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RFA Combined With Chemotherapy for Unresectable Cholangiocarcinoma

Primary Purpose

Cholangiocarcinoma

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
radiofrequency ablation
Chemotherapy drug
Sponsored by
First People's Hospital of Hangzhou
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cholangiocarcinoma focused on measuring biliary tract cancer, radiofrequency ablation, S-1, Gemcitabine

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Obtention of a written informed consent.
  • Patient with histologically proved cholangiocarcinoma ; histologic diagnosis must be proved by biliary brushing, bile cytology, endobiliary biopsy under Spyglass, or by EUS-FNA.
  • Patient with Karnofsky score > 60, ECOG>level 2
  • Patient capable of fill in the quality of life questionnaire
  • For the first time treatment
  • CT, MRCP, EUS and other examinations indicate that the tumor has locally infiltrated large blood vessels and cannot be surgically removed

Exclusion Criteria

  • No written informed consent
  • Patients under or already treated by radiotherapy or chemotherapy treatment for cholangiocarcinoma.
  • Pregnant, parturient or breastfeeding women
  • Serious abnormalities in liver and kidney function and coagulation function
  • The ERCP guide wire cannot pass the stricture due to severe biliary stricture
  • Merge with other malignant tumors
  • Use other treatments that may affect the observation, such as radioactive particles or seed stent implantation, P53 injection, oral chemotherapy, interventional therapy, etc.

Sites / Locations

  • Hangzhou First People's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

RAF combined with gemcitabine and S-1 group

RFA-only gruop

Arm Description

Patients will receive endobiliary radiofrequency ablation ( RFA) followed by plastic stent(s) placement, and be treated with gemcitabine and S-1 within 1 month after RFA.

Patients will only receive endobiliary radiofrequency ablation ( RFA) followed by plastic stent(s) placement

Outcomes

Primary Outcome Measures

survival time
The period from endoscopic treatment to patient death or the last day of study

Secondary Outcome Measures

Adverse events
Number of participants with adverse events; type, frequency and intensity of adverse events
Stent patency time
Take the stent placement as the starting point and the stent occlusion confirmed by ERCP as the end point. Record the time interval between the two point
Progression free survival
evaluate the survival time without disease progression

Full Information

First Posted
August 25, 2021
Last Updated
February 17, 2023
Sponsor
First People's Hospital of Hangzhou
Collaborators
Hangzhou Cancer Hospital, Changhai Hospital, Eastern Hepatobiliary Surgery Hospital, Cancer Institute and Hospital, Chinese Academy of Medical Sciences, Xijing Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05028439
Brief Title
RFA Combined With Chemotherapy for Unresectable Cholangiocarcinoma
Official Title
Endoscopic Radiofrequency Ablation Combined With Gemcitabine and S-1 in Paitiens for Unresectable Cholangiocarcinoma:A Randomized Open-label Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
January 1, 2020 (Actual)
Primary Completion Date
December 1, 2022 (Actual)
Study Completion Date
December 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
First People's Hospital of Hangzhou
Collaborators
Hangzhou Cancer Hospital, Changhai Hospital, Eastern Hepatobiliary Surgery Hospital, Cancer Institute and Hospital, Chinese Academy of Medical Sciences, Xijing Hospital

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
Extrahepatic cholangiocarcinoma is a malignant tumor that is highly malignant and difficult to diagnose and treat early. Endobiliary radiofrequency ablation (RFA) has been reported to be a beneficial treatment option for palliation of malignant biliary strictures. Within the bile duct, RFA appears to be safe and may result in decreased tumor ingrowth. To date, little is known about the role of the addition of systemic chemotherapy to RFA for cholangiocarcinoma. The aim of this study is to compare the efficacy and safety of RAF combined with Gemcitabine and S-1 in patients with unresectable cholangiocarcinoma.
Detailed Description
Over 60 % of common bile duct (CBD) obstructions are due to malignancy, and the majority of neoplasms are unresectable at the time of diagnosis. Biliary drainage with placement of metal or plastic stents for palliation is the therapy of choice in this set of patients. Radiofrequency ablation (RFA) is well established method for treatment of some solid tumors, like liver cancer, lung cancer, etc. Recently, an endoscopically applicable radiofrequency probe, HabibTM EndoHBP catheter, was approved for clinical use. RFA uses a high-frequency alternating current to generate heat and achieve coagulative necrosis when in contact with tissue. Many studies showed RFA with biliary stent was a beneficial treatment option for palliation of malignant biliary strictures. However, most of therapeutic effects were expected to delay bile duct obstruction rather than to decrease the tumor. Recently orally available chemotherapeutic agent, S-1, an oral fluoropyrimidine, was reported as effective in patients with bile duct adenocarcinoma. To date, little is known about the role of the addition of systemic chemotherapy to RFA for cholangiocarcinoma. The aim of this study is to compare the efficacy and safety of RAF combined with Gemcitabine and S-1 in patients with unresectable cholangiocarcinoma

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cholangiocarcinoma
Keywords
biliary tract cancer, radiofrequency ablation, S-1, Gemcitabine

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
RAF combined with gemcitabine and S-1 group
Arm Type
Experimental
Arm Description
Patients will receive endobiliary radiofrequency ablation ( RFA) followed by plastic stent(s) placement, and be treated with gemcitabine and S-1 within 1 month after RFA.
Arm Title
RFA-only gruop
Arm Type
Placebo Comparator
Arm Description
Patients will only receive endobiliary radiofrequency ablation ( RFA) followed by plastic stent(s) placement
Intervention Type
Device
Intervention Name(s)
radiofrequency ablation
Intervention Description
All patients underwent biliary sphincterotomy. Cholangiogram was performed to confirm stricture location, length and diameter. The Habib Endo HPB (Hepatobiliary) probe (EMcision, HitchinHerts, UK) was then advanced over a wire at the level of the biliary stricture and ablation using ERBE generator set at 7-10 watts for a time period of 90-120 s was conducted. A 1- to 2-min resting period after energy delivery was allowed before moving the catheter along the length of the stricture to ablate the rest of the stricture. Plastic stent(s) were placed after RFA depending on the location of the malignant obstruction
Intervention Type
Drug
Intervention Name(s)
Chemotherapy drug
Other Intervention Name(s)
oral fluoropyrimidine
Intervention Description
Gemcitabine 1 000 mg/m2 intravenously on day 1,8; S-1 80 mg/m2 was taken orally twice for two weeks. The curative effect was evaluated comprehensively for each 2 cycles of chemotherapy
Primary Outcome Measure Information:
Title
survival time
Description
The period from endoscopic treatment to patient death or the last day of study
Time Frame
two years
Secondary Outcome Measure Information:
Title
Adverse events
Description
Number of participants with adverse events; type, frequency and intensity of adverse events
Time Frame
one month
Title
Stent patency time
Description
Take the stent placement as the starting point and the stent occlusion confirmed by ERCP as the end point. Record the time interval between the two point
Time Frame
two years
Title
Progression free survival
Description
evaluate the survival time without disease progression
Time Frame
two years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Obtention of a written informed consent. Patient with histologically proved cholangiocarcinoma ; histologic diagnosis must be proved by biliary brushing, bile cytology, endobiliary biopsy under Spyglass, or by EUS-FNA. Patient with Karnofsky score > 60, ECOG>level 2 Patient capable of fill in the quality of life questionnaire For the first time treatment CT, MRCP, EUS and other examinations indicate that the tumor has locally infiltrated large blood vessels and cannot be surgically removed Exclusion Criteria No written informed consent Patients under or already treated by radiotherapy or chemotherapy treatment for cholangiocarcinoma. Pregnant, parturient or breastfeeding women Serious abnormalities in liver and kidney function and coagulation function The ERCP guide wire cannot pass the stricture due to severe biliary stricture Merge with other malignant tumors Use other treatments that may affect the observation, such as radioactive particles or seed stent implantation, P53 injection, oral chemotherapy, interventional therapy, etc.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiaofeng Zhang, M.S
Organizational Affiliation
First People's Hospital of Hangzhou
Official's Role
Study Director
Facility Information:
Facility Name
Hangzhou First People's Hospital
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
31006
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26162420
Citation
Laquiere A, Boustiere C, Leblanc S, Penaranda G, Desilets E, Prat F. Safety and feasibility of endoscopic biliary radiofrequency ablation treatment of extrahepatic cholangiocarcinoma. Surg Endosc. 2016 Mar;30(3):1242-8. doi: 10.1007/s00464-015-4322-7. Epub 2015 Jul 11.
Results Reference
background
PubMed Identifier
24637151
Citation
Butros SR, Shenoy-Bhangle A, Mueller PR, Arellano RS. Radiofrequency ablation of intrahepatic cholangiocarcinoma: feasability, local tumor control, and long-term outcome. Clin Imaging. 2014 Jul-Aug;38(4):490-494. doi: 10.1016/j.clinimag.2014.01.013. Epub 2014 Feb 7.
Results Reference
background
PubMed Identifier
24836747
Citation
Strand DS, Cosgrove ND, Patrie JT, Cox DG, Bauer TW, Adams RB, Mann JA, Sauer BG, Shami VM, Wang AY. ERCP-directed radiofrequency ablation and photodynamic therapy are associated with comparable survival in the treatment of unresectable cholangiocarcinoma. Gastrointest Endosc. 2014 Nov;80(5):794-804. doi: 10.1016/j.gie.2014.02.1030. Epub 2014 May 15.
Results Reference
background

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RFA Combined With Chemotherapy for Unresectable Cholangiocarcinoma

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