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The prevalence and risk factors of inhibitor development of FVIII in previously treated patients with hemophilia A

BACKGROUND: Risk factors for the development of inhibitors in previously untreated patients (PUPs) have been reported; this is not the case in previously treated patients (PTPs) owing to fewer studies. Risk factors may differ for the development of PTP versus PUP inhibitors. We aimed to identify ris...

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Autores principales: Kim, Ju Young, You, Chur Woo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779946/
https://www.ncbi.nlm.nih.gov/pubmed/31730688
http://dx.doi.org/10.5045/br.2019.54.3.204
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author Kim, Ju Young
You, Chur Woo
author_facet Kim, Ju Young
You, Chur Woo
author_sort Kim, Ju Young
collection PubMed
description BACKGROUND: Risk factors for the development of inhibitors in previously untreated patients (PUPs) have been reported; this is not the case in previously treated patients (PTPs) owing to fewer studies. Risk factors may differ for the development of PTP versus PUP inhibitors. We aimed to identify risk factors for PTP inhibitor development. METHODS: Participants were patients at a hemophilia treatment center in Korea with current or past history of factor VIII or factor IX alloantibodies. Observed inhibitors were classified as PUP or PTP inhibitors based on the cumulative number of exposure days. We compared the type and severity of hemophilia, mutation type, and family history of inhibitor between PUPs and PTPs. Events within 3 months before the first inhibitor detection, such as change of the factor concentrate used, short-term high exposure or continuous infusion of factor concentrate, history of surgery, infection, diagnosis of cancer, use of immunosuppressive or immunomodulator agents, and vaccination were compared between PUPs and PTPs. RESULTS: We observed 5 PUP inhibitors and 5 PTP inhibitors in 115 patients with hemophilia A. Events that might be related to the development of inhibitors within 3 months prior to the first inhibitor detection were observed in all 5 PTPs. On the contrary, no such events were observed in any PUPs. The observed events included a change in the factor concentrate used, subsequent chemotherapy, and short-term high exposure to factor concentrates for controlling hemorrhage and surgeries. CONCLUSION: Our results suggest a greater role of nongenetic factors in PTP inhibitor development.
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spelling pubmed-67799462019-10-16 The prevalence and risk factors of inhibitor development of FVIII in previously treated patients with hemophilia A Kim, Ju Young You, Chur Woo Blood Res Original Article BACKGROUND: Risk factors for the development of inhibitors in previously untreated patients (PUPs) have been reported; this is not the case in previously treated patients (PTPs) owing to fewer studies. Risk factors may differ for the development of PTP versus PUP inhibitors. We aimed to identify risk factors for PTP inhibitor development. METHODS: Participants were patients at a hemophilia treatment center in Korea with current or past history of factor VIII or factor IX alloantibodies. Observed inhibitors were classified as PUP or PTP inhibitors based on the cumulative number of exposure days. We compared the type and severity of hemophilia, mutation type, and family history of inhibitor between PUPs and PTPs. Events within 3 months before the first inhibitor detection, such as change of the factor concentrate used, short-term high exposure or continuous infusion of factor concentrate, history of surgery, infection, diagnosis of cancer, use of immunosuppressive or immunomodulator agents, and vaccination were compared between PUPs and PTPs. RESULTS: We observed 5 PUP inhibitors and 5 PTP inhibitors in 115 patients with hemophilia A. Events that might be related to the development of inhibitors within 3 months prior to the first inhibitor detection were observed in all 5 PTPs. On the contrary, no such events were observed in any PUPs. The observed events included a change in the factor concentrate used, subsequent chemotherapy, and short-term high exposure to factor concentrates for controlling hemorrhage and surgeries. CONCLUSION: Our results suggest a greater role of nongenetic factors in PTP inhibitor development. Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2019-09 2019-09-25 /pmc/articles/PMC6779946/ /pubmed/31730688 http://dx.doi.org/10.5045/br.2019.54.3.204 Text en © 2019 Korean Society of Hematology http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Ju Young
You, Chur Woo
The prevalence and risk factors of inhibitor development of FVIII in previously treated patients with hemophilia A
title The prevalence and risk factors of inhibitor development of FVIII in previously treated patients with hemophilia A
title_full The prevalence and risk factors of inhibitor development of FVIII in previously treated patients with hemophilia A
title_fullStr The prevalence and risk factors of inhibitor development of FVIII in previously treated patients with hemophilia A
title_full_unstemmed The prevalence and risk factors of inhibitor development of FVIII in previously treated patients with hemophilia A
title_short The prevalence and risk factors of inhibitor development of FVIII in previously treated patients with hemophilia A
title_sort prevalence and risk factors of inhibitor development of fviii in previously treated patients with hemophilia a
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779946/
https://www.ncbi.nlm.nih.gov/pubmed/31730688
http://dx.doi.org/10.5045/br.2019.54.3.204
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