Cargando…
First open-label, single-arm, prospective study of real-world use of FIX replacement therapy in a predominantly pediatric hemophilia B population in China
BACKGROUND: Nonacog alfa (recombinant factor IX [FIX]) is approved in China for the control and prevention of bleeding events in patients with hemophilia B. This was the first study to assess prophylaxis and on-demand therapy with recombinant FIX replacement in a real-world setting in China. This st...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8154445/ https://www.ncbi.nlm.nih.gov/pubmed/34032739 http://dx.doi.org/10.1097/MD.0000000000026077 |
_version_ | 1783699014725664768 |
---|---|
author | Yang, Renchi Wu, Runhui Sun, Jing Sun, Feifei Rupon, Jeremy Huard, Francois Korth-Bradley, Joan M. Xu, Lihong Luo, Binyu Liu, Yingxue Cathy Rendo, Pablo |
author_facet | Yang, Renchi Wu, Runhui Sun, Jing Sun, Feifei Rupon, Jeremy Huard, Francois Korth-Bradley, Joan M. Xu, Lihong Luo, Binyu Liu, Yingxue Cathy Rendo, Pablo |
author_sort | Yang, Renchi |
collection | PubMed |
description | BACKGROUND: Nonacog alfa (recombinant factor IX [FIX]) is approved in China for the control and prevention of bleeding events in patients with hemophilia B. This was the first study to assess prophylaxis and on-demand therapy with recombinant FIX replacement in a real-world setting in China. This study aimed to evaluate the safety and efficacy of nonacog alfa in Chinese patients with hemophilia B. METHODS: In this open-label, multicenter study (clinicaltrials.gov identifier NCT02336178), patients received on-demand or prophylactic treatment with intravenous nonacog alfa for approximately 6 months or 50 exposure days, whichever occurred first. The primary safety outcome was medically important events (i.e., development of FIX inhibitors, allergic reactions, and thrombotic events). Key secondary efficacy outcomes included the annualized bleeding rate for on-demand treatment and prophylaxis, response to on-demand treatment, the number of infusions per bleeding event, and the number of breakthrough bleeding events within 48 hours of prophylaxis. RESULTS: Seventy male patients (mean [standard deviation] age 7.8 [7.2] years) were enrolled (on-demand, n = 37; prophylaxis, n = 57 [24 patients were included in both groups]). Thirty-eight (54%) patients had up to 50 FIX exposure days before the study. The only medically important event was a transient low-titer FIX inhibitor (incidence 1.4%, 95% confidence interval, 0–7.7). The mean annualized bleeding rate was 26.3 for on-demand treatment and 6.5 for prophylaxis. A mean (standard deviation) of 1.5 (1.7) nonacog alfa infusions were given per bleeding episode; 78.8% of episodes resolved with 1 infusion. Response was “excellent” or “good” for 88% of the on-demand infusions. Twenty-three bleeding events (n = 11 patients) occurred within 48 hours of 2032 prophylaxis doses (1.13%). CONCLUSION: In the real-world setting, nonacog alfa is safe and effective for on-demand treatment and for prophylaxis for patients with hemophilia B in China. |
format | Online Article Text |
id | pubmed-8154445 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-81544452021-05-29 First open-label, single-arm, prospective study of real-world use of FIX replacement therapy in a predominantly pediatric hemophilia B population in China Yang, Renchi Wu, Runhui Sun, Jing Sun, Feifei Rupon, Jeremy Huard, Francois Korth-Bradley, Joan M. Xu, Lihong Luo, Binyu Liu, Yingxue Cathy Rendo, Pablo Medicine (Baltimore) 4800 BACKGROUND: Nonacog alfa (recombinant factor IX [FIX]) is approved in China for the control and prevention of bleeding events in patients with hemophilia B. This was the first study to assess prophylaxis and on-demand therapy with recombinant FIX replacement in a real-world setting in China. This study aimed to evaluate the safety and efficacy of nonacog alfa in Chinese patients with hemophilia B. METHODS: In this open-label, multicenter study (clinicaltrials.gov identifier NCT02336178), patients received on-demand or prophylactic treatment with intravenous nonacog alfa for approximately 6 months or 50 exposure days, whichever occurred first. The primary safety outcome was medically important events (i.e., development of FIX inhibitors, allergic reactions, and thrombotic events). Key secondary efficacy outcomes included the annualized bleeding rate for on-demand treatment and prophylaxis, response to on-demand treatment, the number of infusions per bleeding event, and the number of breakthrough bleeding events within 48 hours of prophylaxis. RESULTS: Seventy male patients (mean [standard deviation] age 7.8 [7.2] years) were enrolled (on-demand, n = 37; prophylaxis, n = 57 [24 patients were included in both groups]). Thirty-eight (54%) patients had up to 50 FIX exposure days before the study. The only medically important event was a transient low-titer FIX inhibitor (incidence 1.4%, 95% confidence interval, 0–7.7). The mean annualized bleeding rate was 26.3 for on-demand treatment and 6.5 for prophylaxis. A mean (standard deviation) of 1.5 (1.7) nonacog alfa infusions were given per bleeding episode; 78.8% of episodes resolved with 1 infusion. Response was “excellent” or “good” for 88% of the on-demand infusions. Twenty-three bleeding events (n = 11 patients) occurred within 48 hours of 2032 prophylaxis doses (1.13%). CONCLUSION: In the real-world setting, nonacog alfa is safe and effective for on-demand treatment and for prophylaxis for patients with hemophilia B in China. Lippincott Williams & Wilkins 2021-05-28 /pmc/articles/PMC8154445/ /pubmed/34032739 http://dx.doi.org/10.1097/MD.0000000000026077 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://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 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) |
spellingShingle | 4800 Yang, Renchi Wu, Runhui Sun, Jing Sun, Feifei Rupon, Jeremy Huard, Francois Korth-Bradley, Joan M. Xu, Lihong Luo, Binyu Liu, Yingxue Cathy Rendo, Pablo First open-label, single-arm, prospective study of real-world use of FIX replacement therapy in a predominantly pediatric hemophilia B population in China |
title | First open-label, single-arm, prospective study of real-world use of FIX replacement therapy in a predominantly pediatric hemophilia B population in China |
title_full | First open-label, single-arm, prospective study of real-world use of FIX replacement therapy in a predominantly pediatric hemophilia B population in China |
title_fullStr | First open-label, single-arm, prospective study of real-world use of FIX replacement therapy in a predominantly pediatric hemophilia B population in China |
title_full_unstemmed | First open-label, single-arm, prospective study of real-world use of FIX replacement therapy in a predominantly pediatric hemophilia B population in China |
title_short | First open-label, single-arm, prospective study of real-world use of FIX replacement therapy in a predominantly pediatric hemophilia B population in China |
title_sort | first open-label, single-arm, prospective study of real-world use of fix replacement therapy in a predominantly pediatric hemophilia b population in china |
topic | 4800 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8154445/ https://www.ncbi.nlm.nih.gov/pubmed/34032739 http://dx.doi.org/10.1097/MD.0000000000026077 |
work_keys_str_mv | AT yangrenchi firstopenlabelsinglearmprospectivestudyofrealworlduseoffixreplacementtherapyinapredominantlypediatrichemophiliabpopulationinchina AT wurunhui firstopenlabelsinglearmprospectivestudyofrealworlduseoffixreplacementtherapyinapredominantlypediatrichemophiliabpopulationinchina AT sunjing firstopenlabelsinglearmprospectivestudyofrealworlduseoffixreplacementtherapyinapredominantlypediatrichemophiliabpopulationinchina AT sunfeifei firstopenlabelsinglearmprospectivestudyofrealworlduseoffixreplacementtherapyinapredominantlypediatrichemophiliabpopulationinchina AT ruponjeremy firstopenlabelsinglearmprospectivestudyofrealworlduseoffixreplacementtherapyinapredominantlypediatrichemophiliabpopulationinchina AT huardfrancois firstopenlabelsinglearmprospectivestudyofrealworlduseoffixreplacementtherapyinapredominantlypediatrichemophiliabpopulationinchina AT korthbradleyjoanm firstopenlabelsinglearmprospectivestudyofrealworlduseoffixreplacementtherapyinapredominantlypediatrichemophiliabpopulationinchina AT xulihong firstopenlabelsinglearmprospectivestudyofrealworlduseoffixreplacementtherapyinapredominantlypediatrichemophiliabpopulationinchina AT luobinyu firstopenlabelsinglearmprospectivestudyofrealworlduseoffixreplacementtherapyinapredominantlypediatrichemophiliabpopulationinchina AT liuyingxuecathy firstopenlabelsinglearmprospectivestudyofrealworlduseoffixreplacementtherapyinapredominantlypediatrichemophiliabpopulationinchina AT rendopablo firstopenlabelsinglearmprospectivestudyofrealworlduseoffixreplacementtherapyinapredominantlypediatrichemophiliabpopulationinchina |