Treatment Outcomes From Erlotinib and Gefitinib in Advanced Epidermal Growth Factor Receptor–Mutated Nonsquamous Non–Small Cell Lung Cancer in Aotearoa New Zealand From 2010 to 2020: Nationwide Whole-of-Patient-Population Retrospective Cohort Study

Abstract BackgroundHealth care system–wide outcomes from routine treatment with erlotinib and gefitinib are incompletely understood. ObjectiveThe aim of the study is to describe the effectiveness of erlotinib and gefitinib during the first decade of their routine u...

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Main Authors: Phyu Sin Aye, Joanne Barnes, George Laking, Laird Cameron, Malcolm Anderson, Brendan Luey, Stephen Delany, Dean Harris, Blair McLaren, Elliott Brenman, Jayden Wong, Ross Lawrenson, Michael Arendse, Sandar Tin Tin, Mark Elwood, Philip Hope, Mark James McKeage
Format: Article
Language:English
Published: JMIR Publications 2025-03-01
Series:JMIR Cancer
Online Access:https://cancer.jmir.org/2025/1/e65118
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Summary:Abstract BackgroundHealth care system–wide outcomes from routine treatment with erlotinib and gefitinib are incompletely understood. ObjectiveThe aim of the study is to describe the effectiveness of erlotinib and gefitinib during the first decade of their routine use for treating advanced epidermal growth factor receptor (EGFR MethodsPatients were identified, and data collated from national pharmaceutical dispensing, cancer registration, and mortality registration electronic databases by deterministic data linkage using National Health Index numbers. Time-to-treatment discontinuation and overall survival were measured from the date of first dispensing of erlotinib or gefitinib and analyzed by Kaplan-Meier curves. Associations of treatment outcomes with baseline factors were evaluated using univariable and multivariable Cox regressions. ResultsOverall, 752 patients were included who started treatment with erlotinib (n=418) or gefitinib (n=334) before October 2020. Median time-to-treatment discontinuation was 11.6 (95% CI 10.8‐12.4) months, and median overall survival was 20.1 (95% CI 18.1‐21.6) months. Shorter time-to-treatment discontinuation was independently associated with high socioeconomic deprivation (hazard ratio [HR] 1.3, 95% CI 1.1‐1.5 compared to the New Zealand Index of Deprivation 1‐4 group), EGFR ConclusionsOutcomes from routine treatment with erlotinib and gefitinib in New Zealand patients with advanced EGFREGFR
ISSN:2369-1999