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Ethnic disparities for survival and mortality in New Zealand patients with head and neck cancer

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Summary:

A retrospective cohort study has found that Māori individuals experienced worse survival outcomes and greater mortality rates from head and neck cancer (HNC) in New Zealand, and present with more advanced disease at a younger age. Anonymised data were obtained from the New Zealand Cancer Registry for 6593 patients diagnosed with HNC between 2010 and 2020. The study population was comprised of 10.7% Māori and 89.3% other ethnicities, predominantly New Zealand European (65.6%). At 5 years after diagnosis, the mortality rate was 39.3% for Māori compared with 35.1% for individuals of other ethnicity (p = 0.03) and 33.3% for New Zealand European individuals (p = 0.002). Mean age of HNC diagnosis was 58.0 years for Māori individuals compared with 64.3 years for individuals of other ethnicity, and mean ages of death were 63.5 vs 72.3 years, respectively. Māori individuals were less likely to have only localised disease at presentation compared with individuals of other ethnicity (14.5% vs 24.0%; p < 0.001), and were more likely to have regional lymph node involvement at diagnosis (39.1% vs 30.5% of patients; p < 0.001).

Comment:
Important that researchers continue to monitor for and report on ethnic inequities along health and healthcare pathways, as we have here for head and neck cancers.
Reference: JAMA Netw Open. 2024;7(6):e2413004.
Independent commentary by Dr. Matire Hardwood

Dr Matire Harwood (Ngapuhi) has worked in Hauora Māori, primary health and rehabilitation settings as clinician and researcher since graduating from Auckland Medical School in 1994. She also holds positions on a number of boards, committees and advisory groups including the Health Research Council. Matire lives in Auckland with her whānau including partner Haunui and two young children Te Rangiura and Waimarie.

Research Review publications are intended for New Zealand health professionals.

Disclaimer: This publication is not intended as a replacement for regular medical education but to assist in the process. The reviews are a summarised interpretation of the published study and reflect the opinion of the writer rather than those of the research group or scientific journal. It is suggested readers review the full trial data before forming a final conclusion on its merits.

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