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Exploring Heterogeneity in Histology-Independent Technologies and the Implications for Cost-Effectiveness

BACKGROUND: The National Institute for Health and Care Excellence and a number of international health technology assessment agencies have recently undertaken appraisals of histology-independent technologies (HITs). A strong and untested assumption inherent in the submissions included identical clin...

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Autores principales: Murphy, Peter, Claxton, Lindsay, Hodgson, Robert, Glynn, David, Beresford, Lucy, Walton, Matthew, Llewellyn, Alexis, Palmer, Stephen, Dias, Sofia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7879234/
https://www.ncbi.nlm.nih.gov/pubmed/33435846
http://dx.doi.org/10.1177/0272989X20980327
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author Murphy, Peter
Claxton, Lindsay
Hodgson, Robert
Glynn, David
Beresford, Lucy
Walton, Matthew
Llewellyn, Alexis
Palmer, Stephen
Dias, Sofia
author_facet Murphy, Peter
Claxton, Lindsay
Hodgson, Robert
Glynn, David
Beresford, Lucy
Walton, Matthew
Llewellyn, Alexis
Palmer, Stephen
Dias, Sofia
author_sort Murphy, Peter
collection PubMed
description BACKGROUND: The National Institute for Health and Care Excellence and a number of international health technology assessment agencies have recently undertaken appraisals of histology-independent technologies (HITs). A strong and untested assumption inherent in the submissions included identical clinical response across all tumour histologies, including new histologies unrepresented in the trial. Challenging this assumption and exploring the potential for heterogeneity has the potential to impact upon cost-effectiveness. METHOD: Using published response data for a HIT, a Bayesian hierarchical model (BHM) was used to identify heterogeneity in response and to estimate the probability of response for each histology included in single-arm studies, which informed the submission for the HIT, larotrectinib. The probability of response for a new histology was estimated. Results were inputted into a simplified response-based economic model using hypothetical parameters. Histology-independent and histology-specific incremental cost-effectiveness ratios accounting for heterogeneity were generated. RESULTS: The results of the BHM show considerable heterogeneity in response rates across histologies. The predicted probability of response estimated by the BHM is 60.9% (95% credible interval 16.0; 91.8%), lower than the naively pooled probability of 74.5%. A mean response probability of 56.9% (0.2; 99.9%) is predicted for an unrepresented histology. Based on the economic analysis, the probability of the hypothetical HIT being cost-effective under the assumption of identical response is 78%. Allowing for heterogeneity, the probability of various approval decisions being cost-effective ranges from 93% to 11%. CONCLUSIONS: Central to the challenge of reimbursement of HITs is the potential for heterogeneity. This study illustrates how heterogeneity in clinical effectiveness can result in highly variable and uncertain estimates of cost-effectiveness. This analysis can help improve understanding of the consequences of histology-independent versus histology-specific decisions.
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spelling pubmed-78792342021-02-22 Exploring Heterogeneity in Histology-Independent Technologies and the Implications for Cost-Effectiveness Murphy, Peter Claxton, Lindsay Hodgson, Robert Glynn, David Beresford, Lucy Walton, Matthew Llewellyn, Alexis Palmer, Stephen Dias, Sofia Med Decis Making Original Articles BACKGROUND: The National Institute for Health and Care Excellence and a number of international health technology assessment agencies have recently undertaken appraisals of histology-independent technologies (HITs). A strong and untested assumption inherent in the submissions included identical clinical response across all tumour histologies, including new histologies unrepresented in the trial. Challenging this assumption and exploring the potential for heterogeneity has the potential to impact upon cost-effectiveness. METHOD: Using published response data for a HIT, a Bayesian hierarchical model (BHM) was used to identify heterogeneity in response and to estimate the probability of response for each histology included in single-arm studies, which informed the submission for the HIT, larotrectinib. The probability of response for a new histology was estimated. Results were inputted into a simplified response-based economic model using hypothetical parameters. Histology-independent and histology-specific incremental cost-effectiveness ratios accounting for heterogeneity were generated. RESULTS: The results of the BHM show considerable heterogeneity in response rates across histologies. The predicted probability of response estimated by the BHM is 60.9% (95% credible interval 16.0; 91.8%), lower than the naively pooled probability of 74.5%. A mean response probability of 56.9% (0.2; 99.9%) is predicted for an unrepresented histology. Based on the economic analysis, the probability of the hypothetical HIT being cost-effective under the assumption of identical response is 78%. Allowing for heterogeneity, the probability of various approval decisions being cost-effective ranges from 93% to 11%. CONCLUSIONS: Central to the challenge of reimbursement of HITs is the potential for heterogeneity. This study illustrates how heterogeneity in clinical effectiveness can result in highly variable and uncertain estimates of cost-effectiveness. This analysis can help improve understanding of the consequences of histology-independent versus histology-specific decisions. SAGE Publications 2021-01-13 2021-02 /pmc/articles/PMC7879234/ /pubmed/33435846 http://dx.doi.org/10.1177/0272989X20980327 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Murphy, Peter
Claxton, Lindsay
Hodgson, Robert
Glynn, David
Beresford, Lucy
Walton, Matthew
Llewellyn, Alexis
Palmer, Stephen
Dias, Sofia
Exploring Heterogeneity in Histology-Independent Technologies and the Implications for Cost-Effectiveness
title Exploring Heterogeneity in Histology-Independent Technologies and the Implications for Cost-Effectiveness
title_full Exploring Heterogeneity in Histology-Independent Technologies and the Implications for Cost-Effectiveness
title_fullStr Exploring Heterogeneity in Histology-Independent Technologies and the Implications for Cost-Effectiveness
title_full_unstemmed Exploring Heterogeneity in Histology-Independent Technologies and the Implications for Cost-Effectiveness
title_short Exploring Heterogeneity in Histology-Independent Technologies and the Implications for Cost-Effectiveness
title_sort exploring heterogeneity in histology-independent technologies and the implications for cost-effectiveness
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7879234/
https://www.ncbi.nlm.nih.gov/pubmed/33435846
http://dx.doi.org/10.1177/0272989X20980327
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