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Native Hawaiian and Pacific Islander People and Cancer

Why disaggregated cancer data, culturally grounded care, and local navigation matter for Native Hawaiian and Pacific Islander communities.

NCI source

National Cancer Institute - AANHPI Cancer Mortality Data

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An older woman stands by a window in a cozy room holding a coat

Key fact

Aggregated data can hide disparities.

The short answer

Native Hawaiian and Pacific Islander communities are distinct populations with different cancer patterns. Grouping them together with Asian American populations can hide important disparities and local needs.

  • Aggregated data can hide disparities.

  • Native Hawaiian and Pacific Islander communities are not one uniform group.

  • Local culture, geography, and access shape care.

  • Community-based navigation can help connect services.

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The full explanation.

The simple version

Native Hawaiian and Pacific Islander people die from cancer at much higher rates than old data showed. For years, health data mixed this group in with the much larger Asian American group. That mix hid a real gap. New research looked at the two groups on their own. It found the truth underneath.

What the new data shows

In 2018, a federal health agency started counting Native Hawaiian and Pacific Islander people on their own. Before, they were counted together with Asian Americans. This change let researchers compare the two groups side by side, for the first time. They used death records from 2018 to 2020. The gap was large. Native Hawaiian and Pacific Islander men died of cancer at a rate 39% higher than Asian American men. Native Hawaiian and Pacific Islander women died of cancer at a rate 73% higher than Asian American women.

Why this stayed hidden so long

The Asian American group in the United States is much bigger. When two groups get mixed into one number, the bigger group's numbers take over. This hid a real, serious gap for years. Experts now say broad race labels can hide real gaps inside them. They want more detailed counts, so gaps like this get found sooner.

What this means for you

This gap is a strong reason to take your own cancer screening seriously. Do not assume broad national numbers match your own risk. Ask your doctor which cancer checks you are due for. Base this on your age, and on your family's health history. Do not rely on averages that may not fit your community.

Things that can get in the way of care

A few things can delay a cancer diagnosis in Pacific Islander communities. One is distance to a cancer center. Another is cost. A third is not knowing which checks to ask for. Some communities live far from a major cancer center, which adds one more hurdle. If a visit or test feels hard to set up, ask for help. Your doctor, or a patient guide at your clinic if one exists, can point you toward support. Many cancer centers offer help with cost and travel, built just for this problem.

Why better data matters going forward

Researchers now want cancer data broken into smaller groups, not lumped together as one broad label. Smaller, clearer groups can show which specific communities need more outreach, more access to screening, or more culturally aware care. One big number, averaged across many different groups, does not serve any single group well.

This pattern shows up in other groups too

Native Hawaiian and Pacific Islander people are not the only group where broad labels have hidden real gaps. Grouping many different communities under one wide category, like "Asian American," can average away real differences in risk, screening rates, and outcomes between the smaller groups inside it. This is part of why more and more health researchers now push for finer detail in how race and ethnicity get reported.

You are not just a statistic

Numbers like these describe a group, not you as a person. Your own risk depends on your family history, your habits, and your access to care, not just which broad category you fall into on a form. Use this data as a reason to ask more questions at your own appointments, not as a fixed prediction about your own health.

What to ask your doctor

Ask what cancer checks fit your age and history. Ask if cost or travel stands between you and a needed test. Ask what help exists if it does. Ask if your clinic tracks detailed race data, since that is part of how future gaps get found and fixed.

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Common questions

Why separate the data?

NCI research shows that combining Asian American and Native Hawaiian and Pacific Islander data can mask substantial differences in cancer mortality.

Are all Pacific Islander communities the same?

No. Communities differ in history, culture, geography, exposures, access, and cancer patterns.

What can help during care?

Local navigators, community health programs, culturally relevant education, and clear travel and referral plans can help make care more accessible.

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Sources last checked: 2026-07-22 what this meansLast updated: 2026-08-05Next planned review: 2027-07-22

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Cancer Explained does not originate medical claims. Every page restates guidance already published by the National Cancer Institute, the CDC, the USPSTF and the FDA, in plain language, with the source cited so you can check the original yourself. AI does the translating and organizing; automated checks test claims, citations, clarity and safety before anything publishes. We do not employ clinicians and do not intend to — our work is translation and navigation, not clinical judgment. Nothing here is personal medical advice, and no page can account for your particular situation.

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Human medical review: not completed. Pages here are not signed off by a clinician before they publish. That is not an oversight we are quietly working around: we restate published guidance and cite it, so the authority belongs to the source rather than to us, and every page names where its claims come from — you can verify us instead of trusting us. Where a volunteer clinician has reviewed a page, their name and credentials appear on it; where no name appears, no clinician has checked it. We are glad to have reviewers and are recruiting them, and we do not hold pages back waiting for one. Use this site to understand your situation and to ask better questions of the people treating you.

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How this page was created

Cancer Explained does not originate medical claims. Every page restates guidance already published by the National Cancer Institute, the CDC, the USPSTF and the FDA, in plain language, with the source cited so you can check the original yourself. AI does the translating and organizing; automated checks test claims, citations, clarity and safety before anything publishes. We do not employ clinicians and do not intend to — our work is translation and navigation, not clinical judgment. Nothing here is personal medical advice, and no page can account for your particular situation.

Editorial status: Source checked This page was written with AI assistance and checked line by line against the sources listed on it. That confirms the sources support what the page says. It is not a medical review, and it does not confirm the page is complete or right for your situation.

Human medical review: not completed. Pages here are not signed off by a clinician before they publish. That is not an oversight we are quietly working around: we restate published guidance and cite it, so the authority belongs to the source rather than to us, and every page names where its claims come from — you can verify us instead of trusting us. Where a volunteer clinician has reviewed a page, their name and credentials appear on it; where no name appears, no clinician has checked it. We are glad to have reviewers and are recruiting them, and we do not hold pages back waiting for one. Use this site to understand your situation and to ask better questions of the people treating you.

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Native Hawaiian and Pacific Islander People and Cancer