Polyprev: Study to Compare Fecal Immunochemical Test With Endoscopic Surveillance After Advanced Adenoma Resection in Fecal Immunochemical Test Colorectal Cancer Screening Programs.
Primary Purpose
Colorectal Cancer
Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Annual FIT
Endoscopic surveillance.
Sponsored by
About this trial
This is an interventional screening trial for Colorectal Cancer focused on measuring Screening program, Endoscopic surveillance, Fecal immunochemical test, Mediterranean diet, Physical activity
Eligibility Criteria
Inclusion Criteria:
- Individuals aged 50 to 65 years.
- Individuals with at least one advanced adenoma (tubulovillous or villous histology, high grade dysplasia or ≥ 10mm), and / or at least three non-advanced adenomas detected and resected completely within the population-based CRC screening program.
Exclusion Criteria:
- Personal history of CRC.
- Colonic lesion ≥10mm resected without histological diagnosis.
- More than 10 adenomas in baseline colonoscopy.
- Serrated polyposis syndrome.
- Two or more first-degree relatives with CRC.
- Hereditary predisposition to CRC.
- Relevant comorbidity with life expectancy inferior to 5 years.
- Colonoscopy with incomplete mucosal examination.
- Incomplete resection of baseline lesions.
- Non-acceptance after reading the informed consent.
Sites / Locations
- Complexo Hospitalario Universitario de OurenseRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Group I
Group II
Arm Description
Annual FIT surveillance
Endoscopic surveillance
Outcomes
Primary Outcome Measures
Rate of invasive CRC
It is the main outcome of the study. Invasive CRC is defined as colonic adenocarcinoma that invades the submucosa. Adenocarcinomas in situ and intramucosal carcinomas will not be considered as invasive CRC.
Rate of interval CRC
Interval CRC is defined as the CRC detected between two organized surveillance (FIT or colonoscopy).
Mortality
The deaths and their cause will be collected: associated with CRC, associated with adverse effects of screening or unrelated.
Rate of advanced colonic lesions
Advanced colonic lesions will be defined as advanced adenomas (at least 10mm, hairy histology or high grade dysplasia) or advanced serrated lesions (at least 10mm or with dysplasia).
Frequency of participation in the surveillance strategy
According to the methodology of the information systems of the screening programs, three categories will be defined: non-participation, irregular participation, regular participation.
Adverse effects
Adverse effects associated with surveillance are defined as complications that require hospitalization. Those related to the surgical treatment of benign colonic lesions will be included as adverse effects.
Secondary Outcome Measures
CRC, adenoma and advanced serrated lesions at three years
Detection of CRC, adenoma and advanced serrated lesion will be collected at 3 years of follow-up.
Physical activity
We will use the International Physical Activity. Questionnaire (IPAQ) to mesure physical activity.
Mediterranean lifestyle
We will use the Mediterranean Lifestyle index (MEDLIFE) to measure overall adherence to the Mediterranean lifestyle.
Preferences of the subjects
We will use a survey with vignette questions to evaluate the values and preferences of the subjects regarding surveillance.
Full Information
NCT ID
NCT04967183
First Posted
July 8, 2021
Last Updated
March 23, 2023
Sponsor
Fundacin Biomedica Galicia Sur
1. Study Identification
Unique Protocol Identification Number
NCT04967183
Brief Title
Polyprev: Study to Compare Fecal Immunochemical Test With Endoscopic Surveillance After Advanced Adenoma Resection in Fecal Immunochemical Test Colorectal Cancer Screening Programs.
Official Title
Polyprev Study: Randomized, Multicenter, Controlled Trial Comparing Fecal Immunochemical Test With Endoscopic Surveillance After Advanced Adenoma Resection in Fecal Immunochemical Test Colorectal Cancer Screening Programs.
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 1, 2022 (Actual)
Primary Completion Date
June 2023 (Anticipated)
Study Completion Date
June 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fundacin Biomedica Galicia Sur
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Colorectal cancer (CRC) screening programs have been implemented to reduce the burden of the disease. When an advanced colonic lesions is detected, it is recommended to perform endoscopic surveillance with different intervals between explorations. Although the reduction in CRC incidence, endoscopic surveillance is producing a considerable increase in the number of colonoscopies. However, participation in CRC screening programs based on the fecal immunochemical test (FIT) could be a non inferior alternative to endoscopic surveillance.
Based on this hypothesis, the research group have designed a randomized clinical trial within the population CRC screening programs to compare FIT surveillance to endoscopic surveillance in patients with advanced lesions resected.
Detailed Description
Colorectal cancer (CRC) is one of the most common malignancies in western countries. CRC screening programs have been implemented in order to reduce the burden of the disease. Screening programs in Spain are based on the biennial detection of fecal hemoglobin with a fecal immunochemical test (FIT) and a diagnostic colonoscopy if positive. The detection of at least one advanced adenoma or serrated lesion defines a high risk situation for metachronous CRC. This group of patients is recommended to perform endoscopic surveillance with different intervals between explorations. Endoscopic surveillance reduces mortality only 1.7% and increases the number of colonoscopies by 62% with an additional cost of € 68,000 for an increase of 0.9 years of life. Moreover, colonoscopy is a procedure associated with potentially serious side effects.
A recently British study shows that with a cut-off of 10 µg/g, FIT has a higher sensitivity and specificity for CRC with a significant cost reduction compared to colonoscopy surveillance. Additionally, most of the population prefers non-invasive faecal tests rather than colonoscopy.
Based on this evidence, the research group have designed a multicenter, randomized clinical trial to compare the 10 year CRC incidence after resection of advanced colonic lesions detected within CRC screening programs between endoscopic surveillance and participation in CRC screening programs based on FIT.
Apart from this purpose, the investigators will also assess the values and preferences regarding surveillance and risk of CRC. Further, the research group will evaluate the relationship between Mediterranean diet and physical activity with the detection of advanced adenomas and CRC.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
Screening program, Endoscopic surveillance, Fecal immunochemical test, Mediterranean diet, Physical activity
7. Study Design
Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients will be identified in population CRC secreening programs of Galicia, the Basque Country, the Region of Valencia and Murcia. We will considered individuals aged 50 to 65 years with at least one advanced adenoma (tubulovillous or villous histology, high grade dysplasia or ≥ 10mm), and / or at least three non-advanced adenomas detected and resected completely within the population-based CRC screening program.
Patients will be randomly allocated to perform an annual FIT and colonoscopy if fecal hemoglobin concentration is ≥10µg/g, or to perform endoscopic surveillance. Patients will be also stratified into two groups: ≥5 adenomas or an adenoma ≥20mm and the rest of patients.
Patients will be followed for a period of 10 years.
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
3788 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Group I
Arm Type
Experimental
Arm Description
Annual FIT surveillance
Arm Title
Group II
Arm Type
Active Comparator
Arm Description
Endoscopic surveillance
Intervention Type
Diagnostic Test
Intervention Name(s)
Annual FIT
Intervention Description
Patients will be offered an annual FIT and colonoscopy will be performed if fecal hemoglobin concentration is ≥10µg / g of feces. After performing a colonoscopy the FIT will be sent to the patient:
After one year if the unscheduled colonoscopy has been incomplete or a lesion requiring endoscopic surveillance has been completely resected.
After five years if the colonoscopy has evaluated the entire mucosa, it is normal or with lesions that do not require endoscopic surveillance (1-2 non-advanced adenomas).
Intervention Type
Procedure
Intervention Name(s)
Endoscopic surveillance.
Intervention Description
First surveillance colonoscopy will be performed in three-year time. If an advanced adenoma or at least three non-advanced adenomas are detected, colonoscopy will be repeated after 3 years. In contrast, if colonoscopy is normal or 1-2 non-advanced adenomas are detected, colonoscopy will be repeated after 5 years.
Primary Outcome Measure Information:
Title
Rate of invasive CRC
Description
It is the main outcome of the study. Invasive CRC is defined as colonic adenocarcinoma that invades the submucosa. Adenocarcinomas in situ and intramucosal carcinomas will not be considered as invasive CRC.
Time Frame
10 years
Title
Rate of interval CRC
Description
Interval CRC is defined as the CRC detected between two organized surveillance (FIT or colonoscopy).
Time Frame
10 years
Title
Mortality
Description
The deaths and their cause will be collected: associated with CRC, associated with adverse effects of screening or unrelated.
Time Frame
10 years
Title
Rate of advanced colonic lesions
Description
Advanced colonic lesions will be defined as advanced adenomas (at least 10mm, hairy histology or high grade dysplasia) or advanced serrated lesions (at least 10mm or with dysplasia).
Time Frame
10 years
Title
Frequency of participation in the surveillance strategy
Description
According to the methodology of the information systems of the screening programs, three categories will be defined: non-participation, irregular participation, regular participation.
Time Frame
10 years
Title
Adverse effects
Description
Adverse effects associated with surveillance are defined as complications that require hospitalization. Those related to the surgical treatment of benign colonic lesions will be included as adverse effects.
Time Frame
10 years
Secondary Outcome Measure Information:
Title
CRC, adenoma and advanced serrated lesions at three years
Description
Detection of CRC, adenoma and advanced serrated lesion will be collected at 3 years of follow-up.
Time Frame
3 years
Title
Physical activity
Description
We will use the International Physical Activity. Questionnaire (IPAQ) to mesure physical activity.
Time Frame
3 years
Title
Mediterranean lifestyle
Description
We will use the Mediterranean Lifestyle index (MEDLIFE) to measure overall adherence to the Mediterranean lifestyle.
Time Frame
3 years
Title
Preferences of the subjects
Description
We will use a survey with vignette questions to evaluate the values and preferences of the subjects regarding surveillance.
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Individuals aged 50 to 65 years.
Individuals with at least one advanced adenoma (tubulovillous or villous histology, high grade dysplasia or ≥ 10mm), and / or at least three non-advanced adenomas detected and resected completely within the population-based CRC screening program.
Exclusion Criteria:
Personal history of CRC.
Colonic lesion ≥10mm resected without histological diagnosis.
More than 10 adenomas in baseline colonoscopy.
Serrated polyposis syndrome.
Two or more first-degree relatives with CRC.
Hereditary predisposition to CRC.
Relevant comorbidity with life expectancy inferior to 5 years.
Colonoscopy with incomplete mucosal examination.
Incomplete resection of baseline lesions.
Non-acceptance after reading the informed consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Joaquín Cubiella, MD PhD
Phone
0034988385824
Email
joaquin.cubiella.fernandez@sergas.es
Facility Information:
Facility Name
Complexo Hospitalario Universitario de Ourense
City
Ourense
ZIP/Postal Code
32002
Country
Spain
Individual Site Status
Recruiting
12. IPD Sharing Statement
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Links:
URL
https://redecan.org/redecan.org/es/444_Estimaciones_Incidencia_y_Supervi_Cancer_en_Espa_na_2014_DEF_DEF3a26.pdf?file=257&area=196
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Polyprev: Study to Compare Fecal Immunochemical Test With Endoscopic Surveillance After Advanced Adenoma Resection in Fecal Immunochemical Test Colorectal Cancer Screening Programs.
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