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Recombinant Human Thrombopoietin Treatment Promotes Hematopoiesis Recovery in Patients with Severe Aplastic Anemia Receiving Immunosuppressive Therapy

Objective. To assess the effectiveness of recombinant human thrombopoietin (rhTPO) in severe aplastic anemia (SAA) patients receiving immunosuppressive therapy (IST). Methods. Eighty-eight SAA patients receiving IST from January 2007 to December 2012 were included in this retrospective analysis. Of...

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Autores principales: Wang, Huaquan, Dong, Qi'e, Fu, Rong, Qu, Wen, Ruan, Erbao, Wang, Guojin, Liu, Hong, Wu, Yuhong, Song, Jia, Xing, Limin, Guan, Jing, Li, Lijuan, Shao, Zonghong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377357/
https://www.ncbi.nlm.nih.gov/pubmed/25861635
http://dx.doi.org/10.1155/2015/597293
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author Wang, Huaquan
Dong, Qi'e
Fu, Rong
Qu, Wen
Ruan, Erbao
Wang, Guojin
Liu, Hong
Wu, Yuhong
Song, Jia
Xing, Limin
Guan, Jing
Li, Lijuan
Shao, Zonghong
author_facet Wang, Huaquan
Dong, Qi'e
Fu, Rong
Qu, Wen
Ruan, Erbao
Wang, Guojin
Liu, Hong
Wu, Yuhong
Song, Jia
Xing, Limin
Guan, Jing
Li, Lijuan
Shao, Zonghong
author_sort Wang, Huaquan
collection PubMed
description Objective. To assess the effectiveness of recombinant human thrombopoietin (rhTPO) in severe aplastic anemia (SAA) patients receiving immunosuppressive therapy (IST). Methods. Eighty-eight SAA patients receiving IST from January 2007 to December 2012 were included in this retrospective analysis. Of these, 40 subjects received rhTPO treatment (15000 U, subcutaneously, three times a week). rhTPO treatment was discontinued when the platelet count returned to normal range. Hematologic response, bone marrow megakaryocyte recovery, and time to transfusion independence were compared. Results. Hematologic response was achieved in 42.5%, 62.5%, and 67.5% of patients receiving rhTPO and 22.9%, 41.6%, and 47.9% of patients not receiving rhTPO at 3, 6, and 9 months after treatment, respectively (P = 0.0665, P = 0.0579, and P = 0.0847, resp.). Subjects receiving rhTPO presented an elevated number of megakaryocytes at 3, 6, and 9 months when compared with those without treatment (P = 0.025, P = 0.021, and P = 0.011, resp.). The time to platelet and red blood cell transfusion independence was shorter in patients who received rhTPO than in those without rhTPO treatment. Overall survival rate presented no differences between the two groups. Conclusion. rhTPO could improve hematologic response and promote bone marrow recovery in SAA patients receiving IST.
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spelling pubmed-43773572015-04-08 Recombinant Human Thrombopoietin Treatment Promotes Hematopoiesis Recovery in Patients with Severe Aplastic Anemia Receiving Immunosuppressive Therapy Wang, Huaquan Dong, Qi'e Fu, Rong Qu, Wen Ruan, Erbao Wang, Guojin Liu, Hong Wu, Yuhong Song, Jia Xing, Limin Guan, Jing Li, Lijuan Shao, Zonghong Biomed Res Int Clinical Study Objective. To assess the effectiveness of recombinant human thrombopoietin (rhTPO) in severe aplastic anemia (SAA) patients receiving immunosuppressive therapy (IST). Methods. Eighty-eight SAA patients receiving IST from January 2007 to December 2012 were included in this retrospective analysis. Of these, 40 subjects received rhTPO treatment (15000 U, subcutaneously, three times a week). rhTPO treatment was discontinued when the platelet count returned to normal range. Hematologic response, bone marrow megakaryocyte recovery, and time to transfusion independence were compared. Results. Hematologic response was achieved in 42.5%, 62.5%, and 67.5% of patients receiving rhTPO and 22.9%, 41.6%, and 47.9% of patients not receiving rhTPO at 3, 6, and 9 months after treatment, respectively (P = 0.0665, P = 0.0579, and P = 0.0847, resp.). Subjects receiving rhTPO presented an elevated number of megakaryocytes at 3, 6, and 9 months when compared with those without treatment (P = 0.025, P = 0.021, and P = 0.011, resp.). The time to platelet and red blood cell transfusion independence was shorter in patients who received rhTPO than in those without rhTPO treatment. Overall survival rate presented no differences between the two groups. Conclusion. rhTPO could improve hematologic response and promote bone marrow recovery in SAA patients receiving IST. Hindawi Publishing Corporation 2015 2015-03-11 /pmc/articles/PMC4377357/ /pubmed/25861635 http://dx.doi.org/10.1155/2015/597293 Text en Copyright © 2015 Huaquan Wang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Wang, Huaquan
Dong, Qi'e
Fu, Rong
Qu, Wen
Ruan, Erbao
Wang, Guojin
Liu, Hong
Wu, Yuhong
Song, Jia
Xing, Limin
Guan, Jing
Li, Lijuan
Shao, Zonghong
Recombinant Human Thrombopoietin Treatment Promotes Hematopoiesis Recovery in Patients with Severe Aplastic Anemia Receiving Immunosuppressive Therapy
title Recombinant Human Thrombopoietin Treatment Promotes Hematopoiesis Recovery in Patients with Severe Aplastic Anemia Receiving Immunosuppressive Therapy
title_full Recombinant Human Thrombopoietin Treatment Promotes Hematopoiesis Recovery in Patients with Severe Aplastic Anemia Receiving Immunosuppressive Therapy
title_fullStr Recombinant Human Thrombopoietin Treatment Promotes Hematopoiesis Recovery in Patients with Severe Aplastic Anemia Receiving Immunosuppressive Therapy
title_full_unstemmed Recombinant Human Thrombopoietin Treatment Promotes Hematopoiesis Recovery in Patients with Severe Aplastic Anemia Receiving Immunosuppressive Therapy
title_short Recombinant Human Thrombopoietin Treatment Promotes Hematopoiesis Recovery in Patients with Severe Aplastic Anemia Receiving Immunosuppressive Therapy
title_sort recombinant human thrombopoietin treatment promotes hematopoiesis recovery in patients with severe aplastic anemia receiving immunosuppressive therapy
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377357/
https://www.ncbi.nlm.nih.gov/pubmed/25861635
http://dx.doi.org/10.1155/2015/597293
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