Colorectal Cancer, Stomach Disease
Conditions
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
Collect two stool samples in two separate days
Screening with one-year interval
One-day sampling
Screening with two-year interval
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
Study design
Eligibility
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
| Measure | Time frame | Description |
|---|---|---|
| Incidence of Stomach Cancer | 5.5 years | 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. |
| Mortality of Stomach Cancer | 5.5 years | 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. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Mortality of Colorectal Cancer | 5.5 years | 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. |
| Incidence of Colorectal Cancer | 5.5 years | 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. |
Other
| Measure | Time frame | Description |
|---|---|---|
| Helicobacter Pylori Eradication Rate | 5.5 years | 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. |
| Detection of Non-advanced Adenoma | 5.5 years | 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. |
| Confirmatory Examination Referral Rate | 5.5 years | 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. |
| Detection of Advanced Adenoma and Cancer | 5.5 years | 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. |
| Participation Rate of HpSA + FIT or FIT Only | 5.5 years | 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. |
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
| Arm | Count |
|---|---|
| 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 |
| Total | 99,314 |
Baseline characteristics
| Characteristic | 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 | FIT Only | Total |
|---|---|---|---|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 1828 Participants | 1495 Participants | 1812 Participants | 1471 Participants | 6104 Participants | 6221 Participants | 18931 Participants |
| Age, Categorical Between 18 and 65 years | 7248 Participants | 7492 Participants | 7220 Participants | 7474 Participants | 25393 Participants | 25556 Participants | 80383 Participants |
| Gastric cancer and colorectal cancer incidence/mortality | 9076 Participants | 8987 Participants | 9032 Participants | 8945 Participants | 31497 Participants | 31777 Participants | 99314 Participants |
| Race/Ethnicity, Customized Asian | 9076 Participants | 8987 Participants | 9032 Participants | 8945 Participants | 31497 Participants | 31777 Participants | 99314 Participants |
| Sex: Female, Male Female | 5206 Participants | 4941 Participants | 5124 Participants | 4990 Participants | 18473 Participants | 18523 Participants | 57257 Participants |
| Sex: Female, Male Male | 3870 Participants | 4046 Participants | 3908 Participants | 3955 Participants | 13024 Participants | 13254 Participants | 42057 Participants |
Adverse events
| Event type | EG000 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 / 9,076 | 0 / 8,987 | 0 / 9,032 | 0 / 8,945 | 34 / 31,497 | 37 / 31,777 |
| other Total, other adverse events | 0 / 9,076 | 0 / 8,987 | 0 / 9,032 | 0 / 8,945 | 0 / 31,497 | 0 / 31,777 |
| serious Total, serious adverse events | 0 / 9,076 | 0 / 8,987 | 0 / 9,032 | 0 / 8,945 | 0 / 31,497 | 0 / 31,777 |
Outcome results
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
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Hp Stool Antigen (HpSA)+FIT | Incidence of Stomach Cancer | 49 Participants |
| FIT Only | Incidence of Stomach Cancer | 59 Participants |
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
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Hp Stool Antigen (HpSA)+FIT | Mortality of Stomach Cancer | 17 Participants |
| FIT Only | Mortality of Stomach Cancer | 23 Participants |
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
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Hp Stool Antigen (HpSA)+FIT | Incidence of Colorectal Cancer | 0 Participants |
| FIT Only | Incidence of Colorectal Cancer | 0 Participants |
| Two-day Sampling With One-year Interval | Incidence of Colorectal Cancer | 0 Participants |
| Two-day Sampling With Two-year Interval | Incidence of Colorectal Cancer | 0 Participants |
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
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Hp Stool Antigen (HpSA)+FIT | Mortality of Colorectal Cancer | 0 Participants |
| FIT Only | Mortality of Colorectal Cancer | 0 Participants |
| Two-day Sampling With One-year Interval | Mortality of Colorectal Cancer | 0 Participants |
| Two-day Sampling With Two-year Interval | Mortality of Colorectal Cancer | 0 Participants |
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
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Hp Stool Antigen (HpSA)+FIT | Confirmatory Examination Referral Rate | 328 Participants |
| FIT Only | Confirmatory Examination Referral Rate | 473 Participants |
| Two-day Sampling With One-year Interval | Confirmatory Examination Referral Rate | 355 Participants |
| Two-day Sampling With Two-year Interval | Confirmatory Examination Referral Rate | 493 Participants |
| Hp Stool Antigen (HpSA) + FIT | Confirmatory Examination Referral Rate | 1724 Participants |
| FIT Only | Confirmatory Examination Referral Rate | 1739 Participants |
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
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Hp Stool Antigen (HpSA)+FIT | Detection of Advanced Adenoma and Cancer | 0 Participants |
| FIT Only | Detection of Advanced Adenoma and Cancer | 0 Participants |
| Two-day Sampling With One-year Interval | Detection of Advanced Adenoma and Cancer | 0 Participants |
| Two-day Sampling With Two-year Interval | Detection of Advanced Adenoma and Cancer | 0 Participants |
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
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Hp Stool Antigen (HpSA)+FIT | Detection of Non-advanced Adenoma | 0 Participants |
| FIT Only | Detection of Non-advanced Adenoma | 0 Participants |
| Two-day Sampling With One-year Interval | Detection of Non-advanced Adenoma | 0 Participants |
| Two-day Sampling With Two-year Interval | Detection of Non-advanced Adenoma | 0 Participants |
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
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Hp Stool Antigen (HpSA)+FIT | Helicobacter Pylori Eradication Rate | 8809 Participants |
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
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Hp Stool Antigen (HpSA)+FIT | Participation Rate of HpSA + FIT or FIT Only | 31497 Participants |
| FIT Only | Participation Rate of HpSA + FIT or FIT Only | 31777 Participants |