Cholangiocarcinoma Clinical Trial
Official title:
Radiofrequency Ablation Plus Stenting Versus Stenting Alone for Treatment of Malignant Biliary Obstruction
Pancreatic cancer and cholangiocarcinoma are the most common causes of malignant biliary
obstruction. They are diseases of increasing incidence and unfavorable prognosis. Only a
minority of patients have a localized disease and are indicated for surgery with a chance of
long-term survival. Locally advanced and metastatic tumors are treated with palliative
chemotherapy or chemoradiotherapy; the results of such treatments are unsatisfactory. The
average survival of patients with unresectable disease is 6 months and only 5 - 10 % of
patients survive 5 years. Chemotherapy and radiotherapy can be used, however only with a
palliative effect. Biliary drainage is an integral part of palliative treatment.
Endoscopically or percutaneously placed stents improve quality of life, decrease cholestasis
and pruritus, but do not significantly improve survival. Biliary stents get occluded over
time, possibly resulting in acute cholangitis and require repeated replacement. Endoluminal
biliary photodynamic therapy (PDT) and radiofrequency ablation (RFA), locally active
endoscopic methods, have been increasingly used in recent years in palliative treatment of
patients with malignant biliary obstruction. In photodynamic therapy, improved survival has
been shown in two randomized controlled trials; however the technique suffers from technical
complexity, high cost and low availability. In RFA, application of low voltage high
frequency current during radiofrequency ablation results in tissue destruction by heat. Its
antitumor effect may also be related to systemic changes in antitumor immunity. The use of
endoluminal biliary RFA has so far been reported only in small retrospective cohorts of
patients.
The aim of this randomized study is to compare efficacy of RFA plus stenting to stenting
alone in palliative treatment of malignant biliary obstruction with survival as primary
outcome. Secondary outcomes are stent patency, immediate and late complications, quality of
life and effects on anti-tumor immunity in the RFA group.
Status | Recruiting |
Enrollment | 140 |
Est. completion date | May 8, 2020 |
Est. primary completion date | May 8, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Age over 18 - Pathologically confirmed malignant bile duct obstruction (cholangiocarcinoma or pancreatic cancer) - Laboratory signs of biliary obstruction - Non-resectable disease (distant metastasis, locally advanced disease, patient related factors) based on a multidisciplinary team decision - Capability of giving informed consent - Life expectancy greater than 3 months Exclusion Criteria: - Unstable for ERC - Inability to give informed consent - Pregnancy - Uncorrected coagulopathy - Concomitant biliary oncological endoluminal therapy (photodynamic therapy, brachytherapy) - Cardiac pacemaker |
Country | Name | City | State |
---|---|---|---|
Czechia | Department of Gastroenterology and Hepatology | Prague |
Lead Sponsor | Collaborator |
---|---|
Institute for Clinical and Experimental Medicine |
Czechia,
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* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Survival | number of days/months of survival (being alive) post intervention | 12 months | |
Secondary | Stent patency | number of days/months of patent stent (not occluded) post intervention | 12 months | |
Secondary | Complications | number of complications related to procedure (bleeding, perforation, cholangitis will be combined to report as a complication) | 30 days | |
Secondary | Quality of life | validated questionnaire investigating quality of live post intervention | 12 months | |
Secondary | Augmentation of antitumor immunity | serum level of HSP 70 and selected cytokines will be measured from blood | 30 days |
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