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High levels of circulating CD34+ cells at autologous stem cell collection are associated with favourable prognosis in multiple myeloma

BACKGROUND: High-dose chemotherapy with autologous stem cell transplantation is a cornerstone in the first-line treatment of multiple myeloma patients. However, only few factors have been identified affecting the outcome in such patients. We hypothesised that varying levels of mobilised CD34+ cells...

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Autores principales: Raschle, J, Ratschiller, D, Mans, S, Mueller, B U, Pabst, T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185945/
https://www.ncbi.nlm.nih.gov/pubmed/21878938
http://dx.doi.org/10.1038/bjc.2011.329
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author Raschle, J
Ratschiller, D
Mans, S
Mueller, B U
Pabst, T
author_facet Raschle, J
Ratschiller, D
Mans, S
Mueller, B U
Pabst, T
author_sort Raschle, J
collection PubMed
description BACKGROUND: High-dose chemotherapy with autologous stem cell transplantation is a cornerstone in the first-line treatment of multiple myeloma patients. However, only few factors have been identified affecting the outcome in such patients. We hypothesised that varying levels of mobilised CD34+ cells confer prognostic information in myeloma patients undergoing high-dose chemotherapy. METHODS: We determined circulating CD34+ cells at the day of peripheral stem cell collection in 158 consecutive myeloma patients between January 2001 and August 2010. Patients were stratified into two groups (super vs normal mobilisers) with a cutoff of 100 000 peripheral CD34+ cells per ml. RESULTS: We found that patients with more than 100 000 peripheral CD34+ cells per ml had a better overall survival (P=0.005) and a prolonged time to progression (P=0.0398) than patients with CD34+ cell counts below 100 000 CD34+ cells per ml. High levels of CD34+ cells were an independent marker for better overall survival and time to progression in a multivariate analysis that included disease stage, response at transplant, light-chain subtype, age, sex, and height. CONCLUSION: Our results suggest that high levels of mobilised peripheral CD34+ cells are associated with favourable outcome in myeloma patients undergoing autologous transplantation.
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spelling pubmed-31859452012-09-27 High levels of circulating CD34+ cells at autologous stem cell collection are associated with favourable prognosis in multiple myeloma Raschle, J Ratschiller, D Mans, S Mueller, B U Pabst, T Br J Cancer Short Communication BACKGROUND: High-dose chemotherapy with autologous stem cell transplantation is a cornerstone in the first-line treatment of multiple myeloma patients. However, only few factors have been identified affecting the outcome in such patients. We hypothesised that varying levels of mobilised CD34+ cells confer prognostic information in myeloma patients undergoing high-dose chemotherapy. METHODS: We determined circulating CD34+ cells at the day of peripheral stem cell collection in 158 consecutive myeloma patients between January 2001 and August 2010. Patients were stratified into two groups (super vs normal mobilisers) with a cutoff of 100 000 peripheral CD34+ cells per ml. RESULTS: We found that patients with more than 100 000 peripheral CD34+ cells per ml had a better overall survival (P=0.005) and a prolonged time to progression (P=0.0398) than patients with CD34+ cell counts below 100 000 CD34+ cells per ml. High levels of CD34+ cells were an independent marker for better overall survival and time to progression in a multivariate analysis that included disease stage, response at transplant, light-chain subtype, age, sex, and height. CONCLUSION: Our results suggest that high levels of mobilised peripheral CD34+ cells are associated with favourable outcome in myeloma patients undergoing autologous transplantation. Nature Publishing Group 2011-09-27 2011-08-30 /pmc/articles/PMC3185945/ /pubmed/21878938 http://dx.doi.org/10.1038/bjc.2011.329 Text en Copyright © 2011 Cancer Research UK https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license 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 license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Short Communication
Raschle, J
Ratschiller, D
Mans, S
Mueller, B U
Pabst, T
High levels of circulating CD34+ cells at autologous stem cell collection are associated with favourable prognosis in multiple myeloma
title High levels of circulating CD34+ cells at autologous stem cell collection are associated with favourable prognosis in multiple myeloma
title_full High levels of circulating CD34+ cells at autologous stem cell collection are associated with favourable prognosis in multiple myeloma
title_fullStr High levels of circulating CD34+ cells at autologous stem cell collection are associated with favourable prognosis in multiple myeloma
title_full_unstemmed High levels of circulating CD34+ cells at autologous stem cell collection are associated with favourable prognosis in multiple myeloma
title_short High levels of circulating CD34+ cells at autologous stem cell collection are associated with favourable prognosis in multiple myeloma
title_sort high levels of circulating cd34+ cells at autologous stem cell collection are associated with favourable prognosis in multiple myeloma
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185945/
https://www.ncbi.nlm.nih.gov/pubmed/21878938
http://dx.doi.org/10.1038/bjc.2011.329
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