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2023

ANUÁRIO DO HOSPITAL
DONA ESTEFÂNIA

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VALUE-BASED DECISION-MAKING FOR ORPHAN DRUGS WITH MULTIPLE CRITERIA DECISION ANALYSIS: BUROSUMAB FOR THE TREATMENT OF X-LINKED HYPOPHOSPHATEMIA

Bjorn Vandewalle, Miguel Amorim, Diogo Ramos, Sofia Azevedo, Inês Alves, Telma Francisco1, Helena Pinto and Sérgio Sousa

1 - Unidade de Nefrologia, Hospital Dona Estefânia, Centro Hospitalar Universitário Lisboa Central, Lisboa

- https://doi.org/10.1080/03007995.2021.1904861

ABSTRACT
Objective: Burosumab is an orphan medicinal product (OMP) approved in Europe for the treatment of X-linked hypophosphatemia (XLH). The aim of this study was to assess the value of burosumab versus conventional therapy for the treatment of paediatric XLH, through a multi-criteria decision analysis (MCDA) framework for health technology assessment (HTA) of OMPs in Portugal.
Methods: The MCDA framework considered 14 criteria related to disease burden, therapeutic value and economic burden. A multidisciplinary panel of national stakeholders participated in a two-phase exercise. In the first phase, relative weights and part-worth utilities for the criteria and their levels were elicited and a reimbursement likelihood function was calibrated through adaptive conjoint analysis. In the second phase, burosumab and conventional therapy were assessed against the criteria, providing a global value score (0-100) and reimbursement likelihood (0–100%) for both.
Results: Of the 14 criteria, disease burden, therapeutic value and economic burden criteria represented 27.29%, 57.17% and 15.53% of the total weight in the decision, respectively. All disease burden and some therapeutic value criteria, typically not included in traditional HTA, represented 47.88% of the total weight. Burosumab was unanimously considered superior to conventional therapy, with an average (range) global value score of 84.96 (82.48–86.54) against 48.06 (43.37–57.68), and reimbursement likelihood of 97.50% (96.78%–98.32%) against 43.66% (31.48%–68.73%), respectively.
Conclusions: MCDA represents a powerful tool in HTA decision-making for OMPs. The results of this MCDA acknowledge burosumab as a disease-modifying drug, deemed superior to conventional therapy for the treatment of paediatric XLH.

Palavras Chave: genetics, inherited kidney disorders, molecular testing, rare kidney diseases, precision medicine.