Challenges for Economic Evaluations of Advanced Therapy Medicinal Products: A Systematic Review
Metadatos
Mostrar el registro completo del ítemAutor
Olry de Labry Lima, Antonio; García Mochón, Leticia; Pérez Troncoso, Daniel; Epstein, David MarkEditorial
Elsevier
Materia
Advanced therapies Cost-effectiveness analysis Health technology assessment
Fecha
2022-08-26Referencia bibliográfica
Antonio Olry de Labry-Lima... [et al.]. Challenges for Economic Evaluations of Advanced Therapy Medicinal Products: A Systematic Review, Value in Health, Volume 26, Issue 1, 2023, Pages 138-150, ISSN 1098-3015, [https://doi.org/10.1016/j.jval.2022.07.004]
Patrocinador
Spanish Government PID2019-105597RA-100Resumen
Objectives: Advanced therapy medicinal products (ATMPs) are drugs for human use for the treatment of chronic, degenerative,
or life-threatening diseases that are based on genes, tissues, or cells. This article aimed to identify and critically review
published economic analyses of ATMPs.
Methods: A systematic review of economic analyses of ATMPs was undertaken. Study characteristics, design, sources of data,
resources and unit costs, modeling and extrapolation methods, study results, and sensitivity analyses were assessed.
Results: A total of 46 economic analyses of ATMP (from 45 articles) were included; 4 were cell therapy medicinal products, 33
gene therapy medicinal products, and 9 tissue-engineered products. 30 therapies had commercial marketing approval; 39
studies were cost-utility analysis, 5 were cost-effectiveness analysis, and 2 were cost only studies. Four studies predicted
that the ATMP offered a step change in the management of the condition and 10 studies estimated that the ATMP would
offer a lower mean cost.
Conclusions: Comparison with historical controls, pooling of data, and use of techniques such as mixture cure fraction models
should be used cautiously. Sensitivity analyses should be used across a plausible range of prices. Clinical studies need to be
designed to align with health technology assessment requirements, including generic quality of life, and payers should aim
for clarity of criteria. Regulators and national payers should aim for compatibility of registers to allow interchange of data.
Given the increasing reliance on industry-funded economic analyses, careful critical review is recommended.