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Uptake to Colorectal Cancer Screening in Familial-risk Population

Primary Purpose

Colorectal Cancer, Screening Uptake of Colonoscopy and FIT

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
annual FIT and colonoscopy in case of a positive test
colonoscopy with sedation
Sponsored by
Hospital Universitario de Canarias
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Colorectal Cancer focused on measuring Immunochemical fecal occult blood test, Colonoscopy, Screening uptake, Screening participation, Familiar risk, Colorectal Cancer

Eligibility Criteria

18 Years - 40 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. FDR with a case index meeting the following conditions: at least one case index < 60 years at diagnosis of the CCR;
  2. having ≥ 2 FDRs with CRC regardless the age of the case index at diagnosis;
  3. having a sibling with CRC;
  4. age <75 years.

Exclusion Criteria:

  1. past CRC screening;
  2. inflammatory bowel disease or past history of colorectal neoplasia;
  3. Family history of hereditary CRC;
  4. Abdominal symptoms;
  5. Colectomy;
  6. Severe comorbidity leading to a poor prognosis (life expectancy < 5 years);
  7. Refusal to participate in the study.

Sites / Locations

  • Federico Sopeña Biarge
  • Cristina Alvarez Urturi, MD
  • Maria Teresa Ocaña Bombardo
  • Inés Castro Novo
  • Patricia Muñoz Garrrido
  • Digestive Service, Huc
  • María Rodriguez Soler

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Fecal occult blood testing

one-time Colonoscopy

Arm Description

Annual FIT and colonoscopy in case of a positive test. Fecal occult blood testing: annual FIT (two rounds) without diet restriction, one stool sample. Positive cut-off = 10 μg Hemoglobin/g feces. Colonoscopy will be performed in case of a positive FIT.

One-time Colonoscopy with sedation

Outcomes

Primary Outcome Measures

Proportion of patients who participate in each screening arm

Secondary Outcome Measures

Efficacy measure: QALYs (Quality adjusted life years).
Costs measure: cost (euros) of the procedures associated with each screening strategy and treatment of advanced neoplastic lesions

Full Information

First Posted
September 29, 2015
Last Updated
August 7, 2020
Sponsor
Hospital Universitario de Canarias
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1. Study Identification

Unique Protocol Identification Number
NCT02567045
Brief Title
Uptake to Colorectal Cancer Screening in Familial-risk Population
Official Title
Uptake to Colorectal Cancer Screening in Familiar-risk Population: A Randomized Controlled Trial Comparing Immunochemical Fecal Occult Blood Test With Colonoscopy
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Completed
Study Start Date
February 25, 2016 (Actual)
Primary Completion Date
December 31, 2019 (Actual)
Study Completion Date
March 24, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital Universitario de Canarias

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a multicenter, controlled, randomized phase III study to compare participation rate with two screening rounds of fecal occult blood test (FIT) versus one-time screening colonoscopy in first degree relatives (FDR) of patients diagnosed of colorectal cancer (CRC). The hypothesis of the study is that annual FIT uptake and colonoscopy when a positive test is higher than that of straightforward colonoscopy. Assuming an uptake of 0.50 for colonoscopy and 0.60 for FIT, a Type I error (alpha) of 5% and a power of 90%, 538 FDRs will be necessary to include in each group.
Detailed Description
This is a multicenter, controlled, randomized phase III study to compare participation rate with two screening rounds of FIT versus one-time screening colonoscopy in FDR of patients diagnosed of CRC. The recruitment process will be programmed through the index case, that will be interviewed to obtain their CRC family history. FDR will be contacted in order to make an appointment in the High-risk CRC Clinic of the participant centers. Randomization will be performed before signing the informed consent to avoid selection bias. A researcher will be responsible to provide detailed information about the study and getting the informed consent. In case of willingness to participate in the study, the FDR will be randomized to one of the following arms: A) One-time colonoscopy; B) annual FIT for two screening rounds and a colonoscopy in case of a positive FIT (cut-off = 10 μg Hemoglobin/g feces). Screening uptake will be defined as the percentage of FDR who participate at least in one of the two FIT screening round in the FIT group or who undergo colonoscopy in the other group. Screening uptake will be calculated under the assumption of intention to screen analysis. The hypothesis of the study is that annual FIT uptake and colonoscopy when a positive test is higher than that of straightforward colonoscopy. Assuming an uptake of 0.50 for colonoscopy and 0.60 for FIT, a Type I error (alpha) of 5% and a power of 90%, 538 FDRs will be necessary to include in each group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer, Screening Uptake of Colonoscopy and FIT
Keywords
Immunochemical fecal occult blood test, Colonoscopy, Screening uptake, Screening participation, Familiar risk, Colorectal Cancer

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
Participants were randomized to either colonoscopy or faecal occult blood test
Allocation
Randomized
Enrollment
260 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Fecal occult blood testing
Arm Type
Experimental
Arm Description
Annual FIT and colonoscopy in case of a positive test. Fecal occult blood testing: annual FIT (two rounds) without diet restriction, one stool sample. Positive cut-off = 10 μg Hemoglobin/g feces. Colonoscopy will be performed in case of a positive FIT.
Arm Title
one-time Colonoscopy
Arm Type
Active Comparator
Arm Description
One-time Colonoscopy with sedation
Intervention Type
Procedure
Intervention Name(s)
annual FIT and colonoscopy in case of a positive test
Intervention Description
FIT and colonoscopy in case of a positive test. Annual interval (2 rounds), without diet restriction, 1 stool sample. Positive cut-off 10 mcg Hemoglobin/g feces.
Intervention Type
Procedure
Intervention Name(s)
colonoscopy with sedation
Intervention Description
One-time Colonoscopy with sedation.
Primary Outcome Measure Information:
Title
Proportion of patients who participate in each screening arm
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Efficacy measure: QALYs (Quality adjusted life years).
Time Frame
2 years
Title
Costs measure: cost (euros) of the procedures associated with each screening strategy and treatment of advanced neoplastic lesions
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: FDR with a case index meeting the following conditions: at least one case index < 60 years at diagnosis of the CCR; having ≥ 2 FDRs with CRC regardless the age of the case index at diagnosis; having a sibling with CRC; age <75 years. Exclusion Criteria: past CRC screening; inflammatory bowel disease or past history of colorectal neoplasia; Family history of hereditary CRC; Abdominal symptoms; Colectomy; Severe comorbidity leading to a poor prognosis (life expectancy < 5 years); Refusal to participate in the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Enrique Quintero, MD, PhD
Organizational Affiliation
Hospital Universitario de Canarias
Official's Role
Study Director
Facility Information:
Facility Name
Federico Sopeña Biarge
City
Zaragoza
State/Province
Aragón
ZIP/Postal Code
50009
Country
Spain
Facility Name
Cristina Alvarez Urturi, MD
City
Barcelona
State/Province
Cataluña
ZIP/Postal Code
08003
Country
Spain
Facility Name
Maria Teresa Ocaña Bombardo
City
Barcelona
State/Province
Cataluña
ZIP/Postal Code
08036
Country
Spain
Facility Name
Inés Castro Novo
City
Ourense
State/Province
Galicia
ZIP/Postal Code
32005
Country
Spain
Facility Name
Patricia Muñoz Garrrido
City
San Sebastián
State/Province
País Vasco, Gipuzcoa
ZIP/Postal Code
20080
Country
Spain
Facility Name
Digestive Service, Huc
City
La Laguna
State/Province
S/C DE Tenerife
ZIP/Postal Code
38320
Country
Spain
Facility Name
María Rodriguez Soler
City
Alicante
ZIP/Postal Code
03010
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
25127679
Citation
Quintero E, Carrillo M, Gimeno-Garcia AZ, Hernandez-Guerra M, Nicolas-Perez D, Alonso-Abreu I, Diez-Fuentes ML, Abraira V. Equivalency of fecal immunochemical tests and colonoscopy in familial colorectal cancer screening. Gastroenterology. 2014 Nov;147(5):1021-30.e1; quiz e16-7. doi: 10.1053/j.gastro.2014.08.004. Epub 2014 Aug 13.
Results Reference
result
PubMed Identifier
22356323
Citation
Quintero E, Castells A, Bujanda L, Cubiella J, Salas D, Lanas A, Andreu M, Carballo F, Morillas JD, Hernandez C, Jover R, Montalvo I, Arenas J, Laredo E, Hernandez V, Iglesias F, Cid E, Zubizarreta R, Sala T, Ponce M, Andres M, Teruel G, Peris A, Roncales MP, Polo-Tomas M, Bessa X, Ferrer-Armengou O, Grau J, Serradesanferm A, Ono A, Cruzado J, Perez-Riquelme F, Alonso-Abreu I, de la Vega-Prieto M, Reyes-Melian JM, Cacho G, Diaz-Tasende J, Herreros-de-Tejada A, Poves C, Santander C, Gonzalez-Navarro A; COLONPREV Study Investigators. Colonoscopy versus fecal immunochemical testing in colorectal-cancer screening. N Engl J Med. 2012 Feb 23;366(8):697-706. doi: 10.1056/NEJMoa1108895. Erratum In: N Engl J Med. 2016 May 12;374(19):1898.
Results Reference
result
PubMed Identifier
19307987
Citation
Pappadopulos E, Jensen PS, Chait AR, Arnold LE, Swanson JM, Greenhill LL, Hechtman L, Chuang S, Wells KC, Pelham W, Cooper T, Elliott G, Newcorn JH. Medication adherence in the MTA: saliva methylphenidate samples versus parent report and mediating effect of concomitant behavioral treatment. J Am Acad Child Adolesc Psychiatry. 2009 May;48(5):501-510. doi: 10.1097/CHI.0b013e31819c23ed.
Results Reference
result
PubMed Identifier
16243849
Citation
Dove-Edwin I, Sasieni P, Adams J, Thomas HJ. Prevention of colorectal cancer by colonoscopic surveillance in individuals with a family history of colorectal cancer: 16 year, prospective, follow-up study. BMJ. 2005 Nov 5;331(7524):1047. doi: 10.1136/bmj.38606.794560.EB. Epub 2005 Oct 21.
Results Reference
result

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Uptake to Colorectal Cancer Screening in Familial-risk Population

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