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Starting soon Observational

EUS-guided CTCs + Multi-omics: Predicting Pancreatic Cancer Recurrence and Metastases

NCT07448376 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2026-03-01
Last updated
2026-03-04

Condition(s) studied

CTCsPancreatic CancerLiver MetastasesRelapseBorderline Resectable Pancreatic CancerResectable Pancreatic CancersEUS

Investigational drug(s) / intervention(s)

CTC

CTC: Obtaining portal vein blood and peripheral blood from patients, extracting circulating tumor cells (CTCs) therein, and performing CTC sorting, thereby assisting clinical evaluation of the applicability of neoadjuvant therapy and prognostic assessment for patients with potentially resectable pancreatic cancer.

Study summary

The investigators conduct a single-center, prospective, observational study to explore the value of EUS-guided portal vein circulating tumor cells (PV-CTCs) and their subtypes combined with multi-omics tests in the early warning of recurrence and metastasis of resectable pancreatic cancer(RPC) and borderline resectable pancreatic cancer (BRPC).

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: 1. Patients with solid masses (diameter \> 1 cm) in the pancreatic area within the accessible range of endoscopic ultrasound, as indicated by clinical symptoms, laboratory tests, and imaging examinations (MRI, CT, B-ultrasound), who require biopsy to clarify the nature of the lesion. 2. Patients diagnosed with resectable pancreatic cancer, borderline resectable pancreatic cancer, locally advanced pancreatic cancer by imaging(CT/MRI). 3. Newly diagnosed pancreatic cancer patients who have not received radiotherapy or chemotherapy. 4. Signed informed consent form. 5. Patients must be able to comply with the trial requirements. Exclusion Criteria: 1. Patients with other active malignant tumors 2. Patients with coagulation dysfunction (PLT 50,000/mm3, INR \> 1.5; roughly estimated, INR \> 1.5 is approximately equivalent to PT \> 18 seconds) 3. Pregnant women 4. Patients with hemorrhagic diseases 5. Patients with a history of taking anticoagulant drugs such as aspirin and warfarin in the past week 6. Patients with absolute contraindications to EUS examination, a history of acute pancreatitis within the past 2 weeks, a history of gastric surgery, pregnancy, severe diseases, or a history of allergy to anesthetics 7. Patients whose EUS examination was terminated early due to esophageal stenosis, obstruction, large space-occupying lesions, rapid changes in the patient's heart rate or respiratory rate, patient intolerance, or a large amount of food residue, etc. 8. Patients with known hepatitis C virus infection 9. Patients with known human immunodeficiency virus (HIV) infection 10. Patients with imaging examinations, EUS results, etc., suggesting pancreatic cystic space-occupying lesions 11. Patients who have received radiotherapy or chemotherapy 12. Patients with incomplete pathological information, unable to make a clear diagnosis, or unable to sign the informed consent form

Primary outcome measure(s)

  • Number of circulating tumor cells in the portal vein — Up to 24 months
    Explore the value of the number of circulating tumor cells in the portal vein in evaluating the applicability of neoadjuvant therapy and guiding treatment decisions for BRPC patients
  • Subpopulation classification of portal vein circulating tumor cells — Up to 24 months
    Explore the application of portal vein circulating tumor cell subset classification in the prognostic evaluation of neoadjuvant therapy in BRPC patients

Trial sites (1)

FacilityCityRegionStatus
Tongji Hospital, Tongji Medical College, HUST Wuhan Hubei
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 NCT07448376 on ClinicalTrials.gov ↗ ← All trials in China