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NCT Number: NCT04214990

Aspirin Use for Gastric Cancer Prevention in the Early Gastric Cancer Patients

This study aimed to investigate the effect of low-dose (100 mg) asprin on the prevention of gastric cancer in the early gastric cancer patients with negative H. pylori status who underwent endoscopic submucosal dissection.

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Key information

Age range

19 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Kosin University Gospel Hospital, Busan, South Korea

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About this study

Aspirin has been widely used as an anti-platelet drug for the primary or secondary prevention of cardiovascular events, including ischemic heart disease and stroke. In 2016, the U.S. Preventive Services Task Force recommended initiating low-dose aspirin use for the primary prevention of cardiovascular diseases and colorectal cancer in adult aged 50 to 59 years who have a 10% or greater 10-year cardiovascular disease risk, are not at increased risk of bleeding, have a life expectancy of at least 10 years, and are willing to take low-dose aspirin daily for at least 10 years. In addition, a meta-analysis reported that long-term aspirin use was associated with reduced the risk of gastrointestinal cancers including colorectal cancer, esophageal cancer, and gastric cancer. However, most studies that reported the cancer prevention effect of long-term aspirin use were conducted as a secondary analysis or subgroup analysis of primary studies investigating the aspirin use for cardiovascular disease prevention. Thus, there is a limitation that appropriate sample sizes and follow-up periods for the cancer prevention effect of aspirin were not considered.

In 2018, we reported that H. pylori treatment reduced the development of metachronous gastric cancer after endoscopic resection in early gastric cancer patients. However, metachronous gastric cancer could develop after successful H. pylori eradication with an annual incidence of 1%-3%. Therefore, we designed a multi-center, double-blind, randomized, placebo-controlled trial to evaluate whether long-term low-dose (100 mg) aspirin uses prevents gastric cancer in early gastric cancer or high-grade dysplasia patients who underwent endoscopic resection.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men and women aged 19-70 years who underwent endoscopic resection for high-grade adenoma or early gastric cancer (category 4 [non-invasive high grade neoplasm] or category 5 [invasive neoplasia] according to the Vienna classification of gastrointestinal epithelial neoplasia [Schlemper RJ, et al. Gut 2000;47:251-255.])
  • Final pathological results after endoscopic resection met the absolute or expanded criteria according to the Japanese Gastric Cancer Treatment guideline 2014 (version 4)
  • Patients who had negative H. pylori status or those who eradicated H. pylori status
  • Willingness to sign an informed consent form

Exclusion criteria

  • Patients who received aspirin for the secondary prevention of cardiovascular diseases or cerebrovascular diseases
  • Regular aspirin uses (more than 3 times a week) with 2 months before screening visit
  • Patients who used anticoagulants or antiplatelet drugs for therapeutic purpose
  • Previous gastrectomy history
  • Current treatment for serious medical condition which could hinder participation (such as severe heart dysfunction, liver cirrhosis, renal failure, COPD or bronchial asthma, or uncontrolled infection)
  • High risk patients for bleeding complications (cerebral aneurysm, vascular malformation, esophageal or gastric varices, or hemophilia, etc)
  • Active peptic ulcer disease (patients who treated peptic ulcer completely could be enrolled)
  • Diagnosis and active treatment for other organ cancer (except carcinoma in situ, and non-melanoma skin cancer) within 5 years
  • Non-curative resection of early gastric cancer after endoscopic resection
  • Aspirin allergy or contraindication of aspirin use
  • Pregnant or lactating women
  • Alcoholism, drug abuse
  • Inadequate patients for study enrollment according to the evaluation of the study physician
  • Inability to provide an informed consent
  • Patients who took a 28-day run-in-period medication less than 80%

Treatment and study plan

Aspirin 100mg

Drug

Daily aspirin 100 mg for 5 years

Placebo oral tablet

Drug

Daily placebo for 5 years

Primary outcomes

  1. The incidence of gastric cancer between the intervention and placebo groups

    Time frame: Until last enrolled patients take 5-year trial medication

    Histologically confirmed gastric cancer detected at follow-up endoscopy or registered at the Korean Cancer Registry

Secondary outcomes

  1. All-cause mortality

    Time frame: Until last enrolled patients take 5-year trial medication

    Mortality from any causes

  2. The incidence of cardiovascular disease and cerebrovascular disease between the intervention and placebo groups

    Time frame: Until last enrolled patients take 5-year trial medication

    Cardiovascular diseases (stable and unstable angina, myocardial infarction); Cerebrovascular diseases (transient ischemic attack, cerebral infarction, other small vascular infarction, etc)

  3. The incidence of other organ cancers between the intervention and placebo groups

    Time frame: Until last enrolled patients take 5-year trial medication

    Cancers detected at follow-up visits or registered at the Korean Cancer Registry

  4. The incidence of gastric dysplasia (adenoma) between the intervention and placebo groups

    Time frame: Until last enrolled patients take 5-year trial medication

    Histologically confirmed gastric dysplasia (adenoma) detected at follow-up endoscopy

  5. Complication related to the aspirin use

    Time frame: Until last enrolled patients take 5-year trial medication

    Gastrointestinal bleeding, intracranial hemorrhage, subarachnoid hemorrhage, and other bleeding complications

  6. Improvement of atrophy and intestinal metaplasia

    Time frame: At the time of 5-year trial medication

    Change in histologic atrophy and intestinal metaplasia grades from enrollment to subsequent endoscopic assessment

Study contacts

Contact information is provided by the study sponsor or research team.

Il Ju Choi, M.D., Ph.D.

CONTACT

[email protected]

+82-31-920-2282

Young-Il Kim, MD

CONTACT

[email protected]

+82-31-920-1712

Sponsors and collaborators

Lead sponsor

National Cancer Center, Korea

Other Gov

Collaborators

  • Asan Medical Center
  • Chilgok Kyungpook National University
  • Chonnam National University Hospital
  • Chung-Ang University Hospital
  • Hallym University Medical Center
  • Incheon St.Mary's Hospital/The Catholic University
  • Kosin University Gospel Hospital
  • Pusan National University Hospital
  • SMG-SNU Boramae Medical Center
  • Samsung Medical Center
  • Seoul National University Bundang Hospital
  • Severance Hospital

Registry information

Official study title

Effect of Low-dose Aspirin for Stomach Cancer Prevention After Endoscopic Resection of Gastric Neoplasm (EASTERN): a Randomized Controlled Trial

Acronym: EASTERN

Important dates

Study start
2020
Primary completion
2031
Study completion
2032
First posted
Jan 2, 2020
Registry last updated
Dec 27, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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