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Completed

NCT Number: NCT05028439

RFA Combined With Chemotherapy for Unresectable Cholangiocarcinoma

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.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hangzhou First People's Hospital

Hangzhou, Zhejiang, 31006, China

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Radiofrequency Ablation

Device

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

Chemotherapy drug

Drug

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

Other names: oral fluoropyrimidine

Primary outcomes

  1. survival time

    Time frame: two years

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

Secondary outcomes

  1. Adverse events

    Time frame: one month

    Number of participants with adverse events; type, frequency and intensity of adverse events

  2. Stent patency time

    Time frame: two years

    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

  3. Progression free survival

    Time frame: two years

    evaluate the survival time without disease progression

Sponsors and collaborators

Lead sponsor

First People's Hospital of Hangzhou

Other

Collaborators

  • Cancer Institute and Hospital, Chinese Academy of Medical Sciences
  • Changhai Hospital
  • Eastern Hepatobiliary Surgery Hospital
  • Hangzhou Cancer Hospital
  • Xijing Hospital

Registry information

Official study title

Endoscopic Radiofrequency Ablation Combined With Gemcitabine and S-1 in Paitiens for Unresectable Cholangiocarcinoma:A Randomized Open-label Clinical Trial

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Aug 31, 2021
Registry last updated
Feb 21, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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