Pancreatic Cancer Research

Clinical trialObservationalUnknown

Acquisition of Portal Venous CTCs and Exosomes From Patients With Pancreatic Cancer by EUS

Acquisition of Portal Venous Circulating Tumor Cells and Exosomes From Patients With Pancreatic Cancer by Endoscopic Ultrasound: a Prospective Study

Outcome
Outcome unknown
Phase
Observational
Status
Unknown
Study type
Observational
Start
1 August 2018
Listed end
September 2020
Enrollment
30 participants
Sites
1
Primary outcomes
The difference of the amount of circulating tumor cells acquisited from portal venous blood between patients with pancreatic cancer and benign pancreatic diseases; The difference of the exosomes acquisited from portal venous blood between patients with pancreatic cancer and benign pancreatic diseases
Sponsor type
Academic / other
Results posted
No
Last update
31 January 2019

These fields come from the trial’s registry entry. A summary of its population, design, endpoints and results, each tied to a quote, has not been written for this trial yet.

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Brief summary public domain (ClinicalTrials.gov)

The investigators are going to explore the diagnostic and prognostic value of circulating tumor cells and exosomes extracted from the portal venous blood obtained with endoscopic ultrasound in pancreatic cancer patients.

Detailed description public domain (ClinicalTrials.gov)

As the prognosis of pancreatic cancer, a kind of malignant tumor, remains poor due to the low diagnostic rate at the early stage, there is still a significant clinical need to determine individualized tumor molecular profiles and personalized risk for recurrence. Circulating tumor cells (CTCs) and exosomes from patients with primary tumors may hold promise in serving as an informative biomarker to address this clinical need. Here in this study, the investigators are going to explore the feasibility and safety of sampling portal venous blood via endoscopic ultrasound (EUS), and detect portal venous CTCs and analyze mRNA markers of exosomes by RNA-seq. The investigators aim to explore the potential molecular mechanisms in tumor microenvironment and mechanisms of drug resistance.