Abstract
Background: This study described the number of patients with psoriasis receiving flexible (continuous/intermittent) dosing with etanercept (ETN) and the real-world economic impact. Methods: BeFlex was a prospective, observational study with a ≥1 year follow-up. Patients ≥18 years with moderate-to-severe psoriasis who were starting or re-starting treatment with ETN in alignment with Belgian reimbursement criteria were included. Cost of ETN was compared with cost of adalimumab, ustekinumab and infliximab using estimates from the National Institute for Sickness and Disability Insurance (INAMI/RIZIV). Results: In the flexible-dosing cohort (n = 121 with dose-regimen data), 66% were treated continuously and 34% intermittently. Baseline characteristics were similar across dosing cohorts. In the per-protocol cohort (n = 138), average ETN treatment duration/year was 40 weeks; 43 weeks continuous and 33 weeks intermittent. The overall mean interruption duration was 3.9 weeks/treatment cycle; 0.2 week continuous and 11.1 weeks intermittent. Mean dose/year was 2065 mg; 2182 mg continuous and 1660 mg intermittent. Flexible ETN dosing reduced the cost by 20% versus INAMI/RIZIV estimates. The theoretical cost of the other continuously-dosed biologics was 28–44% higher than that of flexible ETN. Conclusion: Approximately one-third of Belgian patients received intermittent ETN treatment. Flexible ETN dosing was more cost-effective than treatment with biologic agents that require continuous dosing.
Acknowledgements
We wish to thank all the patients who participated in the BeFlex study and all the investigators and medical staff of the participating centers. We also thank Jacques Bruhwyler of ECSOR for statistical support and Erwin Bruninx of Mediconsult, a paid contractor to Pfizer Inc., for his contribution to the analysis and reporting throughout this project.
Declaration of interest
Siegfried Segaert has served as a consultant and/or speaker and/or clinical investigator for Abbott, Amgen, Janssen, Lilly, MSD, Novartis and Pfizer.
Pierre-Dominique Ghislain has served as a consultant, advisory board member or speaker, provided clinical research support, and has received grants or funding from Pfizer, AbbVie and Merck.
Caroline Boone is a full-time employee of Pfizer.
This research was sponsored by Pfizer Inc. The editorial/medical writing support was provided by Samantha Forster of Engage Scientific Solutions and was funded by Pfizer Inc.