Predictive Modeling Identifies Total Bleeds at 12-Weeks Postswitch to N8-GP Prophylaxis as a Predictor of Treatment Response

Author:

Chowdary Pratima1ORCID,Hampton Kingsley2,Jiménez-Yuste Victor3,Young Guy4,Benchikh el Fegoun Soraya5,Cooper Aidan6,Scalfaro Erik7,Tiede Andreas8ORCID

Affiliation:

1. Katharine Dormandy Haemophilia and Thrombosis Centre, Royal Free Hospital, London, United Kingdom

2. Department of Cardiovascular Science, University of Sheffield, Sheffield, United Kingdom

3. Department of Hematology, La Paz University Hospital-IdiPaz, Autónoma University, Madrid, Spain

4. Hemostasis and Thrombosis Center, Cancer and Blood Disorders Institute, Children's Hospital Los Angeles, University of Southern California Keck School of Medicine, Los Angeles, California, United Sates

5. Global Medical Affairs Biopharm, Novo Nordisk Health Care AG, Zürich, Switzerland

6. Predictive Analytics, Real World Solutions, IQVIA, London, United Kingdom

7. Real World Insights, IQVIA, Basel, Switzerland

8. Department of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hanover, Germany

Abstract

Abstract Background Predicting annualized bleeding rate (ABR) during factor VIII (FVIII) prophylaxis for severe hemophilia A (SHA) is important for long-term outcomes. This study used supervised machine learning-based predictive modeling to identify predictors of long-term ABR during prophylaxis with an extended half-life FVIII. Methods Data were from 166 SHA patients who received N8-GP prophylaxis (50 IU/kg every 4 days) in the pathfinder 2 study. Predictive models were developed to identify variables associated with an ABR of ≤1 versus >1 during the trial's main phase (median follow-up of 469 days). Model performance was assessed using area under the receiver operator characteristic curve (AUROC). Pre-N8-GP prophylaxis models learned from data collected at baseline; post-N8-GP prophylaxis models learned from data collected up to 12-weeks postswitch to N8-GP, and predicted ABR at the end of the outcome period (final year of treatment in the main phase). Results The predictive model using baseline variables had moderate performance (AUROC = 0.64) for predicting observed ABR. The most performant model used data collected at 12-weeks postswitch (AUROC = 0.79) with cumulative bleed count up to 12 weeks as the most informative variable, followed by baseline von Willebrand factor and mean FVIII at 30 minutes postdose. Univariate cumulative bleed count at 12 weeks performed equally well to the 12-weeks postswitch model (AUROC = 0.75). Pharmacokinetic measures were indicative, but not essential, to predict ABR. Conclusion Cumulative bleed count up to 12-weeks postswitch was as informative as the 12-week post-switch predictive model for predicting long-term ABR, supporting alterations in prophylaxis based on treatment response.

Funder

Novo Nordisk A/S

Publisher

Georg Thieme Verlag KG

Subject

Hematology

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