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Therapeutic effects of autologous hematopoietic stem cell transplantation in multiple myeloma patients
The present study aimed to evaluate the effect of autologous hematopoietic stem cell transplantation (ASCT) on the response and outcome of patients with multiple myeloma (MM) and to analyze the factors influencing the prognosis of the disease. Retrospective analysis was performed in 27 patients with...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797248/ https://www.ncbi.nlm.nih.gov/pubmed/24137301 http://dx.doi.org/10.3892/etm.2013.1261 |
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author | FU, CHENGCHENG WANG, JUAN XIN, XUE LIU, HUI XUE, SHENGLI MA, XIAO JIN, ZHENGMING SUN, AINING QIU, HUIYING WU, DEPEI |
author_facet | FU, CHENGCHENG WANG, JUAN XIN, XUE LIU, HUI XUE, SHENGLI MA, XIAO JIN, ZHENGMING SUN, AINING QIU, HUIYING WU, DEPEI |
author_sort | FU, CHENGCHENG |
collection | PubMed |
description | The present study aimed to evaluate the effect of autologous hematopoietic stem cell transplantation (ASCT) on the response and outcome of patients with multiple myeloma (MM) and to analyze the factors influencing the prognosis of the disease. Retrospective analysis was performed in 27 patients with MM who had been treated by ASCT (ASCT group) and 28 patients treated with combined chemotherapy only (non-ASCT group) from May 2004 to August 2011. The impact on the depth of response, progression-free survival (PFS) and overall survival (OS) times, as well as associated prognostic factors of patients with MM, were analyzed. All patients successfully underwent hematopoietic reconstruction without transplantation-related mortality. The complete remission (CR) rate of patients in the ASCT group significantly increased from 25.9% (7/27) before ASCT to 70.4% (19/27) following ASCT (P<0.01). The probability of OS for 5 years was 52.2% for the patients in the ASCT group and 33.1% for those in the non-ASCT group (P>0.05). Univariate analysis in the ASCT group demonstrated that maintenance and consolidation therapies were associated with significant increases in PFS (P=0.01) and OS (P<0.01) times. The present study demonstrated that ASCT further increases the CR rate, prolongs PFS time and potentially increases the OS time. Incorporation of these novel agents, including the protea-some inhibitor bortezomib and the immunomodulatory drugs thalidomide and lenalidomide, into the induction, consolidation and maintenance phases has optimized the anti-myeloma activity of ASCT. |
format | Online Article Text |
id | pubmed-3797248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-37972482013-10-17 Therapeutic effects of autologous hematopoietic stem cell transplantation in multiple myeloma patients FU, CHENGCHENG WANG, JUAN XIN, XUE LIU, HUI XUE, SHENGLI MA, XIAO JIN, ZHENGMING SUN, AINING QIU, HUIYING WU, DEPEI Exp Ther Med Articles The present study aimed to evaluate the effect of autologous hematopoietic stem cell transplantation (ASCT) on the response and outcome of patients with multiple myeloma (MM) and to analyze the factors influencing the prognosis of the disease. Retrospective analysis was performed in 27 patients with MM who had been treated by ASCT (ASCT group) and 28 patients treated with combined chemotherapy only (non-ASCT group) from May 2004 to August 2011. The impact on the depth of response, progression-free survival (PFS) and overall survival (OS) times, as well as associated prognostic factors of patients with MM, were analyzed. All patients successfully underwent hematopoietic reconstruction without transplantation-related mortality. The complete remission (CR) rate of patients in the ASCT group significantly increased from 25.9% (7/27) before ASCT to 70.4% (19/27) following ASCT (P<0.01). The probability of OS for 5 years was 52.2% for the patients in the ASCT group and 33.1% for those in the non-ASCT group (P>0.05). Univariate analysis in the ASCT group demonstrated that maintenance and consolidation therapies were associated with significant increases in PFS (P=0.01) and OS (P<0.01) times. The present study demonstrated that ASCT further increases the CR rate, prolongs PFS time and potentially increases the OS time. Incorporation of these novel agents, including the protea-some inhibitor bortezomib and the immunomodulatory drugs thalidomide and lenalidomide, into the induction, consolidation and maintenance phases has optimized the anti-myeloma activity of ASCT. D.A. Spandidos 2013-10 2013-08-16 /pmc/articles/PMC3797248/ /pubmed/24137301 http://dx.doi.org/10.3892/etm.2013.1261 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles FU, CHENGCHENG WANG, JUAN XIN, XUE LIU, HUI XUE, SHENGLI MA, XIAO JIN, ZHENGMING SUN, AINING QIU, HUIYING WU, DEPEI Therapeutic effects of autologous hematopoietic stem cell transplantation in multiple myeloma patients |
title | Therapeutic effects of autologous hematopoietic stem cell transplantation in multiple myeloma patients |
title_full | Therapeutic effects of autologous hematopoietic stem cell transplantation in multiple myeloma patients |
title_fullStr | Therapeutic effects of autologous hematopoietic stem cell transplantation in multiple myeloma patients |
title_full_unstemmed | Therapeutic effects of autologous hematopoietic stem cell transplantation in multiple myeloma patients |
title_short | Therapeutic effects of autologous hematopoietic stem cell transplantation in multiple myeloma patients |
title_sort | therapeutic effects of autologous hematopoietic stem cell transplantation in multiple myeloma patients |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797248/ https://www.ncbi.nlm.nih.gov/pubmed/24137301 http://dx.doi.org/10.3892/etm.2013.1261 |
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