Skip to content

Screening for Stomach Diseases and Colorectal Neoplasms With the Fecal Testing

Screening for Stomach Diseases and Colorectal Neoplasms With the Fecal Testing: a Population-based Randomized Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01741363
Enrollment
99314
Registered
2012-12-04
Start date
2014-01-01
Completion date
2020-12-31
Last updated
2024-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer, Stomach Disease

Keywords

iFOBT, one-day sample, two-day sample, Helicobacter pylori stool antigen

Brief summary

1. 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. 2. 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: 1. 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; 2. 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. The primary outcomes were gastric cancer incidence and mortality rates as well as colorectal cancer incidence and mortality rates.

Interventions

OTHERFIT(Eiken OC-Sensor) Two-day sampling

Collect two stool samples in two separate days

OTHERFIT(Eiken OC-Sensor) One-year interval

Screening with one-year interval

OTHERFIT(Eiken OC-Sensor) One-day sampling

One-day sampling

OTHERFIT(Eiken OC-Sensor) Two-year interval

Screening with two-year interval

OTHERHpSA (Firstep Helicobacter pylori Antigen Rapid Test)

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.

HPSA+FIT compared with FIT alone.

Sponsors

Ministry of Health and Welfare, Taiwan
CollaboratorOTHER_GOV
National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
50 Years to 69 Years
Healthy volunteers
Yes

Inclusion criteria

* 50 to 69 years average-risk subjects for FIT * 50 to 69 years subjects for HpSA

Exclusion criteria

(for the FIT-based RCT): * Subjects who are unwilling to participate * Subjects ineligible for colonoscopy (for the one-day vs two day FIT screening)

Design outcomes

Primary

MeasureTime frameDescription
Incidence of Stomach Cancer5.5 yearsNumber of incident stomach cancer The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.
Mortality of Stomach Cancer5.5 yearsNumber of stomach cancer death The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.

Secondary

MeasureTime frameDescription
Mortality of Colorectal Cancer5.5 yearsNumber of colorectal cancer death The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.
Incidence of Colorectal Cancer5.5 yearsNumber of incident colorectal cancer The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.

Other

MeasureTime frameDescription
Helicobacter Pylori Eradication Rate5.5 yearsSubjects who received anti-H. pylori treatment. The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.
Detection of Non-advanced Adenoma5.5 yearsNumber of non-advanced adenoma from study population The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.
Confirmatory Examination Referral Rate5.5 yearsSubjects 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) The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.
Detection of Advanced Adenoma and Cancer5.5 yearsNumber of Advanced Adenoma and Colorectal Cancer The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.
Participation Rate of HpSA + FIT or FIT Only5.5 yearsNumber of participants from invitation population The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.

Countries

Taiwan

Participant flow

Recruitment details

2014/04/01 First patient first visit

Pre-assignment details

2018/09/27 Last patient last visit

Participants by arm

ArmCount
One-day Sampling With One-year Interval
FIT one-day sampling with one-year interval FIT(Eiken OC-Sensor) One-year interval: Screening with one-year interval FIT(Eiken OC-Sensor) One-day sampling: One-day sampling
9,076
One-day Sampling With Two-year Interval
FIT one-day sampling with two-year interval FIT(Eiken OC-Sensor) One-day sampling: One-day sampling FIT(Eiken OC-Sensor) Two-year interval: Screening with two-year interval
8,987
Two-day Sampling With One-year Interval
FIT two-day sampling with one-year interval FIT(Eiken OC-Sensor) Two-day sampling: Collect two stool samples in two separate days FIT(Eiken OC-Sensor) One-year interval: Screening with one-year interval
9,032
Two-day Sampling With Two-year Interval
FIT two-day sampling with two-year interval FIT(Eiken OC-Sensor) Two-day sampling: Collect two stool samples in two separate days FIT(Eiken OC-Sensor) Two-year interval: Screening with two-year interval
8,945
Hp Stool Antigen (HpSA)+FIT
HpSA for detection of upper gastrointestinal tract diseases and upper endoscopy for H. pylori carriers; HPSA combined with FIT HpSA (Firstep Helicobacter pylori Antigen Rapid Test): 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.
31,497
FIT Only
HPSA+FIT compared with FIT alone.
31,777
Total99,314

Baseline characteristics

CharacteristicOne-day Sampling With One-year IntervalOne-day Sampling With Two-year IntervalTwo-day Sampling With One-year IntervalTwo-day Sampling With Two-year IntervalHp Stool Antigen (HpSA)+FITFIT OnlyTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
1828 Participants1495 Participants1812 Participants1471 Participants6104 Participants6221 Participants18931 Participants
Age, Categorical
Between 18 and 65 years
7248 Participants7492 Participants7220 Participants7474 Participants25393 Participants25556 Participants80383 Participants
Gastric cancer and colorectal cancer incidence/mortality9076 Participants8987 Participants9032 Participants8945 Participants31497 Participants31777 Participants99314 Participants
Race/Ethnicity, Customized
Asian
9076 Participants8987 Participants9032 Participants8945 Participants31497 Participants31777 Participants99314 Participants
Sex: Female, Male
Female
5206 Participants4941 Participants5124 Participants4990 Participants18473 Participants18523 Participants57257 Participants
Sex: Female, Male
Male
3870 Participants4046 Participants3908 Participants3955 Participants13024 Participants13254 Participants42057 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
EG004
affected / at risk
EG005
affected / at risk
deaths
Total, all-cause mortality
0 / 9,0760 / 8,9870 / 9,0320 / 8,94534 / 31,49737 / 31,777
other
Total, other adverse events
0 / 9,0760 / 8,9870 / 9,0320 / 8,9450 / 31,4970 / 31,777
serious
Total, serious adverse events
0 / 9,0760 / 8,9870 / 9,0320 / 8,9450 / 31,4970 / 31,777

Outcome results

Primary

Incidence of Stomach Cancer

Number of incident stomach cancer The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.

Time frame: 5.5 years

Population: Average risk population

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Hp Stool Antigen (HpSA)+FITIncidence of Stomach Cancer49 Participants
FIT OnlyIncidence of Stomach Cancer59 Participants
Primary

Mortality of Stomach Cancer

Number of stomach cancer death The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.

Time frame: 5.5 years

Population: Average risk population

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Hp Stool Antigen (HpSA)+FITMortality of Stomach Cancer17 Participants
FIT OnlyMortality of Stomach Cancer23 Participants
Secondary

Incidence of Colorectal Cancer

Number of incident colorectal cancer The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.

Time frame: 5.5 years

Population: Average risk population

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Hp Stool Antigen (HpSA)+FITIncidence of Colorectal Cancer0 Participants
FIT OnlyIncidence of Colorectal Cancer0 Participants
Two-day Sampling With One-year IntervalIncidence of Colorectal Cancer0 Participants
Two-day Sampling With Two-year IntervalIncidence of Colorectal Cancer0 Participants
Secondary

Mortality of Colorectal Cancer

Number of colorectal cancer death The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.

Time frame: 5.5 years

Population: Average risk population

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Hp Stool Antigen (HpSA)+FITMortality of Colorectal Cancer0 Participants
FIT OnlyMortality of Colorectal Cancer0 Participants
Two-day Sampling With One-year IntervalMortality of Colorectal Cancer0 Participants
Two-day Sampling With Two-year IntervalMortality of Colorectal Cancer0 Participants
Other Pre-specified

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) The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.

Time frame: 5.5 years

Population: subjects with positive stool test

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Hp Stool Antigen (HpSA)+FITConfirmatory Examination Referral Rate328 Participants
FIT OnlyConfirmatory Examination Referral Rate473 Participants
Two-day Sampling With One-year IntervalConfirmatory Examination Referral Rate355 Participants
Two-day Sampling With Two-year IntervalConfirmatory Examination Referral Rate493 Participants
Hp Stool Antigen (HpSA) + FITConfirmatory Examination Referral Rate1724 Participants
FIT OnlyConfirmatory Examination Referral Rate1739 Participants
Other Pre-specified

Detection of Advanced Adenoma and Cancer

Number of Advanced Adenoma and Colorectal Cancer The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.

Time frame: 5.5 years

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Hp Stool Antigen (HpSA)+FITDetection of Advanced Adenoma and Cancer0 Participants
FIT OnlyDetection of Advanced Adenoma and Cancer0 Participants
Two-day Sampling With One-year IntervalDetection of Advanced Adenoma and Cancer0 Participants
Two-day Sampling With Two-year IntervalDetection of Advanced Adenoma and Cancer0 Participants
Other Pre-specified

Detection of Non-advanced Adenoma

Number of non-advanced adenoma from study population The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.

Time frame: 5.5 years

Population: Average risk population

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Hp Stool Antigen (HpSA)+FITDetection of Non-advanced Adenoma0 Participants
FIT OnlyDetection of Non-advanced Adenoma0 Participants
Two-day Sampling With One-year IntervalDetection of Non-advanced Adenoma0 Participants
Two-day Sampling With Two-year IntervalDetection of Non-advanced Adenoma0 Participants
Other Pre-specified

Helicobacter Pylori Eradication Rate

Subjects who received anti-H. pylori treatment. The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.

Time frame: 5.5 years

Population: subjects with HpSA positive test

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Hp Stool Antigen (HpSA)+FITHelicobacter Pylori Eradication Rate8809 Participants
Other Pre-specified

Participation Rate of HpSA + FIT or FIT Only

Number of participants from invitation population The recruitment period of participants was from January 1, 2014 to September 27, 2018. Final follow-up occurred December 31, 2020. For outcome measurement, the average follow-up time of the study participants was 5.5 years.

Time frame: 5.5 years

Population: Average risk population

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Hp Stool Antigen (HpSA)+FITParticipation Rate of HpSA + FIT or FIT Only31497 Participants
FIT OnlyParticipation Rate of HpSA + FIT or FIT Only31777 Participants

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026