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NCT05195281Recruiting

Pancreatic Cancer Evolution Upon Treatment

Source: ClinicalTrials.gov · Last updated 15 Jan 2026

Brief summary (registry, in English)

This project aims at evaluating the different subtypes of pancreatic cancer on EUS-tissue acquisition of pancreatic cancer patients, and their possible modifications throughout time. The study takes advantage of a systematic evaluation of pancreatic cancers through diagnostic EUS-guided fine needle biopsy (FNB) sampling of the mass performed during a restaging EUS. FNB samples represent a valuable source of cancer cells, both for the histological diagnosis and as the source of tumor macromolecules, including DNA and RNA. Study design This is a prospective study enrolling patients with non-metastatic pancreatic cancer who already underwent diagnostic EUS with tissue acquisition and rapid on-site evaluation (ROSE) by cytologist positive for pancreatic cancer, with a first sample acquired for diagnostic purposes and a second sample stored for RNA extraction acquired with the already approved protocol BIOGASTRO. As recommended by guidelines, patients will follow the standard pathway of treatment, being sent to chemotherapy and will then undergo restaging of the lesion and re-evaluation of vascular invasion by CT and EUS. During this second session of EUS a new specimen of the tumor will be sampled for diagnostic purposes, with a second pass undergoing for RNA extraction.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
80 (estimated)
First submitted
29 Nov 2021
Start date
14 Jul 2021
Primary completion date
28 Sept 2027
Lead sponsor
IRCCS San Raffaele
NCT number
NCT05195281

What you commit to

  • Study type: Interventional
  • Planned participants: 80
  • From 14 Jul 2021 to the primary completion date, 28 Sept 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Cytology positive for malignancies other than PDAC

Other

  • Patients not willing to sign informed consent
  • Pregnancy and breastfeeding
  • Patient undergoing progression at re-staging CT scan

Who the study is looking for

  • Age ≥ 18 years
  • Willing to sign informed consent
  • Patient with CT scan or MRI or EUS defining the lesion as locally advanced
  • Patient who already underwent EUS-TA for solid lesion of the pancreas positive for pancreatic ductal adenocarcinoma (PDAC)
  • Patient undergoing neoadjuvant chemotherapy
  • Patient primarily followed at San Raffaele Hospital

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
IRCCS San Raffaele Hospital
Coordinator of this site? Confirm its status
MilanItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.