Skip to content

NON-COlorectal Liver METastases Undergoing Liver Resection

Electronic Dataset of NON-COlorectal Liver METastases Undergoing Liver Resection

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06542926
Acronym
NONCOLMET
Enrollment
300
Registered
2024-08-07
Start date
2025-01-01
Completion date
2029-06-30
Last updated
2024-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Liver Metastases

Brief summary

Liver metastases (LM) are common in various types of malignant diseases, either at the diagnosis of the primary tumour or at a later time point. While the resection of colorectal LM (CRLM) is a well-established procedure, with survival rates superior to chemotherapy alone, controversial data still exist on liver resection for non-colorectal LM (NCRLM) (2, 3). These patients comprise a diverse and heterogeneous group usually excluded from surgery due to advanced tumour stage or the presence of concomitant extrahepatic disease. To date, no randomized clinical trial on the surgical treatment of NCRLM has been conducted, and only few retrospective reports are available.The scope of this research project is to develop a large registry of patients undergoing liver surgery for non-colorectal liver metastases.

Interventions

PROCEDUREliver resection

Resection of non-colorectal liver metastases

Sponsors

Azienda Ospedaliero Universitaria Maggiore della Carita
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Signature informed consent * Age ≥ 18 years * Histologically confirmed diagnosis of NCRLM (first diagnosis or relapse) * Liver resection performed.

Exclusion criteria

* ASA IV * Severe psychiatric pathology * Unable to follow a clinical examination pattern during observation. * Patient submitted exclusively to interventional locoregional procedures other than liver resection.

Design outcomes

Primary

MeasureTime frameDescription
Overall SurvivalFrom date of enrollment until the date of death from any cause assessed up to 36 monthsOverall Survival defined as the time elapsed between the date of resective surgery and the date of death for any reason. Patients who are surviving at the end of observation will be considered censored at the date of the last available follow-up.

Secondary

MeasureTime frameDescription
Disease-free SurvivalFrom date of enrollement until the date of first documented progression assessed up to 36 monthsDisease-free Survival defined as the time from resective surgery to the date of first relapse or last available follow-up, whichever occurs first

Contacts

Primary ContactMatteo Donadon, MD, PhD
matteo.donadon@uniupo.it003903213733045

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026