DOES THE ADOPTION OF A SOCIETAL PERSPECTIVE IMPROVE ACCESS TO PREVENTATIVE MIGRAINE THERAPIES?
Author(s)
Farhana Haque Anisha, BSc1, Holly Jones, BSc1, Fern Woodhouse, MChem MSc2.
1Costello Medical, London, United Kingdom, 2Costello Medical, Cambridge, United Kingdom.
1Costello Medical, London, United Kingdom, 2Costello Medical, Cambridge, United Kingdom.
OBJECTIVES: Healthcare systems and governments globally are shifting from reactive treatment to proactive disease prevention. The long-term and broader societal value of preventative therapies may not be adequately captured in current HTA frameworks. We assess how differences in HTA methodological approaches, particularly adopting a societal perspective, could influence reimbursement decisions, focusing on calcitonin gene-related peptide (CGRP) therapies for migraine prevention as a case study.
METHODS: Published evaluations for six CGRP therapies (galcanezumab, erenumab, fremanezumab, eptinezumab, atogepant and rimegepant) were identified for HTA bodies focused on cost-effectiveness: NICE, SMC, ICER, CDA-AMC, PBAC and ZIN. Key methodological characteristics, decision-making metrics and reimbursement outcomes were extracted.
RESULTS: Of 32 appraisals, productivity costs were included in six base case analyses, all conducted by ZIN. Of these, four were reimbursed for the manufacturer-defined population albeit narrower than the licensed population; separately, four required reassessments after initial evidence was insufficient for decision-making, with key uncertainties around estimation and substantiation of productivity costs. Scenario analyses including productivity costs were explored in eight appraisals, but had limited influence on outcomes despite ICER reductions: CDA-AMC did not comment on these scenarios; broader uncertainty drove a decrease in the willingness-to-pay threshold for NICE; similarly, perceived long-term value for money was reduced by uncertainty for ICER. Reimbursement rates were similar between appraisals assessing productivity losses (base case or scenario) and those that did not (100% vs 94.4%, excluding ICER assessments), although 6% fewer appraisals assessing productivity losses were recommended for the full manufacturer-defined population. This likely reflects differences in manufacturer-defined populations across HTA bodies rather than a direct effect of including productivity costs.
CONCLUSIONS: Despite widespread acknowledgement of productivity losses, a societal perspective was rarely adopted. Where adopted, including productivity costs reduced ICERs but these reductions were generally not reflected in final decision-making, with evidence uncertainty remaining a key barrier to demonstrating value.
METHODS: Published evaluations for six CGRP therapies (galcanezumab, erenumab, fremanezumab, eptinezumab, atogepant and rimegepant) were identified for HTA bodies focused on cost-effectiveness: NICE, SMC, ICER, CDA-AMC, PBAC and ZIN. Key methodological characteristics, decision-making metrics and reimbursement outcomes were extracted.
RESULTS: Of 32 appraisals, productivity costs were included in six base case analyses, all conducted by ZIN. Of these, four were reimbursed for the manufacturer-defined population albeit narrower than the licensed population; separately, four required reassessments after initial evidence was insufficient for decision-making, with key uncertainties around estimation and substantiation of productivity costs. Scenario analyses including productivity costs were explored in eight appraisals, but had limited influence on outcomes despite ICER reductions: CDA-AMC did not comment on these scenarios; broader uncertainty drove a decrease in the willingness-to-pay threshold for NICE; similarly, perceived long-term value for money was reduced by uncertainty for ICER. Reimbursement rates were similar between appraisals assessing productivity losses (base case or scenario) and those that did not (100% vs 94.4%, excluding ICER assessments), although 6% fewer appraisals assessing productivity losses were recommended for the full manufacturer-defined population. This likely reflects differences in manufacturer-defined populations across HTA bodies rather than a direct effect of including productivity costs.
CONCLUSIONS: Despite widespread acknowledgement of productivity losses, a societal perspective was rarely adopted. Where adopted, including productivity costs reduced ICERs but these reductions were generally not reflected in final decision-making, with evidence uncertainty remaining a key barrier to demonstrating value.
Conference/Value in Health Info
2026-11, ISPOR Europe 2026, Vienna, Austria
Value in Health, Volume 29, Issue 12S
Code
HTA384
Topic
Economic Evaluation, Health Technology Assessment
Topic Subcategory
Value Frameworks & Dossier Format
Disease
No Additional Disease & Conditions/Specialized Treatment Areas