Screening for Stomach Diseases and Colorectal Neoplasms With the Fecal Testing
Primary Purpose
Colorectal Cancer, Stomach Disease
Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
FIT(Eiken OC-Sensor) Two-day sampling
FIT(Eiken OC-Sensor) One-year interval
FIT(Eiken OC-Sensor) One-day sampling
FIT(Eiken OC-Sensor) Two-year interval
HpSA (Firstep Helicobacter pylori Antigen Rapid Test)
Sponsored by
About this trial
This is an interventional prevention trial for Colorectal Cancer focused on measuring iFOBT, one-day sample, two-day sample, Helicobacter pylori stool antigen
Eligibility Criteria
Inclusion Criteria:
- 50 to 75 years average-risk subjects for FIT
- 50 to 75 years subjects for HpSA
Exclusion Criteria:
- Subjects who are unwilling to participate
- Subjects ineligible for endoscopy
Sites / Locations
- National Taiwan University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm Type
Experimental
Active Comparator
Experimental
Experimental
Experimental
Arm Label
one-day sampling with one-year interval
one-day sampling with two-year interval
two-day sampling with one-year interval
two-day sampling with two-year interval
Hp stool antigen (HpSA)+FIT
Arm Description
FIT one-day sampling with one-year interval
FIT one-day sampling with two-year interval
FIT two-day sampling with one-year interval
FIT two-day sampling with two-year interval
HpSA for detection of upper gastrointestinal tract diseases and upper endoscopy for H. pylori carriers; HPSA combined with FIT
Outcomes
Primary Outcome Measures
Detection rate for advanced adenoma and cancer
Detection rate for advanced adenoma per 1000 screened subjects and detection rate for invasive cancers per 1000 screened subjects
Detection rate of upper gastrointestinal tract diseases
Detection rate for important upper gastrointestinal tract lesions and important upper gastrointestinal tract neoplastic lesions per 1000 screened subjects.
Secondary Outcome Measures
Participation rate for the FIT and/or HpSA
participation rate=tested population/ target or invited population
Detection rates for non-advanced adenoma
Detection rate for non-advanced adenoma per 1000 screened subjects
Confirmatory examination referral rate
Subjects who received confirmatory examinations (colonoscopy or flexible sigmoidoscopy plus double contrast barium enema for lower gastrointestinal tract disease; esophagogastroduodenoscopy for upper gastrointestinal tract disease) / subjects with positive stool test (FIT or HpSA)
Mortality rate from colorectal cancer
Number of colorectal cancer death / person-year of each study arm
Incidence of colorectal cancer
Number of incident colorectal cancer / person-year of each study arm
Incidence of stomach cancer
Number of incident stomach cancer / person-year of each study arm
Mortality rate from stomach cancer
Number of stomach cancer death / person-year of each study arm
Helicobacter pylori eradication rate
Subjects who received anti-H. pylori treatment.
Full Information
NCT ID
NCT01741363
First Posted
October 5, 2012
Last Updated
October 23, 2015
Sponsor
National Taiwan University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01741363
Brief Title
Screening for Stomach Diseases and Colorectal Neoplasms With the Fecal Testing
Official Title
Screening for Stomach Diseases and Colorectal Neoplasms With the Fecal Testing: a Population-based Randomized Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2015
Overall Recruitment Status
Unknown status
Study Start Date
July 2012 (undefined)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Taiwan University Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The abundant results from this trial will be helpful for assessing the feasibility of increasing stool sampling and shortening screening interval in population setting for lower and upper gastrointestinal tract lesions, their long-term effects, and the respective cost-effectiveness.
The study will evaluate the value of population-based screen and treatment for H. pylori infection when the HPSA is combined with the FIT.
Detailed Description
Growing body of evidences have shown that fecal immunochemical test (FIT) outperform guaiac fecal occult blood test (gFOBT) in terms of sensitivity, neoplasm detection rate and public participation. Though direct outcome evidence is still lacking for FIT, it is anticipated to have higher colorectal cancer (CRC) mortality and incidence reduction compared with gFOBT. In Taiwan, nation-wide CRC screening program has been launched since the year of 2004 ,which provides biennial FIT screening for adults aged 50 to 69 years. Currently available data from the Bureau of Health Promotion has shown a significant stage-shift effect, an early indicator of screening effectiveness, by this screening program.
Nevertheless, the aforementioned advantages of FIT, missed neoplasms and interval cancer still exists under the current one-day stool sampling method with biennial screening interval, which might affect the effectiveness of overall screening program. Increase the number of stool samples or shortening of screening interval may be helpful for early detection of clinically significant neoplasms but it remains unclear whether such an approach may lower the screenee compliance or public participation. Moreover, its impact on the demand of confirmatory colonoscopy and cost-effectiveness of the whole screening program is still largely unknown and need to be further investigated.
In this study, we firstly aim to randomly allocate screening attendee to one of the following four arms: one-day sampling with annual screening, one-day sampling with biennial screening, two-day sampling with annual screening, and two-day sampling with biennial screening. Participation rate, positive rates of FIT, detection rate for neoplasms, positive predictive value, and long-term outcome including cancer incidence and mortality will be calculated and compared among four groups.
Secondly, in the Taiwanese population, which is a typical presentation of Asian populations, although the incidence of colorectal cancer is rapidly increasing, Helicobacter pylori-related upper gastrointestinal pathologies remain highly prevalent, which may imply that mass screening solely based on FIT could be insufficient as significant upper GI pathologies can be missed. Since the FIT does not predict upper GI pathologies, the adjunct of an「Helicobacter pylori stool-antigen test (HpSA) 」 may be a potential candidate to realize a pan-detecting assay based on stool samples in a population in which both lower and upper GI lesions are equally prevalent. Therefore, in the present study, we will also evaluate the value of simultaneous FIT and HpSA test in the community-based mass screening. We invited subjects in a randomized study to receive the FIT or the FIT plus HPSA. Those who are tested positive for HPSA will receive upper endoscopic examination and anti-H. pylori treatment. For the short-term indicators, we will evaluate the participation rate and diagnostic yield when the HPSA is added. For the long-term indicators, we will compare the incidence and mortality of gastric cancer as well as complicated peptic ulcers.
To summary, this study includes two randomized trials:
To make a comparison between one-day sampling with annual screening, one-day sampling with biennial screening, two-day sampling with annual screening, and two-day sampling with biennial screening using FIT;
To make a comparison between FIT plus HpSA and FIT alone for screening.
Finally, the cost-effectiveness analysis will be also conducted using previously established Markov model of CRC natural history and stomach diseases (such as dyspepsia, peptic ulcer disease, and gastric cancer) using the results ascertained from this trial.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer, Stomach Disease
Keywords
iFOBT, one-day sample, two-day sample, Helicobacter pylori stool antigen
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
40000 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
one-day sampling with one-year interval
Arm Type
Experimental
Arm Description
FIT one-day sampling with one-year interval
Arm Title
one-day sampling with two-year interval
Arm Type
Active Comparator
Arm Description
FIT one-day sampling with two-year interval
Arm Title
two-day sampling with one-year interval
Arm Type
Experimental
Arm Description
FIT two-day sampling with one-year interval
Arm Title
two-day sampling with two-year interval
Arm Type
Experimental
Arm Description
FIT two-day sampling with two-year interval
Arm Title
Hp stool antigen (HpSA)+FIT
Arm Type
Experimental
Arm Description
HpSA for detection of upper gastrointestinal tract diseases and upper endoscopy for H. pylori carriers; HPSA combined with FIT
Intervention Type
Other
Intervention Name(s)
FIT(Eiken OC-Sensor) Two-day sampling
Intervention Description
Collect two stool samples in two separate days
Intervention Type
Other
Intervention Name(s)
FIT(Eiken OC-Sensor) One-year interval
Intervention Description
Screening with one-year interval
Intervention Type
Other
Intervention Name(s)
FIT(Eiken OC-Sensor) One-day sampling
Intervention Description
One-day sampling
Intervention Type
Other
Intervention Name(s)
FIT(Eiken OC-Sensor) Two-year interval
Intervention Description
Screening with two-year interval
Intervention Type
Other
Intervention Name(s)
HpSA (Firstep Helicobacter pylori Antigen Rapid Test)
Intervention Description
HpSA for detection of upper gastrointestinal diseases; screen and treat for H. pylori infection. Upper endoscopy for H. pylori carriers. HPSA+FIT compared with FIT alone.
Primary Outcome Measure Information:
Title
Detection rate for advanced adenoma and cancer
Description
Detection rate for advanced adenoma per 1000 screened subjects and detection rate for invasive cancers per 1000 screened subjects
Time Frame
6 years
Title
Detection rate of upper gastrointestinal tract diseases
Description
Detection rate for important upper gastrointestinal tract lesions and important upper gastrointestinal tract neoplastic lesions per 1000 screened subjects.
Time Frame
6 years
Secondary Outcome Measure Information:
Title
Participation rate for the FIT and/or HpSA
Description
participation rate=tested population/ target or invited population
Time Frame
6 years
Title
Detection rates for non-advanced adenoma
Description
Detection rate for non-advanced adenoma per 1000 screened subjects
Time Frame
6 years
Title
Confirmatory examination referral rate
Description
Subjects who received confirmatory examinations (colonoscopy or flexible sigmoidoscopy plus double contrast barium enema for lower gastrointestinal tract disease; esophagogastroduodenoscopy for upper gastrointestinal tract disease) / subjects with positive stool test (FIT or HpSA)
Time Frame
6 years
Title
Mortality rate from colorectal cancer
Description
Number of colorectal cancer death / person-year of each study arm
Time Frame
Anticipated 10 years
Title
Incidence of colorectal cancer
Description
Number of incident colorectal cancer / person-year of each study arm
Time Frame
Anticipated 10 years
Title
Incidence of stomach cancer
Description
Number of incident stomach cancer / person-year of each study arm
Time Frame
Anticipated 10 years
Title
Mortality rate from stomach cancer
Description
Number of stomach cancer death / person-year of each study arm
Time Frame
Anticipated 10 years
Title
Helicobacter pylori eradication rate
Description
Subjects who received anti-H. pylori treatment.
Time Frame
6 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
50 to 75 years average-risk subjects for FIT
50 to 75 years subjects for HpSA
Exclusion Criteria:
Subjects who are unwilling to participate
Subjects ineligible for endoscopy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Han-Mo Chiu, M.D., Ph.D.
Phone
+886-2-23123456 ext 63354
Email
hanmochiu@ntu.edu.tw
First Name & Middle Initial & Last Name or Official Title & Degree
Yi-Chia Lee, M.D., Ph.D.
Phone
+886-2-23123456 ext 63351
Email
yichialee@ntu.edu.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Han-Mo Chiu, M.D., Ph.D.
Organizational Affiliation
Department of Internal Medicine & Health Management Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Yi-Chia Lee, M.D., Ph.D.
Organizational Affiliation
National Taiwan University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Taiwan University Hospital
City
Taipei
ZIP/Postal Code
10002
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Han-Mo Chiu, M.D., Ph.D.
Phone
+886-2-23123456 ext 63354
Ext
63354
Email
hanmochiu@ntu.edu.tw
First Name & Middle Initial & Last Name & Degree
Yi-Chia Lee, M.D., Ph.D.
Phone
+886-2-23123456 ext 63351
Ext
63351
Email
yichialee@ntu.edu.tw
First Name & Middle Initial & Last Name & Degree
Han-Mo Chiu, M.D., Ph.D.
12. IPD Sharing Statement
Citations:
PubMed Identifier
33444571
Citation
Lee YC, Chiang TH, Chiu HM, Wu MS, Yeh YP, Hsiu-Hsi Chen T; Collaborators of the Taiwan Community-Based Integrated Screening Group. Community-Based Gastric Cancer Screening Coupled With a National Colorectal Cancer Screening Program: Baseline Results. Gastroenterology. 2021 May;160(6):2159-2161.e4. doi: 10.1053/j.gastro.2021.01.008. Epub 2021 Jan 11. No abstract available.
Results Reference
derived
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Screening for Stomach Diseases and Colorectal Neoplasms With the Fecal Testing
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