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艾曲泊帕、重组人血小板生成素联合标准免疫抑制治疗重型再生障碍性贫血16例疗效及安全性分析

OBJECTIVE: To evaluate the efficacy and safety of combination therapy of eltrombopag, recombinant human thrombopoietin (rhTPO), and standard immunosuppressive therapy (IST) for severe aplastic anemia (SAA). METHODS: A total of 16 cases with SAA treated with IST combined with eltrombopag and rhTPO we...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770875/
https://www.ncbi.nlm.nih.gov/pubmed/35045674
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.12.010
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collection PubMed
description OBJECTIVE: To evaluate the efficacy and safety of combination therapy of eltrombopag, recombinant human thrombopoietin (rhTPO), and standard immunosuppressive therapy (IST) for severe aplastic anemia (SAA). METHODS: A total of 16 cases with SAA treated with IST combined with eltrombopag and rhTPO were retrospectively analyzed. RESULTS: At 3 months, the total response rate was 81.3%, and the complete hematological response rate was 37.5%. At 6 months, the total response rate was 87.5%, and the complete hematological response rate was 50.0%. The median time of platelet transfusion independence was 35 (16–78) days, the median time of red blood cell transfusion independence was 47.5 (15–105) days, the median platelet transfusion was 5.5 (3–20) U, and the median red blood cell transfusion was 6.5 (2–16) U. CONCLUSION: The combination of eltrombopag and rhTPO can improve the hematological response rate of IST for SAA and the quality of hematological remission with minimal toxic effects.
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spelling pubmed-87708752022-02-13 艾曲泊帕、重组人血小板生成素联合标准免疫抑制治疗重型再生障碍性贫血16例疗效及安全性分析 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To evaluate the efficacy and safety of combination therapy of eltrombopag, recombinant human thrombopoietin (rhTPO), and standard immunosuppressive therapy (IST) for severe aplastic anemia (SAA). METHODS: A total of 16 cases with SAA treated with IST combined with eltrombopag and rhTPO were retrospectively analyzed. RESULTS: At 3 months, the total response rate was 81.3%, and the complete hematological response rate was 37.5%. At 6 months, the total response rate was 87.5%, and the complete hematological response rate was 50.0%. The median time of platelet transfusion independence was 35 (16–78) days, the median time of red blood cell transfusion independence was 47.5 (15–105) days, the median platelet transfusion was 5.5 (3–20) U, and the median red blood cell transfusion was 6.5 (2–16) U. CONCLUSION: The combination of eltrombopag and rhTPO can improve the hematological response rate of IST for SAA and the quality of hematological remission with minimal toxic effects. Editorial office of Chinese Journal of Hematology 2021-12 /pmc/articles/PMC8770875/ /pubmed/35045674 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.12.010 Text en 2021年版权归中华医学会所有 https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 License.
spellingShingle 论著
艾曲泊帕、重组人血小板生成素联合标准免疫抑制治疗重型再生障碍性贫血16例疗效及安全性分析
title 艾曲泊帕、重组人血小板生成素联合标准免疫抑制治疗重型再生障碍性贫血16例疗效及安全性分析
title_full 艾曲泊帕、重组人血小板生成素联合标准免疫抑制治疗重型再生障碍性贫血16例疗效及安全性分析
title_fullStr 艾曲泊帕、重组人血小板生成素联合标准免疫抑制治疗重型再生障碍性贫血16例疗效及安全性分析
title_full_unstemmed 艾曲泊帕、重组人血小板生成素联合标准免疫抑制治疗重型再生障碍性贫血16例疗效及安全性分析
title_short 艾曲泊帕、重组人血小板生成素联合标准免疫抑制治疗重型再生障碍性贫血16例疗效及安全性分析
title_sort 艾曲泊帕、重组人血小板生成素联合标准免疫抑制治疗重型再生障碍性贫血16例疗效及安全性分析
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770875/
https://www.ncbi.nlm.nih.gov/pubmed/35045674
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.12.010
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