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Kinectics of Distribution of Doxorubicin-Lipiodol Emulsion in c-TACE (CineDoxo)

Primary Purpose

Hepato Cellular Carcinoma

Status
Completed
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
Super selective transarterial chemoembolization of CHC, with doxorubicin reconstituted in 5cc iso-osmolar ionic iodinated contrast media
Super selective transarterial chemoembolization of CHC, with doxorubicin reconstituted in 5cc normal saline
Sponsored by
University Hospital, Strasbourg, France
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Hepato Cellular Carcinoma focused on measuring Conventional transarterial chemoembolization (c-TACE), Doxorubicin, Kinetics of distribution

Eligibility Criteria

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

Inclusion Criteria:

  • Adult (>18)
  • Informed consent
  • CHC Child-Pugh stage A or B, BCLC stage B
  • Referred for chemoembolization of a non-surgery-candidate CHC
  • Blood test results compatible with cTACE (INR ≤ 1,5, ASAT/ALAT<5N, albumine>2,5g/dl)

Exclusion Criteria:

  • Contraindication to cTACE, angiography, confocal laser endomicroscopy or liver biopsy Hyperthyroidism
  • Contraindication to the use of fluorescein, Ariblastine,Lipiodol, Visipaque, Gelita spon, Avitene
  • extra hepatic metastasis
  • Subcapsular or exophytic tumor impeding direct percutaneous access through healthy liver tissue
  • Waiting list for liver transplant
  • Complete portal venous thrombosis or flow inversion
  • Pregnancy or breast feeding
  • Protected major (Guardianship)
  • Patient in situation of exclusion (determined by a previous or ongoing study)
  • Subject incapacity to understand informed consent

Sites / Locations

  • University Hospital, Strasbourg, france

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Iodinate contrast

Normal saline

Arm Description

Doxorubicin solution reconstituted in 5 mL iso-osmolar ionic iodinated contrast media

Doxorubicin solution reconstituted in 5 mL normal saline

Outcomes

Primary Outcome Measures

Histological analysis of biopsy samples for the evaluation of the kinetics of distribution of doxorubicine in tumor compartments depending on the solvent used for drug reconstitution
Biopsy samples of liver tumor tissue. Histological analysis will provide a quantification of the doxorubicin drug in tumor compartment.
Histological analysis of biopsy samples for the evaluation of the kinetics of distribution of doxorubicine in tumor compartments depending on the solvent used for drug reconstitution
Biopsy samples of liver tumor tissue. Histological analysis will provide a quantification of the doxorubicin drug in tumor compartment.
Histological analysis of biopsy samples for the evaluation of the kinetics of distribution of doxorubicine in tumor compartments depending on the solvent used for drug reconstitution
Biopsy samples of liver tumor tissue. Histological analysis will provide a quantification of the doxorubicin drug in tumor compartment.
Histological analysis of biopsy samples for the evaluation of the kinetics of distribution of doxorubicine in tumor compartments depending on the solvent used for drug reconstitution
Biopsy samples of liver tumor tissue. Histological analysis will provide a quantification of the doxorubicin drug in tumor compartment.

Secondary Outcome Measures

In vivo evaluation of the kinetics of distribution of doxorubicine in tumoral tissue with confocal laser endomicroscopy, depending on the solvent used for drug reconstitution
Continuous image recording (videos) through the course of the cTACE drug injection, from 1 minute before drug injection starts to the time when cTACE drug injection is completed
In vivo evaluation of the kinetics of distribution of doxorubicine in tumoral tissue with confocal laser endomicroscopy, depending on the solvent used for drug reconstitution
Continuous image recording (videos) through the course of the cTACE drug injection, from 1 minute before drug injection starts to the time when cTACE drug injection is completed
In vivo evaluation of the kinetics of distribution of doxorubicine in tumoral tissue with confocal laser endomicroscopy, depending on the solvent used for drug reconstitution
Continuous image recording (videos) through the course of the cTACE drug injection, from 1 minute before drug injection starts to the time when cTACE drug injection is completed
In vivo evaluation of the kinetics of distribution of doxorubicine in tumoral tissue with confocal laser endomicroscopy, depending on the solvent used for drug reconstitution
Continuous image recording (videos) through the course of the cTACE drug injection, from 1 minute before drug injection starts to the time when cTACE drug injection is completed

Full Information

First Posted
October 2, 2018
Last Updated
July 24, 2020
Sponsor
University Hospital, Strasbourg, France
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1. Study Identification

Unique Protocol Identification Number
NCT03706157
Brief Title
Kinectics of Distribution of Doxorubicin-Lipiodol Emulsion in c-TACE
Acronym
CineDoxo
Official Title
Kinectics of Distribution of Doxorubicin-Lipiodol Emulsion in c-TACE: a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
November 26, 2018 (Actual)
Primary Completion Date
October 9, 2019 (Actual)
Study Completion Date
October 9, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Strasbourg, France

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
Conventional transarterial chemoembolization with Doxorubicin (c-TACE) is the gold standard treatment for Hepato Cellular Carcinoma (HCC) stage B (BCLC) / stages A and B (Child-Pugh). Clinical recommendations for cTACE indicate that the doxorubicin solution may be reconstituted in either aqueous solution or iso-osmolar ionic iodinated contrast media. There is no consensus on which solvent should be used. Hence, the clinical evaluation of Lipiodol cTACE would benefit from a standardization in the reconstitution of the drug. In this study, the comparison of the kinetics of distribution of the drug within the tumor micro-environment is expected to allow for comparison of drug solvents. This pilot study aims at evaluating the kinetics of distribution of the drug within the tumor micro-environment, for the two main solvents used in reconstituting the drug, namely normal saline and contrast media. The kinetics of distribution in the tumor will be evaluated primarily through regular biopsy sampling, and secondary with confocal laser endomicroscopy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepato Cellular Carcinoma
Keywords
Conventional transarterial chemoembolization (c-TACE), Doxorubicin, Kinetics of distribution

7. Study Design

Primary Purpose
Other
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Iodinate contrast
Arm Type
Active Comparator
Arm Description
Doxorubicin solution reconstituted in 5 mL iso-osmolar ionic iodinated contrast media
Arm Title
Normal saline
Arm Type
Active Comparator
Arm Description
Doxorubicin solution reconstituted in 5 mL normal saline
Intervention Type
Drug
Intervention Name(s)
Super selective transarterial chemoembolization of CHC, with doxorubicin reconstituted in 5cc iso-osmolar ionic iodinated contrast media
Intervention Description
Super selective transarterial chemoembolization of CHC, with doxorubicin reconstituted in 5cc iso-osmolar ionic iodinated contrast media
Intervention Type
Drug
Intervention Name(s)
Super selective transarterial chemoembolization of CHC, with doxorubicin reconstituted in 5cc normal saline
Intervention Description
Super selective transarterial chemoembolization of CHC, with doxorubicin reconstituted in 5cc normal saline
Primary Outcome Measure Information:
Title
Histological analysis of biopsy samples for the evaluation of the kinetics of distribution of doxorubicine in tumor compartments depending on the solvent used for drug reconstitution
Description
Biopsy samples of liver tumor tissue. Histological analysis will provide a quantification of the doxorubicin drug in tumor compartment.
Time Frame
T0: 1 min before cTACE drug injection star
Title
Histological analysis of biopsy samples for the evaluation of the kinetics of distribution of doxorubicine in tumor compartments depending on the solvent used for drug reconstitution
Description
Biopsy samples of liver tumor tissue. Histological analysis will provide a quantification of the doxorubicin drug in tumor compartment.
Time Frame
T1 : 2 min after cTACE drug injection started
Title
Histological analysis of biopsy samples for the evaluation of the kinetics of distribution of doxorubicine in tumor compartments depending on the solvent used for drug reconstitution
Description
Biopsy samples of liver tumor tissue. Histological analysis will provide a quantification of the doxorubicin drug in tumor compartment.
Time Frame
T2: 1 second after half of cTACE drug has been injected
Title
Histological analysis of biopsy samples for the evaluation of the kinetics of distribution of doxorubicine in tumor compartments depending on the solvent used for drug reconstitution
Description
Biopsy samples of liver tumor tissue. Histological analysis will provide a quantification of the doxorubicin drug in tumor compartment.
Time Frame
T3: 1 min after cTACE drug injection is completed
Secondary Outcome Measure Information:
Title
In vivo evaluation of the kinetics of distribution of doxorubicine in tumoral tissue with confocal laser endomicroscopy, depending on the solvent used for drug reconstitution
Description
Continuous image recording (videos) through the course of the cTACE drug injection, from 1 minute before drug injection starts to the time when cTACE drug injection is completed
Time Frame
1 min before cTACE drug injection starts,
Title
In vivo evaluation of the kinetics of distribution of doxorubicine in tumoral tissue with confocal laser endomicroscopy, depending on the solvent used for drug reconstitution
Description
Continuous image recording (videos) through the course of the cTACE drug injection, from 1 minute before drug injection starts to the time when cTACE drug injection is completed
Time Frame
2 min after cTACE drug injection started,
Title
In vivo evaluation of the kinetics of distribution of doxorubicine in tumoral tissue with confocal laser endomicroscopy, depending on the solvent used for drug reconstitution
Description
Continuous image recording (videos) through the course of the cTACE drug injection, from 1 minute before drug injection starts to the time when cTACE drug injection is completed
Time Frame
1 second after half of cTACE drug has been injected,
Title
In vivo evaluation of the kinetics of distribution of doxorubicine in tumoral tissue with confocal laser endomicroscopy, depending on the solvent used for drug reconstitution
Description
Continuous image recording (videos) through the course of the cTACE drug injection, from 1 minute before drug injection starts to the time when cTACE drug injection is completed
Time Frame
1 min after cTACE drug injection is completed,

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult (>18) Informed consent CHC Child-Pugh stage A or B, BCLC stage B Referred for chemoembolization of a non-surgery-candidate CHC Blood test results compatible with cTACE (INR ≤ 1,5, ASAT/ALAT<5N, albumine>2,5g/dl) Exclusion Criteria: Contraindication to cTACE, angiography, confocal laser endomicroscopy or liver biopsy Hyperthyroidism Contraindication to the use of fluorescein, Ariblastine,Lipiodol, Visipaque, Gelita spon, Avitene extra hepatic metastasis Subcapsular or exophytic tumor impeding direct percutaneous access through healthy liver tissue Waiting list for liver transplant Complete portal venous thrombosis or flow inversion Pregnancy or breast feeding Protected major (Guardianship) Patient in situation of exclusion (determined by a previous or ongoing study) Subject incapacity to understand informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Iuian 03 69 55 15 27, MD
Organizational Affiliation
University Hospital, Strasbourg, France
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital, Strasbourg, france
City
Strasbourg
ZIP/Postal Code
67000
Country
France

12. IPD Sharing Statement

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Kinectics of Distribution of Doxorubicin-Lipiodol Emulsion in c-TACE

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