<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang SC</submitter><funding>Ministry of Science and Technology, Taiwan</funding><funding>National Cheng Kung University Hospital</funding><pagination>e0231413</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7141611</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(4)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Comparison of the effectiveness and cost-effectiveness of three first-line EGFR-tyrosine kinase inhibitors (TKIs) would improve patients' clinical benefits and save costs. Using real-world data, this study attempted to directly compare the effectiveness and cost-effectiveness of first-line afatinib, erlotinib, and gefitinib.&lt;h4>Methods&lt;/h4>During May 2011-December 2017, all patients with non-small cell lung cancer (NSCLC) visiting a tertiary center were invited to fill out the EuroQol five-dimension (EQ-5D) questionnaires and World Health Organization Quality of Life, brief version (WHOQOL-BREF), and received follow-ups for survival and direct medical costs. A total of 379 patients with EGFR mutation-positive advanced NSCLC under first-line TKIs were enrolled for analysis. After propensity score matching for the patients receiving afatinib (n = 48), erlotinib (n = 48), and gefitinib (n = 96), we conducted the study from the payers' perspective with a lifelong time horizon.&lt;h4>Results&lt;/h4>Patients receiving afatinib had the worst lifetime psychometric scores, whereas the differences in quality-adjusted life expectancy (QALE) were modest. Considering 3 treatments together, afatinib was dominated by erlotinib. Erlotinib had an incremental cost-effectiveness of US$17,960/life year and US$12,782/QALY compared with gefitinib. Acceptability curves showed that erlotinib had 58.6% and 78.9% probabilities of being cost-effective given a threshold of 1 Taiwanese per capita GDP per life year and QALY, respectively.&lt;h4>Conclusion&lt;/h4>Erlotinib appeared to be cost-effective. Lifetime psychometric scores may provide additional information for effectiveness evaluation.</pubmed_abstract><journal>PloS one</journal><pubmed_title>Comparative effectiveness and cost-effectiveness of three first-line EGFR-tyrosine kinase inhibitors: Analysis of real-world data in a tertiary hospital in Taiwan.</pubmed_title><pmcid>PMC7141611</pmcid><funding_grant_id>NCKUH-10902047</funding_grant_id><funding_grant_id>MOST107-2320-B-006-069 and MOST108-2918-I-006-006</funding_grant_id><pubmed_authors>Yang SC</pubmed_authors><pubmed_authors>Wang JD</pubmed_authors><pubmed_authors>Hsu JC</pubmed_authors><pubmed_authors>Lai WW</pubmed_authors><pubmed_authors>Su WC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparative effectiveness and cost-effectiveness of three first-line EGFR-tyrosine kinase inhibitors: Analysis of real-world data in a tertiary hospital in Taiwan.</name><description>&lt;h4>Introduction&lt;/h4>Comparison of the effectiveness and cost-effectiveness of three first-line EGFR-tyrosine kinase inhibitors (TKIs) would improve patients' clinical benefits and save costs. Using real-world data, this study attempted to directly compare the effectiveness and cost-effectiveness of first-line afatinib, erlotinib, and gefitinib.&lt;h4>Methods&lt;/h4>During May 2011-December 2017, all patients with non-small cell lung cancer (NSCLC) visiting a tertiary center were invited to fill out the EuroQol five-dimension (EQ-5D) questionnaires and World Health Organization Quality of Life, brief version (WHOQOL-BREF), and received follow-ups for survival and direct medical costs. A total of 379 patients with EGFR mutation-positive advanced NSCLC under first-line TKIs were enrolled for analysis. After propensity score matching for the patients receiving afatinib (n = 48), erlotinib (n = 48), and gefitinib (n = 96), we conducted the study from the payers' perspective with a lifelong time horizon.&lt;h4>Results&lt;/h4>Patients receiving afatinib had the worst lifetime psychometric scores, whereas the differences in quality-adjusted life expectancy (QALE) were modest. Considering 3 treatments together, afatinib was dominated by erlotinib. Erlotinib had an incremental cost-effectiveness of US$17,960/life year and US$12,782/QALY compared with gefitinib. Acceptability curves showed that erlotinib had 58.6% and 78.9% probabilities of being cost-effective given a threshold of 1 Taiwanese per capita GDP per life year and QALY, respectively.&lt;h4>Conclusion&lt;/h4>Erlotinib appeared to be cost-effective. Lifetime psychometric scores may provide additional information for effectiveness evaluation.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2024-11-20T23:38:49.96Z</modification><creation>2020-05-22T16:46:44Z</creation></dates><accession>S-EPMC7141611</accession><cross_references><pubmed>32267879</pubmed><doi>10.1371/journal.pone.0231413</doi></cross_references></HashMap>