2021
DOI: 10.1177/0272989x21994553
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Validity of Surrogate Endpoints and Their Impact on Coverage Recommendations: A Retrospective Analysis across International Health Technology Assessment Agencies

Abstract: Background Surrogate endpoints (i.e., intermediate endpoints intended to predict for patient-centered outcomes) are increasingly common. However, little is known about how surrogate evidence is handled in the context of health technology assessment (HTA). Objectives 1) To map methodologies for the validation of surrogate endpoints and 2) to determine their impact on acceptability of surrogates and coverage decisions made by HTA agencies. Methods We sought HTA reports where evaluation relied on a surrogate from… Show more

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Cited by 24 publications
(18 citation statements)
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“…The regulatory (FDA or EMA) statements are usually used as a reference for the validation of surrogate end points by HTA agencies. However, regulators are more focused on safety and shorter-term efficacy while HTA agencies should focus more on a longer-term perspective to assess clinical effectiveness and cost-effectiveness, where the considerations on the acceptance of surrogate end points may be different between them (40). HTA agencies are suggested to develop more detailed methodological guidance for the selection of end points and validation of surrogate end points for the cancer diseases (39).…”
Section: Discussionmentioning
confidence: 99%
“…The regulatory (FDA or EMA) statements are usually used as a reference for the validation of surrogate end points by HTA agencies. However, regulators are more focused on safety and shorter-term efficacy while HTA agencies should focus more on a longer-term perspective to assess clinical effectiveness and cost-effectiveness, where the considerations on the acceptance of surrogate end points may be different between them (40). HTA agencies are suggested to develop more detailed methodological guidance for the selection of end points and validation of surrogate end points for the cancer diseases (39).…”
Section: Discussionmentioning
confidence: 99%
“…For example, there are still issues with respect to surrogate to final outcomes which is recognized by the majority of the respondents in this survey. Previous recommendations surrounding transparency and quantification of exploration of uncertainty have been published both in general (22,23) and for several tumors types like breast cancer (24) and colorectal cancer (25). While extensive guidance is available from different HTA organizations (26,27), the issue of extrapolation is still perceived by public sector respondents as black boxes.…”
Section: Implications For Researchmentioning
confidence: 99%
“…The second dimension of difference is the outcomes that are considered. And I think the regulatory bodies will accept surrogate outcomes, 17,18 not necessarily final outcomes for patients. Also, they tend not to focus very much on quality of life measures, although that's increasing.…”
Section: Chapter 7: the Wider Stakeholder Environment [1006]mentioning
confidence: 99%