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16 December 2003, Vol 139, No. 12>
Summaries for Patients | 16 December 2003

Using Risks To Tailor Screening for Colorectal Cancer FREE

[+] Article and Author Information

The summary below is from the full report titled “Using Risk for Advanced Proximal Colonic Neoplasia To Tailor Endoscopic Screening for Colorectal Cancer.” It is in the 16 December 2003 issue of Annals of Internal Medicine (volume 139, pages 959-965). The authors are T.F. Imperiale, D.R. Wagner, C.Y. Lin, G.N. Larkin, J.D. Rogge, and D.F. Ransohoff.


Ann Intern Med. 2003;139(12):I-10. doi:10.7326/0003-4819-139-12-200312160-00001
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What is the problem and what is known about it so far?

Cancer of the colon or rectum is called colorectal cancer. It is the second leading cause of death from cancer in the United States. Polyps (outgrowths of the wall of the colon) precede most colorectal cancers. Screening procedures can detect and remove polyps before they become cancers and also detect early cancers that may be cured with surgery. For example, doctors can use a short flexible tube to look for polyps in the lower half of the colon (sigmoidoscopy) or a longer tube to look at the entire colon (colonoscopy). They can take tissue samples (biopsies) and remove polyps with either procedure. Many doctors use sigmoidoscopy to screen for polyps and/or cancer. If this exam finds polyps, they then do colonoscopy to check for more polyps in the upper part of the colon. Methods that identify people with low risk for polyps in the upper colon might help doctors and patients decide when sigmoidoscopy alone is enough.

Why did the researchers do this particular study?

To find a way of identifying people with low risks for colorectal cancer in the upper colon for whom sigmoidoscopy screening might be sufficient.

Who was studied?

3025 adults age 50 years and older who participated in a company-based screening program. None had symptoms of colorectal cancer.

How was the study done?

Participants were screened with colonoscopy. The location and size of any polyps that were found were noted before their removal. Pathologists examined removed tissue to identify advanced growths (precancerous polyps or cancer). The researchers first looked at data from the 1994 people who were screened between September 1995 and December 1998. They identified factors that were associated with an increased probability of finding advanced growths in the upper part of the colon. They developed a risk index that scored and summed those factors. They then tested how well the risk index worked using data from 1031 people who were screened between January 1999 and June 2001.

What did the researchers find?

In people examined between 1995 and 1998, the researchers found that three factors increased the probability of finding advanced growths in the upper part of the colon. These factors were older age, male sex, and certain types and sizes of polyps in the lower part of the colon. Using these factors, the researchers scored risk for advanced growths in the upper colon as low (0 to 1 point), intermediate (2 to 3 points), and high (4 to 7 points). The risk index worked in the second group of people examined between 1999 and 2001. Advanced growths in the upper part of the colon were found in 0.4%, 1.9%, and 3.8% of those classified as low, intermediate, and high risk, respectively.

What were the limitations of the study?

The risk index was derived in people who had the location of polyps assessed at colonoscopy rather than from people who had polyps in the lower colon detected at sigmoidoscopy. The index needs testing in additional populations.

What are the implications of the study?

A risk index may identify low-risk people whose probability of advanced growth in the upper colon is about 1 in 250 (0.4%). The index may help identify people who don't need colonoscopy after sigmoidoscopy.

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Citing articles are presented as examples only. In non-demo SCM6 implementation, integration with CrossRef’s “Cited By” API will populate this tab (http://www.crossref.org/citedby.html).
Compression-Only CPR: Pushing the Science Forward
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AAM 2010;304:1493-1495.
All you need to read in the other general jounals
BMJ 2010;341:c5893-c1494.

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