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NCT07109440Recruiting

The Role of the Imaging FAPI PET/CT in Exploring the Microenvironment of Colorectal Cancer Liver Metastases

The Role of FAPI PET/CT in Exploring the Microenvironment of Colorectal Cancer Liver Metastases: Non-randomized Phase II Molecular Imaging Study

Source: ClinicalTrials.gov · Last updated 7 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

FAPI PET/CT molecular imaging represents a cutting-edge advancement in oncological imaging, particularly for the preoperative assessment of colorectal liver metastases (CRLM). Fibroblast activation protein inhibitors (FAPIs), which are the focus of this imaging modality, selectively target cancer-associated fibroblasts, a critical component of the tumor microenvironment. FAPI PET/CT could be useful in the detection of HGP (Histological Growth Pattern) and in the changes during neoadjuvant chemotherapy prior to surgery

Status (registry)
Recruiting
Study type
Interventional
Enrollment
50 (estimated)
First submitted
15 Jul 2025
Start date
9 May 2025
Primary completion date
Dec 2027
Lead sponsor
Jules Bordet Institute
NCT number
NCT07109440

What you commit to

  • Study type: Interventional
  • Planned participants: 50
  • From 9 May 2025 to the primary completion date, Dec 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

  • Subjects with another significant medical condition which, in the investigator's opinion, may interfere with the completion of the study.

Other

  • Non-resectable liver metastases
  • Pregnant and lactating women

Who the study is looking for

  • Age above 18 years.
  • Liver metastasis on standard imaging for the initial assessment (MRI, FDG PET/CT)
  • Naïve for treatment or after neoadjuvant chemotherapy
  • Scheduled for liver metastasis resection
  • ECOG Performance status ≤2.
  • Signed written informed consent

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
Institut Jules Bordet
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BrusselsBelgiumRecruiting

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