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Challenges in the Evaluation of Emerging Highly Specialised Technologies: Is There a Role for Living HTA?

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Specialty Public Health
Date 2023 Oct 12
PMID 37824056
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Abstract

There is currently deep uncertainty about the clinical benefits and cost effectiveness of highly specialised technologies (HSTs), like gene and cell therapies. These treatments are novel, typically have high upfront costs, the patient populations are small and heterogenous, there is minimal information on their long-term safety and effectiveness, and data are limited and often of poor quality. With the increasing number of these technologies and their high cost burden on governments and health care providers, policy makers are currently walking a decision tightrope. On the one hand, an unfavourable funding decision could potentially limit patient access to life-saving treatments, while on the other, a favourable decision could result in unsustainable budget impacts and perhaps poorer patient health outcomes. Health technology assessment (HTA) is meant to determine the value of a health technology in order to promote an equitable, efficient, and high-quality health system. However, standard HTA processes have failed to mitigate the deep uncertainties associated with these technologies. In this paper, we propose a Living HTA framework to address these challenges. This framework includes a one-off process for making explicit the societal values associated with HSTs. These would inform the decision-making approach, data collection and the development of disease-specific reference models to be used by industry sponsors as the basis for their submissions for public funding. Coverage with an evidence development mechanism is also proposed by which data can be collected in real time to update the reference model on a rolling basis, thereby allowing re-assessment of the clinical and cost effectiveness of individual HSTs. The HTA would be 'live' until the results indicate there is sufficient certainty for the funding decision to be confirmed, the price changed or the funding removed.

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References
1.
Rodriguez-Santana I, DasMahapatra P, Burke T, Hakimi Z, Bartelt-Hofer J, Nazir J . Health-related quality of life, direct medical and societal costs among children with moderate or severe haemophilia in Europe: multivariable models of the CHESS-PAEDs study. Orphanet J Rare Dis. 2022; 17(1):150. PMC: 8981697. DOI: 10.1186/s13023-022-02301-0. View

2.
Shah N, Lee D, Yates B, Yuan C, Shalabi H, Martin S . Long-Term Follow-Up of CD19-CAR T-Cell Therapy in Children and Young Adults With B-ALL. J Clin Oncol. 2021; 39(15):1650-1659. PMC: 8274806. DOI: 10.1200/JCO.20.02262. View

3.
OSullivan G, Philips J, Rasko J . Clinical gene technology in Australia: building on solid foundations. Med J Aust. 2022; 217(2):65-70. PMC: 9540640. DOI: 10.5694/mja2.51629. View

4.
Anagnostou T, Riaz I, Hashmi S, Murad M, Kenderian S . Anti-CD19 chimeric antigen receptor T-cell therapy in acute lymphocytic leukaemia: a systematic review and meta-analysis. Lancet Haematol. 2020; 7(11):e816-e826. DOI: 10.1016/S2352-3026(20)30277-5. View

5.
Stafinski T, Glennie J, Young A, Menon D . HTA decision-making for drugs for rare diseases: comparison of processes across countries. Orphanet J Rare Dis. 2022; 17(1):258. PMC: 9264608. DOI: 10.1186/s13023-022-02397-4. View