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Prospective Evaluation of the Ablation Therapy With Bipolar Radio Frequency for Nonresectable Bile Duct Cancer (RFA-BILIAIRE)

Primary Purpose

Nonresectable Bile Duct Cancer

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Ablation Therapy
Sponsored by
Institut Paoli-Calmettes
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nonresectable Bile Duct Cancer

Eligibility Criteria

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

Inclusion Criteria:

  • Age ≥ 18 years,
  • Bile duct cancer nonresectable
  • Type I, II ou III of Bismuth classification with cholangio-MRI and/or endoscopic cholangiography
  • Laboratory values : prothrombin time ≥ 50%, platelets ≥ 50 000, aPTT < 3 (Authorized transfusions)
  • Written informed consent,
  • Affiliation to Social Security System.

Exclusion Criteria:

  • Intra-pancreatic mass and/or Wirsung dilation,
  • Bile duct cancer,
  • Visceral metastasis (extrahepatic),
  • Initial metallic prosthesis,
  • Woman pregnant or susceptible to the being,
  • Patients deprived of liberty or placed Under the authority of a tutor,
  • Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol or follow-up schedule.

Sites / Locations

  • Institut Paoli-Calmettes

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Ablation Therapy With Bipolar Radio Frequency

Arm Description

Outcomes

Primary Outcome Measures

Rate of success of the use of a treatment based on radiofrequency for all the target stenosis.
Evaluation of the success of the use of bipolary radiofrequency for all target stenosis after each procedure

Secondary Outcome Measures

Technic efficiency (Measure the duration of biliary permeability in the time)
Ablation Therapy
Number of intervention for biliary drainage on the duration of the follow-up
Biliary drainage intervention
Global morbidity to 30 days
Morbidity
Specific morbidity to 30 days
Complications after intervention((cholecystitis, haemorrhage, pancreatitis, angiocholitis, intestinal perforation),
Overall survival
Overall survival

Full Information

First Posted
November 14, 2017
Last Updated
June 22, 2023
Sponsor
Institut Paoli-Calmettes
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1. Study Identification

Unique Protocol Identification Number
NCT03679338
Brief Title
Prospective Evaluation of the Ablation Therapy With Bipolar Radio Frequency for Nonresectable Bile Duct Cancer
Acronym
RFA-BILIAIRE
Official Title
Prospective Evaluation of the Ablation Therapy With Bipolar Radio Frequency for Nonresectable Bile Duct Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
March 22, 2018 (Actual)
Primary Completion Date
March 18, 2021 (Actual)
Study Completion Date
March 11, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut Paoli-Calmettes

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
90 % of the patients with bile duct cancer are not justifiable of a surgical resection with curative aim for oncologic reasons ( metastatic extensions), for reasons of resectability (canalar extension, vascular) or still for surgically reasons (age, comorbidity). The palliative care of these patients consists at first in assuring an effective biliary drainage, infectious complications being one of the main causes of death. The biliary drainage allows to improve the survival of these patients. It bases by the implementation, by the endoscopic or percutaneous way of biliary, generally metallic prosthesis the duration of average permeability of which is of approximately 6 months. The standard oncologic treatment is the administration of a chemotherapy exclusive or associated with a radiotherapy. The radiotherapy and the radio chemotherapy did not show efficiency on the survival superior to the exclusive biliary drainage. The first-line exclusive chemotherapy bases on the gemcitabine-cisplatin association with a median survival of 11,6 months. No study allows to justify the administration of a chemotherapy of the second line. Thus the preservation of the permeability of the biliary ways is today, the most important factor to improve the survival of these patients. Therefore, the addition of a treatment allowing to obtain a local tumoral response to the insertion of biliary prosthesis would allow to increase the duration of permeability of the biliary prosthesis and would limit the local evolution. Endoductal destruction tumoral technics were thus developed in this indication: Dynamic phototherapy which demonstrated, during preliminary studies, a certain efficiency both on the tumoral response estimated on the improvement of the tumoral stenosis as on the survival in case of cholangiocarcinoma bile ducts not resectables. However, the improvement of the survival was not confirmed by wider randomized studies. A study randomized of phase III was interrupted prematurely because of a survival decreased in the experimental arm. The radium therapy and the brachytherapy were estimated in this indication with results interesting on series limited in size, but is not used in routine because of its cost and of technics difficulties. Ablation therapy technics (radio frequency, microwaves, radium therapy) percutaneous by radiological or surgical way proved their efficiency for the treatment of hepatocarcinoma and liver metastasis. The hepatic radio frequency was estimated, during trials of phases II, for peripheral cholangiocarcinoma intra hepatic (developed at a distance main bile ducts) with interesting tumoral rates of necrosis. However, the direct percutaneous access of the cholangiocarcinoma of the biliary ways is not practicable because of the risk of iatrogenic biliary fistula. Therefore, systems allowing to realize ablation therapy by endoductal radio frequency are from now on available. It is miniaturized bipolar probes which are inserted into bile ducts by reactionary way (retrograde cholangiography), or anterograde percutaneous. Two systems (Habib ®, ELLRA ®) are at present available and were estimated during in vitro and in vivo studies, to the animal and in man. The purposes of this study are to estimate the feasibility, the efficiency and the morbidity of the biliary radio frequency for the treatment of the extra hepatic cholangiocarcinoma non resectable (resection or transplantation).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nonresectable Bile Duct Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ablation Therapy With Bipolar Radio Frequency
Arm Type
Other
Intervention Type
Device
Intervention Name(s)
Ablation Therapy
Intervention Description
Ablation Therapy With Bipolar Radio frequency
Primary Outcome Measure Information:
Title
Rate of success of the use of a treatment based on radiofrequency for all the target stenosis.
Description
Evaluation of the success of the use of bipolary radiofrequency for all target stenosis after each procedure
Time Frame
1 day
Secondary Outcome Measure Information:
Title
Technic efficiency (Measure the duration of biliary permeability in the time)
Description
Ablation Therapy
Time Frame
From date of end of the treatment and the date of the first one re-permeabilisation of the prosthesis (until end of follow-up: 1 year)
Title
Number of intervention for biliary drainage on the duration of the follow-up
Description
Biliary drainage intervention
Time Frame
From day of intervention until follow-up (during 1 year)
Title
Global morbidity to 30 days
Description
Morbidity
Time Frame
From day of intervention until 30 days
Title
Specific morbidity to 30 days
Description
Complications after intervention((cholecystitis, haemorrhage, pancreatitis, angiocholitis, intestinal perforation),
Time Frame
From day of intervention until 30 days
Title
Overall survival
Description
Overall survival
Time Frame
From day of intervention until 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years, Bile duct cancer nonresectable Type I, II ou III of Bismuth classification with cholangio-MRI and/or endoscopic cholangiography Laboratory values : prothrombin time ≥ 50%, platelets ≥ 50 000, aPTT < 3 (Authorized transfusions) Written informed consent, Affiliation to Social Security System. Exclusion Criteria: Intra-pancreatic mass and/or Wirsung dilation, Bile duct cancer, Visceral metastasis (extrahepatic), Initial metallic prosthesis, Woman pregnant or susceptible to the being, Patients deprived of liberty or placed Under the authority of a tutor, Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol or follow-up schedule.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
BORIES Erwan, MD
Organizational Affiliation
Institut Paoli-Calmettes
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institut Paoli-Calmettes
City
Marseille
ZIP/Postal Code
13009
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
http://www.institutpaolicalmettes.fr
Description
Institut Paoli-Calmettes

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Prospective Evaluation of the Ablation Therapy With Bipolar Radio Frequency for Nonresectable Bile Duct Cancer

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