Treatment and Survival Outcomes for Indigenous and Non-Indigenous Australians Within the Victorian Lung Cancer Registry: A Retrospective Cross-Sectional Cohort Study
Details
Publication Year 2026-07,Volume 224,Issue #7,Page e70232
Journal Title
Medical Journal of Australia
Publication Type
Research article
Abstract
OBJECTIVES: Our goal was to explore and compare risk factors, patterns of management and survival outcomes in Indigenous compared with non-Indigenous Australian patients using the Victorian Lung Cancer Registry (VLCR). STUDY TYPE: A retrospective observational cohort study of the VLCR. SETTING: Data collected from the VLCR between 18 January 2011 and 24 January 2024. PARTICIPANTS: Primary lung cancer patients in the VLCR. MAIN OUTCOME MEASURES: Patient, disease and management characteristics of Indigenous and non-Indigenous Australian patients. Impacts of patient and clinical variables on treatment and survival, measured by multivariable Cox regression and propensity-matched survival analysis. RESULTS: We included 186 Indigenous and 17,439 non-Indigenous Australian patients. Indigenous Australian lung cancer patients were younger in age {median, 62 years (interquartile range [IQR], 55-69 years) vs. median, 71 years (IQR, 63-77 years); p < 0.001}, had lower socio-economic status (lowest quintile, 57 patients [31%] vs. 3274 patients [19%]; p < 0.001), were more likely to be current smokers (118 patients [65%] vs. 5963 patients [35%]; p < 0.001) and had higher levels of respiratory comorbidity (64 patients [34%] vs. 4088 patients [23%]; p < 0.001). There were no statistically significant differences in receipt of guideline-concordant treatment (82 patients [51%] vs. 8036 patients [56%]; p = 0.12) and survival outcomes (median survival, 1.4 vs. 1.5 years; hazard ratio, 1.06 [95% confidence interval, 0.88-1.27]). CONCLUSION: We found lung cancer patients of Indigenous status were more likely to have demographic disadvantage and clinical risk factors that may contribute to discrepancies in management compared with patients of non-Indigenous status. Identifying barriers to healthcare and treatment in the Indigenous Australian population is an important research priority to improve disparities between the two populations.; The Known: The confirmation of equity for Indigenous Australians is a critical objective of Australian cancer registries targeting healthcare improvement. The New: Indigenous Australian patients with lung cancer had increased radiotherapy and a non‐significant decrease in surgery and guideline‐concordant treatment in comparison to non‐Indigenous Australian patients. Indigenous Australian NSCLC patients had similar median survival to non‐Indigenous Australian NSCLC patients (1.4 vs. 1.5 years). The Implications: Clinical quality registries have strong capability in describing disparity for vulnerable populations. The earlier age of lung cancer diagnosis raises concerns regarding screening eligibility for Indigenous Australians in the Lung Cancer Screening Program.; eng
Publisher
Wiley
Keywords
Humans; Middle Aged; Female; *Lung Neoplasms/mortality/therapy/ethnology; Retrospective Studies; Male; Registries; Aged; Victoria/epidemiology; Cross-Sectional Studies; Risk Factors; Survival Analysis; Australia/epidemiology; cancer; lung diseases
Department(s)
Medical Oncology; Radiation Oncology
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Creation Date: 2026-07-14 12:09:29
Last Modified: 2026-07-14 12:09:34
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