European Polyp Surveillance Trial (EPoS)

Asociación Española de Gastroenterología

Status: Active, not recruiting

Conditions: Colorectal Neoplasms

Treatments: Procedure: Colonoscopy

Study type: Interventional

Funder types: Other

Identifiers

NCT02319928

AEG-EPOS-1

Details and patient eligibility

About

This protocol describes the epos (ancient greek (Επος) for "story") of a group of related clinical trials aiming at addressing one of the most important unsolved challenges in the prevention of colorectal cancer (one of our major cancer killers); the surveillance of patients with premalignant polyps in the large bowel.

This project is timely because large scale colorectal cancer screening programmes are currently rolled out in most Western countries. These programmes are diagnosing large numbers of individuals with premalignant polyps (adenomas and serrated polyps). This creates both a diagnostic and resource dilemma, because the optimal surveillance strategy for these individuals to reduce future cancer risk is currently unknown..

The EPoS trials will randomize or register more than 20,000 individuals in different European countries to different surveillance colonoscopy intervals to disentangle the most effective and cost-effective surveillance strategy for the population. Subjects will be randomized according to their presenting polyp chracteristics The EPoS I trial randomizes patients with low-risk adenomas into 5 or 10-year surveillance; ; EPoS II randomizes patients with high-risk adenomas into 3 or 5-yearly surveillance ; EPoS III will include patients with serrated polyps in a one-arm study with surveillance after 5 and 10 years. The primary endpoint for all three trials is incidence of colorectal cancer after 10 years of follow-up.

This EPoS trials are the largest in polyp surveillance ever conducted. They address a clinical problem affecting hundreds of thousand individuals in Europe and the US each year, it has a large size, and should thus provide definitive results.

Enrollment: 20,000 estimated patients

Sex: All

Ages: 40 to 74 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Cecal intubation (preferably documented by images/videoof the apendiceal orifice and the ileocecal valve; but not required).
• Adequate colonic cleansing, with Boston Bowel Cleansing Score equal or higher than 2 points in all colonic segments.
• Complete excision of all polyps at baseline colonoscopy findings (as judged by the trial endoscopists).

Exclusion criteria

• Lack of consent
• History of CRC or adenomas
• History of serrated polyps ≥ 10 mm in diameter at any colorectal location or ≥ 5 mm if located proximal to the splenic flexure
• Incomplete colonoscopy
• Incomplete endoscopic excision of polyps
• Genetic cancer syndrome (adenomatous or serrated polyposis syndrome; Lynch or Lynch-like syndrome)
• Inflammatory bowel disease
• History of surgical colon resection for any reason
• Severe co-morbidity with reduced life expectancy (NYHA 3-4)
• On-going cytotoxic treatment or radiotherapy for malignant disease
• Long-lasting attention and nursing services (somatic or psychosocial, mental retardation).

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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20,000 participants in 2 patient groups

Short-term surveillance

Active Comparator group

Description:

Short-term surveillance. Colonoscopy at 5+10 years in low-risk adenomas or 3+5 years in high-risk adenomas.

Treatment:

Procedure: Colonoscopy

Long-term surveillance

Experimental group

Description:

Long-term surveillance. Colonoscopy at 10 years in low-risk adenomas or 5 years in high-risk adenomas.

Treatment:

Procedure: Colonoscopy