Population-based prostate cancer outcomes registries – what have we learned and where are we heading?

Wee Loon Ong, Krupa Krishnaprasad, Jonathan Bensley, Michelle Steeper, Kerri Beckmann, Sibilah Breen, Michelle King, Stephen Mark, Michael O'Callaghan, Manish Patel, Emma Tod, Jeremy Millar, the Prostate Cancer Outcomes Registry Australia and New Zealand (PCOR-ANZ)

Research output: Contribution to journalComment/debate

1 Citation (Scopus)

Abstract

The Australia and New Zealand Prostate Cancer Outcomes Registry (PCOR-ANZ) has now entered its ninth year of operation since establishment in 2015. The PCOR-ANZ represents a unique, huge, and rich dataset which can, and should, be optimally utilised to monitor, benchmark, and improve the quality of prostate cancer care in Australia and New Zealand (ANZ). The PCOR-ANZ 2023 Annual Report was recently published, detailing the activities for the period of 2015–2021. Here, we provide a summary of key findings and plans moving forward.
Original languageEnglish
Pages (from-to)9-11
Number of pages3
JournalBJU International
Volume134
Issue numberS2
Early online date19 Aug 2024
DOIs
Publication statusPublished - Dec 2024

Keywords

  • Prostate cancer
  • Patient outcomes
  • Patient registries

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