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Clinical Trial
. 2022 Oct;54(10):948-958.
doi: 10.1055/a-1795-4673. Epub 2022 Apr 11.

Post-polypectomy surveillance interval and advanced neoplasia detection rates: a multicenter, retrospective cohort study

Affiliations
Clinical Trial

Post-polypectomy surveillance interval and advanced neoplasia detection rates: a multicenter, retrospective cohort study

Amanda J Cross et al. Endoscopy. 2022 Oct.

Abstract

Background: Longer post-polypectomy surveillance intervals are associated with increased colorectal neoplasia detection at surveillance in some studies. We investigated this association to inform optimal surveillance intervals.

Methods: Patients who underwent colonoscopy and post-polypectomy surveillance at 17 UK hospitals were classified as low/high risk by baseline findings. We compared detection rates of advanced adenomas (≥ 10 mm, tubulovillous/villous, high grade dysplasia), high risk findings (HRFs: ≥ 2 serrated polyps/[adenomas] of which ≥ 1 is ≥ 10 mm or has [high grade] dysplasia; ≥ 5 serrated polyps/adenomas; or ≥ 1 nonpedunculated polyp ≥ 20 mm), or colorectal cancer (CRC) at surveillance colonoscopy by surveillance interval (< 18 months, 2, 3, 4, 5, 6 years). Risk ratios (RRs) were estimated using multivariable regression.

Results: Of 11 214 patients, 7216 (64 %) were low risk and 3998 (36 %) were high risk. Among low risk patients, advanced adenoma, HRF, and CRC detection rates at first surveillance were 7.8 %, 3.7 %, and 1.1 %, respectively. Advanced adenoma detection increased with increasing surveillance interval, reaching 9.8 % with a 6-year interval (P trend < 0.001). Among high risk patients, advanced adenoma, HRF, and CRC detection rates at first surveillance were 15.3 %, 10.0 %, and 1.5 %, respectively. Advanced adenoma and CRC detection rates (P trends < 0.001) increased with increasing surveillance interval; RRs (95 % confidence intervals) for CRC were 1.54 (0.68-3.48), 4.44 (1.95-10.08), and 5.80 (2.51-13.40) with 3-, 4-, and 5-year intervals, respectively, versus an interval of < 18 months.

Conclusions: Metachronous neoplasia was uncommon among low risk patients, even with long surveillance intervals, supporting recommendations for no surveillance in these patients. For high risk patients, a 3-year surveillance interval would ensure timely CRC detection.

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Conflict of interest statement

AJC, as Chief Investigator, was the recipient of all the funding. MDR reports personal fees from Swiss SCWeb AG, Pentax, and Norgine, and a grant from Olympus, outside the submitted work. All other authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Study profile flow diagram. 1  Not mutually exclusive. 2  Mutually exclusive groups. Among the 395 patients with a single PMP of unknown size, 90 PMPs were also of unknown shape. Of the 611 patients with 2–4 PMPs and ≥ 1 PMP of unknown size, 99 patients also had ≥ 1 PMP of unknown dysplasia. 3  Of the 46 patients lost to follow-up, 22 were lost because they had no surveillance and could not be traced through national data sources, 20 because they had all examinations after emigrating, and 4 because their date of birth was unknown. 4  High risk patients were those with any of the following at baseline: ≥ 2 PMPs, of which ≥ 1 was a serrated polyp (or adenoma) ≥ 10 mm or with (high grade) dysplasia; ≥ 5 PMPs; or ≥ 1 large (≥ 20 mm) nonpedunculated PMP. Low risk patients were those with none of these findings at baseline. Of those classified as high risk, 85 % had ≥ 2 PMPs of which ≥ 1 was a serrated polyp (or adenoma) ≥ 10 mm or with (high grade) dysplasia, 8 % had ≥ 5 PMPs only, and 8 % had a large nonpedunculated PMP only. CRC, colorectal cancer; PMP, premalignant polyp.

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