multivariable analysis of patients receiving only non-myeloablative transplants, decreased overall survival and PFS were associated with relapse after a prior autograft and a β2 microglobulin >4.0. Transplant mortality was reduced and only influenced by a prior tandem autograft. |
format | Online Article Text |
id | pubmed-3376198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-33761982013-10-01 Allo-SCT for multiple myeloma: a review of outcomes at a single transplant center Bensinger, W Rotta, M Storer, B Chauncey, T Holmberg, L Becker, P Sandmaier, B M Storb, R Maloney, D Bone Marrow Transplant Article Allogeneic stem cell transplant for multiple myeloma (MM) is one treatment associated with long-term disease-free survival. The high incidence of treatment-related mortality and relapses, however, are important reasons for controversy about the role of allografting in the management of MM. We reviewed our results of allografting for MM spanning a period of 34 years in order to better define long-term outcomes and identify areas of progress as well as areas requiring improvement. A total of 278 patients received allogeneic marrow or PBSCs after high-dose myeloablative (N=144) or reduced intensity, non-myeloablative (N=134) regimens. In multivariable analysis, adjusting for differences in patient groups, reduced intensity/non-myeloablative transplants were associated with significantly less acute GVHD, lower transplant mortality, better PFS and overall survival. There were no significant differences in relapse, progression or chronic GVHD, when adjusted. In multivariable analysis of patients receiving only non-myeloablative transplants, decreased overall survival and PFS were associated with relapse after a prior autograft and a β2 microglobulin >4.0. Transplant mortality was reduced and only influenced by a prior tandem autograft. Nature Publishing Group UK 2012-02-13 2012 /pmc/articles/PMC3376198/ /pubmed/22327126 http://dx.doi.org/10.1038/bmt.2012.1 Text en © Macmillan Publishers Limited 2012 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Bensinger, W Rotta, M Storer, B Chauncey, T Holmberg, L Becker, P Sandmaier, B M Storb, R Maloney, D Allo-SCT for multiple myeloma: a review of outcomes at a single transplant center |
title | Allo-SCT for multiple myeloma: a review of outcomes at a single transplant center |
title_full | Allo-SCT for multiple myeloma: a review of outcomes at a single transplant center |
title_fullStr | Allo-SCT for multiple myeloma: a review of outcomes at a single transplant center |
title_full_unstemmed | Allo-SCT for multiple myeloma: a review of outcomes at a single transplant center |
title_short | Allo-SCT for multiple myeloma: a review of outcomes at a single transplant center |
title_sort | allo-sct for multiple myeloma: a review of outcomes at a single transplant center |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376198/ https://www.ncbi.nlm.nih.gov/pubmed/22327126 http://dx.doi.org/10.1038/bmt.2012.1 |
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