PCOR-TAS is a Clinical Quality Registry that collects information about treatments and outcomes for men diagnosed with prostate cancer in Tasmania since 2015. It captures data about diagnosis, relevant treatments, procedures, interventions and quality of life to improve the quality of care provided to men with prostate cancer in Tasmania. Patient Reported Outcome Measures are collected at 12 months after treatment, or diagnosis if the patient receives no active treatment.

PCOR-ANZ (Prostate Cancer Outcomes Registry - Australia and New Zealand) is a large-scale prostate cancer registry that collects information on the care provided and the outcomes for men diagnosed with prostate cancer in Australia and New Zealand. PCOR-TAS is one of the state-based registries that contributes data into the PCOR-ANZ. Patients are recruited from across Tasmania including men diagnosed at both public and private health care providers. Participation is voluntary and participants can opt out at any time.

Participation by clinicians, hospitals and patients is voluntary and as such it does not have population coverage.

To collect population-based clinical data, with the aim of improving the quality of care provided to men with prostate cancer

Tasmania state data

Opt-out registry

Privacy Act (1988)

Health Records Act (2001)