Background
LGBTQIA+ people affected by cancer represent a growing, medically underserved population, experiencing greater dissatisfaction with cancer care, lower quality of life, and heightened levels of psychologic distress compared to their non-LGBTIQA+ individuals. Although 5.7% of Victorian adults identify as LGBTIQA+, comprehensive data on cancer prevalence, risk and outcomes of the population is lacking due to insufficient sexual orientation and gender identity (SOGI) data collection.
Objectives
To understand the demographic characteristics and estimated cancer prevalence among LGBTIQA+ populations in Western and Central Melbourne, explore challenges faced by CALD individuals affected by cancer, identify service gaps and propose actionable recommendations for improving outcomes.
Methodology
This review utilised a mixed-methods approach, analysing data from the Australian Bureau of Statistics, the Victorian Population Health Survey 2017, the Victorian Admitted Episode Data and semi-structured interviews with patients and service providers. Participants were recruited via convenience sampling, and interviews were transcribed, coded and thematically analysed.
Key Findings
Recommendations
Conclusion
Addressing the unique challenges faced by LGBTIQA+ cancer patients require the implementation of appropriate recommendations to effectively serve the diverse patient population.