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Risk of Metachronous Advanced Colorectal Neoplastic Among Individuals With Varying Numbers of Non-Advanced Adenomas Detected During Screening Colonoscopy

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Fudan University

Status

Completed

Conditions

Colorectal Adenoma

Treatments

Other: No Intervention: Observational Cohort

Study type

Observational

Funder types

Other

Identifiers

NCT07302139
2025K369

Details and patient eligibility

About

A retrospective observational study to evaluate the risk of metachronous advanced colorectal neoplastic (ACRN) among individuals with varying numbers of non-advanced adenomas (NAA) detected during screening colonoscopy

Full description

Colorectal cancer (CRC) is the third most commonly diagnosed malignancy worldwide and the second leading cause of cancer-related mortality. In recent years, with increasing westernization of diet and lifestyle, both the incidence and prevalence of CRC in China have risen sharply. CRC has become the most common gastrointestinal malignancy in the country, ranking second in incidence and fifth in mortality among all cancers. Screening colonoscopy and appropriate surveillance intervals can substantially reduce CRC-related deaths.

The latest 2020 U.S. Multi-Society Task Force (USMSTF) guidelines classify patients with 1-2 non-advanced adenomas (NAAs), 3-4 NAAs, and >4 NAAs as having low-, intermediate-, and high-risk colonoscopic findings, respectively, and recommend surveillance intervals of 7-10 years, 3-5 years, and 3 years for these groups. However, accumulating evidence suggests that the risk of developing metachronous advanced colorectal neoplastic lesions (ACRN) in individuals with 3-4 NAAs may be comparable to those with only 1-2 NAAs, raising concerns regarding the appropriateness of current surveillance recommendations.

Using a real-world, endoscopy database, this study systematically evaluates the association between different NAA counts and the subsequent risk of ACRN, providing evidence to inform optimization of post-polypectomy surveillance intervals.

Enrollment

2,955 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • First-time screening colonoscopy
  • Only non-advanced adenomas (no villous features, no high-grade dysplasia, and diameter <10 mm) were detected during first-time screening colonoscopy
  • Individuals with at least one surveillance colonoscopy
  • Complete electronic medical record and pathology information

Exclusion criteria

  • Inadequate bowel preparation (BBPS < 6)
  • Emergency colonoscopy
  • History of colorectal cancer
  • Incomplete pathology information or incompletely resected polyps
  • Screening colonoscopies performed by endoscopists with a low dynamic adenoma detection rate (ADR < 15%)
  • Follow-up duration < 6 months

Trial design

2,955 participants in 3 patient groups

Individuals with <3 NAAs detected during screening colonoscopy
Description:
Individuals with \<3 non-advanced adenomas detected during screening colonoscopy
Treatment:
Other: No Intervention: Observational Cohort
Individuals with 3-4 NAAs detected during screening colonoscopy
Description:
Individuals with 3-4 non-advanced adenomas detected during screening colonoscopy
Treatment:
Other: No Intervention: Observational Cohort
Individuals with >4 NAAs detected during screening colonoscopy
Description:
Individuals with \>4 non-advanced adenomas detected during screening colonoscopy
Treatment:
Other: No Intervention: Observational Cohort

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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