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Long-term outcome after allogeneic stem cell transplantation in multiple myeloma
The role of allogeneic hematopoietic stem cell transplantation (allo-SCT) in multiple myeloma is controversial. We analyzed the results of 205 patients transplanted in one center during 2000–2017. Transplantation was performed on 75 patients without a previous autologous SCT (upfront-allo), on 74 as...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116307/ https://www.ncbi.nlm.nih.gov/pubmed/33866396 http://dx.doi.org/10.1007/s00277-021-04514-y |
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author | Luoma, Sini Silvennoinen, Raija Rauhala, Auvo Niittyvuopio, Riitta Martelin, Eeva Lindström, Vesa Heiskanen, Jouni Volin, Liisa Ruutu, Tapani Nihtinen, Anne |
author_facet | Luoma, Sini Silvennoinen, Raija Rauhala, Auvo Niittyvuopio, Riitta Martelin, Eeva Lindström, Vesa Heiskanen, Jouni Volin, Liisa Ruutu, Tapani Nihtinen, Anne |
author_sort | Luoma, Sini |
collection | PubMed |
description | The role of allogeneic hematopoietic stem cell transplantation (allo-SCT) in multiple myeloma is controversial. We analyzed the results of 205 patients transplanted in one center during 2000–2017. Transplantation was performed on 75 patients without a previous autologous SCT (upfront-allo), on 74 as tandem transplant (auto-allo), and on 56 patients after relapse. Median overall survival (OS) was 9.9 years for upfront-allo, 11.2 years for auto-allo, and 3.9 years for the relapse group (p = 0.015). Progression-free survival (PFS) was 2.4, 2.4, and 0.9 years, respectively (p < 0.001). Non-relapse mortality at 5 years was 8% overall, with no significant difference between the groups. Post-relapse survival was 4.1 years for upfront-allo and auto-allo, and 2.6 years for the relapse group (p = 0.066). Survival of high-risk patients was reduced. In multivariate analysis, the auto-allo group had improved OS and chronic graft-versus-host disease was advantageous in terms of PFS, OS, and relapse incidence. Late relapses occurred in all groups. Allo-SCT resulted in long-term survival in a small subgroup of patients. Our results indicate that auto-allo-SCT is feasible and could be considered for younger patients in the upfront setting. |
format | Online Article Text |
id | pubmed-8116307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-81163072021-05-26 Long-term outcome after allogeneic stem cell transplantation in multiple myeloma Luoma, Sini Silvennoinen, Raija Rauhala, Auvo Niittyvuopio, Riitta Martelin, Eeva Lindström, Vesa Heiskanen, Jouni Volin, Liisa Ruutu, Tapani Nihtinen, Anne Ann Hematol Original Article The role of allogeneic hematopoietic stem cell transplantation (allo-SCT) in multiple myeloma is controversial. We analyzed the results of 205 patients transplanted in one center during 2000–2017. Transplantation was performed on 75 patients without a previous autologous SCT (upfront-allo), on 74 as tandem transplant (auto-allo), and on 56 patients after relapse. Median overall survival (OS) was 9.9 years for upfront-allo, 11.2 years for auto-allo, and 3.9 years for the relapse group (p = 0.015). Progression-free survival (PFS) was 2.4, 2.4, and 0.9 years, respectively (p < 0.001). Non-relapse mortality at 5 years was 8% overall, with no significant difference between the groups. Post-relapse survival was 4.1 years for upfront-allo and auto-allo, and 2.6 years for the relapse group (p = 0.066). Survival of high-risk patients was reduced. In multivariate analysis, the auto-allo group had improved OS and chronic graft-versus-host disease was advantageous in terms of PFS, OS, and relapse incidence. Late relapses occurred in all groups. Allo-SCT resulted in long-term survival in a small subgroup of patients. Our results indicate that auto-allo-SCT is feasible and could be considered for younger patients in the upfront setting. Springer Berlin Heidelberg 2021-04-17 2021 /pmc/articles/PMC8116307/ /pubmed/33866396 http://dx.doi.org/10.1007/s00277-021-04514-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Luoma, Sini Silvennoinen, Raija Rauhala, Auvo Niittyvuopio, Riitta Martelin, Eeva Lindström, Vesa Heiskanen, Jouni Volin, Liisa Ruutu, Tapani Nihtinen, Anne Long-term outcome after allogeneic stem cell transplantation in multiple myeloma |
title | Long-term outcome after allogeneic stem cell transplantation in multiple myeloma |
title_full | Long-term outcome after allogeneic stem cell transplantation in multiple myeloma |
title_fullStr | Long-term outcome after allogeneic stem cell transplantation in multiple myeloma |
title_full_unstemmed | Long-term outcome after allogeneic stem cell transplantation in multiple myeloma |
title_short | Long-term outcome after allogeneic stem cell transplantation in multiple myeloma |
title_sort | long-term outcome after allogeneic stem cell transplantation in multiple myeloma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116307/ https://www.ncbi.nlm.nih.gov/pubmed/33866396 http://dx.doi.org/10.1007/s00277-021-04514-y |
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