NCT07180641

Brief Summary

The investigators designed this observational, retrospective, multicenter study including all patients who underwent surgery for non-colorectal liver metastases between January 2010 and December 2022, with the aim of establishing a series of recommendations for the treatment of liver metastases from various extrahepatic primary tumors

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,039

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2010

Longer than P75 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2010

Completed
13 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2022

Completed
2.7 years until next milestone

First Submitted

Initial submission to the registry

August 25, 2025

Completed
24 days until next milestone

First Posted

Study publicly available on registry

September 18, 2025

Completed
Last Updated

September 18, 2025

Status Verified

September 1, 2025

Enrollment Period

13 years

First QC Date

August 25, 2025

Last Update Submit

September 11, 2025

Conditions

Keywords

Non-colorectal non-neuroendocrine liver metastasesLiver metastasesLiver resectionHepatectomy

Outcome Measures

Primary Outcomes (2)

  • Overall Survival

    Time from the date of liver resection for non-colorectal metastases to death from any cause. Survival will be assessed for up to 5 years postoperatively

    5 years from liver resection

  • Progression-Free Survival

    Time from the date of liver resection for non-colorectal metastases to the date of documented disease progression or death from any cause, whichever occurs first. Patients without progression or death will be censored at the last follow-up

    5 years from surgery

Secondary Outcomes (5)

  • Postoperative Morbidity Rate

    90 days from surgery

  • Postoperative Mortality Rate

    90 days from surgery

  • Recurrence Pattern

    Up to 5 years from liver resection

  • Length of hospital stay

    Perioperative/Periprocedural

  • R0 Resection Rate

    At surgery

Study Arms (1)

Patients with non-colorectal liver metastases

Patients who underwent liver resection for non-colorectal liver metastases from January 2010 to December 2022

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Adult patients scheduled for liver surgery due to non-colorectal liver metastases, regardless of the primary tumor origin, via open or minimally invasive approach, from January 2010 to December 2022

You may qualify if:

  • Patients scheduled for liver surgery due to non-colorectal liver metastases, regardless of the primary tumor origin, via open or minimally invasive approach

You may not qualify if:

  • Patients undergoing surgery for colorectal liver metastases, emergency surgical interventions and patients younger than 18 years old.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 25, 2025

First Posted

September 18, 2025

Study Start

January 1, 2010

Primary Completion

December 31, 2022

Study Completion

December 31, 2022

Last Updated

September 18, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will share

The data will be shared with all investigators who have participated in this multicenter study and who have expressed interest in its follow-up and execution. The data will be shared anonymously, as each patient is assigned a unique anonymized identification number unrelated to their clinical records. Access to the data will be available for a period of five years following the end of recruitment, which was June 2025. There is no official repository; interested investigators must contact me directly, and I will provide them with unique and private access to the data

Shared Documents
STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE
Time Frame
5 years following the end of recruitment, which was June 2025
Access Criteria
All investigators who have participated in this multicenter study and who have expressed interest in its follow-up and execution.