A Personalized Surveillance and Intervention Protocol for Patients With Familial Adenomatous Polyposis That Have Undergone (Procto)Colectomy
NCT ID: NCT04678011
Last Updated: 2025-10-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
1000 participants
OBSERVATIONAL
2021-11-24
2026-11-30
Brief Summary
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Detailed Description
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After both types of prophylactic colorectal surgery, subtotal colectomy with IRA/ISA or proctocolectomy with IPAA, patients will require life-long surveillance because disease progression and development of new adenomas in retained rectum, pouch or residual rectal cuff will occur.
The 10-years risk of developing one or more adenomas in the rectum after IRA is 100% compared to 33% in the pouch after IPAA. The risk of developing rectal cancer after IRA was found to be 9% and 11% in two large studies with a median follow-up of 12.8 and 15 years, respectively. One study showed that the 10-years risk of developing a carcinoma in the pouch was 1%. As patients are usually operated at a young age, and nowadays have a long life-expectancy, the actual cumulative life-time risk will presumably be higher.
The recently published ESGE (European Society of Gastrointestinal Endoscopy) polyposis guideline recommends a one to two yearly endoscopic surveillance interval after prophylactic colorectal surgery in FAP, both for patients that underwent IRA/ISA and IPAA, with removal of all polyps \>5mm. This recommendation is based on expert-opinion, since no studies have been reported comparing the efficacy and safety of different surveillance intervals. No advices are provided on which patients will benefit from which surveillance interval.
With the proposed study, the investigators aim to provide evidence for personalized endoscopic surveillance for patients with FAP that have undergone (procto)colectomy with construction of an IRA/ISA or IPAA with the goal to prevent development of advanced neoplasia (AN) by endoscopically removing lesions before they progress to AN.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Personalized surveillance and intervention protocol
Personalized surveillance and intervention protocol
This study uses one arm. Participants will undergo endoscopic surveillance with intervals between 6 months and 2 years, depending on severity of polyposis and performed endoscopic interventions.
Interventions
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Personalized surveillance and intervention protocol
This study uses one arm. Participants will undergo endoscopic surveillance with intervals between 6 months and 2 years, depending on severity of polyposis and performed endoscopic interventions.
Eligibility Criteria
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Inclusion Criteria
* Have undergone prophylactic (procto)colectomy with IRA/ISA or IPAA
* Age 18 years or older
Exclusion Criteria
* Cancer at baseline endoscopy
* Need for surgery
18 Years
ALL
No
Sponsors
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Leiden University Medical Center
OTHER
The Netherlands Cancer Institute
OTHER
St Mark's Hospital Foundation
OTHER
Hospital Clinic of Barcelona
OTHER
Hôpital Edouard Herriot
OTHER
Maria Sklodowska-Curie National Research Institute of Oncology
OTHER
Hospital General Universitario de Alicante
OTHER
University Medical Center Mainz
OTHER
IRCCS Azienda Ospedaliero-Universitaria di Bologna
OTHER
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
OTHER
Responsible Party
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Prof. Evelien Dekker, MD, PhD
Prof. dr. Evelien Dekker, MD, PhD
Locations
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Academic Medical Centre
Amsterdam, North Holland, Netherlands
Countries
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Facility Contacts
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Other Identifiers
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W20_182
Identifier Type: -
Identifier Source: org_study_id
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