โœ‰ย  info@nzbtr.org.nz

๐Ÿ“ย  Centre for Brain Research, University of Auckland

New Zealand Brain Tumour Registry emblem
Registry data ๐Ÿ—“ Expected 2027

National Data Overview

Our first national summary of brain tumour epidemiology: case numbers, demographics, and outcomes across Aotearoa.

Prepared by NZ Brain Tumour Registry
National Data Overview cover: one of the first registry reports, on brain tumour epidemiology across Aotearoa

About this report

The National Data Overview will be the Registry’s first national summary of brain tumour epidemiology in Aotearoa. It will describe how many people are diagnosed each year, the types and grades of tumour recorded, and how diagnosis and treatment vary by age, ethnicity and region.

What it will cover

  • Incidence and trends over time
  • Tumour types, grades and molecular subtypes
  • Treatment pathways and time to treatment
  • Outcomes, including survival and recurrence
  • Equity of access across regions and population groups

Timing

Publication is expected in 2027, once the first full period of national data has been collected, checked and reviewed by the governance group. Subscribe on the homepage to be notified when it is released.


More reports

Other publications

National Data Overview cover: one of the first registry reports, on brain tumour epidemiology across Aotearoa
Registry data

National Data Overview

Our first national summary of brain tumour epidemiology: case numbers, demographics, and outcomes across Aotearoa.

๐Ÿ—“ Expected 2027

Research Collaboration Guide cover: partnering on research, trials and quality improvement
Research

Research Collaboration Guide

How to partner with the registry for research, clinical trials, and quality improvement projects.

๐Ÿ—“ Expected 2027

Service Planning Brief cover: brain tumour burden and service distribution
Planning

Service Planning Brief

Evidence for the health sector: brain tumour burden, geographic distribution, and service recommendations.

๐Ÿ—“ Expected 2027