# Risk of advanced neoplasia after removal of colorectal adenomas with high-grade dysplasia

**Authors:** Degao He, Kai Wang, Yanhong Zhang, Xuefei Jiang, Hao Chen, Junguo Chen, Danlin Liu, Guanman Li, Jiancong Hu, Xiaosheng He

PMC · DOI: 10.1007/s00464-024-10898-5 · 2024-05-28

## TL;DR

This study finds that patients who had colorectal adenomas with high-grade dysplasia removed are at increased risk for advanced neoplasia and colorectal cancer, but regular colonoscopies can reduce this risk.

## Contribution

The study provides the first detailed long-term risk assessment for patients with adenomas with high-grade dysplasia after removal.

## Key findings

- The 10-year cumulative incidence of advanced neoplasia was 39.1% and colorectal cancer was 5.5%.
- Participation in surveillance colonoscopies significantly reduced the risk of both advanced neoplasia and colorectal cancer.
- 73% of colorectal cancers that developed were deficient mismatch repair CRCs.

## Abstract

Many studies reported the presence of adenomas with high-grade dysplasia (HGD) at index colonoscopy increased the incidence of advanced neoplasia (AN) and colorectal cancer (CRC) following. However, the conclusion remains obscure due to lack of studies on the specific population of adenomas with HGD. This study aimed to assess the long-term risk of AN and CRC after removal of adenomas with HGD.

A total of 814 patients who underwent adenomas with HGD removal between 2010 and 2019 were retrospectively analyzed. The outcomes were the incidences of AN and CRC during surveillance colonoscopy. Cox proportional hazards models were utilized to identify risk factors associated with AN and CRC.

During more than 2000 person-years of follow-up, we found that AN and CRC incidence densities were 44.3 and 4.4 per 1000 person-years, respectively. The 10-year cumulative incidence of AN and CRC were 39.1% and 5.5%, respectively. In the multivariate model, synchronous low-risk polyps (HR 1.80, 95% CI 1.10–2.93) and synchronous high-risk polyps (HR 3.99, 95% CI 2.37–6.72) were risk factors for AN, whereas participation in surveillance colonoscopy visits (HR 0.56, 95% CI 0.36–0.88 for 1 visit; HR 0.10, 95% CI 0.06–0.19 for ≥ 2 visits) were associated with decreased AN incidence. Additionally, elevated baseline carcinoembryonic antigen (CEA) level (HR 10.19, 95% CI 1.77–58.59) was a risk factor for CRC, while participation in ≥ 2 surveillance colonoscopy visits (HR 0.11, 95% CI 0.02–0.56) were associated with decreased CRC incidence. Interestingly, for 11 patients who developed CRC after removal of adenomas with HGD, immunohistochemistry revealed that 8 cases (73%) were deficient mismatch repair CRCs.

Patients who have undergone adenoma with HGD removal are at higher risk of developing AN and CRC, while surveillance colonoscopy can reduce the risk. Patients with synchronous polyps, or with elevated baseline CEA level are considered high-risk populations and require more frequent surveillance.

The online version contains supplementary material available at 10.1007/s00464-024-10898-5.

## Linked entities

- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Diseases:** polyps (MESH:D011127), dysplasia (MESH:D015792), AN (MESH:D009369), HGD (MESH:D008228), CRC (MESH:D015179), adenoma (MESH:D000236)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11219408/full.md

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Source: https://tomesphere.com/paper/PMC11219408