Do Australian adolescents' and young adults' experiences of cancer care influence their quality of life?

Abstract

Objective: To examine the relationship between the cancer care experiences of adolescents and young adults (AYAs) and their quality of life. Methods: Two hundred and nine AYAs completed a cross-sectional, self-report survey distributed through the population-based cancer registries in 2 Australian states (New South Wales and Victoria). Eligible AYAs were 15 to 24 years old when diagnosed with any cancer (excluding early-stage melanoma) and were 3 to 24 months post-diagnosis. Questions examined whether particular care experiences occurred for the patient at different points in the cancer care pathway, including diagnosis, treatment, inpatient care, and at the end of treatment. Quality of life..