Pilot Comparing ctDNA IDV vs. SPV Sample in Pts Undergoing Biopsies for Hepatobiliary and Pancreatic Cancers

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of California, Irvine

About this trial

This is a prospective pilot protocol investigating whether ctDNA detection be improved by sampling the cancer draining vein versus the standard practice of sampling from a peripheral vein in patients who are undergoing biopsies for hepatobiliary and pancreatic cancers.

Eligibility criteria

Qualifiers

18 years of age or older

Have or are undergoing work-up for hepatobiliary and/or pancreatic carcinoma (such as hepatocellular carcinoma, cholangiocarcinoma, ampullary carcinoma, pancreatic carcinoma)

Scheduled for an image-guided percutaneous or trans-jugular biopsy of a lesion

Must be able to provide a written informed consent

Disqualifiers

Patients unable to hold reasonably still on a procedure table or hold their breath during imaging or needle passes

Patients with a gross body weight over 375 pounds (upper limit of the CT and angiography tables)

Patients with uncorrectable coagulopathy

Platelet count < 30,000/ul

Trial design

Treatments tested in this trial

  • ctDNA Blood Collection

Treatment groups

15 Participants
are divided into 1 treatment group