PCOR-NSW is a Clinical Quality Registry that collects information about treatments and outcomes for men diagnosed with prostate cancer in NSW since 2015. It captures data about diagnosis, treatment and long term quality outcomes to help identify whether there are trends or gaps that exist in service provision across NSW, Australia and Internationally. 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-NSW is the New South Wales arm of the Prostate Cancer Outcomes Registry Australia and New Zealand (PCOR-ANZ). The Cancer Institute NSW has established PCOR-NSW in partnership with the NSW Agency for Clinical Innovation. Patients are recruited from across NSW 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 nor will it likely ever have. The Quality statement published on our website provides more information on limitations.

To provide data regarding diagnosis, treatment and long term quality outcomes to help identify whether there are trends or gaps that exist in service provision across Australia and New Zealand.

NSW data

Opt-out registry

Privacy Act (1988)

Health Records Act (2001)