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Differences in Incremental Cost-Effectiveness Ratios for Common Versus Rare Conditions: A Case from Oncology
BACKGROUND: Incremental cost-effectiveness ratios (ICERs) are used to assess the value for money of new drugs. Many believe that ICERs for drugs that treat rare diseases are much higher than those of common drugs. Our objective was to compare the proportion of ICERs that are cost effective for rare...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691840/ https://www.ncbi.nlm.nih.gov/pubmed/29441496 http://dx.doi.org/10.1007/s41669-017-0022-7 |
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author | Jayasundara, Kavisha Krahn, Murray Mamdani, Muhammad Hoch, Jeffrey S. Grootendorst, Paul |
author_facet | Jayasundara, Kavisha Krahn, Murray Mamdani, Muhammad Hoch, Jeffrey S. Grootendorst, Paul |
author_sort | Jayasundara, Kavisha |
collection | PubMed |
description | BACKGROUND: Incremental cost-effectiveness ratios (ICERs) are used to assess the value for money of new drugs. Many believe that ICERs for drugs that treat rare diseases are much higher than those of common drugs. Our objective was to compare the proportion of ICERs that are cost effective for rare and common cancers. METHODS: We used the Tufts Medical Center Cost-Effectiveness Analysis (CEA) Registry to identify cost-effectiveness studies of pharmaceutical interventions for cancers. Studies that assessed FDA-approved ‘orphan drugs’ were categorized as assessing rare cancers. The proportion of common and rare cancer drugs that were cost effective at various ICER thresholds were compared along with study characteristics. Logistic regressions were conducted to assess important predictors of cost effectiveness. RESULTS: We identified 303 studies that reported 701 ICERs. Seventy nine percent (n = 240) of studies evaluated drugs for common cancers. At a threshold of US$50,000/QALY, 58% (n = 321) of ICERs for drugs treating common cancers and 64% (n = 94) of ICERs for drugs treating rare cancers were cost effective (p = 0.23). At US$100,000/QALY, 74% (n = 409) of ICERs for common cancers and 78% (n = 115) of ICERs for rare cancers were cost effective (p = 0.35). Results from the logistic regressions demonstrated that rarity was not a statistically significant predictor of cost effectiveness at both thresholds with publication year, study sponsorship, and cancer type as covariates. CONCLUSIONS: The proportion of ICERs that were cost effective at both thresholds does not appear to be significantly different between the two groups. Rarity is not statistically significantly associated with cost effectiveness, even when adjusted for important covariates. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s41669-017-0022-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5691840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-56918402017-12-18 Differences in Incremental Cost-Effectiveness Ratios for Common Versus Rare Conditions: A Case from Oncology Jayasundara, Kavisha Krahn, Murray Mamdani, Muhammad Hoch, Jeffrey S. Grootendorst, Paul Pharmacoecon Open Original Research Article BACKGROUND: Incremental cost-effectiveness ratios (ICERs) are used to assess the value for money of new drugs. Many believe that ICERs for drugs that treat rare diseases are much higher than those of common drugs. Our objective was to compare the proportion of ICERs that are cost effective for rare and common cancers. METHODS: We used the Tufts Medical Center Cost-Effectiveness Analysis (CEA) Registry to identify cost-effectiveness studies of pharmaceutical interventions for cancers. Studies that assessed FDA-approved ‘orphan drugs’ were categorized as assessing rare cancers. The proportion of common and rare cancer drugs that were cost effective at various ICER thresholds were compared along with study characteristics. Logistic regressions were conducted to assess important predictors of cost effectiveness. RESULTS: We identified 303 studies that reported 701 ICERs. Seventy nine percent (n = 240) of studies evaluated drugs for common cancers. At a threshold of US$50,000/QALY, 58% (n = 321) of ICERs for drugs treating common cancers and 64% (n = 94) of ICERs for drugs treating rare cancers were cost effective (p = 0.23). At US$100,000/QALY, 74% (n = 409) of ICERs for common cancers and 78% (n = 115) of ICERs for rare cancers were cost effective (p = 0.35). Results from the logistic regressions demonstrated that rarity was not a statistically significant predictor of cost effectiveness at both thresholds with publication year, study sponsorship, and cancer type as covariates. CONCLUSIONS: The proportion of ICERs that were cost effective at both thresholds does not appear to be significantly different between the two groups. Rarity is not statistically significantly associated with cost effectiveness, even when adjusted for important covariates. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s41669-017-0022-7) contains supplementary material, which is available to authorized users. Springer International Publishing 2017-04-25 /pmc/articles/PMC5691840/ /pubmed/29441496 http://dx.doi.org/10.1007/s41669-017-0022-7 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Article Jayasundara, Kavisha Krahn, Murray Mamdani, Muhammad Hoch, Jeffrey S. Grootendorst, Paul Differences in Incremental Cost-Effectiveness Ratios for Common Versus Rare Conditions: A Case from Oncology |
title | Differences in Incremental Cost-Effectiveness Ratios for Common Versus Rare Conditions: A Case from Oncology |
title_full | Differences in Incremental Cost-Effectiveness Ratios for Common Versus Rare Conditions: A Case from Oncology |
title_fullStr | Differences in Incremental Cost-Effectiveness Ratios for Common Versus Rare Conditions: A Case from Oncology |
title_full_unstemmed | Differences in Incremental Cost-Effectiveness Ratios for Common Versus Rare Conditions: A Case from Oncology |
title_short | Differences in Incremental Cost-Effectiveness Ratios for Common Versus Rare Conditions: A Case from Oncology |
title_sort | differences in incremental cost-effectiveness ratios for common versus rare conditions: a case from oncology |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691840/ https://www.ncbi.nlm.nih.gov/pubmed/29441496 http://dx.doi.org/10.1007/s41669-017-0022-7 |
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