Abstract

Introduction: The significant therapeutic potential of the advanced therapies (ATs) has predetermined the increased interests in their development mainly in the context of rare diseases most of which are genetically determined. However, there are still many challenges in front of the health insurance funds related to the cost-effectiveness and budget impact issues of these therapies. Our aim was to review and analyze the potential of low- and middle-income countries for health technology assessment (HTA) of advanced therapies focusing on Bulgaria, Romania and Poland as reference countries. A literature review of the existing good practices related to HTA of advanced therapies across the world and comparison with the national reality were performed. A list of challenges and issues from the point of view of the payer institution of all analyzed countries was performed. Pilot recommendations on how to overcome the barriers were created based on the existing practices and the potential of the national system.Discussion: 15 out of 80 articles identified in PubMed were found as applicable to the study scope as most of them were published in the period 2019–2021. Undoubtedly, the main challenges correspond to the high treatment costs, the uncertainty in clinical effectiveness, and poor HTA methodological approaches applicable for ATs worldwide. The issues identified for low and middle-income countries are similar having as well the lack of enough qualified health economists for the purposes of assessment and appraisal of HTA dossiers of the advanced therapies, lack of adequate existing separate financial programs for those therapies, and not preparedness of the health system and the society as a whole for such therapies.Conclusions: Despite the difficulties and challenges, the advanced therapies can be defined as a futuristic therapy for which great discoveries are yet to come. Therefore, each country should consider the implementation of reliable and nationally oriented programs for HTA and adequate financial coverage of these therapies.

Highlights

  • The significant therapeutic potential of the advanced therapies (ATs) has predetermined the increased interests in their development mainly in the context of rare diseases most of which are genetically determined

  • The advanced therapy medicinal products (ATMPs) are a fast-growing field with the innovative potential to modify the treatment of a wide range of pathologies rare but common oncology, cardiovascular, musculoskeletal and immune diseases etc. for which the conventional approaches are ineffective [1]

  • Many recommendations were given in the scientific literature how to cope with the barriers and challenges such as early dialogue between Health Technology Assessment (HTA) Agencies and other stakeholders, patients’ registries in the post-authorization period, outcomebased managed entry agreements, adopt societal perspective in a long-term period etc. [6, 7]

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Summary

Introduction

The significant therapeutic potential of the advanced therapies (ATs) has predetermined the increased interests in their development mainly in the context of rare diseases most of which are genetically determined. The recent proposal for joint HTA increase the authority of European Medicines Agency (EMA) in providing scientific advice in the field and earlier joint creation of evidence that will satisfy the marketing authorization and market access of innovative therapies [8].

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