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Clinical Effect and Safety of PDT and RFA for Unresectable EHCC

Primary Purpose

Cholangiocarcinoma

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Photodynamic therapy
radiofrequency ablation
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 extrahepatic cholangiocarcinoma, Photodynamic therapy, radiofrequency ablation

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • histologically or cytologically confirmed cholangiocarcinoma;
  • unresectable cholangiocarcinoma due to local infiltration of major vessels according to computed tomography (CT), magnetic resonance cholangiopancreatography (MRCP), or endoscopic ultrasound(EUS);
  • no previous treatment;
  • adequate bone marrow and organ function (white blood cells>4.0×109/L, hemoglobin>90 g/L, and platelets>75×109/L, serum creatinine<2.0 mg/dl);
  • a Karnofsky performance status (KPS) score ≥ 50;
  • signed written informed consent.

Exclusion Criteria:

  • imaging examination (CT, MRCP, EUS) showed distant metastasis of liver, lung and other organs;
  • coexistent with other malignant tumors;
  • pregnant or nursing women;
  • previous gastrointestinal diversion;
  • participation in another study during the month before enrollment in this study;
  • alcohol and/or substance abuse or potentially poor compliance per a doctor's judgment.

Sites / Locations

  • Jianfeng Yang

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

PDT group

RFA group

Arm Description

Patients in PDT group underwnt PDT

Patients in RFA group underwent RFA

Outcomes

Primary Outcome Measures

Overall survival (OS)
OS was defined as the time from initial RFA to death or the end of the study.

Secondary Outcome Measures

Adverse events
Number of patients with adverse events
Progression-free survival (PFS)
PFS was measured from randomization until the date of disease progression or death

Full Information

First Posted
March 6, 2020
Last Updated
August 27, 2021
Sponsor
First People's Hospital of Hangzhou
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1. Study Identification

Unique Protocol Identification Number
NCT04301999
Brief Title
Clinical Effect and Safety of PDT and RFA for Unresectable EHCC
Official Title
Clinical Effect and Safety of Photodynamic Therapy With Radiofrequency Ablation for Unresectable Extrahepatic Cholangiocarcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Completed
Study Start Date
March 1, 2020 (Actual)
Primary Completion Date
August 27, 2021 (Actual)
Study Completion Date
August 27, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
First People's Hospital of Hangzhou

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
The prognosis of patients with advanced unresectable EHCC is very poor with a median survival of 3 to 6 months. Active control of tumor growth is the key to extending stent patency and survival for patients with unresectable locally advanced EHCC. Photodynamic therapy (PDT) is by far the only modality that has shown to improve stent patency as well as over survival (OS) in patients with cholangiocarcinoma. In recent years, many studies have shown that endoscopic radiofrequency ablation (RFA) extends stent patency and possibly the survival of patients with malignant biliary obstruction. However, there are few reports comparing the clinical efficacy and advers event of these two endoscopic treatment.
Detailed Description
Extrahepatic cholangiocarcinoma (EHCC) originates from the hepatic hilar region to the lower common bile duct. The prognosis of patients with advanced unresectable EHCC is very poor with a median survival of 3 to 6 months. Active control of tumor growth is the key to extending stent patency and survival for patients with unresectable locally advanced EHCC. Photodynamic therapy (PDT) is by far the only modality that has shown to improve stent patency as well as over survival (OS) in patients with cholangiocarcinoma. In an attempt to improve stent patency placed for malignant biliary obstruction, enthusiasm for endoscopic retrograde cholangio-pancreatography (ERCP)-guided radiofrequency ablation (RFA) has been increasing in recent years. The HABIBTM EndoHBP catheter is an endoscopic bipolar RFA catheter with proven safety and effectiveness for biliary RFA of cholangiocarcinoma. Many studies have shown that endoscopic RFA extends stent patency and possibly the survival of patients with malignant biliary obstruction. However, there are few reports comparing the clinical efficacy and advers event of these two endoscopic treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cholangiocarcinoma
Keywords
extrahepatic cholangiocarcinoma, Photodynamic therapy, radiofrequency ablation

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
PDT group
Arm Type
Active Comparator
Arm Description
Patients in PDT group underwnt PDT
Arm Title
RFA group
Arm Type
Experimental
Arm Description
Patients in RFA group underwent RFA
Intervention Type
Procedure
Intervention Name(s)
Photodynamic therapy
Other Intervention Name(s)
PDT
Intervention Description
The PDT optical fiber was inserted through the dilation catheterand advanced toward the bile duct stenosis point under visualradiography. The dilation catheter was then withdrawn to leavethe PDT optical fiber directly across the stricture. Photoactivation was performed at 640 nm using a diode laser at a light dose of 180 J/cm2at power density of300 mW/cm2 and irradiation time of 600 s.
Intervention Type
Procedure
Intervention Name(s)
radiofrequency ablation
Other Intervention Name(s)
RFA
Intervention Description
an RFA electrode (Habib EndoHPB, EMcision, HitchinHerts, UK) was advanced along the guide wire into the bile duct and to the biliary stricture under X-ray fluoroscopic guidance. A 400 kHz RF generator (RITA 1500X, Angio Dynamics, USA) was connected for RFA at 7-10 W for 90 seconds.
Primary Outcome Measure Information:
Title
Overall survival (OS)
Description
OS was defined as the time from initial RFA to death or the end of the study.
Time Frame
two years
Secondary Outcome Measure Information:
Title
Adverse events
Description
Number of patients with adverse events
Time Frame
two years
Title
Progression-free survival (PFS)
Description
PFS was measured from randomization until the date of disease progression or death
Time Frame
two years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: histologically or cytologically confirmed cholangiocarcinoma; unresectable cholangiocarcinoma due to local infiltration of major vessels according to computed tomography (CT), magnetic resonance cholangiopancreatography (MRCP), or endoscopic ultrasound(EUS); no previous treatment; adequate bone marrow and organ function (white blood cells>4.0×109/L, hemoglobin>90 g/L, and platelets>75×109/L, serum creatinine<2.0 mg/dl); a Karnofsky performance status (KPS) score ≥ 50; signed written informed consent. Exclusion Criteria: imaging examination (CT, MRCP, EUS) showed distant metastasis of liver, lung and other organs; coexistent with other malignant tumors; pregnant or nursing women; previous gastrointestinal diversion; participation in another study during the month before enrollment in this study; alcohol and/or substance abuse or potentially poor compliance per a doctor's judgment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jianfeng Yang
Organizational Affiliation
First People's Hospital of Hangzhou
Official's Role
Principal Investigator
Facility Information:
Facility Name
Jianfeng Yang
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310006
Country
China

12. IPD Sharing Statement

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Clinical Effect and Safety of PDT and RFA for Unresectable EHCC

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