Cancer surveillance in longstanding ulcerative colitis: endoscopic appearances help predict cancer risk

Matthew D. Rutter

Gut · 2004 · 444 citations · 13 references

DOIFull text

Open access

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TL;DR

Colorectal cancer risk is elevated in ulcerative colitis, yet colonoscopic appearances vary widely among patients. The study aimed to identify colonoscopic markers that could stratify colorectal cancer risk in ulcerative colitis patients. A matched case‑control study collected data on post‑inflammatory polyps, scarring, strictures, backwash ileitis, shortened or tubular colons, severe inflammation, and normal‑appearing colonoscopies from 68 neoplasia cases and 136 controls. Post‑inflammatory polyps, strictures, shortened or tubular colons, and severe inflammation were independently associated with neoplasia, whereas a normal‑appearing colonoscopy was linked to a cancer risk comparable to the general population, suggesting surveillance could be extended to five years in such patients.

Abstract

The risk of colorectal cancer is increased in ulcerative colitis (UC). Patients with UC have diverse colonoscopic appearances. Determining colonoscopic markers for cancer risk could allow patient risk stratification.Following on from an earlier study which demonstrated a correlation between inflammation severity and neoplasia risk, a case control study was performed to look for colonoscopic markers of colorectal neoplasia risk in UC. Each patient with neoplasia detected between 1988 and 2002 was matched with two non-dysplastic colitic controls. Data were collected on post-inflammatory polyps, scarring, strictures, backwash ileitis, a shortened, tubular, or featureless colon, severe inflammation, and normal looking surveillance colonoscopies.Cases (n = 68) and controls (n = 136) were well matched. On univariate analysis, cases were significantly more likely to have post-inflammatory polyps (odds ratio (OR) 2.14 (95% confidence interval 1.24-3.70)), strictures (OR 4.22; 1.08-15.54), shortened colons (OR 10.0; 1.17-85.6), tubular colons (OR 2.03; 1.00-4.08), or segments of severe inflammation (OR 3.38; 1.41-10.13), and less likely to have had a macroscopically normal looking colonoscopy (OR 0.40; 0.21-0.74). After multivariate analysis, a macroscopically normal looking colonoscopy (OR 0.38; 0.19-0.73), post-inflammatory polyps (2.29; 1.28-4.11), and strictures (4.62; 1.03-20.8) remained significant. The five year risk of colorectal cancer following a normal looking colonoscopy was no different from that of matched general population controls.Macroscopic colonoscopic features help predict neoplasia risk in UC. Features of previous/ongoing inflammation signify an increased risk. A macroscopically normal looking colonoscopy returns the cancer risk to that of the general population: it should be possible to reduce surveillance frequency to five years in this cohort.

References

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