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HepaT1ca: Quantifying Liver Health in Surgical Candidates for Liver Malignancies (Hepatica)

Primary Purpose

Liver Cancer, Surgery, Liver Regeneration

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Multiparameter magnetic resonance imaging
Sponsored by
University of Edinburgh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Liver Cancer focused on measuring LiverMultiScan, multiparameter MRI, functional liver remnant, liver resection, hepatic resection, portal vein embolisation, preoperative liver function, postoperative liver failure

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients being considered for liver resection

Exclusion Criteria:

  • i. Patients under the age of 18 years will be excluded from the present study. ii. Prisoners will be excluded from the present study. iii. Persons unable to have an MRI scan (including but not limited to claustrophobia, implanted metallic devices, metal foreign body) iv. Adults with incapacity v. Non-provision of consent

Sites / Locations

  • Hampshire Hospitals Foundation Trust
  • NHS Lothian Royal Infirmary of Edinburgh

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Main cohort

Nested cohort PVE

Nested cohort neoadjuvant chemotherapy

Nested cohort TACE

Arm Description

Patients undergoing liver resection

Patients undergoing liver resection after portal vein embolisation

Patients undergoing liver resection after neoadjuvant chemotherapy

Patients undergoing trans arterial chemoembolisation for presumed hepatocellular carcinoma

Outcomes

Primary Outcome Measures

Correlation between the pre-operative liver health assessment score and the post-operative liver function composite integer-based risk score.
Correlation between the pre-operative liver health assessment score (Hepatica score - calculated by weighting future remnant liver volume by liver inflammation and fibrosis (LIF) score) and the post-operative liver function composite integer-based risk (Hyder-Pawlik) score.

Secondary Outcome Measures

To compare LiverMultiScan image interpretations with histological findings
To compare LiverMultiScan image interpretations with clinical outcome after surgery in three domains: post-operative liver function, surgery-specific complication rate, and overall complication rate
• To evaluate LiverMultiScan image interpretations correlated with post-operative length of stay.
• To compare LiverMultiScan image interpretations with histological findings in the resected liver specimen in four domains: fibrosis, inflammation, fat content and iron load as title

Full Information

First Posted
June 30, 2017
Last Updated
October 3, 2019
Sponsor
University of Edinburgh
Collaborators
Hampshire Hospitals NHS Foundation Trust, Perspectum
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1. Study Identification

Unique Protocol Identification Number
NCT03213314
Brief Title
HepaT1ca: Quantifying Liver Health in Surgical Candidates for Liver Malignancies
Acronym
Hepatica
Official Title
HepaT1ca: Quantifying Liver Health in Surgical Candidates for Liver Malignancies
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
September 7, 2017 (Actual)
Primary Completion Date
March 31, 2019 (Actual)
Study Completion Date
March 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Edinburgh
Collaborators
Hampshire Hospitals NHS Foundation Trust, Perspectum

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This observational clinical cohort study aims to evaluate the clinical utility of LiverMultiScan in quantifying liver health prior to liver resection or TACE. The results will enable further developments in scanning protocols and software, and clearly define the relevance of applying this technology as part of the pre-operative assessment of the patient being considered for liver resection or TACE.
Detailed Description
The liver is unique among the abdominal organs for the capacity to regenerate post-operatively. However, a minimum functional liver remnant (FLR) is required for patients to survive the initial perioperative period. At present, the assessment of the FLR is based on volume alone, in the context of clinical judgment and surrogate markers of liver function based on blood tests. Recently, Perspectum Diagnostics have developed and validated LiverMultiScan, an MRI-based technology that can non-invasively quantify fibroinflammatory disease in addition to steatosis and iron content. In this project, we plan to use LiverMultiScan as an additional direct measurement of liver health prior to resectional surgery or transarterial chemoembolization (TACE), so that liver volume and function can be combined. For example, surgery with a predicted FLR of 21% might be survivable if the liver tissue was in extremely good health, whereas surgery with a predicted FLR of 40% might be lethal if the liver tissue was in poor health. Occasionally, portal vein embolization (PVE) is performed to promote hypertrophy of the FLR. Furthermore, non-resectional intervention, for example TACE for primary liver cancers, is well-tolerated by patients with healthy livers, but can lead to serious liver decompensation and liver failure if TACE is delivered to a liver in poor health. Currently, the available imaging modalities are limited in their ability to assess liver health in liver resection or TACE candidates. Liver fat content (steatosis) can be assessed with CT, or more accurately with MRI. However, fibroinflammatory disease, which has been shown to correlate with post-resection morbidity, typically requires an invasive biopsy to diagnose accurately. This research project will support the definition, development and technical validation of Hepatica, which aims to build on the MRI technology underlying LiverMultiScan and develop the additional functionality required to meet this clinical need.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Cancer, Surgery, Liver Regeneration, Colorectal Cancer Metastatic
Keywords
LiverMultiScan, multiparameter MRI, functional liver remnant, liver resection, hepatic resection, portal vein embolisation, preoperative liver function, postoperative liver failure

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Nested cohort study
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
149 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Main cohort
Arm Type
Experimental
Arm Description
Patients undergoing liver resection
Arm Title
Nested cohort PVE
Arm Type
Experimental
Arm Description
Patients undergoing liver resection after portal vein embolisation
Arm Title
Nested cohort neoadjuvant chemotherapy
Arm Type
Experimental
Arm Description
Patients undergoing liver resection after neoadjuvant chemotherapy
Arm Title
Nested cohort TACE
Arm Type
Experimental
Arm Description
Patients undergoing trans arterial chemoembolisation for presumed hepatocellular carcinoma
Intervention Type
Diagnostic Test
Intervention Name(s)
Multiparameter magnetic resonance imaging
Other Intervention Name(s)
LiverMultiScan
Intervention Description
LiverMultiScan before and after surgery to assess liver health prior to liver resection and in the regenerative phase.
Primary Outcome Measure Information:
Title
Correlation between the pre-operative liver health assessment score and the post-operative liver function composite integer-based risk score.
Description
Correlation between the pre-operative liver health assessment score (Hepatica score - calculated by weighting future remnant liver volume by liver inflammation and fibrosis (LIF) score) and the post-operative liver function composite integer-based risk (Hyder-Pawlik) score.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
To compare LiverMultiScan image interpretations with histological findings
Description
To compare LiverMultiScan image interpretations with clinical outcome after surgery in three domains: post-operative liver function, surgery-specific complication rate, and overall complication rate
Time Frame
24 months
Title
• To evaluate LiverMultiScan image interpretations correlated with post-operative length of stay.
Description
• To compare LiverMultiScan image interpretations with histological findings in the resected liver specimen in four domains: fibrosis, inflammation, fat content and iron load as title
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients being considered for liver resection Exclusion Criteria: i. Patients under the age of 18 years will be excluded from the present study. ii. Prisoners will be excluded from the present study. iii. Persons unable to have an MRI scan (including but not limited to claustrophobia, implanted metallic devices, metal foreign body) iv. Adults with incapacity v. Non-provision of consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Damian J Mole, MBChB PhD
Organizational Affiliation
University of Edinburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hampshire Hospitals Foundation Trust
City
Basingstoke
Country
United Kingdom
Facility Name
NHS Lothian Royal Infirmary of Edinburgh
City
Edinburgh
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Controlled access of study data through a reasonable request to the study management team, after a reasonable embargo period after completion of the study
Citations:
PubMed Identifier
33264327
Citation
Mole DJ, Fallowfield JA, Sherif AE, Kendall T, Semple S, Kelly M, Ridgway G, Connell JJ, McGonigle J, Banerjee R, Brady JM, Zheng X, Hughes M, Neyton L, McClintock J, Tucker G, Nailon H, Patel D, Wackett A, Steven M, Welsh F, Rees M; HepaT1ca Study Group. Quantitative magnetic resonance imaging predicts individual future liver performance after liver resection for cancer. PLoS One. 2020 Dec 2;15(12):e0238568. doi: 10.1371/journal.pone.0238568. eCollection 2020.
Results Reference
derived
PubMed Identifier
30208871
Citation
Mole DJ, Fallowfield JA, Kendall TJ, Welsh F, Semple SI, Bachtiar V, Kelly M, Wigmore SJ, James Garden O, Wilman HR, Banerjee R, Rees M, Brady M. Study protocol: HepaT1ca - an observational clinical cohort study to quantify liver health in surgical candidates for liver malignancies. BMC Cancer. 2018 Sep 12;18(1):890. doi: 10.1186/s12885-018-4737-3.
Results Reference
derived

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HepaT1ca: Quantifying Liver Health in Surgical Candidates for Liver Malignancies

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