Too many people in the United States are dying of colorectal cancer (CRC). The #2 cancer killer in the United States, it impacts Black Americans disproportionately. Compared to White adults, Black adults aged 50 and above get colon cancer at a rate that’s 23% higher than White adults and have a 31% higher risk of dying from the disease.1 These disparities persist despite progress in screening and treatment and are particularly frustrating because CRC is highly treatable when caught in early stages and even preventable when pre-cancers are identified and removed through screening. These differences in incidence and mortality persist even while we have made progress to make screening more accessible to all. A 2019 NIH study showed that a similar proportion of Black and White Americans are up to date with CRC screening2, a meaningful improvement since 20053. If screening access and uptake are now so similar, why do these disparities persist?
The question to be asked is this: could a difference in the CRC screenings themselves be contributing to these disparities? New research shows the answer is yes.
Recent data published in the Journal of the National Cancer Institute demonstrate that the quality and full completion of a screening for colorectal cancer can have profound impacts on outcomes. In this first-of-its-kind modeling study, which was funded by Exact Sciences, my colleagues and I examined the impact of screening colonoscopy quality and completion of follow-up colonoscopy after a positive stool test on CRC incidence and mortality for Black adults.
Studies show Black adults in the United States are more likely to receive a lower-quality screening colonoscopy than White adults4-8. They are also less likely to complete a colonoscopy after a positive stool screening test for colon cancer (such as Cologuard or a FIT test)9-16. Colonoscopy quality is assessed by “adenoma detection rate,” which measures the proportion of screening exams wherein the endoscopist finds a pre-cancerous lesion that can then be removed as a preventive step. Follow-up colonoscopy after a positive stool test is important because it’s needed to complete the screening process. These factors can contribute to disparities in outcomes because finding and removing pre-cancerous growths and early cancers is crucial to improving health outcomes from screening 17-18.
Our study modeled scenarios to look at how improving the quality of a screening colonoscopy (measured by adenoma detection rate) and completion of follow-up colonoscopy after a positive stool test would impact the rates at which Black adults get or die from colorectal cancer. We were surprised to find that eliminating difference in these two areas could cut the gap in CRC incidence and mortality between Black and White Americans in half. Together, eliminating the Black-White differences in colonoscopy quality and follow-up colonoscopy rates would eliminate 49% of the gap in CRC incidence and 59% of the difference in mortality, respectively. This new evidence reveals two under-recognized areas where taking direct action can help lower incidence and mortality of CRC in Black adults.
So, now what? We must continue to build on the progress of the last 10 years to get every eligible adult over age 45 screened for CRC. But we must also ensure everyone gets a high-quality screening with the potential to identify and effectively treat pre-cancers and early-stage cancers. This study provides clear direction on two areas of focus that can make a meaningful difference: Detecting precancerous growths with the initial screening test and working to ensure people have access to high quality colonoscopies to complete screening if they start with a stool test and have a positive result. Improving these two areas won’t be easy. However, if we – healthcare providers, government, industry, advocacy, researchers, payers, and all committed stakeholders – make this a public health priority, we have a real chance to improve healthcare and CRC outcomes for Black adults.
Dr. Oguzhan Alagoz is the Procter & Gamble Bascom Professor in the Department of Industrial & Systems and Engineering and the Department of Population Health Sciences at the University of Wisconsin-Madison.
Sources:
- National Cancer Institute. Surveillance, Epidemiology, and End Results http://seer.cancer.gov/.
- Sabatino SA, Thompson TD, White MC, et al. Cancer Screening Test Use―US, 2019. American Journal of Preventive Medicine 2022;63(3):431-439.
- Klabunde CN, Cronin KA, Breen N, et al. Trends in colorectal cancer test use among vulnerable populations in the United States. Cancer Epidemiology, Biomarkers & Prevention 2011;20(8):1611-1621.
- Diamond SJ, Enestvedt BK, Jiang Z, et al. Adenoma detection rate increases with each decade of life after 50 years of age. Gastrointestinal endoscopy 2011;74(1):135-140.
- Fedewa SA, Flanders WD, Ward KC, et al. Racial and ethnic disparities in interval colorectal cancer incidence: a population-based cohort study. Annals of Internal Medicine 2017;166(12):857-866.
- David Y, Ottaviano L, Park J, et al. Confounders in adenoma detection at initial screening colonoscopy: a factor in the assessment of racial disparities as a risk for colon cancer. Journal of cancer therapy 2019;10(4):269.
- Jawitz NG, Gellad ZF, Lin L, et al. Patient, physician, and procedure characteristics are independently predictive of polyp detection rates in clinical practice. Digestive Diseases and Sciences 2021;66:2570-2577.
- Schottinger JE, Jensen CD, Ghai NR, et al. Association of physician adenoma detection rates with postcolonoscopy colorectal cancer. JAMA 2022;327(21):2114-2122.
- Laiyemo AO, Doubeni C, Pinsky PF, et al. Race and colorectal cancer disparities: health-care utilization vs different cancer susceptibilities. Journal of the National Cancer Institute 2010;102(8):538-546.
- Laiyemo AO, Doubeni C, Pinsky PF, et al. Occurrence of distal colorectal neoplasia among whites and blacks following negative flexible sigmoidoscopy: An analysis of PLCO Trial. Journal of General Internal Medicine 2015;30:1447-1453.
- Burnett-Hartman AN, Mehta SJ, Zheng Y, et al. Racial/ethnic disparities in colorectal cancer screening across healthcare systems. American Journal of Preventive Medicine 2016;51(4):e107-e115.
- Issaka RB, Singh MH, Oshima SM, et al. Inadequate utilization of diagnostic colonoscopy following abnormal FIT results in an integrated safety-net system. Official journal of the American College of Gastroenterology| ACG 2017;112(2):375-382.
- Elangovan A, Skeans J, Lalani I, et al. Disparities in colorectal cancer screening practices in a Midwest urban safety-net healthcare system. Digestive Diseases and Sciences 2021;66:2585-2594.
- Coronado GD, Dickerson JF, Burnett-Hartman AN, et al. Reduced Implementation and Completion of Average-Risk Annual Fecal Immunochemical Test Colorectal Cancer Screening in Black Patients Aged 45–49 Years. Clinical Gastroenterology and Hepatology 2022.
- Mohl JT, Ciemins EL, Miller-Wilson L-A, et al. Rates of Follow-up Colonoscopy After a Positive Stool-Based Screening Test Result for Colorectal Cancer Among Health Care Organizations in the US, 2017-2020. JAMA Network Open 2023;6(1):e2251384-e2251384.
- Ciemins EL, Mohl JT, Moreno CA, et al. Development of a Follow-Up Measure to Ensure Complete Screening for Colorectal Cancer. JAMA Network Open 2024;7(3):e242693-e242693.
- Fendrick, A. M., Kisiel, J. B., Brooks, D., Vahdat, V., Estes, C., Ebner, D. W., & Limburg, P. (2023). A call to action to increase uptake of follow-up colonoscopy after initial positive stool-based colorectal cancer screening. Population health management, 26(6), 448-450.
- Fendrick, A. M., Borah, B. J., Ozbay, A. B., Saoud, L., & Limburg, P. J. (2022). Life-years gained resulting from screening colonoscopy compared with follow-up colonoscopy after a positive stool-based colorectal screening test. Preventive Medicine Reports, 26, 101701.
Dr. Oguzhan Alagoz
Dr. Oguzhan Alagoz is the Procter & Gamble Bascom Professor in the Department of Industrial & Systems and Engineering and the Department of Population Health Sciences at the University of Wisconsin-Madison.