🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in China / NCT06893133
Recruiting Observational

ctDNA-MRD Monitoring After Resection in Gastric Cancer

NCT06893133 · tracked via the Priya Life Science China tracker
Sponsor
Peking University
Phase
Observational
Started
2025-04-08
Last updated
2026-04-21

Condition(s) studied

Gastric Cancer

Study summary

Numerous studies have demonstrated that circulating tumor DNA (ctDNA)-based molecular residual disease (MRD) detection has significant clinical value in postoperative recurrence monitoring, adjuvant treatment decision-making, and early intervention. Our previous retrospective study, using fixed ctDNA-MRD, confirmed that postoperative ctDNA-MRD can predict recurrence risk. Therefore, we plan to conduct a further prospective, multicenter, observational study, utilizing a combination of personalized ctDNA-MRD and fixed MRD panels, to dynamically monitor gastric cancer patients who have received neoadjuvant therapy followed by curative resection. The study will systematically analyze the correlation between ctDNA-MRD status and tumor recurrence and metastasis, assess its sensitivity and specificity in recurrence prediction, and compare its early warning advantage over traditional imaging techniques in predicting recurrence.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
Accepted
Inclusion Criteria: 1. Patients have received neoadjuvant therapy and radical resection (R0). 2. Pathologically confirmed ypTNM stage II-III gastric or gastroesophageal junction adenocarcinoma. 3. Patients must be able to provide sufficient fresh tissue/biopsies or minimum 5-10 FFPE sections for NGS-WES analysis. 4. Patients must be able to follow the study visit schedule and be willing to cooperate with the study by providing blood samples at the indicated time point. Exclusion Criteria: 1. Patients who could not receive enhanced CT, gastroscopy and other routine review after surgery. 2. Patients who could not perform WES or ctDNA-MRD detection for various reasons after surgery. 3. Other cases considered unsuitable for inclusion by researchers.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Peking University Cancer Hospital & Institute Beijing Beijing Municipality Recruiting

More Peking University trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06893133 on ClinicalTrials.gov ↗ ← All trials in China