Abstract

Gene therapy is an emerging type of treatment that may aim to provide a cure to individuals with a genetic mutation known to be causative of a specific disease. A diagnosis of the causative mutation must precede treatment with a in vivo gene therapy. Both achieving a genomic-based diagnosis and treatment with a gene therapy may result in substantial expenditures for health care systems. Uncertainties around the health care costs, risks, and benefits derived from diagnosis and treatment with a subsequent gene therapy suggests a need for developing an evidence base, underpinned by opportunity cost, to inform if, and how, these health technologies should be introduced into health care systems funded by finite budgets. This article discusses why current methods to evaluate health technologies (decision-analytic model-based cost-effectiveness analysis from the perspective of a health care system over a lifetime time horizon) are appropriate to quantify the costs and consequences of using genomic-based diagnostic tests and gene therapies in combination, rather than as separate interventions, within clinical practice. Evaluating the economic impact of test-and-treatment strategies will ensure that the opportunity cost of these health technologies is quantified fully for decision-makers who are responsible for allocating limited resources in health care systems.

Highlights

  • Gene therapy is an emerging type of treatment that aims to provide a definitive cure to individuals with a genetic mutation known to be causative of a specific disease

  • In Europe, gene therapies are categorized under the regulatory remit of a broader classification called “advanced therapy medicinal products” (ATMPs) [4]

  • The current discussions about the need to produce evidence to understand the economic impact of introducing expensive gene therapies have focused on the cost-effectiveness of the therapy component in isolation

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Summary

Introduction

Gene therapy is an emerging type of treatment that aims to provide a definitive cure to individuals with a genetic mutation known to be causative of a specific disease. A definitive diagnosis, informed by a genomic-based testing strategy, that provides information about the specific causative genetic mutation must precede treatment in order to identify the population of patients who will benefit from a in vivo gene therapy. Strategies to identify causative genetic mutations have improved following the development of next-generation sequencing (NGS) technologies [13] These NGS technologies have stimulated the clinical application of genomic-based diagnostic tests [14]. A genomic-based diagnostic test that directs patients to a relevant gene therapy is similar to the use of the term “companion diagnostic”. Genomic-based diagnostic tests enter clinical practice when there is evidence that a specific gene may be responsible for a defined phenotype (the genetic condition) and are not developed with the intent of being companion diagnostics. These frameworks currently do not consider evidence of the opportunity cost imposed by a new genomic-based diagnostic test

Opportunity Cost and Value Assessment Frameworks
Conclusions
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