Actively Recruiting
Effectiveness of Risk-based Sequential Screening for Esophageal and Gastric Cancer
Led by Peking University Cancer Hospital & Institute · Updated on 2025-01-24
21000
Participants Needed
1
Research Sites
544 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To evaluate the feasibility, applicability, effectiveness, and health-economic value of the risk-based sequential screening modality for esophageal and gastric cancers, the investigators aim to initiate a community-based randomized controlled trial in Xun County, Henan Province, which is a high-risk region of upper gastrointestinal cancer (UGIC) in northern China. A total of 258 target villages from all the 11 communities (townships and streets) in Xun County will be randomly selected and assigned to the sequential screening group and the universal screening group at a ratio of 2:1 and the total sample size will be 21,000. In the sequential screening group, participants in the top 50% risk level (i.e., stratified as the high-risk subgroup) will be offered a standard upper gastrointestinal endoscopic screening. In contrast, all participants in the universal screening group will receive the endoscopic examination. The surveillance strategy for participants with screening-detected premalignant lesions in the sequential screening group will be tailored based on individualized risk assessment using endoscopic characteristics, pathological diagnosis, and biomarkers. Surveillance for participants in the universal screening group will adhere to current guidelines for UGIC screening and clinical treatment. Detection rates of upper gastrointestinal malignant lesions, early-stage malignant lesions and premalignant lesions, and health-economic indicators such as the unit cost per detected malignant lesions will be compared between the two groups.
CONDITIONS
Official Title
Effectiveness of Risk-based Sequential Screening for Esophageal and Gastric Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Permanent residency in the target villages in Xun County, Henan Province, China
- Aged 50 to 69 at the enrollment
- Voluntarily participate in this study and provide informed consent
You will not qualify if you...
- History of endoscopic examination within 5 years prior to the initial interview
- History of cancer
- History of mental disorder
- Positive for hepatitis B virus (HBV), hepatitis C virus (HCV), or human immunodeficiency virus (HIV)
- Severe cardiovascular and cerebrovascular diseases
- Severe respiratory disease, dyspnea, or asthmaticus status
- Retropharyngeal abscess, severe spinal deformity, or aortic aneurysm
- Physical debility unable to tolerate endoscopic examination or difficulty with sedation and self-control
- Acute phase of corrosive inflammation or suspected perforation of the upper gastrointestinal tract
- Massive ascites, severe abdominal distension, or severe esophageal varices
- Pregnancy
- Severe history of allergies
- Propensity for bleeding (coagulopathy)
- Others unable to tolerate the clinical examinations involved in this study
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Trial Site Locations
Total: 1 location
1
Department of genetics, Peking University Cancer Hospital & Institute
Beijing, Beijing Municipality, China, 100142
Actively Recruiting
Research Team
Z
Zhonghu He
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SCREENING
Number of Arms
2
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