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

U

University of Edinburgh

Status

Completed

Conditions

Surgery
Colorectal Cancer Metastatic
Liver Regeneration
Liver Cancer

Treatments

Diagnostic Test: Multiparameter magnetic resonance imaging

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT03213314
AC17009
223180 (Other Identifier)

Details and patient eligibility

About

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.

Full 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.

Enrollment

149 patients

Sex

All

Ages

18+ years old

Volunteers

No 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

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

149 participants in 4 patient groups

Main cohort
Experimental group
Description:
Patients undergoing liver resection
Treatment:
Diagnostic Test: Multiparameter magnetic resonance imaging
Nested cohort PVE
Experimental group
Description:
Patients undergoing liver resection after portal vein embolisation
Treatment:
Diagnostic Test: Multiparameter magnetic resonance imaging
Nested cohort neoadjuvant chemotherapy
Experimental group
Description:
Patients undergoing liver resection after neoadjuvant chemotherapy
Treatment:
Diagnostic Test: Multiparameter magnetic resonance imaging
Nested cohort TACE
Experimental group
Description:
Patients undergoing trans arterial chemoembolisation for presumed hepatocellular carcinoma
Treatment:
Diagnostic Test: Multiparameter magnetic resonance imaging

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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