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Switching to nonacog beta pegol in hemophilia B: Outcomes from a Canadian real-world, multicenter, retrospective study.
Matino, Davide; Iorio, Alfonso; Keepanasseril, Arun; Germini, Federico; Caillaud, Alexandre; Carcao, Manuel; Hews-Girard, Julia; Iserman, Emma; James, Paula; Lee, Adrienne; Phua, Chai W; Sun, Haowei Linda; Teitel, Jerome; Poon, Man-Chiu.
Affiliation
  • Matino D; McMaster University Hamilton ON Canada.
  • Iorio A; McMaster University Hamilton ON Canada.
  • Keepanasseril A; McMaster University Hamilton ON Canada.
  • Germini F; McMaster University Hamilton ON Canada.
  • Caillaud A; BioPharm Medical Affairs Novo Nordisk Canada Inc. Mississauga ON Canada.
  • Carcao M; The Hospital for Sick Children University of Toronto Toronto ON Canada.
  • Hews-Girard J; Foothills Medical Centre Alberta Health Services Calgary AB Canada.
  • Iserman E; McMaster University Hamilton ON Canada.
  • James P; Queen's University Kingston ON Canada.
  • Lee A; University of Calgary Calgary AB Canada.
  • Phua CW; Western University London ON Canada.
  • Sun HL; University of Alberta Edmonton AB Canada.
  • Teitel J; St Michael's Hospital University of Toronto Toronto ON Canada.
  • Poon MC; Cumming School of Medicine University of Calgary Calgary AB Canada.
Res Pract Thromb Haemost ; 6(3): e12661, 2022 Mar.
Article in En | MEDLINE | ID: mdl-35386274
Background: The Canadian Bleeding Disorders Registry (CBDR) captures data from 24 hemophilia treatment centers and patients directly. Nonacog beta pegol (N9-GP) was approved in Canada in 2018. Objectives: To assess treatment outcomes following switching to N9-GP in a real-world setting. Methods: CBDR data for Canadian male patients (aged 7-72 years) with hemophilia B receiving prophylactic N9-GP for ≥6 months as of March 31, 2021, were included. To allow comparison with the previously used products, only patients for whom data were available in the CBDR for at least 6 months before the switch to N9-GP were included in this retrospective analysis. Results: Forty-two patients were included in the analysis (total observation period: 148.0 patient-years). The distribution of disease severity was 62% severe, 36% moderate, 2% mild, with 62% of patients previously receiving recombinant factor IX-Fc-fusion protein (rFIXFc) and 38% previously receiving standard half-life (SHL) recombinant factor IX (rFIX). During a median follow-up period of 2.3 years on N9-GP prophylaxis, 232 bleeds were reported in 30 patients, 29% of patients reported zero bleeds. The median overall annualized bleeding rate on N9-GP was 0.73 for patients switching from rFIXFc (previously 1.44) and 2.10 for patients switching from SHL rFIX (previously 6.06). Median total annualized factor consumption (IU/kg) was lower with N9-GP than with previous SHL rFIX (2152 vs 3018) and previous rFIXFc (1766 vs 2278). Conclusions: Results from this first real-world study of N9-GP in patients with hemophilia B suggest optimal bleeding control with low factor consumption after switching to N9-GP, irrespective of the previous product.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Observational_studies Language: En Journal: Res Pract Thromb Haemost Year: 2022 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Observational_studies Language: En Journal: Res Pract Thromb Haemost Year: 2022 Type: Article