Abstract
Introduction
In Western Washington (WA), colorectal cancer (CRC) mortality between 2012 and 2016 was highest in American Indian/Alaska Natives (AI/AN) and African-Americans (AA) at 20.7 and 18.7, respectively, compared with non-Hispanic Whites at 14.1/100,000 people. We hypothesized that time from billed encounters for CRC-associated symptoms to endoscopy completion or CRC stage at diagnosis contributed to observed differences.
Methods
Using administrative insurance claims linked to WA cancer registry data, we performed a retrospective cohort study of patients diagnosed with CRC between 2011 and 2017, with continuous insurance for 15 months prior to diagnosis and a billed encounter for CRC-associated symptoms. We determined the wait-time (days) and stage at diagnosis and conducted logistic regression analysis to identify the factors associated with endoscopy completion.
Results
Of the 3461 CRC patients identified, 57% had stage 2 or 3 disease with no differences in stage by race, and 84% completed an endoscopy after a billed encounter for CRC-associated symptoms. The median wait-time to endoscopy was 52 days (IQR 14–218) without differences by race. Compared with patients diagnosed with stage 1 CRC, patients with stage 4 CRC were more likely to complete an endoscopy within the first quartile of time (22.2% vs. 17.4%, p < 0.01). Living arrangement, insurance type, and comorbidity, but not race, were significant factors associated with endoscopy completion.
Conclusions
We found no statistically significant differences in time from billed CRC-associated symptoms to endoscopy completion or in CRC stage among AA and AI/AN compared to Whites. This suggests that other factors are more likely to contribute to observed mortality disparities.
Similar content being viewed by others
References
Siegel RL, Miller KD, Jemal A. Cancer statistics, 2019. CA Cancer J Clin. 2019;69(1):7–34. https://doi.org/10.3322/caac.21551.
Yabroff KR, Gansler T, Wender RC, Cullen KJ, Brawley OW. Minimizing the burden of cancer in the United States: goals for a high-performing health care system. CA Cancer J Clin. 2019;69(3):166–83. https://doi.org/10.3322/caac.21556.
Williams R, White P, Nieto J, Vieira D, Francois F, Hamilton F. Colorectal cancer in African Americans: an update. Clin Transl Gastroenterol. 2016;7(7):e185. https://doi.org/10.1038/ctg.2016.36.
Guadagnolo BA, Petereit DG, Coleman CN. Cancer care access and outcomes for American Indian populations in the United States: challenges and models for progress. Semin Radiat Oncol. 2017;27(2):143–9. https://doi.org/10.1016/j.semradonc.2016.11.006.
Burnett-Hartman AN, Adams SV, Bansal A, McDougall JA, Cohen SA, Karnopp A, et al. Indian health service care system and cancer stage in American Indians and Alaska natives. J Health Care Poor Underserved. 2018;29(1):245–52. https://doi.org/10.1353/hpu.2018.0017.
White A, Joseph D, Rim SH, Johnson CJ, Coleman MP, Allemani C. Colon cancer survival in the United States by race and stage (2001-2009): findings from the CONCORD-2 study. Cancer. 2017;123(Suppl 24):5014–36. https://doi.org/10.1002/cncr.31076.
Centers for Disease Control and Prevention. National Center for Chronic Disease Prevention and Health Promotion, Division of Population Health. BRFSS Prevalence & Trends Data. 2015. https://www.cdc.gov/brfss/brfssprevalence/. Accessed February 3 2020.
Rauscher GH, Johnson TP, Cho YI, Walk JA. Accuracy of self-reported cancer-screening histories: a meta-analysis. Cancer Epidemiol Biomark Prev. 2008;17(4):748–57. https://doi.org/10.1158/1055-9965.EPI-07-2629.
Lee W, Nelson R, Mailey B, Duldulao MP, Garcia-Aguilar J, Kim J. Socioeconomic factors impact colon cancer outcomes in diverse patient populations. J Gastrointest Surg. 2012;16(4):692–704. https://doi.org/10.1007/s11605-011-1809-y.
Berg GD, Gurley VF. Development and validation of 15-month mortality prediction models: a retrospective observational comparison of machine-learning techniques in a national sample of Medicare recipients. BMJ Open. 2019;9(7):e022935. https://doi.org/10.1136/bmjopen-2018-022935.
HICOR. Community Cancer Care in Washington State Quality and Cost Report 2018. Fred Hutchinson Cancer Research Center, Seattle, WA. 2018. https://www.fredhutch.org/content/dam/public/labs-projects/hicor/CCCReport/HICOR%20Community%20Cancer%20Care%20Report%20May%202018.pdf. Accessed December 5 2018.
Healthcare Delivery Research Program NCI. National Cancer Institute comorbidity index overview. https://healthcaredelivery.cancer.gov/seermedicare/considerations/comorbidity.html. Accessed Feb 07 2019.
Corley DA, Jensen CD, Quinn VP, Doubeni CA, Zauber AG, Lee JK, et al. Association between time to colonoscopy after a positive fecal test result and risk of colorectal cancer and cancer stage at diagnosis. JAMA. 2017;317(16):1631–41. https://doi.org/10.1001/jama.2017.3634.
Zapka JG, Taplin SH, Solberg LI, Manos MM. A framework for improving the quality of cancer care: the case of breast and cervical cancer screening. Cancer Epidemiol Biomark Prev. 2003;12(1):4–13.
Janssen RM, Takach O, Nap-Hill E, Enns RA. Time to endoscopy in patients with colorectal cancer: analysis of wait-times. Can J Gastroenterol Hepatol. 2016;2016:8714587. https://doi.org/10.1155/2016/8714587.
Singh H, Shu E, Demers A, Bernstein CN, Griffith J, Fradette K. Trends in time to diagnosis of colon cancer and impact on clinical outcomes. Can J Gastroenterol. 2012;26(12):877–80.
Ramos M, Esteva M, Cabeza E, Llobera J, Ruiz A. Lack of association between diagnostic and therapeutic delay and stage of colorectal cancer. Eur J Cancer. 2008;44(4):510–21. https://doi.org/10.1016/j.ejca.2008.01.011.
Torring ML, Frydenberg M, Hamilton W, Hansen RP, Lautrup MD, Vedsted P. Diagnostic interval and mortality in colorectal cancer: U-shaped association demonstrated for three different datasets. J Clin Epidemiol. 2012;65(6):669–78. https://doi.org/10.1016/j.jclinepi.2011.12.006.
Pruitt SL, Harzke AJ, Davidson NO, Schootman M. Do diagnostic and treatment delays for colorectal cancer increase risk of death? Cancer Causes Control. 2013;24(5):961–77. https://doi.org/10.1007/s10552-013-0172-6.
Meester RG, Zauber AG, Doubeni CA, Jensen CD, Quinn VP, Helfand M, et al. Consequences of increasing time to colonoscopy examination after positive result from fecal colorectal cancer screening test. Clin Gastroenterol Hepatol. 2016;14(10):1445–51 e8. https://doi.org/10.1016/j.cgh.2016.05.017.
May FP, Glenn BA, Crespi CM, Ponce N, Spiegel BMR, Bastani R. Decreasing black-White disparities in colorectal cancer incidence and stage at presentation in the United States. Cancer Epidemiol Biomark Prev. 2017;26(5):762–8. https://doi.org/10.1158/1055-9965.EPI-16-0834.
Adams SV, Burnett-Hartman AN, Karnopp A, Bansal A, Cohen SA, Warren-Mears V, et al. Cancer stage in American Indians and Alaska natives enrolled in Medicaid. Am J Prev Med. 2016;51(3):368–72. https://doi.org/10.1016/j.amepre.2016.02.016.
Day LW, Kwon A, Inadomi JM, Walter LC, Somsouk M. Adverse events in older patients undergoing colonoscopy: a systematic review and meta-analysis. Gastrointest Endosc. 2011;74(4):885–96. https://doi.org/10.1016/j.gie.2011.06.023.
Issaka RB, Inadomi JM. Low-value colorectal cancer screening: too much of a good thing? JAMA Netw Open. 2018;1(8):e185445. https://doi.org/10.1001/jamanetworkopen.2018.5445.
Osborn R, Moulds D, Squires D, Doty MM, Anderson C. International survey of older adults finds shortcomings in access, coordination, and patient-centered care. Health Aff (Millwood). 2014;33(12):2247–55. https://doi.org/10.1377/hlthaff.2014.0947.
Kaiser Family Foundation. Profile of Medicare beneficiaries by race and ethnicity: a chartpack. 2016. https://www.kff.org/medicare/report/profile-of-medicare-beneficiaries-by-race-and-ethnicity-a-chartpack/. Accessed February 3 2020.
El-Haddad B, Dong F, Kallail KJ, Hines RB, Ablah E. Association of marital status and colorectal cancer screening participation in the USA. Color Dis. 2015;17(5):O108–14. https://doi.org/10.1111/codi.12926.
Bureau USC. Quick facts. 2018. https://www.census.gov/quickfacts/map/IPE120213/53. Accessed November 1 2019.
Guarantor of the Article
Rachel Issaka, MD, MAS
Funding
This research was supported by the National Institutes of Health/National Cancer Institute Cancer Center Support Grant P30 CA015704. The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Author information
Authors and Affiliations
Contributions
Study concept and design: Issaka.
Acquisition of data: Issaka, Li, Fedorenko.
Statistical analysis: Issaka, Li.
Drafting of the manuscript: Issaka.
Critical revision of the manuscript for important intellectual content: All authors.
Approval of the final manuscript: All authors.
Corresponding author
Ethics declarations
Financial Disclosures
No financial disclosures were reported by the authors of this paper.
Ethical Approval
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional research committee (Fred Hutchinson Institutional Review Board, IR File #8694) and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
Conflict of Interest
All authors declare that they have no conflict of interest.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
ESM 1
(DOCX 20 kb)
Rights and permissions
About this article
Cite this article
Issaka, R.B., Li, L., Fedorenko, C. et al. Racial Disparities in Colorectal Cancer Mortality: the Role of Endoscopy Wait-Time and Stage at Diagnosis. J. Racial and Ethnic Health Disparities 7, 967–974 (2020). https://doi.org/10.1007/s40615-020-00721-x
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s40615-020-00721-x