Skip to main content
Log in

Screening Women Aged 50–59 for CRC Using Fecal Occult Blood Test Produces Outcomes Similar to Men Undergoing Screening Colonoscopy

  • Original Article
  • Published:
Digestive Diseases and Sciences Aims and scope Submit manuscript

Abstract

Background

Average-risk women aged 50–59 years have a lower incidence and mortality of colorectal cancer relative to age-matched men, calling into question the benefit of screening colonoscopy in this age group.

Aims

We aimed to determine whether FOBT is an effective initial screening test in 50–59-year-old women.

Methods

We conducted a cross-sectional study using a computerized endoscopic report generator. We identified 320,906 individuals who had average-risk screening colonoscopy and 32,369 who had colonoscopy for positive FOBT. The primary outcome was the positive predictive value (PPV) of FOBT for large polyp(s) greater than 9 mm, as a surrogate for advanced neoplasia.

Results

Among patients aged 50–59 years undergoing screening colonoscopy, men were more likely than women to have large polyps (6.3 vs 4.2%, p < 0.0001). Black women undergoing screening colonoscopy had higher rates of large polyps compared to non-Black women. The PPV in FOBT-positive men aged 50–54 (11.5%) and 55–59 (14.4%) was higher than in women aged 50–54 (6.1%) and 55–59 (5.4%). Despite this lower PPV, women aged 50–54 with a positive FOBT had a similar rate of large polyps as 50–54-year-old men undergoing screening colonoscopy (6.1 vs 6.3%, p = 0.626).

Conclusions

CRC screening with FOBT identifies 50–59-year-old men and women with a higher risk of large polyps. Since younger women have a lower risk of large polyps than men, screening with FOBT in 50–59-year-old non-Black women could be an effective screening strategy, with outcomes similar to the use of screening colonoscopy in 50–59-year-old men.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Siegel RL, Miller KD, Jemal A. Cancer statistics. CA Cancer J Clin. 2016;66:7–30.

    Article  PubMed  Google Scholar 

  2. American Cancer Society. Cancer Facts and Figures 2016. http://www.cancer.org/acs/groups/content/@research/documents/document/acspc-047079.pdf. Accessed January 1, 2016.

  3. Levin B, Lieberman DA, McFarland B, et al. Screening and surveillance for early detection of colorectal cancer and adenomatous polyps, 2008: a joint guideline from the American Cancer Society, the US Multi-Society Task Force on Colorectal Cancer, and the American College of Radiology. Gastroenterology. 2008;134:1570–1595.

    Article  CAS  PubMed  Google Scholar 

  4. Rex DK, Johnson DA, Anderson JC, et al. American College of Gastroenterology guidelines for colorectal cancer screening 2008. Am J Gastroenterol. 2009;104:739–750.

    Article  PubMed  Google Scholar 

  5. Qaseem A, Denberg TD, Hopkins RH Jr, et al. Screening for colorectal cancer: a guidance statement from the American College of Physicians. Ann Intern Med. 2012;156:378–386.

    Article  PubMed  Google Scholar 

  6. US Preventive Services Task Force, Bibbins-Domingo K, Grossman DC, et al. Screening for colorectal cancer: US preventive services task force recommendation statement. JAMA. 2016;315:2564–2575.

    Article  CAS  Google Scholar 

  7. Klabunde CN, Joseph DA, King JB, et al. Vital signs: colorectal cancer screening test use—United States, 2012. MMWR Morb Mortal Wkly Rep. 2013;62:881–888.

    PubMed Central  Google Scholar 

  8. Shapiro JA, Klabunde CN, Thompson TD, et al. Patterns of colorectal cancer test use, including CT colonography, in the 2010 National Health Interview Survey. Cancer Epidemiol Biomark Prev. 2012;21:895–904.

    Article  Google Scholar 

  9. SEER*Explorer. National Cancer Institute. https://seer.cancer.gov/explorer/. Updated April 14, 2017. Accessed April 23, 2017.

  10. Regula J, Rupinski M, Kraszewska E, et al. Colonoscopy in colorectal-cancer screening for detection of advanced neoplasia. N Engl J Med. 2006;355:1863–1872.

    Article  CAS  PubMed  Google Scholar 

  11. Schoenfeld P, Cash B, Flood A, et al. Colonoscopic screening of average-risk women for colorectal neoplasia. N Engl J Med. 2005;352:2061–2068.

    Article  CAS  PubMed  Google Scholar 

  12. Lieberman DA, Williams JL, Holub JL, et al. Race, ethnicity, and sex affect risk for polyps > 9 mm in average-risk individuals. Gastroenterology. 2014;147:351–358.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Ferlitsch M, Reinhart K, Pramhas S, et al. Sex-specific prevalence of adenomas, advanced adenomas and colorectal cancer in individuals undergoing screening colonoscopy. JAMA. 2011;306:1352–1358.

    Article  CAS  PubMed  Google Scholar 

  14. Mandel JS, Bond JH, Church TR, et al. Reducing mortality from colorectal cancer by screening for fecal occult blood. Minnesota Colon Cancer Control Study. N Engl J Med. 1993;328:1365–1371.

    Article  CAS  PubMed  Google Scholar 

  15. Hardcastle JD, Chamberlain JO, Robinson MH, et al. Randomised controlled trial of faecal-occult-blood screening for colorectal cancer. Lancet. 1996;348:1472–1477.

    Article  CAS  PubMed  Google Scholar 

  16. Kronborg O, Fenger C, Olsen J, et al. Randomised study of screening for colorectal cancer with faecal-occult-blood test. Lancet. 1996;348:1467–1471.

    Article  CAS  PubMed  Google Scholar 

  17. Winawer SJ, Zauber AG, Ho MN, et al. Prevention of colorectal cancer by colonoscopic polypectomy. N Engl J Med. 1993;329:1977–1981.

    Article  CAS  PubMed  Google Scholar 

  18. Sonnenberg A, Amorosi SL, Lacey MJ, et al. Patterns of endoscopy in the United States: analysis of data from the Centers for Medicare and Medicaid Services and the National Endoscopic Database. Gastrointest Endosc. 2008;67:489–496.

    Article  PubMed  Google Scholar 

  19. Lieberman D, Moravec M, Holub J, et al. Polyp size and advanced histology in patients undergoing colonoscopy screening: implications for CT Colonography. Gastroenterology. 2008;135:1100–1105.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Lieberman DA, Holub JL, Moravec MD, et al. Prevalence of colon polyps detected by colonoscopy screening in asymptomatic black and white patients. JAMA. 2008;300:1417–1422.

    Article  CAS  PubMed  Google Scholar 

  21. Brenner H, Hoffmeister M, Birkner B, et al. Men with negative results of guaiac-based fecal occult blood test have higher prevalence of colorectal neoplasms than women with positive results. Int J Cancer. 2014;134:2927–2934.

    Article  CAS  PubMed  Google Scholar 

  22. Ferlitsch M, Heinze G, Salzl P, et al. Sex is a stronger predictor of colorectal adenoma and advanced adenoma than fecal occult blood test. Med Oncol. 2014;31:151.

    Article  PubMed  Google Scholar 

  23. Inadomi JM, Vijan S, Janz NK, et al. Adherence to colorectal cancer screening: a randomized clinical trial of competing strategies. Arch Intern Med. 2012;172:575–582.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Auge J, Pellise M, Escudero JM, et al. Risk stratification for advanced colorectal neoplasia according to fecal hemoglobin concentration in a colorectal cancer screening program. Gastroenterology. 2014;147:628–636.

    Article  CAS  PubMed  Google Scholar 

  25. Van Hees F, Zauber AG, van Veldhuizen H, et al. The value of models in informing resource allocation in colorectal cancer screening—the case of the Netherlands. Gut. 2015;64:1985–1997.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Decker K, Demers A, Nugent Z, et al. Longitudinal rates of colon cancer screening use in Winnipeg, Canada: the experience of a universal health-care system with an organized colon screening program. Am J Gastroenterol. 2015;110:1640–1646.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Chan AT, Giovannucci EL. Primary prevention of colorectal cancer. Gastroenterology. 2010;138:2029–2043.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgments

This project was supported with funding from NIDDK U01DK57132 and R33-DK61778-01. In addition, the practice network (Clinical Outcomes Research Initiative) has received support from the following entities to support the infrastructure of the practice-based network: AstraZeneca, Novartis, Bard International, Pentax USA, ProVation, Endosoft, GIVEN Imaging, and Ethicon. The commercial entities had no involvement in this research.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to David A. Lieberman.

Ethics declarations

Conflict of interest

Dr. Lieberman is the executive director of CORI, a non-profit organization that receives funding from federal and industry sources. This potential conflict of interest has been reviewed and managed by the OHSU and Portland VA Conflict of Interest in Research Committees. All other authors have no potential conflicts of interests to disclose.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Mooers, H.M., Holub, J.L. & Lieberman, D.A. Screening Women Aged 50–59 for CRC Using Fecal Occult Blood Test Produces Outcomes Similar to Men Undergoing Screening Colonoscopy. Dig Dis Sci 63, 2780–2785 (2018). https://doi.org/10.1007/s10620-018-5156-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10620-018-5156-7

Keywords

Navigation