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Validation of the revised IPSS at transplant in patients with myelodysplastic syndrome/transformed acute myelogenous leukemia receiving allogeneic stem cell transplantation: a retrospective analysis of the EBMT chronic malignancies working party

The International Prognostic Scoring System has been revised (IPSS-R) to predict prognosis of patients with myelodysplastic syndromes at diagnosis. To validate the use of the IPSS-R assessed before transplant rather than at diagnosis we performed a retrospective analysis of the EBMT database. A tota...

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Autores principales: Scheid, C, de Wreede, L, van Biezen, A, Koenecke, C, Göhring, G, Volin, L, Maertens, J, Finke, J, Passweg, J, Beelen, D, Cornelissen, J J, Itälä-Remes, M, Chevallier, P, Russell, N, Petersen, E, Milpied, N, Richard Espiga, C, Peniket, A, Sierra, J, Mufti, G, Crawley, C, Veelken, J H, Ljungman, P, Cahn, J Y, Alessandrino, E P, de Witte, T, Robin, M, Kröger, N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5671928/
https://www.ncbi.nlm.nih.gov/pubmed/28892084
http://dx.doi.org/10.1038/bmt.2017.171
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author Scheid, C
de Wreede, L
van Biezen, A
Koenecke, C
Göhring, G
Volin, L
Maertens, J
Finke, J
Passweg, J
Beelen, D
Cornelissen, J J
Itälä-Remes, M
Chevallier, P
Russell, N
Petersen, E
Milpied, N
Richard Espiga, C
Peniket, A
Sierra, J
Mufti, G
Crawley, C
Veelken, J H
Ljungman, P
Cahn, J Y
Alessandrino, E P
de Witte, T
Robin, M
Kröger, N
author_facet Scheid, C
de Wreede, L
van Biezen, A
Koenecke, C
Göhring, G
Volin, L
Maertens, J
Finke, J
Passweg, J
Beelen, D
Cornelissen, J J
Itälä-Remes, M
Chevallier, P
Russell, N
Petersen, E
Milpied, N
Richard Espiga, C
Peniket, A
Sierra, J
Mufti, G
Crawley, C
Veelken, J H
Ljungman, P
Cahn, J Y
Alessandrino, E P
de Witte, T
Robin, M
Kröger, N
author_sort Scheid, C
collection PubMed
description The International Prognostic Scoring System has been revised (IPSS-R) to predict prognosis of patients with myelodysplastic syndromes at diagnosis. To validate the use of the IPSS-R assessed before transplant rather than at diagnosis we performed a retrospective analysis of the EBMT database. A total of 579 patients had sufficient information available to calculate IPSS-R at transplant. Median overall survival (OS) from transplant was significantly different according to IPSS-R: very low 23.6 months, low 55.0 months, intermediate 19.7 months, high 13.5 months, very high 7.8 months (P<0.001). In a multivariate Cox model the following parameters were significant risk factors for OS: IPSS-R, graft source, age and prior treatment. Median relapse free survival also showed significant differences according to IPSS-R: very low: 23.6 months, low: 24.8 months, intermediate 10.6 months, high 7.9 months, very high 5.5 months (P<0.001). Multivariate risk factors for relapse-free survival (RFS) were: IPSS-R, reduced intensity conditioning, graft source and prior treatment. A trend for an increased relapse incidence was noted for very high risk IPSS-R. We conclude that the IPSS-R at transplant is a useful prognostic score for predicting OS and RFS after transplantation, capturing both disease evolution and response to prior treatment before transplant.
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spelling pubmed-56719282017-11-09 Validation of the revised IPSS at transplant in patients with myelodysplastic syndrome/transformed acute myelogenous leukemia receiving allogeneic stem cell transplantation: a retrospective analysis of the EBMT chronic malignancies working party Scheid, C de Wreede, L van Biezen, A Koenecke, C Göhring, G Volin, L Maertens, J Finke, J Passweg, J Beelen, D Cornelissen, J J Itälä-Remes, M Chevallier, P Russell, N Petersen, E Milpied, N Richard Espiga, C Peniket, A Sierra, J Mufti, G Crawley, C Veelken, J H Ljungman, P Cahn, J Y Alessandrino, E P de Witte, T Robin, M Kröger, N Bone Marrow Transplant Original Article The International Prognostic Scoring System has been revised (IPSS-R) to predict prognosis of patients with myelodysplastic syndromes at diagnosis. To validate the use of the IPSS-R assessed before transplant rather than at diagnosis we performed a retrospective analysis of the EBMT database. A total of 579 patients had sufficient information available to calculate IPSS-R at transplant. Median overall survival (OS) from transplant was significantly different according to IPSS-R: very low 23.6 months, low 55.0 months, intermediate 19.7 months, high 13.5 months, very high 7.8 months (P<0.001). In a multivariate Cox model the following parameters were significant risk factors for OS: IPSS-R, graft source, age and prior treatment. Median relapse free survival also showed significant differences according to IPSS-R: very low: 23.6 months, low: 24.8 months, intermediate 10.6 months, high 7.9 months, very high 5.5 months (P<0.001). Multivariate risk factors for relapse-free survival (RFS) were: IPSS-R, reduced intensity conditioning, graft source and prior treatment. A trend for an increased relapse incidence was noted for very high risk IPSS-R. We conclude that the IPSS-R at transplant is a useful prognostic score for predicting OS and RFS after transplantation, capturing both disease evolution and response to prior treatment before transplant. Nature Publishing Group 2017-11 2017-09-11 /pmc/articles/PMC5671928/ /pubmed/28892084 http://dx.doi.org/10.1038/bmt.2017.171 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Original Article
Scheid, C
de Wreede, L
van Biezen, A
Koenecke, C
Göhring, G
Volin, L
Maertens, J
Finke, J
Passweg, J
Beelen, D
Cornelissen, J J
Itälä-Remes, M
Chevallier, P
Russell, N
Petersen, E
Milpied, N
Richard Espiga, C
Peniket, A
Sierra, J
Mufti, G
Crawley, C
Veelken, J H
Ljungman, P
Cahn, J Y
Alessandrino, E P
de Witte, T
Robin, M
Kröger, N
Validation of the revised IPSS at transplant in patients with myelodysplastic syndrome/transformed acute myelogenous leukemia receiving allogeneic stem cell transplantation: a retrospective analysis of the EBMT chronic malignancies working party
title Validation of the revised IPSS at transplant in patients with myelodysplastic syndrome/transformed acute myelogenous leukemia receiving allogeneic stem cell transplantation: a retrospective analysis of the EBMT chronic malignancies working party
title_full Validation of the revised IPSS at transplant in patients with myelodysplastic syndrome/transformed acute myelogenous leukemia receiving allogeneic stem cell transplantation: a retrospective analysis of the EBMT chronic malignancies working party
title_fullStr Validation of the revised IPSS at transplant in patients with myelodysplastic syndrome/transformed acute myelogenous leukemia receiving allogeneic stem cell transplantation: a retrospective analysis of the EBMT chronic malignancies working party
title_full_unstemmed Validation of the revised IPSS at transplant in patients with myelodysplastic syndrome/transformed acute myelogenous leukemia receiving allogeneic stem cell transplantation: a retrospective analysis of the EBMT chronic malignancies working party
title_short Validation of the revised IPSS at transplant in patients with myelodysplastic syndrome/transformed acute myelogenous leukemia receiving allogeneic stem cell transplantation: a retrospective analysis of the EBMT chronic malignancies working party
title_sort validation of the revised ipss at transplant in patients with myelodysplastic syndrome/transformed acute myelogenous leukemia receiving allogeneic stem cell transplantation: a retrospective analysis of the ebmt chronic malignancies working party
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5671928/
https://www.ncbi.nlm.nih.gov/pubmed/28892084
http://dx.doi.org/10.1038/bmt.2017.171
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