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Rituximab as first-line treatment for acquired thrombotic thrombocytopenic purpura

OBJECTIVE: To investigate the efficacy and safety of rituximab (RTX) as first-line treatment of acquired thrombotic thrombocytopenic purpura (aTTP). METHODS: Twenty-five patients with acute aTTP and/or severe a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS13...

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Autores principales: Chen, Haifei, Fu, Ailin, Wang, Jing, Wu, Tianqin, Li, Zhengyang, Tang, Jieqing, Shen, Hongshi, Zhu, Jingjing, Li, Jie, Zhu, Qian, Qing, Longmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536423/
https://www.ncbi.nlm.nih.gov/pubmed/28639502
http://dx.doi.org/10.1177/0300060517695646
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author Chen, Haifei
Fu, Ailin
Wang, Jing
Wu, Tianqin
Li, Zhengyang
Tang, Jieqing
Shen, Hongshi
Zhu, Jingjing
Li, Jie
Zhu, Qian
Qing, Longmei
author_facet Chen, Haifei
Fu, Ailin
Wang, Jing
Wu, Tianqin
Li, Zhengyang
Tang, Jieqing
Shen, Hongshi
Zhu, Jingjing
Li, Jie
Zhu, Qian
Qing, Longmei
author_sort Chen, Haifei
collection PubMed
description OBJECTIVE: To investigate the efficacy and safety of rituximab (RTX) as first-line treatment of acquired thrombotic thrombocytopenic purpura (aTTP). METHODS: Twenty-five patients with acute aTTP and/or severe a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS13) deficiency were admitted to our centre from April 2009 to March 2015. Fourteen patients received RTX plus standard therapy (plasma exchange and corticosteroids) at acute episodes. Haemoglobin, platelet count, schistocytes, lactate dehydrogenase levels, ADAMTS13 activity and its inhibitors, and the ratio of B lymphocytes in the peripheral blood, were monitored. The number of plasma exchange (PEXs), total plasma volume, remission time, relapse ratio, and adverse effects were recorded. RESULTS: The median number of PEXs was 5 (2–17) sessions and median total plasma volume was 168.43 ml/kg (62.86–469.52 ml/kg). Patients achieved haematological remission at a median of 15 days (5–22 days), and the median time of immunological remission was 2 weeks (2–8 weeks) with a median follow-up of 13 months (3–61 months). ADAMTS13 activity significantly increased after 2 weeks. The B lymphocyte percentage in peripheral blood was reduced 1 week after the first dose of RTX infusion compared with before treatment (2.21% ± 5.23% vs 18.47% ± 7.34%, P = 0.000 [the result of statistical software]), and began to gradually increase 9 months later. Severe adverse effects and relapsing TTP were not observed during therapy and follow-up. However, one patient who had sustained immunological remission died of severe pneumonia 7 months later. CONCLUSION: Although our study was limited by its small sample number and it was a non-controlled, clinical trial, it showed potential benefits of RTX therapy for acute aTTP. RTX may be administered as a first-line therapy for lowering patients’ relapse rate in the long term. Randomized, controlled trials of RTX for aTTP are required.
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spelling pubmed-55364232017-10-03 Rituximab as first-line treatment for acquired thrombotic thrombocytopenic purpura Chen, Haifei Fu, Ailin Wang, Jing Wu, Tianqin Li, Zhengyang Tang, Jieqing Shen, Hongshi Zhu, Jingjing Li, Jie Zhu, Qian Qing, Longmei J Int Med Res Clinical Note OBJECTIVE: To investigate the efficacy and safety of rituximab (RTX) as first-line treatment of acquired thrombotic thrombocytopenic purpura (aTTP). METHODS: Twenty-five patients with acute aTTP and/or severe a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS13) deficiency were admitted to our centre from April 2009 to March 2015. Fourteen patients received RTX plus standard therapy (plasma exchange and corticosteroids) at acute episodes. Haemoglobin, platelet count, schistocytes, lactate dehydrogenase levels, ADAMTS13 activity and its inhibitors, and the ratio of B lymphocytes in the peripheral blood, were monitored. The number of plasma exchange (PEXs), total plasma volume, remission time, relapse ratio, and adverse effects were recorded. RESULTS: The median number of PEXs was 5 (2–17) sessions and median total plasma volume was 168.43 ml/kg (62.86–469.52 ml/kg). Patients achieved haematological remission at a median of 15 days (5–22 days), and the median time of immunological remission was 2 weeks (2–8 weeks) with a median follow-up of 13 months (3–61 months). ADAMTS13 activity significantly increased after 2 weeks. The B lymphocyte percentage in peripheral blood was reduced 1 week after the first dose of RTX infusion compared with before treatment (2.21% ± 5.23% vs 18.47% ± 7.34%, P = 0.000 [the result of statistical software]), and began to gradually increase 9 months later. Severe adverse effects and relapsing TTP were not observed during therapy and follow-up. However, one patient who had sustained immunological remission died of severe pneumonia 7 months later. CONCLUSION: Although our study was limited by its small sample number and it was a non-controlled, clinical trial, it showed potential benefits of RTX therapy for acute aTTP. RTX may be administered as a first-line therapy for lowering patients’ relapse rate in the long term. Randomized, controlled trials of RTX for aTTP are required. SAGE Publications 2017-03-21 2017-06 /pmc/articles/PMC5536423/ /pubmed/28639502 http://dx.doi.org/10.1177/0300060517695646 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Clinical Note
Chen, Haifei
Fu, Ailin
Wang, Jing
Wu, Tianqin
Li, Zhengyang
Tang, Jieqing
Shen, Hongshi
Zhu, Jingjing
Li, Jie
Zhu, Qian
Qing, Longmei
Rituximab as first-line treatment for acquired thrombotic thrombocytopenic purpura
title Rituximab as first-line treatment for acquired thrombotic thrombocytopenic purpura
title_full Rituximab as first-line treatment for acquired thrombotic thrombocytopenic purpura
title_fullStr Rituximab as first-line treatment for acquired thrombotic thrombocytopenic purpura
title_full_unstemmed Rituximab as first-line treatment for acquired thrombotic thrombocytopenic purpura
title_short Rituximab as first-line treatment for acquired thrombotic thrombocytopenic purpura
title_sort rituximab as first-line treatment for acquired thrombotic thrombocytopenic purpura
topic Clinical Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536423/
https://www.ncbi.nlm.nih.gov/pubmed/28639502
http://dx.doi.org/10.1177/0300060517695646
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