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Platelet response during the second cycle of decitabine treatment predicts response and survival for myelodysplastic syndrome patients
Despite the efficacy of decitabine to myelodysplastic syndrome (MDS), there is a wide range of responses, and no definite predictive marker has been identified. This study aimed to describe the efficacy of decitabine and to identify potential predictors of response and survival in patients with MDS....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4599296/ https://www.ncbi.nlm.nih.gov/pubmed/25938546 |
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author | Jung, Hyun Ae Maeng, Chi Hoon Kim, Moonjin Kim, Sungmin Jung, Chul Won Jang, Jun Ho |
author_facet | Jung, Hyun Ae Maeng, Chi Hoon Kim, Moonjin Kim, Sungmin Jung, Chul Won Jang, Jun Ho |
author_sort | Jung, Hyun Ae |
collection | PubMed |
description | Despite the efficacy of decitabine to myelodysplastic syndrome (MDS), there is a wide range of responses, and no definite predictive marker has been identified. This study aimed to describe the efficacy of decitabine and to identify potential predictors of response and survival in patients with MDS. We retrospectively analyzed clinical data of MDS patients at Samsung Medical Center between August 2008 and August 2011. The response assessment was conducted using the International Working Group (IWG) response criteria for MDS. We analyzed 101 MDS patients (total 613 cycles) who received decitabine for a median of four cycles. The overall response was 52.5% (n = 53/101). The median time to any response was two cycles with the median overall survival of 16.7 months. Patients who showed hematologic improvement had significantly longer survival than those who did not (9.8 vs. 22.9 months, p = 0.004). The difference in OS was evident in the Intermediate-2/High risk group (p = 0.002) but not in the Intermediate-1 risk group (p = 0.145). Multivariate analysis confirmed that platelet response (no platelet transfusions for at least 3 days) during the second cycle of treatment was an independent predictor for response, OS and Leukemia free survival. Based on the results of this study, for patients with hematological improvement, recovery of platelet count by the second cycle of therapy can be used as an early predictive marker of improved survival and an increased response rate. |
format | Online Article Text |
id | pubmed-4599296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-45992962015-10-26 Platelet response during the second cycle of decitabine treatment predicts response and survival for myelodysplastic syndrome patients Jung, Hyun Ae Maeng, Chi Hoon Kim, Moonjin Kim, Sungmin Jung, Chul Won Jang, Jun Ho Oncotarget Clinical Research Paper Despite the efficacy of decitabine to myelodysplastic syndrome (MDS), there is a wide range of responses, and no definite predictive marker has been identified. This study aimed to describe the efficacy of decitabine and to identify potential predictors of response and survival in patients with MDS. We retrospectively analyzed clinical data of MDS patients at Samsung Medical Center between August 2008 and August 2011. The response assessment was conducted using the International Working Group (IWG) response criteria for MDS. We analyzed 101 MDS patients (total 613 cycles) who received decitabine for a median of four cycles. The overall response was 52.5% (n = 53/101). The median time to any response was two cycles with the median overall survival of 16.7 months. Patients who showed hematologic improvement had significantly longer survival than those who did not (9.8 vs. 22.9 months, p = 0.004). The difference in OS was evident in the Intermediate-2/High risk group (p = 0.002) but not in the Intermediate-1 risk group (p = 0.145). Multivariate analysis confirmed that platelet response (no platelet transfusions for at least 3 days) during the second cycle of treatment was an independent predictor for response, OS and Leukemia free survival. Based on the results of this study, for patients with hematological improvement, recovery of platelet count by the second cycle of therapy can be used as an early predictive marker of improved survival and an increased response rate. Impact Journals LLC 2015-04-23 /pmc/articles/PMC4599296/ /pubmed/25938546 Text en Copyright: © 2015 Jung et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Clinical Research Paper Jung, Hyun Ae Maeng, Chi Hoon Kim, Moonjin Kim, Sungmin Jung, Chul Won Jang, Jun Ho Platelet response during the second cycle of decitabine treatment predicts response and survival for myelodysplastic syndrome patients |
title | Platelet response during the second cycle of decitabine treatment predicts response and survival for myelodysplastic syndrome patients |
title_full | Platelet response during the second cycle of decitabine treatment predicts response and survival for myelodysplastic syndrome patients |
title_fullStr | Platelet response during the second cycle of decitabine treatment predicts response and survival for myelodysplastic syndrome patients |
title_full_unstemmed | Platelet response during the second cycle of decitabine treatment predicts response and survival for myelodysplastic syndrome patients |
title_short | Platelet response during the second cycle of decitabine treatment predicts response and survival for myelodysplastic syndrome patients |
title_sort | platelet response during the second cycle of decitabine treatment predicts response and survival for myelodysplastic syndrome patients |
topic | Clinical Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4599296/ https://www.ncbi.nlm.nih.gov/pubmed/25938546 |
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