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New Zealand Cancer Registry (NZCR)
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Sample details

The NZCR is a national, population-based registry that has recorded all primary malignant cancer diagnoses in New Zealand since 1948, with over 27,000 new cases registered annually from across the country. Participant data is passively collected through mandatory reporting from pathology laboratories, hospital discharge summaries, death certificates, and autopsy reports. Follow-up is conducted passively and continuously through linkage with national mortality and hospital datasets, with no fixed follow-up intervals.

Study design
Registry

Number of participants at first data collection

28,275 (new cancer registrations as of 2022)

Recruitment is ongoing

Age at first data collection

Varied (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Cancer patients
Ethnically diverse populations
Patients and clinical populations
Population-based sample
Dataset details

Country

New Zealand

Year of first data collection

1948

Primary Institutions

Health New Zealand - Te Whatu Ora

Links

tewhatuora.govt.nz/for-health-professionals/clinical-guidance/diseases-and-conditions/cancer/new-zealand-cancer-registry-nzcr

doi.org/10.1016/j.canep.2014.06.008

Profile paper DOI
Not available

Funders

Health New Zealand - Te Whatu Ora

Ongoing?
Yes

Data types collected

dataLinkage
Quantitative data collection
  • Secondary data
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
  • Mortality data
Features

Engagement

  • None
  • Keywords

    Administrative data
    Breast cancer
    Cancer
    Diagnostic information
    Epidemiology
    Ethnic disparity
    Hospital discharges
    Morbidity and mortality
    Pathology
    Population health
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