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.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | Cancer Research Antwerp Academic / other |
| Drugs / interventions | bevacizumab, chemotherapy, immunotherapy |
| Locations | 1 site (Wilrijk, Antwerp) |
| Status | Recruiting |
| Started | September 8, 2020 |
| Main results expected | December 2027 |
| Study ends | May 2028 |
| Registry record updated | August 24, 2026 |
| Trial ID | NCT07781306 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
- Study coordinator: Peter Vermeulen, MD, PhD
- Email: peter.vermeulen@zas.be
- Phone: 0032493194745
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Guaraná Supplement for Cancer-Related Fatigue in People Undergoing Treatment
This study tests whether taking guaraná capsules helps reduce cancer-related fatigue and improve quality of life in adults with breast, lung, colorectal, or gastric cancer who are actively receiving treatment.
-
First-in-human STRO-006 in adults with certain recurrent or metastatic solid tumors
This study tests STRO-006 alone and with pembrolizumab in adults with certain head and neck, lung, esophageal, gastric, colorectal cancers to see if it is safe and shows early anticancer activity.
-
Oral, Fecal and Tumor Microbiome Atlas in Colombian Patients With Advanced Solid Tumors Receiving First-Line Immunotherapy
This study tests how the oral, gut, and tumor microbiomes relate to response to first-line immunotherapy in Colombian adults with advanced solid cancers.
-
Precision navigation to boost cancer screening participation in high-risk communities
This study tests whether a personalized navigation program helps adults aged 45–74 in Chinese communities who are at high risk for several cancers to complete recommended free cancer screenings.
-
Targeted radiopharmaceuticals for GRPR-positive cancers in adults
A phase 1 study tests two targeted radiopharmaceuticals, radiolabeled Lu-177 and Ac-225 compounds, to treat GRPR-expressing breast, prostate, colorectal, and other solid tumors in adults who have not benefited from standard therapies.
-
IM-1617 in people with advanced solid cancers
A first-in-human study will test IM-1617 to see if it is safe and helps treat solid tumors that have spread or cannot be removed.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.