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Monitoring Minimal Residual Disease in Gastric Cancer by Liquid Biopsy Study Description

Monitoring Minimal Residual Disease in Gastric Cancer by Liquid Biopsy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05029869
Enrollment
100
Registered
2021-09-01
Start date
2021-10-04
Completion date
2026-12-30
Last updated
2025-08-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ctDNA, Gastric Cancer

Brief summary

This study aims to evaluate the use of Next Generation Sequencing (NGS) to detect circulating tumor DNA in gastric cancer patients after gastrectomy

Detailed description

Gastric cancer is the fourth most common cancer in Vietnam with high mortality rate. Patients at early stages undergo radical gastrectomy with curative intent, but the remaining tumor cells, termed as minimal residual disease (MRD), can later cause relapse. Conventional methods to monitor MRD such as imaging and blood tests for biomarkers such as CEA are not sensitive and specific enough. ctDNA has recently emerged as a promising noninvasive marker with high accuracy to monitor MRD and detect relapse in many cancers such as breast and colorectal cancers. However, its application in gastric cancer has not been extensively evaluated. Therefore, this study aims to use advanced NGS technologies to detect ctDNA in liquid biopsy as a biomarker to monitor MRD after radical gastrectomy.

Interventions

DIAGNOSTIC_TESTctDNA

The blood samples for ctDNA and other tumor markers will be first collected within 14 days before surgery, and then be tested after gastrectomy in scheduled interval

Sponsors

University Medical Center Ho Chi Minh City (UMC)
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Male or Female patients aged 18 years and older 2. Histologically proven primary gastric adenocarcinoma before surgery 3. Clinical stage is locally advanced cT2-4a any N and M0 4. In initial evaluation, patient can undergo radical gastrectomy and lymphadenectomy 5. No preoperative therapy, including chemotherapy and radiotherapy 6. No known cancer diagnosis within last five years 7. Signed informed consent

Exclusion criteria

1. Gastrectomy cannot be achieved during operation due to metastasis 2. Patient fails to follow-up and provide postoperative samples

Design outcomes

Primary

MeasureTime frameDescription
The sensitivity of MRD detection using ctDNA as the biomarker2 years after surgeryThe percentage of positive ctDNA detection among participants who experience disease recurrence or metastasis
The specificity of MRD detection using ctDNA as the biomarker2 years after surgeryThe percentage of positive ctDNA detection among participants who do not experience disease recurrence or metastasis

Secondary

MeasureTime frameDescription
Leading time between ctDNA detection and cancer recurrence detected by conventional methods2 years after surgeryTime is measured between first positive ctDNA detection and first cancer recurrence detected by conventional methods
Mean ctDNA level (MTM/ml) of gastric cancer before operationWithin 14 days before operationThe mean ctDNA level in gastric cancer patients before operation
Mutation profile of gastric cancerWithin 14 days before operationProfiling of the most frequent gene mutations

Countries

Vietnam

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 29, 2026