Exploratory Study on the Application of Molecular Residual Disease (MRD) in Postoperative Treatment of Gastric Cancer

NCT ID: NCT07034742

Last Updated: 2025-06-24

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: EARLY_PHASE1
• Total Enrollment: 136 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-06-01
• Study Completion Date: 2028-01-01

Brief Summary

Gastric cancer is one of the most prevalent and lethal malignancies in China. The majority of patients are diagnosed at the locally advanced stage. Despite standard treatment involving radical resection combined with adjuvant chemotherapy, approximately 40% of patients experience recurrence and metastasis, with peritoneal metastasis accounting for nearly half of these cases.

Building upon our team's previous establishment of next-generation sequencing (NGS) technology for detecting molecular residual disease (MRD) in peritoneal lavage fluid and blood, this project aims to guide systemic chemotherapy with or without intraperitoneal chemotherapy for locally advanced gastric cancer patients based on the results of peritoneal lavage fluid MRD testing. We will investigate whether intraperitoneal chemotherapy can reduce the peritoneal metastasis rate in patients testing positive for MRD in peritoneal lavage fluid. The ultimate goal is to propose a novel diagnostic and therapeutic strategy for post-operative adjuvant treatment of gastric cancer, addressing this critical clinical challenge.

Patients testing negative for MRD in peritoneal lavage fluid will be enrolled in an observational cohort study. This cohort will explore the concordance between blood-based MRD positivity and actual clinical recurrence and metastasis. The objectives are to determine whether blood-based MRD can predict the occurrence of non-peritoneal metastasis after surgery and whether it can be used to evaluate the efficacy of post-operative systemic chemotherapy.

Conditions

Gastric Adenocarcinoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

GC patients

Group Type: EXPERIMENTAL

Intraperitoneal chemotherapy PLUS systemic chemotherapy

Intervention Type: DRUG

Intraperitoneal chemotherapy (fluorouracil + nab-paclitaxel + cisplatin + interleukin-2) PLUS systemic chemotherapy (SOX regimen: oxaliplatin + tegafur-gimeracil-oteracil potassium)

Interventions

Intraperitoneal chemotherapy PLUS systemic chemotherapy

Intraperitoneal chemotherapy (fluorouracil + nab-paclitaxel + cisplatin + interleukin-2) PLUS systemic chemotherapy (SOX regimen: oxaliplatin + tegafur-gimeracil-oteracil potassium)

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Histologically confirmed adenocarcinoma, mucinous adenocarcinoma, or signet ring cell carcinoma of the stomach or gastroesophageal junction (GEJ).
• Clinical stage cT4NanyM0, deemed suitable for radical resection.
• Age between 18 and 75 years.
• ECOG performance status of 0 or 1.
• No prior neoadjuvant therapy and strong patient/family preference for primary surgery.
• Adequate organ function defined as:

Absolute neutrophil count (ANC) > 1.5 x 10⁹/L (or > 1500/µL)；Hemoglobin (Hb) > 90 g/L；Platelet count (PLT) > 100 x 10⁹/L (or > 100,000/µL)；Alanine aminotransferase (ALT) and Aspartate aminotransferase (AST) < 2.5 x Upper Limit of Normal (ULN)；Total bilirubin (TBIL) < 1.5 x ULN；Serum creatinine (Cr) < 1.0 x ULN

• Good compliance and willingness to undergo long-term follow-up.
• Provision of signed written informed consent.

Exclusion Criteria

• Pathological specimens containing >10% of other histological components (e.g., squamous cell carcinoma, neuroendocrine carcinoma, etc.).
• Uncontrolled gastrointestinal obstruction or recurrent bleeding.
• Inability to swallow oral medications.
• Active infection requiring systemic therapy.
• Moderate to severe cirrhosis due to any cause.
• Cardiac function classified as NYHA class > I.
• History of myocardial infarction, unstable angina, stroke, or uncontrolled arrhythmia.
• Anticipated inability to tolerate postoperative adjuvant chemotherapy.
• Concurrent medical conditions that contraindicate chemotherapy.
• Pregnancy or lactation; history of psychiatric illness; poor compliance.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Cancer Institute and Hospital, Chinese Academy of Medical Sciences

OTHER

Sponsor Role: lead

Responsible Party

Dong Bing Zhao

MD

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Chaoyang District, Panjiayuan Nanli NO.17

Beijing, , China

Site Status: RECRUITING

Countries

China

Central Contacts

Dongbing Zhao

Role: CONTACT

dbzhao@cicams.ac.cn

010-87787120

Other Identifiers

25/099-5045

Identifier Type: -

Identifier Source: org_study_id