Clinical trial Recruiting at 1 site Observational Ages 18 and up

Prospective look at liver metastases imaging and tissue patterns in colorectal and breast cancer

Official title: Prospective Complete Histopathological Characterization of Liver Metastases From Colorectal and Breast Carcinoma to Predict the Histopathological Growth Patterns by Medical Imaging - PrOspEctive Metastases Imaging (POEM)

Run by Cancer Research Antwerp · NCT07781306 · Data updated 2026-11-12

This observational study tests whether 3D maps of histopathological growth patterns in liver metastases align with imaging features from MRI/CT in patients undergoing liver surgery.

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Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment50 (estimated)
SponsorCancer Research Antwerp
Academic / other
Drugs / interventionsbevacizumab, chemotherapy, immunotherapy
Locations1 site (Wilrijk, Antwerp)
StatusRecruiting
StartedSeptember 8, 2020
Main results expectedDecember 2027
Study endsMay 2028
Registry record updatedAugust 24, 2026
Trial IDNCT07781306 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) with liver metastases from colorectal or breast cancer who are scheduled for surgical removal of the metastases and can provide informed consent.

Probably not a fit

Patients without suitable imaging timelines or who do not undergo surgery may not benefit from the study findings.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This non-interventional study collects imaging data and tissue samples from patients with liver metastases from colorectal or breast cancer who are having liver metastases surgically removed. Researchers compare the histopathological growth patterns, particularly desmoplastic versus other patterns, with imaging characteristics to see if imaging can reflect underlying biology. An optional biobanking activity may collect remnant tissue for further study, using tissue that would otherwise be discarded. The goal is to improve understanding of how imaging relates to tumor behavior and to potentially inform future patient care.

Why it matters

Potential benefit: Better matching of imaging features to tumor biology could improve future treatment planning for liver metastases.

How similar studies have gone: Prior work has shown that histopathological growth patterns correlate with imaging in liver metastases, supporting further exploration in this observational setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. ≥ 18 years old.
2. Patients with liver metastatic colorectal or breast carcinoma undergoing a surgical excision of the liver metastases
3. Therapy-naive patients as well as patients with neo-adjuvant therapy are eligible for inclusion
4. Willingness of the patient to participate in this study demonstrated by signed written informed consent

Exclusion Criteria:

1. Patients without MRI or CT of the liver prior to surgery
2. Time interval between medical imaging, CT and/or MRI is more than 12 weeks (nb: time interval is preferably less than 4 weeks but this is not an exclusion criterium)
3. Prior radiofrequency ablation (RFA) or transarterial chemoembolization (TACE) on the liver metastasis that would be operated

Where it's running

  • GZA St Augustinus
    Wilrijk, Antwerp, Belgium
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.