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Effects of H. Pylori Eradication on the Gastric Preneoplastic Lesion and Neoplasm After ESD

Primary Purpose

Helicobacter Pylori Infection, Early Gastric Cancer, Endoscopic Resection

Status
Active
Phase
Phase 3
Locations
Korea, Republic of
Study Type
Interventional
Intervention
7 day H.pylori eradication Omeprazole or Rabeprazole, Clarithromycin, Amoxicillin
Placebo, Omeprazole or Rabeprazole, Clarithromycin
Sponsored by
National Cancer Center, Korea
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Helicobacter Pylori Infection focused on measuring H. pylori eradication, Atrophy, Intestinal metaplasia, Endoscopic resection, Stomach neoplasm

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Early Gastric cancer or high grade dysplasia confirmed by endoscopy

    • Histologically confirmed well or moderately differentiated adenocarcinoma, or high grade dysplasia
    • Submucosal invasion is not suspected
    • No evidence of ulceration or ulcer scar within the lesion
  • Helicobacter pylori infection was confirmed by histological evaluation and rapid urease test
  • Pre op CT stage: IA (T1N0M0) according to UICC TNM classification system
  • Informed consent should be signed

Exclusion Criteria:

  • Recurrent gastric cancer
  • Previous serious side effect to antibiotics
  • H. pylori eradication treatment history
  • Poorly differentiated adenocarcinoma or Signet ring cell carcinoma
  • Undergoing operation due to complication of EMR
  • Undergoing operation due to remnant cancer
  • Other malignancy within the past 5 years
  • Pregnant or nursing women
  • Serious concurrent infection or nonmalignant disease such as liver cirrhosis, renal failure, cardiovascular diseases
  • Psychiatric disorder that would preclude compliance

Sites / Locations

  • National Cancer Center, Korea

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

7 day H.pylori eradication

Placebo

Arm Description

Treatment: Omeprazole 20 mg or Rabeprazole 10 mg bid + clarithromycin 500 mg and amoxicillin 1,000 mg bid for 7 days

Omeprazole 20 mg or Rabeprazole 10 mg bid + Placebo for two antibiotics (clarithromycin and amoxicillin) bid for 7 days

Outcomes

Primary Outcome Measures

Improvement (histological) of glandular atrophy
Improvement of glandular atrophy at the corpus lesser curvature
Incidence of metachronous gastric cancer
Comparison of metachronous gastric cancer according to the allocated treatment

Secondary Outcome Measures

Incidence of new gastric dysplasia
Comparison of new gastric dysplasia according to the allocated treatment
Overall survival
Comparison of overall survival according to the allocated treatment

Full Information

First Posted
March 13, 2015
Last Updated
April 8, 2022
Sponsor
National Cancer Center, Korea
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1. Study Identification

Unique Protocol Identification Number
NCT02407119
Brief Title
Effects of H. Pylori Eradication on the Gastric Preneoplastic Lesion and Neoplasm After ESD
Official Title
Effect of Helicobacter Pylori Eradication on Glandular Atrophy and Metachronous Cancer in Patients Undergoing Endoscopic Mucosal Resection for Gastric Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 2003 (undefined)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
June 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Cancer Center, Korea

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study evaluates whether Helicobacter pylori eradication improves precancerous lesions including glandular atrophy and intestinal metaplasia as well as metachronous cancers or dysplasias after endoscopic mucosal resection for gastric cancer.
Detailed Description
Helicobacter pylori is a primary etiological agent leading to chronic gastritis and peptic ulcer. The organism is also associated with gastric cancer in epidemiological studies. However detailed mechanism of carcinogenesis remains unknown. Histolopathological studies indicate that chronic H. pylori infection progresses over decades through stages of chronic gastritis, atrophy, intestinal metaplasia, dysplasia and cancer. Gastric atrophy and intestinal metaplasia are considered as precancerous lesions, but whether H. pylori eradication improves these lesions and prevents metachronous gastric cancer is controversial. And the issue has not been evaluated in gastric cancer patients. However, despite the conflicting evidences from two open labelled randomized controlled trials, current guidelines from various regions recommend H. pylori eradication treatment in patients who were treated for gastric cancer by surgically or endoscopically. Thus, it is important to evaluate whether H. pylori eradication can improve known precancerous lesion, i.e. glandular atrophy and intestinal metaplasia in gastric cancer patients. Such histological improvement can eventually reduce secondary gastric cancer development and provide evidence for current guidelines.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Helicobacter Pylori Infection, Early Gastric Cancer, Endoscopic Resection
Keywords
H. pylori eradication, Atrophy, Intestinal metaplasia, Endoscopic resection, Stomach neoplasm

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
470 (Actual)

8. Arms, Groups, and Interventions

Arm Title
7 day H.pylori eradication
Arm Type
Active Comparator
Arm Description
Treatment: Omeprazole 20 mg or Rabeprazole 10 mg bid + clarithromycin 500 mg and amoxicillin 1,000 mg bid for 7 days
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Omeprazole 20 mg or Rabeprazole 10 mg bid + Placebo for two antibiotics (clarithromycin and amoxicillin) bid for 7 days
Intervention Type
Drug
Intervention Name(s)
7 day H.pylori eradication Omeprazole or Rabeprazole, Clarithromycin, Amoxicillin
Other Intervention Name(s)
7 day Proton pump inhibitor (PPI)-based standard triple therapy
Intervention Description
Omeprazole 20 mg or Rabeprazole 10 mg bid for 7 days, Clarithromycin 500 mg bid for 7 days, Amoxicillin 1,000 mg bid for 7 days.
Intervention Type
Drug
Intervention Name(s)
Placebo, Omeprazole or Rabeprazole, Clarithromycin
Other Intervention Name(s)
Placebo
Intervention Description
Omeprazole 20 mg or Rabeprazole 10 mg bid for 7 days, Placebo for clarithromycin 500 mg bid for 7 days, Placebo for amoxicillin 1,000 mg bid for 7 days.
Primary Outcome Measure Information:
Title
Improvement (histological) of glandular atrophy
Description
Improvement of glandular atrophy at the corpus lesser curvature
Time Frame
3 years after enrollment
Title
Incidence of metachronous gastric cancer
Description
Comparison of metachronous gastric cancer according to the allocated treatment
Time Frame
3 years after last patient enrollment
Secondary Outcome Measure Information:
Title
Incidence of new gastric dysplasia
Description
Comparison of new gastric dysplasia according to the allocated treatment
Time Frame
3 years after last patient enrollment
Title
Overall survival
Description
Comparison of overall survival according to the allocated treatment
Time Frame
3 years after last patient enrollment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Early Gastric cancer or high grade dysplasia confirmed by endoscopy Histologically confirmed well or moderately differentiated adenocarcinoma, or high grade dysplasia Submucosal invasion is not suspected No evidence of ulceration or ulcer scar within the lesion Helicobacter pylori infection was confirmed by histological evaluation and rapid urease test Pre op CT stage: IA (T1N0M0) according to UICC TNM classification system Informed consent should be signed Exclusion Criteria: Recurrent gastric cancer Previous serious side effect to antibiotics H. pylori eradication treatment history Poorly differentiated adenocarcinoma or Signet ring cell carcinoma Undergoing operation due to complication of EMR Undergoing operation due to remnant cancer Other malignancy within the past 5 years Pregnant or nursing women Serious concurrent infection or nonmalignant disease such as liver cirrhosis, renal failure, cardiovascular diseases Psychiatric disorder that would preclude compliance
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Il Ju Choi, MD, PhD
Organizational Affiliation
National Cancer Center, Korea
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Cancer Center, Korea
City
Goyang
State/Province
Gyeonggi
ZIP/Postal Code
410-769
Country
Korea, Republic of

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
29562147
Citation
Choi IJ, Kook MC, Kim YI, Cho SJ, Lee JY, Kim CG, Park B, Nam BH. Helicobacter pylori Therapy for the Prevention of Metachronous Gastric Cancer. N Engl J Med. 2018 Mar 22;378(12):1085-1095. doi: 10.1056/NEJMoa1708423.
Results Reference
derived

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Effects of H. Pylori Eradication on the Gastric Preneoplastic Lesion and Neoplasm After ESD

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