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Regression Analysis to Estimate the Factor VIII Activity of Patients with Hemophilia A Without Inhibitor who Received Emicizumab Therapy

BACKGROUND:  Emicizumab, a bispecific monoclonal antibody for hemophilia A (HA), has strong pharmacodynamic effects in several coagulation assays resulting in dosing difficulties with Factor VIII (FVIII) concentrates during bleeding emergencies. MATERIALS AND METHODS: Single and multiple regression...

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Autores principales: Hatayama, Yuki, Motokura, Toru, Hosoda, Yuzuru, Suzuki, Sayaka, Namba, Hiroya, Kato, Konami, Kojima, Nao, Horie, Takuya, Iwamoto, Takuya, Yamashita, Noriko, Ichikawa, Hitomi, Fukuda, Tetsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894944/
https://www.ncbi.nlm.nih.gov/pubmed/35225012
http://dx.doi.org/10.1177/10760296221082992
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author Hatayama, Yuki
Motokura, Toru
Hosoda, Yuzuru
Suzuki, Sayaka
Namba, Hiroya
Kato, Konami
Kojima, Nao
Horie, Takuya
Iwamoto, Takuya
Yamashita, Noriko
Ichikawa, Hitomi
Fukuda, Tetsuya
author_facet Hatayama, Yuki
Motokura, Toru
Hosoda, Yuzuru
Suzuki, Sayaka
Namba, Hiroya
Kato, Konami
Kojima, Nao
Horie, Takuya
Iwamoto, Takuya
Yamashita, Noriko
Ichikawa, Hitomi
Fukuda, Tetsuya
author_sort Hatayama, Yuki
collection PubMed
description BACKGROUND:  Emicizumab, a bispecific monoclonal antibody for hemophilia A (HA), has strong pharmacodynamic effects in several coagulation assays resulting in dosing difficulties with Factor VIII (FVIII) concentrates during bleeding emergencies. MATERIALS AND METHODS: Single and multiple regression models were studied to estimate FVIII activity using 27 archived plasma samples from three patients with HA without inhibitor under emicizumab treatment. Explanatory variables were FVIII chromogenic assay (CSA), Ad|min1|, Ad|min2|, the number of seconds of APTT, and the FVIII one-stage assay (OSA), which were measured without idiotype antibodies. The response variable was FVIII OSA measured with idiotype antibodies. RESULTS: In the simple linear model, the FVIII CSA regression coefficient was 1.04 and the intercept was −14.55 (r(2) = 0.95; p < 0.001). In the multiple regression model, FVIII OSA and FVIII CSA were selected based on the Akaike Information Criterion, with regression coefficients of 1.74 and 1.15, respectively, and an intercept of −92.03 (r(2) = 0.96, p < 0.001). CONCLUSIONS: The regression models can estimate the FVIII:C levels in patients with HA receiving emicizumab and would be useful in a bleeding emergency and/or surgery.
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spelling pubmed-88949442022-03-05 Regression Analysis to Estimate the Factor VIII Activity of Patients with Hemophilia A Without Inhibitor who Received Emicizumab Therapy Hatayama, Yuki Motokura, Toru Hosoda, Yuzuru Suzuki, Sayaka Namba, Hiroya Kato, Konami Kojima, Nao Horie, Takuya Iwamoto, Takuya Yamashita, Noriko Ichikawa, Hitomi Fukuda, Tetsuya Clin Appl Thromb Hemost Original Manuscript BACKGROUND:  Emicizumab, a bispecific monoclonal antibody for hemophilia A (HA), has strong pharmacodynamic effects in several coagulation assays resulting in dosing difficulties with Factor VIII (FVIII) concentrates during bleeding emergencies. MATERIALS AND METHODS: Single and multiple regression models were studied to estimate FVIII activity using 27 archived plasma samples from three patients with HA without inhibitor under emicizumab treatment. Explanatory variables were FVIII chromogenic assay (CSA), Ad|min1|, Ad|min2|, the number of seconds of APTT, and the FVIII one-stage assay (OSA), which were measured without idiotype antibodies. The response variable was FVIII OSA measured with idiotype antibodies. RESULTS: In the simple linear model, the FVIII CSA regression coefficient was 1.04 and the intercept was −14.55 (r(2) = 0.95; p < 0.001). In the multiple regression model, FVIII OSA and FVIII CSA were selected based on the Akaike Information Criterion, with regression coefficients of 1.74 and 1.15, respectively, and an intercept of −92.03 (r(2) = 0.96, p < 0.001). CONCLUSIONS: The regression models can estimate the FVIII:C levels in patients with HA receiving emicizumab and would be useful in a bleeding emergency and/or surgery. SAGE Publications 2022-02-28 /pmc/articles/PMC8894944/ /pubmed/35225012 http://dx.doi.org/10.1177/10760296221082992 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) 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 Original Manuscript
Hatayama, Yuki
Motokura, Toru
Hosoda, Yuzuru
Suzuki, Sayaka
Namba, Hiroya
Kato, Konami
Kojima, Nao
Horie, Takuya
Iwamoto, Takuya
Yamashita, Noriko
Ichikawa, Hitomi
Fukuda, Tetsuya
Regression Analysis to Estimate the Factor VIII Activity of Patients with Hemophilia A Without Inhibitor who Received Emicizumab Therapy
title Regression Analysis to Estimate the Factor VIII Activity of Patients with Hemophilia A Without Inhibitor who Received Emicizumab Therapy
title_full Regression Analysis to Estimate the Factor VIII Activity of Patients with Hemophilia A Without Inhibitor who Received Emicizumab Therapy
title_fullStr Regression Analysis to Estimate the Factor VIII Activity of Patients with Hemophilia A Without Inhibitor who Received Emicizumab Therapy
title_full_unstemmed Regression Analysis to Estimate the Factor VIII Activity of Patients with Hemophilia A Without Inhibitor who Received Emicizumab Therapy
title_short Regression Analysis to Estimate the Factor VIII Activity of Patients with Hemophilia A Without Inhibitor who Received Emicizumab Therapy
title_sort regression analysis to estimate the factor viii activity of patients with hemophilia a without inhibitor who received emicizumab therapy
topic Original Manuscript
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894944/
https://www.ncbi.nlm.nih.gov/pubmed/35225012
http://dx.doi.org/10.1177/10760296221082992
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