Asian American Breast Cancer: Rising Rates and Disparities Across Asian American and Pacific Islander Communities
Breast cancer affects people in every community, but risk and outcomes are not the same for everyone. Breast cancer rates are rising faster in Asian American and Pacific Islander (AAPI) women than in any other racial or ethnic group in the United States.
AAPI communities are incredibly diverse and include people with roots in East Asia, Southeast Asia, South Asia, and the Pacific Islands. Each group has different genetic backgrounds, cultures, and access to care. As a result, breast cancer risk, age at diagnosis, cancer subtype, and survival outcomes can vary widely within the AAPI community.
Understanding these differences is essential to improving outcomes. In recent years, researchers have begun to uncover how factors such as screening, language barriers, cultural stigma, breast density, and tumor biology contribute to breast cancer disparities among AAPI women.
Research in this area seeks to clarify why breast cancer rates are rising in AAPI communities and why outcomes differ across groups. BCRF-funded research is working to close these gaps—so that progress in breast cancer care reaches everyone, not just a few.
Key Takeaways
- In recent years, breast cancer incidence rates rose more quickly for Asian American and Pacific Islander (AAPI) women in the U.S. than for other groups.
- AAPI women are not one single group. Breast cancer risk, stage at diagnosis, and outcomes can vary widely across different AAPI communities, so care and screening recommendations may also vary.
- Barriers such as limited access to screening, language differences, and cultural stigma about having breast cancer can delay diagnosis and worsen outcomes for some AAPI women.
- BCRF funds research to improve prevention, early detection, and treatment— progress in breast cancer care that can also benefit AAPI women.
Breast cancer is rising among AAPI women, but outcomes vary significantly among subgroups. Here’s what’s driving the disparities
Advances in early detection and treatment have helped breast cancer mortality rates drop significantly over the last 30 years. But for Asian American and Pacific Islander (AAPI) women, the picture is more complicated. While their survival outcomes tend to be better overall, recent data show that breast cancer cases are rising faster in this community than in any other racial or ethnic group.
Yet, AAPI women are not a monolithic group, and examining data across different subpopulations reveals significant disparities in risk, diagnosis, and outcomes. Some groups experience disproportionately higher rates of late-stage diagnosis, while others face lower survival rates despite medical advancements. It’s a complex reality that’s impacted by genetics, access to care, differences in breast cancer subtypes, and cultural norms around screening.
Here, we look at both the progress and the ongoing challenges in breast cancer outcomes for AAPI women, as well as the factors driving these disparities.
How does breast cancer impact AAPI women?
Breast cancer is the most common cancer in AAPI women. While historically considered a lower-risk group, AAPI women are now experiencing the fastest-rising incidence rates of the disease.
Data compiled by the American Cancer Society (ACS) show that while the overall breast cancer incidence rate rose one percent annually from 2012 to 2021, it increased 2.5 to 2.7 percent for AAPI women every year during the same period. Among AAPI women under 50, cases have surged by 50 percent since 2000, placing their incidence rate on par with white women for the highest rate of any racial or ethnic group. According to the CDC, breast cancer makes up the highest proportion of new cancer diagnoses among Asian Americans, Native Hawaiians, and Pacific Islanders.
AAPI women experience a few key differences in screening, age at diagnosis, and subtype of breast cancer. AAPI women:
- Are less likely to be up to date on their annual breast screening, compared to other racial groups
- Are more likely to be diagnosed at a younger age: The median age at the time of diagnosis is 58 for AAPI women, which is younger than that of Black, American Indian/Alaska Native, and white women, but a year older than Hispanic women.
- Experience higher rates of HER2-positive breast cancer, which can be more aggressive, than all racial and ethnic groups
- Are more likely to be diagnosed with breast cancer at a later stage, compared to their white counterparts
However, overall breast cancer outcomes tend to be better among AAPI women than those of most other ethnic groups. According to the CDC, breast cancer death rates among AAPI women dropped from 12.7 percent in 1999 to 11.4 percent in 2020. As of 2024, AAPI women had the lowest breast cancer mortality rate of all racial and ethnic groups studied, ranging from 12 to 14 per 100,000 women, according to the ACS.
Differences among AAPI ethnic groups
While AAPI women as a whole tend to have better breast cancer outcomes than some other racial and ethnic groups, it’s important to remember that the term AAPI doesn’t refer to a single, uniform community. It’s an umbrella term that includes people from dozens of ethnic backgrounds, each with their own genetic risks, cultural beliefs, and access to healthcare.
These differences can play a big role in the overall risk of breast cancer and certain subtypes, diagnosis, and outcomes. What holds true for women of one ethnic background may not apply to another, even if they’re both characterized as members of the AAPI community. Looking at AAPI women as a single group can conceal important disparities in breast cancer risk and care.
The prevalence of breast cancer among AAPI women varies significantly by subgroup. According to ACS data, it accounts for 17 percent of all cancer cases in Hmong women, while in Fijian women, it makes up 44 percent of all cancer diagnoses—more than twice as much.
What’s more, certain breast cancer subtypes affect some AAPI women at higher rates than those of other racial and ethnic groups. A 2015 analysis of the California Cancer Registry found that Korean, Filipina, Vietnamese, and Chinese women had a significantly higher risk of a HER2-positive breast cancer diagnosis than non-Hispanic white women.
A previous study evaluated data on 346 Asian breast cancer patients at two New York City institutions. It reported that Chinese and Japanese women had a higher proportion of hormone receptor–positive breast cancers (66.7 percent and 80 percent, respectively), which have the best prognosis, than Filipinos and Koreans. It also found that the more-difficult-to-treat triple-negative breast cancer (TNBC) affected Koreans at a higher rate than other ethnic groups.
Differences in when breast cancer is diagnosed also vary among AAPI subpopulations, with some groups more likely to receive an earlier-stage diagnosis than others. Localized-stage breast cancer accounts for 73 percent of breast cancer cases in Japanese women, compared to just 47 percent in Samoan women.
This could play a role in survival rates among different AAPI subpopulations. A 2022 study published in JCO Oncology Practice found that while the 10-year survival rate of AAPI women with stage 0 through 2 breast cancer was 91 percent overall, it was just 83 percent for Native Hawaiian and other Pacific Islanders. According to ACS data, the five-year relative survival rate for breast cancer varies significantly among AAPI subpopulations, ranging from 94 percent in Japanese women to between 72 percent and 74 percent in Tongan, Chamorro/Guamanian, and Samoan women.
More nuanced research on each of the subpopulations within the AAPI community could help identify specific risk factors, improve screening rates, and promote better outcomes.
What drives breast cancer disparities among AAPI women?
No single factor is responsible for the disparate impact of breast cancer among AAPI women. Instead, these differences may be shaped by a combination of systemic challenges, along with genetic and cultural issues that vary widely across ethnic subgroups.
The stigma surrounding breast cancer in AAPI communities may also contribute to delayed diagnoses and poorer outcomes, says Dr. Scarlett Gomez, a BCRF investigator. Cultural beliefs and fear of social repercussions may discourage some women from getting regular screenings or following up on symptoms, potentially increasing the chances of a late-stage diagnosis in certain AAPI populations. Socio-economic challenges, such as finances, language barriers, and access to healthcare, further complicate this issue.
Dense breast tissue, which is prevalent among Asian women, presents another challenge in detecting early-stage breast cancer. Women with dense breasts have a higher risk of developing breast cancer because dense breast tissue can make interpreting mammograms more difficult and detecting suspicious areas and tumors more challenging. This means that some AAPI women may require additional imaging, such as breast ultrasounds or breast magnetic resonance imaging (MRI), for more accurate breast cancer detection. But some patients may not be aware of having dense breasts or may have limited access to these screening services, both potentially contributing to higher rates of later-stage diagnosis in some subpopulations.
Certain genetic predispositions may contribute to disparities in breast cancer subtypes and outcomes among AAPI women. This may explain the higher rates of TNBC among Koreans and HER2-positive breast cancer among Korean, Filipina, Vietnamese, and Chinese women.
The lack of research focused on AAPI women and breast cancer has significant consequences for prevention, diagnosis, and treatment. While Asian Americans comprise about seven percent of the U.S. population, a 2019 study reported that less than one percent of funding from the National Institutes of Health was directed to research regarding this community between 1992 and 2018. In fact, overall very little research has been dedicated to investigating the causes of cancer in this group. This lack of attention can lead to missed opportunities for early detection, less effective screening guidelines, and a failure to develop targeted interventions that address the unique risks faced by AAPI women. It also perpetuates the misconception that breast cancer isn’t a burden among AAPI women.
How BCRF is advancing research on AAPI breast cancer risk and outcomes
Because risk factors, tumor biology, and access to care can differ widely across AAPI subgroups, closing the gap in outcomes depends on research that reflects this diversity.
Today, important challenges remain. Many AAPI women are still underrepresented in clinical trials. Health data are often grouped into a single “Asian” category, which can hide meaningful differences between ethnic communities. Long-term outcomes are also less likely to be tracked by specific subgroup, limiting what researchers can learn about survival, recurrence, and quality of life over time.
BCRF-funded research is working to change this.
Through support for leading scientists around the world, BCRF funding has the potential to help advance studies that:
- Disaggregate AAPI data to better understand subgroup-specific risk factors
- Explore genetic factors and tumor biology that contribute to aggressive breast cancers across different populations
- Examine how screening access, language barriers, and timing of diagnosis affect survival and long-term health
- Expand the inclusion of AAPI women in clinical trials to ensure new treatments are tested across diverse populations
This work has direct, real-world impact. It helps clinicians assess risk more accurately, supports strategies for earlier detection, guides the development of treatments tailored to specific cancer subtypes, and improves the overall quality of care for patients and families.
Research progress depends on sustained support from individuals and communities. Those who want to help advance more inclusive breast cancer research can make a one-time or monthly gift, give in honor or memory of a loved one, or start a community fundraiser to support BCRF’s work. There are also opportunities to find and attend BCRF events or create a personal fundraising page to rally friends, family, or colleagues around the cause.
Continued investment in this research is essential to ensuring better outcomes, longer lives, and more equitable care for future generations of AAPI women.
Research on AAPI women and breast cancer
We need more research to understand the driving factors behind the rising incidence rate of breast cancer in AAPI women, as well as the gaps in early-stage diagnosis, care, and outcomes in subpopulations.
BCRF makes significant investments in research to reduce breast cancer disparities and improve outcomes for racial groups—like AAPI women—who are disproportionately impacted by the disease in unique ways.
We’re currently supporting Dr. Gomez’s work to understand how structural and social determinants of health impact breast cancer risk among AAPI women specifically. Across a multitude of projects, BCRF investigators are working to better understand and treat HER2-positive and triple-negative breast cancers, improve screening for women with dense breasts, and understand why incidence rates are rising among younger women. Such research stands to benefit AAPI women at this critical juncture—when their incidence rates are on the rise.
Donate to BCRF today to support vital research and breakthroughs for Asian American and Pacific Islander women with breast cancer.
Frequently asked questions about AAPI women and breast cancer
Breast cancer rates are actually rising fastest among AAPI women in the United States. Risk varies widely across AAPI subgroups, which was often hidden in earlier research because they were seen as a single population.
Researchers point to post-immigration lifestyle changes, longer life expectancy, and improved screening as contributing factors. Limited data collection and underfunding of AAPI-specific research have also delayed recognition of these trends.
Some AAPI subgroups are more likely to be diagnosed with aggressive breast cancers such as HER2-positive or triple-negative breast cancer. Ongoing research is seeking to clarify how genetics and tumor biology are involved.
In some communities, yes. Barriers can include limited access to care, language differences, cultural stigma, and lack of targeted health outreach. Historically, public health research and education efforts focused more on Black and white populations, leaving gaps in awareness for many AAPI groups.
BCRF funds research that examines breast cancer risk and outcomes across diverse populations, including AAPI women. BCRF also funds research that seeks a deep understanding of the genetic and tumor factors that play a role in aggressive breast cancers that affect AAPI women. Overall, BCRF-funded research across the continuum of the disease can inform breast cancer care in AAPI subgroups. And BCRF’s efforts to actively expand the inclusion of AAPI women in clinical trials will ensure that clinical findings are relevant to them.
People can support more inclusive breast cancer research by donating, giving in honor or memory of a loved one, starting a fundraiser, or participating in BCRF events. Every contribution helps advance research that improves prevention, detection, and care for all communities.
Selected References
American Cancer Society. (2024a). Breast cancer facts & figures 2024-2025. https://www.cancer.org/content/dam/cancer-org/research/cancer-facts-and-statistics/breast-cancer-facts-and-figures/2024/breast-cancer-facts-and-figures-2024.pdf
American Cancer Society. (2024b). Cancer Facts & Figures for Asian American, Native Hawaiian, & other Pacific Islander People 2024-2026 [Report]. https://www.cancer.org/content/dam/cancer-org/research/cancer-facts-and-statistics/aanhpi-cancer-facts-and-figures/aanhpi-cff.pdf
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Cancer and Asian Americans. (n.d.). Office of Minority Health. https://minorityhealth.hhs.gov/cancer-and-asian-americans
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Ðoàn, L. N., Takata, Y., Sakuma, K. K., & Irvin, V. L. (2019). Trends in clinical research including Asian American, Native Hawaiian, and Pacific Islander participants funded by the US National Institutes of Health, 1992 to 2018. JAMA Network Open, 2(7), e197432. https://doi.org/10.1001/jamanetworkopen.2019.7432
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