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Blood concentration of cyclosporine during early post-transplant period may have influence on the occurrence of chronic graft versus host disease in patients who received allogeneic hematopoietic stem cell transplantation
INTRODUCTION: It has rarely been studied that how the blood level of CsA affect the incidence of chronic GVHD after allogeneic hematopoietic stem cell transplantation (allo-HSCT). METHODS: A total of 183 patients who underwent allo-HSCT from an HLA-matched or haplo matched family donors between 2006...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312356/ https://www.ncbi.nlm.nih.gov/pubmed/27494893 http://dx.doi.org/10.18632/oncotarget.10988 |
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author | Park, Silvia Kim, Kihyun Jang, Jun Ho Kim, Seok Jin Kim, Won Seog Jung, Chul Won |
author_facet | Park, Silvia Kim, Kihyun Jang, Jun Ho Kim, Seok Jin Kim, Won Seog Jung, Chul Won |
author_sort | Park, Silvia |
collection | PubMed |
description | INTRODUCTION: It has rarely been studied that how the blood level of CsA affect the incidence of chronic GVHD after allogeneic hematopoietic stem cell transplantation (allo-HSCT). METHODS: A total of 183 patients who underwent allo-HSCT from an HLA-matched or haplo matched family donors between 2006 and 2014 were reviewed. RESULTS: The average monthly CsA blood concentration (CsA(avr), ng/ml) was calculated in each patient: 0-1, 1-2, and 2-3 months after allo-HSCT. CsA(avr) at the first month showed significant association with the occurrence of moderate to severe cGVHD in multivariate analysis adjusted for gender, age, total body irradiation, anti-thymocyte globulin, acute GVHD ≥ grade 2 and CsA(avr) levels of other periods. The risk of cGVHD development was lowest in patients with CsA(avr) of 200-250 ng/ml when compared to those with CsA(avr) of ≥ 250 or < 200 ng/ml (p=0.003). CONCLUSIONS: CsA level between 200 and 250 mg/ml during the first month after transplantation was significantly associated with the decreased risk of moderate to severe cGVHD. |
format | Online Article Text |
id | pubmed-5312356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53123562017-03-06 Blood concentration of cyclosporine during early post-transplant period may have influence on the occurrence of chronic graft versus host disease in patients who received allogeneic hematopoietic stem cell transplantation Park, Silvia Kim, Kihyun Jang, Jun Ho Kim, Seok Jin Kim, Won Seog Jung, Chul Won Oncotarget Research Paper INTRODUCTION: It has rarely been studied that how the blood level of CsA affect the incidence of chronic GVHD after allogeneic hematopoietic stem cell transplantation (allo-HSCT). METHODS: A total of 183 patients who underwent allo-HSCT from an HLA-matched or haplo matched family donors between 2006 and 2014 were reviewed. RESULTS: The average monthly CsA blood concentration (CsA(avr), ng/ml) was calculated in each patient: 0-1, 1-2, and 2-3 months after allo-HSCT. CsA(avr) at the first month showed significant association with the occurrence of moderate to severe cGVHD in multivariate analysis adjusted for gender, age, total body irradiation, anti-thymocyte globulin, acute GVHD ≥ grade 2 and CsA(avr) levels of other periods. The risk of cGVHD development was lowest in patients with CsA(avr) of 200-250 ng/ml when compared to those with CsA(avr) of ≥ 250 or < 200 ng/ml (p=0.003). CONCLUSIONS: CsA level between 200 and 250 mg/ml during the first month after transplantation was significantly associated with the decreased risk of moderate to severe cGVHD. Impact Journals LLC 2016-08-01 /pmc/articles/PMC5312356/ /pubmed/27494893 http://dx.doi.org/10.18632/oncotarget.10988 Text en Copyright: © 2016 Park 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 | Research Paper Park, Silvia Kim, Kihyun Jang, Jun Ho Kim, Seok Jin Kim, Won Seog Jung, Chul Won Blood concentration of cyclosporine during early post-transplant period may have influence on the occurrence of chronic graft versus host disease in patients who received allogeneic hematopoietic stem cell transplantation |
title | Blood concentration of cyclosporine during early post-transplant period may have influence on the occurrence of chronic graft versus host disease in patients who received allogeneic hematopoietic stem cell transplantation |
title_full | Blood concentration of cyclosporine during early post-transplant period may have influence on the occurrence of chronic graft versus host disease in patients who received allogeneic hematopoietic stem cell transplantation |
title_fullStr | Blood concentration of cyclosporine during early post-transplant period may have influence on the occurrence of chronic graft versus host disease in patients who received allogeneic hematopoietic stem cell transplantation |
title_full_unstemmed | Blood concentration of cyclosporine during early post-transplant period may have influence on the occurrence of chronic graft versus host disease in patients who received allogeneic hematopoietic stem cell transplantation |
title_short | Blood concentration of cyclosporine during early post-transplant period may have influence on the occurrence of chronic graft versus host disease in patients who received allogeneic hematopoietic stem cell transplantation |
title_sort | blood concentration of cyclosporine during early post-transplant period may have influence on the occurrence of chronic graft versus host disease in patients who received allogeneic hematopoietic stem cell transplantation |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312356/ https://www.ncbi.nlm.nih.gov/pubmed/27494893 http://dx.doi.org/10.18632/oncotarget.10988 |
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