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Colorectal Liver Metastases: Novel Assessment Tools for Technical Resectability

Conditions
Liver Metastasis Colon Cancer
Cancer Metastatic
Colorectal Cancer
Cancer
Registration Number
NCT04270851
Lead Sponsor
University of Manchester
Brief Summary

The CoNoR study aims to assess whether the use of the LiMAx test and the HepaT1ca pre-operative planning magnetic resonance scan impact upon technical resectability decision-making in colorectal liver metastases (CLM).

Detailed Description

The CoNoR Study will occur via 4 workstreams:

1. Systematic review of all published criteria for colorectal liver metastases (CLM) technical resectability (systematic review protocol published on PROSPERO database: https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=136748

2. Expert interviews: Interviews with liver surgeons and radiologists to assess current standard practice in CLM technical resectability decision-making and role for novel assessment tools

3. Online questionnaire: Online international questionnaire of liver surgeons to assess current standard practice in CLM technical resectability decision-making and role for novel assessment tools, in additional to identifying clinical scenarios in which these tools may be of greatest benefit

4. Online case-based survey: Recruitment of 10-20 participants with 'difficult decisions' regarding technical resectability, and consent to use results from pre-operative assessments to create anonymised online case-based survey. Participants will consent to have two additional pre-operative assessments: the LiMAx tests and the HepaT1ca magnetic resonance scan. These results from these additional tests will also be used in the online survey, We will recruit international liver surgeons to complete this online survey, where they will be asked to provide an opinion on technical resectability for each individual case scenario, and to specify their operative plan, both before and after seeing the results of these novel assessment tools. We will assess for change in decision-making on resectability, and change in operative plan after seeing these test results. We will also assess for level of agreement between liver surgeons on each scenario, and identify where they difficult decisions persist.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
20
Inclusion Criteria
  1. Patients over 16 years of age with histologically verified adenocarcinoma of the colon or rectum and radiological evidence of liver metastases
  2. Discussion at regional hepatobiliary multidisciplinary team meeting
  3. Hepatobiliary surgical opinion that their case represents a potentially difficult decision regarding technical resectability
  4. Ability to provide written informed consent
Exclusion Criteria
  1. Presence of a medical or psychiatric condition impairing the ability to give informed consent
  2. Presence of any other serious uncontrolled medical condition
  3. Patients under 16 years old
  4. Contra-indications to magnetic resonance scanning

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in decision making on technical resectabilityOne year

Liver surgeons will view the standard pre-operative assessment results and decide if each case scenario is 'technically resectable.' They will then view the results from these two additional pre-operative tests (LiMAx and HepaT1ca), and decide again. We will measure for any change in decision making after viewing the novel test results.

Secondary Outcome Measures
NameTimeMethod
Change in operative planOne Year

Liver surgeons will view the standard pre-operative assessment results and specify their operative plan for each clinical scenario. They will then view the results from these two additional pre-operative tests (LiMAx and HepaT1ca), and specify their operative plan again. We will measure for any change in decision making in their operative plan after viewing the novel test results.

Level of agreement between liver surgeons on technical resectabilityOne Year

For all participating surgeons, we will measure the level of agreement between them when they decide if each case scenario is technically resectable.

Trial Locations

Locations (1)

The Christie NHS Foundation Trust

🇬🇧

Manchester, Greater Manchester, United Kingdom

The Christie NHS Foundation Trust
🇬🇧Manchester, Greater Manchester, United Kingdom

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