The American Cancer Society (ACS) believes everyone should have a fair and just opportunity to prevent, find, treat, and survive cancer. That belief guides the ACS to conduct and support research to help understand cancer inequalities and create strategies for overcoming them.
Watch this video to witness cancer disparities and cancer care inequities in real life.
To learn more about the American Cancer Society's (ACS) focus on ending health disparities, see:
Cancer is a disease that can affect anyone, but it doesn’t affect everyone equally. Many social structures and practices can limit a person’s access to health care needed to prevent, treat, and survive cancer. These obstacles may include racism, discrimination, poverty, lack of access to healthy and affordable foods, low quality education and housing, and jobs with inadequate pay.
A health disparity is when the quality of health care differs between people because of discrimination based on:
Health care disparities can affect every step of cancer care — from prevention and screening to the quality of life after cancer treatment, which means disparities in care can affect who develops and dies from cancer.
Last summer, Extramural Discovery Science funded the first American Cancer Society DICR Internship program at 8 universities.
This 10-week summer cancer research experience aims to increase diversity and inclusion in the cancer workforce for under-represented minorities who are rising sophomores, juniors, and seniors with an interest in any STEM (science, technology, engineering, and mathematics) discipline.
Learn more about the ACS Diversity in Cancer Research (DICR) Internship program
The American Cancer Society (ACS) employs full-time researchers and funds scientists across the United States who relentlessly search for answers to help us better understand cancer, including cancer health disparities. Here are some highlights of their work.
“Despite some progress in recent decades, cancer disparities are still a major issue in the United States, and they may further widen because of increasing costs of novel treatments and advanced medical technologies.
“Much more work needs to be done to enhance health equity and mitigate cancer disparities.” —Farhad Islami, MD, PhD
See the highlight about Dr. Islami's published study.
“We consistently found a link between lower Medicaid eligibility limits and worse survival after a cancer diagnosis. And that was true whether the cancer was found at an early or late stage.
“This could be explained for multiple reasons. Having health insurance may make receiving guideline-based treatment easier to receive and complete and may improve access to timely care as well as specialized survivorship care, psychosocial care, and end-of-life and hospice care.”
—Jingxuan Zhao, MPH
See the highlight about Jingxuan Zhao's published study.
ACS Grantee from Wayne State University of Medicine/Karmanos Cancer Institute in Detroit
“Research has shown that certain groups of people are more at risk for experiencing financial toxicity: African American/Black populations, people with limited incomes, and those younger than age 65. We developed the DISCO app to help decrease that risk for such patients in Detroit.
“Our goal is to prompt high-quality and timely discussions about costs between oncologists and patients and to improve patient knowledge and self-efficacy surrounding treatment costs. We also want to increase referrals to social workers and financial navigators, who can help cancer patients better predict and manage the costs of their care.”
—Lauren Hamel, PhD
See the highlight about Dr. Hamel's study.
“We’ve found this in some of our participants—the belief that God is punishing the person for past deeds by giving them cancer.
“And this is not only unsettling for the patient; it’s unsettling for providers. So how do you approach this and not offend the person? . . . How do you turn it around from persecution to an opportunity for meaning-making?”
—Mark Lazenby, PhD, APRN, FAAN
Listen to the podcast with Dr. Lazenby and Aasim Padela, MD, also an ACS grantee.
The American Cancer Society funds scientists who conduct research about cancer at medical schools, universities, research institutes, and hospitals throughout the United States. We use a rigorous and independent peer review process to select the most innovative research projects proposals to fund.
Epidemiology researchers in the ACS Population Science department continually analyze data from the Cancer Prevention Study II (CPS-II) and CPS-3 to better understand factors that contribute to disparities.
Currently, we’re looking at how:
We’re also adding new questions to the 2021 survey that will help us understand perceived discrimination and its impact on health by asking participants where, why, and when they have felt discrimination.
“Most population studies that examine risk factors for developing cancer, like physical inactivity, only allow participants to select from very broad racial/ethnicity categories, largely ‘Black, white, and other.’ But there’s so much diversity in each of these categories – especially ‘other’ – that needs to be identified and studied.
“With CPS-3, we allow participants to select from more specific racial/ethnic groups. By doing so, we found some disparities in physical activity related to participants’ race and birthplace. Other scientists can use our results to identify demographic groups for future research to explore group-specific barriers and facilitators of physical activity and to create culturally tailored messaging, programs, and policy work.” —Erika Rees-Punia, PhD, MPH, Principal Scientist, Epidemiology & Behavioral Research, ACS
Every 3 years, the American Cancer Society (ACS) publishes the report Cancer Facts & Figures for African American/Black People and its accompanying scientific paper in the ACS peer-reviewed journal, CA: A Cancer Journal for Clinicians.
These publications provide the most recent data on cancer newly diagnosed cases (incidence), mortality, survival, screening, and risk factors for Black people in the United States.
For most types of cancers, Black people have the highest death rate and shortest survival rate of any racial/ethnic group. This is due to disproportionate numbers of Black people living below the national poverty level and underlying systemic discrimination that reduce access to cancer screening, which is care that allows for early detection, and appropriate, high-quality treatment. In 2022, there will be an estimated 224,080 new cancer cases and 73,680 cancer deaths among Black people.
Facts about Black Women & Cancer
Facts about Black Men & Cancer
For Spanish-speaking readers >>Datos y Estadísticas sobre el Cáncer entre los Hispanos/Latinos
Every 3 years, Kimberly Miller, MPH, a research scientist at the American Cancer Society (ACS), publishes the report Cancer Facts & Figures for Hispanics/Latinos (Spanish edition available Winter 2021) and also is the lead author for a scientific paper published in the ACS peer-reviewed journal, CA: A Cancer Journal for Clinicians.
These publications provide updated cancer information on cancer occurrence and risk factors in the Hispanic/Latino population, as well as information about prevention, early detection, and treatment.
For Hispanic people, compared to non-Hispanic White people:
Hispanic/Latino people born in the US may have cancer incidence rates more like non-Hispanic white people—or even higher. This is partly due to US acculturation—the adoption of attitudes, values, customs, beliefs, and behaviors of people in the US. When combined with socioeconomic disparities and systemic racism, acculturation leads to a higher burden of cancer risk factors, such as obesity and type 2 diabetes in US-born Hispanic people.
Certain Hispanic/Latino subpopulations have substantially varying cancer rates and risk factors. For example, lung cancer incidence rates are higher in Cuban men than in other Hispanic groups combined due to higher historical smoking rates.
Hispanic/Latino children and adolescents have higher rates of leukemia than all other racial and ethnic groups in the US. They have nearly double the rate in Black children, who experience the lowest rates.
The American Cancer Society Cancer Action Network (ACS CAN) is the nonprofit, nonpartisan advocacy affiliate of the American Cancer Society. Its role is to support evidence-based policy and legislative solutions designed to eliminate cancer as a major health problem. American Cancer Society (ACS) researchers collaborate with ACS CAN staff to explore how and why certain groups of people in the US are not benefitting from health care services such as cancer prevention, early detection, and treatment.
ACS CAN is attacking disparities by changing or adding new evidence-based public health policies at the local, state, and federal levels. The goal of ACS CAN is to reduce these disparities and improve health outcomes for all US population groups regardless of race, ethnicity, gender, age, sexual orientation, socioeconomic status, or zip code.
For more information, visit the ACSCAN web site at www.fightcancer.org
“Medicaid recipients in many states . . . are essentially barred from enrolling in clinical trials. ACS CAN developed some model legislation over the past year, and our state colleagues have worked to get that introduced. And we actually got legislation passed in three states—Colorado, Minnesota, and Illinois—which would require their state Medicaid plans to cover those routine care costs of cancer clinical trials."
—Mark Fleury, PhD, Policy Principal at ACS CAN
American Cancer Society (ACS) researchers and the researchers we fund through extramural grants are working to better understand what health disparities exist, what causes them, and how to decrease them.
Our research shows that while overall cancer mortality rates are dropping, populations who are marginalized are bearing a disproportionate burden of preventable death and disease. If we are to further reduce deaths from cancer, we need to make sure everyone has the ability to benefit from the advances in the prevention and treatment of cancer.
A partnership and 3-year grant (2021 to 2023) with the Robert Wood Johnson Foundation (RWJF) is helping us do just that. RWJF is the nation's largest philanthropic organization dedicated solely to health in the United States. They’re committed to working with others to build a “Culture of Health” that provides everyone with a fair and just opportunity to be as healthy as possible.
The purpose of RWJF’s partnership with ACS and our nonprofit, nonpartisan affiliate, the American Cancer Society Cancer Action Network (ACS CAN) is to advance the culture of health equity, integrate it into our organization, and make it a shared value for ACS and ACS CAN volunteers, staff, partners, and the community at the national, state, and local levels. We are doing this through trainings and other educational opportunities for volunteers and staff to deepen their health equity knowledge and skills.
We are also piloting Health Equity Community Projects, a collaboration between ACS, ACS CAN, and community partners in select cohorts across the nation. The goal of this partnership is to explore, identify, and implement community-driven solutions that address specific social and structural factors around cancer disparities.
From advocating for change to fundraising for research, we’re working hard to address cancer health disparities.