Abstract

We previously performed a randomized controlled trial (RCT) comparing targeted and random biopsy in neoplasia detection in patients with ulcerative colitis (UC), which showed the short-term effectiveness of targeted biopsy with one-time colonoscopy. In this retrospective cohort study, we investigated the long-term effectiveness of targeted biopsy in tertiary care hospitals, using the follow-up data from patients with UC for ≥ 8 years who had enrolled in the initial RCT. The primary outcome was death from colorectal cancer (CRC). Secondary outcomes were advanced neoplasia (CRC or high-grade dysplasia) and colectomy due to neoplasia after the RCT. We compared these outcomes between target and random groups. Data on 195 of the 221 patients (88.2%) enrolled in the previous RCT were collected from 28 institutions between 2008 and 2019. No patients died of CRC in either group, with a median 8.8-year follow-up demonstrating a robustness for targeted biopsy in terms of CRC death prevention. Advanced neoplasia was detected in four and three patients in the target and random groups, respectively. Colectomy was required due to neoplasia in three patients in each group. The chance of developing CRC in patients with a negative colonoscopy was low, and the targeted biopsy appeared effective in this population. Conversely, patients found with low-grade dysplasia at initial RCT have 10-fold higher risk of progression to high-grade dysplasia and/or CRC. Ten extracolonic malignancies were observed during the follow-up, resulting in four deaths. Panchromoendoscopy was used only in 4.6% and targeted biopsy was only performed in 59.1% of colonoscopies. We recommend targeted biopsy rather than > 33 random biopsies in real-world settings under adequate observation by specialists.

Highlights

  • Ulcerative colitis (UC) is an inflammatory bowel diseases (IBD), manifesting as chronic inflammation of the colorectum

  • We investigated the cumulative rate of advanced neoplasia [colorectal cancer (CRC) or high-grade dysplasia (HGD)] in patients who had no dysplasia and those who were found to have low-grade dysplasia (LGD) at the time of the initial randomized controlled trial (RCT)

  • One patient who died from cancer of unknown primary was originally in the random group, and no dysplasia was detected at the time of the initial RCT

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Summary

Introduction

Ulcerative colitis (UC) is an inflammatory bowel diseases (IBD), manifesting as chronic inflammation of the colorectum. Medications such as 5-aminosalicylic acid, steroids, immunomodulators, and biological agents alleviate the inflammation, they cannot completely cure the disease [1]. Patients with long-standing UC are at increased risk for the development of colorectal cancer (CRC). The use of thiopurines in these patients may increase the risk of lymphoproliferative diseases and non-melanoma skin cancers in Caucasian populations [7,8], such an effect may not be extrapolated to the Asian population because of racial differences affecting the incidence of these malignancies [9]

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