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Combined Fluorocholine Positron Emission Tomography and Magnetic Resonance Imaging (FCH-PET/MRI) in Curative Treatment of a Hepatocellular Carcinoma (TOMIC)

Primary Purpose

Patients Eligible to a Curative Treatment for Primary HCC

Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
PET/MRI system (SIEMENS AG, Munich, Germany; distributed in France by SIEMENS S.A.S, Saint-Denis, France)
Sponsored by
Hospices Civils de Lyon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Patients Eligible to a Curative Treatment for Primary HCC focused on measuring FCH-PET/MRI, primary HCC, curative treatment, resection, thermo-ablation, transplantation

Eligibility Criteria

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

Inclusion Criteria:

  • Age ≥18 years old
  • Primary HCC proven by histological or imaging examinations (LIRAD 4 or 5)
  • Eligible for curative treatment (Barcelona criteria) i.e. hepatic transplantation according to Milan criteria, surgical resection, or thermo-ablation, according to a multidisciplinary decision care committee
  • Affiliated to, or a beneficiary of, a social security system
  • Written informed consent.

Exclusion Criteria:

  • Patient refusing curative treatment
  • Patient with HCC not eligible for curative treatment according to conventional imaging (CT, MRI)
  • Patient with performance status >1
  • Contraindication to MRI
  • Pregnant or lactating woman
  • Adult ward of court (under guardianship or trusteeship)

Sites / Locations

  • CHU de Grenoble, Servide d'Hépato-gastro-entérologieRecruiting
  • HCL, Hôpital Edouard Herriot, service d'hépato-gastro-entérologieRecruiting
  • HCL, Hôpital de la Croix-Rousse, service d'Hépato-gastro-entérologieRecruiting
  • Hospices Civils de Lyon, Groupement Hospitalier Lyon Sud, Service de radiologie digestive

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

FCH-PET/MRI

Arm Description

FCH-PET/MRI exam performed in addition to the usual examinations for monitoring hepatocellular carcinoma.

Outcomes

Primary Outcome Measures

Specificity of FCH-PET/MRI for the detection of preoperative lesions
Specificity of FCH-PET/MRI for the detection of preoperative lesions not visible with conventional imaging techniques and confirmed as being HCC Specificity of preoperative FCH-PET/MRI will be calculated as a ratio of the number of patients with negative FCH-PET/MRI and no additional lesions in histopathology and/or no progressive lesions confirmed at follow-up, to the total number of patients with no additional lesions in histopathology and/or no progressive lesions confirmed at follow-up.

Secondary Outcome Measures

Progression-free survival rates of patients with and without additional lesions visible on FCH-PET/MRI
Sensitivity of preoperative FCH-PET/MRI for detecting HCC lesions
Sensitivity of preoperative FCH-PET/MRI will be determined as a ratio of the number of patients with positive imaging and additional lesions in histopathology and/or progressive lesions confirmed at follow-up, to the total number of patients with additional lesions in histopathology and/or progressive lesions confirmed at follow-up.
Positive and negative predictive value of FCH-PET/MRI
Positive predictive value will be calculated from the number of patients with positive imaging and additional lesions in histopathology and/or progressive lesions confirmed at follow-up, and the total number of patients with positive imaging. Negative predictive value will be calculated from the number of patients with negative imaging and no additional lesions in histopathology and/or progressive lesions confirmed at follow-up, and the total number of patients with negative imaging.
Specificity and sensitivity of FCH-PET/MRI compared with preoperative MRI findings for extra-hepatic HCC lesions and for intra-hepatic HCC lesions
FCH-PET/MRI findings (positive or negative, and standardized uptake value ratio between lesions and liver or tissue) compared to HCC differentiation by histopathology
Costs of performing FCH-PET/MRI
Direct observation of the realization of FCH-PET/MRI, to be able to reconstitute, in the most reliable way, the cost of the examination (micro-costing method).
Incremental cost-effectiveness ratio
Modeling of the patient pathway in terms of resource consumption and efficacy, including the completion of FCH-PET/MRI compared to the usual strategy of patient care
Costs avoided and induced by performing FCH-PET/MRI

Full Information

First Posted
June 29, 2016
Last Updated
January 12, 2021
Sponsor
Hospices Civils de Lyon
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1. Study Identification

Unique Protocol Identification Number
NCT02824185
Brief Title
Combined Fluorocholine Positron Emission Tomography and Magnetic Resonance Imaging (FCH-PET/MRI) in Curative Treatment of a Hepatocellular Carcinoma
Acronym
TOMIC
Official Title
Potential Interest of Combined Fluorocholine Positron Emission Tomography and Magnetic Resonance Imaging (FCH-PET/MRI) for the Selection of Patients Proposed for Curative Treatment of a Hepatocellular Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Unknown status
Study Start Date
June 14, 2017 (Actual)
Primary Completion Date
December 14, 2021 (Anticipated)
Study Completion Date
August 14, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospices Civils de Lyon

4. Oversight

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

5. Study Description

Brief Summary
Hepatocellular carcinoma (HCC) is the fifth most common cancer in terms of incidence and the second in terms of mortality. At an early stage, which is based on a low number and size of liver nodules and the absence of extra-hepatic locations (Milan criteria), a curative treatment can be performed, i.e. liver transplantation, surgical resection, or thermo-ablation. These treatments can lead to severe complications, so patients benefiting from them must be carefully selected. The correct identification of all HCC lesions at the time of the therapeutic decision is crucial. MRI is the reference examination for diagnosis but its field of exploration is limited to the upper abdominal area and its sensitivity decreases for nodules of less than two centimetres. Such lesions could actually be HCC that will cause early post-operative progression. Positron Emission Tomography (PET; functional imaging) with fluorodeoxyglucose can provide prognostic information but impacts initial staging in less than 5% of cases. However, PET with fluorocholine (FCH), available in France since 2010, could detect intra- and extra-hepatic HCC lesions not identified by conventional imaging, potentially impacting patient management (e.g. 52% of patients in a small case study). FCH-PET/MRI could therefore be the ideal examination for the initial staging of HCC, combining in a single multimodality investigation the reference morphological imaging technique and an efficient functional one. The hypothesis of this study is that FCH-PET/MRI is able to detect, in patients eligible for curative treatment, additional preoperative intra- and extra-hepatic early or metastatic HCC unseen or equivocal with conventional imaging (CT and MRI) and responsible for recurrence or disease progression at 6 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Patients Eligible to a Curative Treatment for Primary HCC
Keywords
FCH-PET/MRI, primary HCC, curative treatment, resection, thermo-ablation, transplantation

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
82 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
FCH-PET/MRI
Arm Type
Experimental
Arm Description
FCH-PET/MRI exam performed in addition to the usual examinations for monitoring hepatocellular carcinoma.
Intervention Type
Device
Intervention Name(s)
PET/MRI system (SIEMENS AG, Munich, Germany; distributed in France by SIEMENS S.A.S, Saint-Denis, France)
Intervention Description
A PET/MRI examination will be performed once for all included patients, using injected fluorocholine, with a dose of 3MBq/kg, up to 2 months before HCC treatment.
Primary Outcome Measure Information:
Title
Specificity of FCH-PET/MRI for the detection of preoperative lesions
Description
Specificity of FCH-PET/MRI for the detection of preoperative lesions not visible with conventional imaging techniques and confirmed as being HCC Specificity of preoperative FCH-PET/MRI will be calculated as a ratio of the number of patients with negative FCH-PET/MRI and no additional lesions in histopathology and/or no progressive lesions confirmed at follow-up, to the total number of patients with no additional lesions in histopathology and/or no progressive lesions confirmed at follow-up.
Time Frame
6 months post-treatment
Secondary Outcome Measure Information:
Title
Progression-free survival rates of patients with and without additional lesions visible on FCH-PET/MRI
Time Frame
24 months post-treatment
Title
Sensitivity of preoperative FCH-PET/MRI for detecting HCC lesions
Description
Sensitivity of preoperative FCH-PET/MRI will be determined as a ratio of the number of patients with positive imaging and additional lesions in histopathology and/or progressive lesions confirmed at follow-up, to the total number of patients with additional lesions in histopathology and/or progressive lesions confirmed at follow-up.
Time Frame
6 months post-treatment
Title
Positive and negative predictive value of FCH-PET/MRI
Description
Positive predictive value will be calculated from the number of patients with positive imaging and additional lesions in histopathology and/or progressive lesions confirmed at follow-up, and the total number of patients with positive imaging. Negative predictive value will be calculated from the number of patients with negative imaging and no additional lesions in histopathology and/or progressive lesions confirmed at follow-up, and the total number of patients with negative imaging.
Time Frame
6 months post-treatment
Title
Specificity and sensitivity of FCH-PET/MRI compared with preoperative MRI findings for extra-hepatic HCC lesions and for intra-hepatic HCC lesions
Time Frame
FCH-PET/MRI examination, up to 2 months before treatment
Title
FCH-PET/MRI findings (positive or negative, and standardized uptake value ratio between lesions and liver or tissue) compared to HCC differentiation by histopathology
Time Frame
FCH-PET/MRI examination, up to 2 months before treatment
Title
Costs of performing FCH-PET/MRI
Description
Direct observation of the realization of FCH-PET/MRI, to be able to reconstitute, in the most reliable way, the cost of the examination (micro-costing method).
Time Frame
FCH-PET/MRI examination, up to 2 months before treatment
Title
Incremental cost-effectiveness ratio
Description
Modeling of the patient pathway in terms of resource consumption and efficacy, including the completion of FCH-PET/MRI compared to the usual strategy of patient care
Time Frame
24 months post-treatment
Title
Costs avoided and induced by performing FCH-PET/MRI
Time Frame
24 months post-treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥18 years old Primary HCC proven by histological or imaging examinations (LIRAD 4 or 5) Eligible for curative treatment (Barcelona criteria) i.e. hepatic transplantation according to Milan criteria, surgical resection, or thermo-ablation, according to a multidisciplinary decision care committee Affiliated to, or a beneficiary of, a social security system Written informed consent. Exclusion Criteria: Patient refusing curative treatment Patient with HCC not eligible for curative treatment according to conventional imaging (CT, MRI) Patient with performance status >1 Contraindication to MRI Pregnant or lactating woman Adult ward of court (under guardianship or trusteeship)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pierre-Jean VALETTE, Pr
Phone
(0)4 72 11 75 44
Ext
+33
Email
pierre-jean.valette@chu-lyon.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Soumia BAYARASSOU, Clinical Research Assistant
Phone
(0)4 72 11 51 69
Ext
+33
Email
soumia.bayarassou01@chu-lyon.fr
Facility Information:
Facility Name
CHU de Grenoble, Servide d'Hépato-gastro-entérologie
City
La Tronche
ZIP/Postal Code
38700
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Thomas DECAENS, MD
First Name & Middle Initial & Last Name & Degree
Thomas DECAENS, MD
Facility Name
HCL, Hôpital Edouard Herriot, service d'hépato-gastro-entérologie
City
Lyon
ZIP/Postal Code
69003
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jérôme DUMORTIER, MD
First Name & Middle Initial & Last Name & Degree
Jérôme DUMORTIER, MD
First Name & Middle Initial & Last Name & Degree
Pierre-Jean VALETTE, MD
First Name & Middle Initial & Last Name & Degree
Hélène GIMONET, MD
Facility Name
HCL, Hôpital de la Croix-Rousse, service d'Hépato-gastro-entérologie
City
Lyon
ZIP/Postal Code
69004
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Philippe MERLE, MD
First Name & Middle Initial & Last Name & Degree
Philippe MERLE, MD
Facility Name
Hospices Civils de Lyon, Groupement Hospitalier Lyon Sud, Service de radiologie digestive
City
Pierre-Bénite
ZIP/Postal Code
69495
Country
France
Individual Site Status
Active, not recruiting

12. IPD Sharing Statement

Learn more about this trial

Combined Fluorocholine Positron Emission Tomography and Magnetic Resonance Imaging (FCH-PET/MRI) in Curative Treatment of a Hepatocellular Carcinoma

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