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D. Murray

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Review Open access Sep 2026

Mapping population-based cancer registries in Europe: coverage, data availability, and capacity for real-world data generation

Background Population-based cancer registries (PBCRs) are essential for cancer surveillance and control yet their capacity and coverage vary across Europe. This study presents the first descriptive results of a survey mapping European PBCRs, with a particular focus on registry coverage, data availability, timeliness, a...

V. Zadnik, A. Konjević, M. Jurtela et al. · 1 citation
Open access Sep 2026

Socioeconomic differences in prostate cancer diagnosis and stage following the introduction of Rapid Access Prostate Clinics in Ireland

Background Rapid Access Prostate Clinics (RAPCs) were introduced in Ireland in 2009 to centralise and standardise prostate cancer (PCa) diagnosis within designated cancer centres. While RAPCs aim to improve diagnostic organisation following general practitioner referral, access remains influenced by socioeconomic diffe...

C. Haugh, S. Walter, P. Sweeney et al. · 0 citations
Open access Sep 2026

Data resource profile: National Cancer Registry Ireland

Background National Cancer Registry Ireland (NCRI) is the state agency responsible for collecting and analysing data on all cancer patients to help improve health outcomes in Ireland. Established by the Minister for Health under Statutory Instrument 19/1991, it began collecting data in 1994 from both public and private...

M. T. Redaniel, J. Kelly, J. McDevitt et al. · 0 citations
Open access Sep 2026

Cancer Patients Mortality From Other Causes: A European Population‐Based Study

Analysis of mortality from all causes other than the index cancer among cancer patients compared to the general population finds elevated mortality among cancer patients compared to the general population.

Gemma Gatta, R. Capocaccia, S. Rossi et al. · 0 citations

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