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Clinical Trials/NCT04511559
NCT04511559
Not yet recruiting
Not Applicable

Methylation Analysis of Circulating Tumor DNA in Early Diagnosis and Prognostic Stratification in Patients With Gastric Cancer

Shanghai Zhongshan Hospital0 sites540 target enrollmentOctober 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stomach Neoplasms
Sponsor
Shanghai Zhongshan Hospital
Enrollment
540
Primary Endpoint
Analysis ctDNA methylation status and its Correlation to early diagnosis and prognostic evaluation of gastric cancer.
Status
Not yet recruiting
Last Updated
5 years ago

Overview

Brief Summary

The primary purpose of this trial is to describe the profile of ctDNA methylation in gastric cancer. The second purpose is to demonstrate the correlation between the plasma ctDNA methylation status and the diagnosis and prognosis of patients with early and intermediate stage gastric cancer.

Detailed Description

Gastric cancer represents one of the common malignant tumors in China, with high incidence and mortality rates. Surgery is the conventional treatment option for early and intermediate stage gastric cancer, but the diagnosis in the early stage of gastric cancer remains a challenge to clinical practitioners. Circulating tumor DNA (ctDNA) is tumor-derived fragmented DNA with an average size of 166 bp, mixed with cell-free DNA (cfDNA) of other sources in blood circulation. ctDNA is reflecting the most up-to-date status of the tumor genome. Hence, it is considered as a novel biomarker for tumors, which can be qualitative, quantitative, and used for disease monitoring. This study is designed to evaluate the potential clinical utility of circulating tumor DNA (ctDNA) as a clinical index in the diagnosis and prognosis of gastric cancer. The primary purpose of this trial is to describe the profile of ctDNA methylation in gastric cancer. The second purpose is to demonstrate the correlation between the plasma ctDNA methylation status and the diagnosis and prognosis of patients with early and intermediate stage gastric cancer.

Registry
clinicaltrials.gov
Start Date
October 1, 2020
End Date
May 1, 2025
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Shanghai Zhongshan Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • The subject is scheduled to undergo an endoscopy because of medical indications.
  • The subject must have personally signed and dated the patient informed consent form indicating that he/she has been informed of all pertinent aspects of the study.
  • The subject must be willing and able to comply with all study procedures.

Exclusion Criteria

  • The subject who is unable to undergo gastroscopy.
  • The subject with previous total or partial gastrectomy.
  • The subject has other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may interfere with the interpretation of study results and in the judgment of the investigator would make the subject unsuitable for entry into the study.
  • The subject is unwilling or unable to provide signed informed consent.
  • The subject who is pregnant.

Outcomes

Primary Outcomes

Analysis ctDNA methylation status and its Correlation to early diagnosis and prognostic evaluation of gastric cancer.

Time Frame: 1-2 years

We will develop the linear model and a threshold value differentiating gastric cancer from control based on the 100 patient training set.

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