CholangiocarcinomaNCT03166436
RFA for Malignant Biliary Obstruction
A study testing Radiofrequency ablation and Biliary stenting in people with Cholangiocarcinoma and Pancreas Cancer, run by Institute for Clinical and Experimental Medicine at 1 site in Czechia.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Cholangiocarcinoma, Pancreas Cancer
- What is being tested?
- Radiofrequency ablation and Biliary stenting
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 140 participants
- Where
- 1 siteCzechia
- Study dates
- 8 Jun 2017to 8 May 2020
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 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
Who cannot join
- Unstable for ERC
- Inability to give informed consent
- Pregnancy
- Uncorrected coagulopathy
- Concomitant biliary oncological endoluminal therapy (photodynamic therapy, brachytherapy)
- Cardiac pacemaker
Trial locations and contacts
1 site in 1 country.
Czechia1 site, 1 recruiting
- Recruiting
Department of Gastroenterology and Hepatology
Prague, 14021
Tomas Hucl, MD, PhD, 00420261362600, tomas.hucl@ikem.cz
Petra Truxova, Ing, 00420261362619, petra.truxova@ikem.cz
About this study
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.
Read the detailed description
Cholangiocarcinoma and pancreatic cancer are by far the two most common causes of malignant bile duct obstruction. Cholangiocarcinoma is an adenocarcinoma originating in the bile duct whereas pancreatic cancer is an adenocarcinoma derived from pancreatic ductal cells. The incidence rates of both diseases have been rising over the past decades. Both diseases still have a very unfavorable prognosis with 5 year survival rates as low as 5-10%. Surgery represents the only therapeutic modality with a curative potential, however most patients are non-eligible for surgical treatment at the time of diagnosis. Patients present with either distant metastases, have a locally advanced disease or are unfit for surgery because of advanced age and/or co-morbidities. The prognosis of patients with unresectable bile duct or pancreatic cancer is poor with a median survival time of about 6 months. Chemotherapy and radiotherapy provide only a slight survival benefit and thus have only palliative intent.
Most patients with cholangiocarcinoma and pancreatic cancer present with bile duct obstruction in the course of their disease. Bile duct obstruction relief is an important part of palliation therapy. Endoscopic retrograde cholangiography with bile duct stenting is the method of choice with a high rate of technical success and a lower complication rate compared to surgery. Biliary stents are either plastic or metal (self-expandable metal stents, SEMS). SEMS can be covered, uncovered or partially covered. Plastic stents are cheaper and easier to exchange but have a shorter patency compared to metal stents. Metal stents have been shown to improve survival of patients with proximal malignant biliary obstruction. Both plastic and metal become occluded in a significant proportion of patients, especially in those with a longer life expectancy. Stent occlusion is often an acute event leading to sepsis and a prompt intervention is required. Failure of achieving adequate drainage may result in severe cholangitis and death.
Photodynamic therapy has been used for bile duct tumor ablation for more than a decade. It is a two stage process in which a photosensitizing agent is taken by the tumor tissue and is than activated by light of a specific wave length. Two randomized trials showed improved survival of patients treated with PDT plus stenting compared to stenting alone. However, side effects of photodynamic therapy such as phototoxicity, high costs and limited availability restrict the use of PDT.
Radiofrequency ablation (RFA), by means of alternating high-frequency current, generates heat that results in coagulation necrosis of tissue. It is widely used to treat liver tumors or dysplastic Barrett's esophagus. Endoluminal biliary RFA has become possible upon availability of narrow ERCP RFA catheters and represents a new modality of intraductal tumor ablation. The probe can be introduced over a 0.035-inch wire through a standard endoscope, thus allowing endoscopic ablation of malignant bile duct obstruction. The bipolar catheter has multiple circumferential electrodes at the distal tip. The coagulative effect is delivered in the area between the two electrodes.
A few human non-randomized case series investigating the safety and efficiency of RFA were reported. Steel at al reported their results in 22 patients with malignant bile duct obstruction (16 patients with pancreatic cancer and 6 patients with cholangiocarcinoma). Immediate, 30 day complication rates and 90 day stent patency were evaluated as primary parameters. Intraductal RFA was followed by a SEMS placement. One patient developed asymptomatic elevation of amylase, one patients developed rigors and two patients developed cholecystitis requiring cholecystectomy. All except 3 patients achieved 90 day stent patency.
In a recent study of Sharaiha et al, 26 patients with pancreatic or bile duct cancer underwent RFA followed by plastic or metal stent placement. They were compared to 40 matched controls who underwent only stenting. Technical success rate was 100%. Multivariable Cox proportional regression analysis showed RFA to be an independent predictor of survival [HR 0.29 (0.11-0.76), p = 0.012] together with age and receipt of chemotherapy [HR 1.04 (1.01-1.07), p = 0.011; HR 0.26 (0.10-0.70), p = 0.007]. Surprisingly, SEMS patency rates were the same across all groups.
In an Austrian national retrospective study, 84 ablations were performed in 58 patients in 11 centers. Cholangiocarcinoma was present in 45 patients. Technical feasibility was 100%, however multiple complications occurred (1 liver infarct, 5 cholangitis, 3 hemobilia, 2 sepsis, 1 gall-bladder empyema, 1 liver coma).
RFA was also investigated in pancreatic cancers only. In a retrospective comparison of 23 patients and 46 controls, the median survival was better in the RFA group (226 vs. 123 days, p=0,01). The median stent patency was not different.
The safety profile of RFA seems to be acceptable, however severe complications have occured. In the study of Tal et al, 3 cases of bleeding were reported, two of them resulted in death. In all of these patients, plastic stents were used.
Increasing evidence indicates that RFA might stimulate anti-tumor immunity. Active anti-cancer immune responses depend on efficient presentation of tumor antigens and cytokine-mediated stimulatory signaling. Tumor cells are generally regarded as poor stimulators of T-cells. In contrast, antigen-presenting cells (APCs) are highly specialized in this function and are therefore important in the process of stimulation of T-cell responses to tumors. RFA has been shown to stimulate anti-tumor immunity through the induction of heat shock proteins, especially HSP 70. HSPs have the capacity to affect the immunogenicity of tumor cells, to chaperone antigenic peptides and deliver them into APCs, thus activate and regulate innate and adaptive immunity.
Based on the available evidence, RFA seems to be a technically feasible technique of malignant bile duct stricture ablation with a favorable safety profile. Retrospective case series have reported improved stent patency and survival in cholangiocarcinoma and pancreatic cancer patients following RFA. Thus, endoluminal RFA may represent a novel treatment modality in patients with malignant biliary obstruction. For this to happen, however, prospectively obtained comparative data with established treatment, i.e. biliary stenting, regarding safety and efficiency are necessary.
The investigators aim to compare endoscopic radiofrequency ablation plus stenting vs. stenting alone for malignant bile duct obstruction not eligible for surgical resection in a randomized controlled trial.
- Conditions
- Cholangiocarcinoma, Pancreas Cancer
- Being tested
- Radiofrequency ablation, Biliary stenting
- Medical subject headings
- Cholangiocarcinoma, Pancreatic Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Radiofrequency ablationProcedure or surgery
radiofrequency ablation
Biliary stentingProcedure or surgery
biliary stenting
| Study group | Role | What they receive |
|---|---|---|
| RFA plus stenting | Experimental | Endoluminal radiofrequency ablation followed by biliary stenting Receives: Procedure: Radiofrequency ablation; Procedure: Biliary stenting |
| Stenting alone | Active comparator | Biliary stenting alone Receives: Procedure: Biliary stenting |
What is being measured
The primary outcome is the main question the study is designed to answer.
Survival
number of days/months of survival (being alive) post intervention
Measured: 12 months
Secondary outcomes (4)
Stent patency
number of days/months of patent stent (not occluded) post intervention
Measured: 12 months
Complications
number of complications related to procedure (bleeding, perforation, cholangitis will be combined to report as a complication)
Measured: 30 days
Quality of life
validated questionnaire investigating quality of live post intervention
Measured: 12 months
Augmentation of antitumor immunity
serum level of HSP 70 and selected cytokines will be measured from blood
Measured: 30 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 May 2017
- Study start8 Jun 2017 (estimated)
- Primary completion8 May 2019 (estimated)
- Study completion8 May 2020 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (20)Papers the sponsor has linked to this study.
- Other trials for CholangiocarcinomaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Randomized controlled study
- Masking
- None (open label)
- Enrolment
- 140 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Institute for Clinical and Experimental Medicine
- Sponsor type
- Other government
- Responsible party
- Principal investigator, Tomas Hucl, Institute for Clinical and Experimental Medicine
- Investigators
- Tomas Hucl, MD, PhD, Principal investigator, Institute for Clinical and Experimental Medicine
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03166436
- Sponsor's protocol ID
- IKEM RFA CCA PC
- Status last verified
- May 2017
- First submitted
- 14 May 2017
- Last updated
- 30 May 2017
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Ilyas SI, Gores GJ. Pathogenesis, diagnosis, and management of cholangiocarcinoma. Gastroenterology. 2013 Dec;145(6):1215-29. doi: 10.1053/j.gastro.2013.10.013. Epub 2013 Oct 15.
PubMed 24140396Khan SA, Davidson BR, Goldin RD, Heaton N, Karani J, Pereira SP, Rosenberg WM, Tait P, Taylor-Robinson SD, Thillainayagam AV, Thomas HC, Wasan H; British Society of Gastroenterology. Guidelines for the diagnosis and treatment of cholangiocarcinoma: an update. Gut. 2012 Dec;61(12):1657-69. doi: 10.1136/gutjnl-2011-301748. Epub 2012 Aug 15.
PubMed 22895392Rerknimitr R, Angsuwatcharakon P, Ratanachu-ek T, Khor CJ, Ponnudurai R, Moon JH, Seo DW, Pantongrag-Brown L, Sangchan A, Pisespongsa P, Akaraviputh T, Reddy ND, Maydeo A, Itoi T, Pausawasdi N, Punamiya S, Attasaranya S, Devereaux B, Ramchandani M, Goh KL; Asia-Pacific Working Group on Hepatobiliary Cancers. Asia-Pacific consensus recommendations for endoscopic and interventional management of hilar cholangiocarcinoma. J Gastroenterol Hepatol. 2013 Apr;28(4):593-607. doi: 10.1111/jgh.12128.
PubMed 23350673Vincent A, Herman J, Schulick R, Hruban RH, Goggins M. Pancreatic cancer. Lancet. 2011 Aug 13;378(9791):607-20. doi: 10.1016/S0140-6736(10)62307-0. Epub 2011 May 26.
PubMed 21620466Davids PH, Groen AK, Rauws EA, Tytgat GN, Huibregtse K. Randomised trial of self-expanding metal stents versus polyethylene stents for distal malignant biliary obstruction. Lancet. 1992 Dec 19-26;340(8834-8835):1488-92. doi: 10.1016/0140-6736(92)92752-2.
PubMed 1281903Sangchan A, Kongkasame W, Pugkhem A, Jenwitheesuk K, Mairiang P. Efficacy of metal and plastic stents in unresectable complex hilar cholangiocarcinoma: a randomized controlled trial. Gastrointest Endosc. 2012 Jul;76(1):93-9. doi: 10.1016/j.gie.2012.02.048. Epub 2012 May 15.
PubMed 22595446Ortner ME, Caca K, Berr F, Liebetruth J, Mansmann U, Huster D, Voderholzer W, Schachschal G, Mossner J, Lochs H. Successful photodynamic therapy for nonresectable cholangiocarcinoma: a randomized prospective study. Gastroenterology. 2003 Nov;125(5):1355-63. doi: 10.1016/j.gastro.2003.07.015.
PubMed 14598251Zoepf T, Jakobs R, Arnold JC, Apel D, Riemann JF. Palliation of nonresectable bile duct cancer: improved survival after photodynamic therapy. Am J Gastroenterol. 2005 Nov;100(11):2426-30. doi: 10.1111/j.1572-0241.2005.00318.x.
PubMed 16279895Curley SA, Izzo F. Radiofrequency ablation of primary and metastatic hepatic malignancies. Int J Clin Oncol. 2002 Apr;7(2):72-81. doi: 10.1007/s101470200010.
PubMed 12018113Shaheen NJ, Overholt BF, Sampliner RE, Wolfsen HC, Wang KK, Fleischer DE, Sharma VK, Eisen GM, Fennerty MB, Hunter JG, Bronner MP, Goldblum JR, Bennett AE, Mashimo H, Rothstein RI, Gordon SR, Edmundowicz SA, Madanick RD, Peery AF, Muthusamy VR, Chang KJ, Kimmey MB, Spechler SJ, Siddiqui AA, Souza RF, Infantolino A, Dumot JA, Falk GW, Galanko JA, Jobe BA, Hawes RH, Hoffman BJ, Sharma P, Chak A, Lightdale CJ. Durability of radiofrequency ablation in Barrett's esophagus with dysplasia. Gastroenterology. 2011 Aug;141(2):460-8. doi: 10.1053/j.gastro.2011.04.061. Epub 2011 May 6.
PubMed 21679712Zacharoulis D, Lazoura O, Sioka E, Potamianos S, Tzovaras G, Nicholls J, Koukoulis G, Habib N. Habib EndoHPB: a novel endobiliary radiofrequency ablation device. An experimental study. J Invest Surg. 2013 Feb;26(1):6-10. doi: 10.3109/08941939.2012.681832. Epub 2012 Dec 28.
PubMed 23273142Steel AW, Postgate AJ, Khorsandi S, Nicholls J, Jiao L, Vlavianos P, Habib N, Westaby D. Endoscopically applied radiofrequency ablation appears to be safe in the treatment of malignant biliary obstruction. Gastrointest Endosc. 2011 Jan;73(1):149-53. doi: 10.1016/j.gie.2010.09.031.
PubMed 21184881Sharaiha RZ, Natov N, Glockenberg KS, Widmer J, Gaidhane M, Kahaleh M. Comparison of metal stenting with radiofrequency ablation versus stenting alone for treating malignant biliary strictures: is there an added benefit? Dig Dis Sci. 2014 Dec;59(12):3099-102. doi: 10.1007/s10620-014-3264-6. Epub 2014 Jul 18.
PubMed 25033929Monga A, Gupta R, Ramchandani M, Rao GV, Santosh D, Reddy DN. Endoscopic radiofrequency ablation of cholangiocarcinoma: new palliative treatment modality (with videos). Gastrointest Endosc. 2011 Oct;74(4):935-7. doi: 10.1016/j.gie.2010.10.018. Epub 2010 Dec 18. No abstract available.
PubMed 21168839Dolak W, Schreiber F, Schwaighofer H, Gschwantler M, Plieschnegger W, Ziachehabi A, Mayer A, Kramer L, Kopecky A, Schrutka-Kolbl C, Wolkersdorfer G, Madl C, Berr F, Trauner M, Puspok A; Austrian Biliary RFA Study Group. Endoscopic radiofrequency ablation for malignant biliary obstruction: a nationwide retrospective study of 84 consecutive applications. Surg Endosc. 2014 Mar;28(3):854-60. doi: 10.1007/s00464-013-3232-9. Epub 2013 Oct 3.
PubMed 24196547
Study at a glance
From the registry record, last updated by the sponsor on 30 May 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Radiofrequency Ablation Plus Stenting Versus Stenting Alone for Treatment of Malignant Biliary Obstruction
- ClinicalTrials.gov ID
- NCT03166436
- Acronym / sponsor ID
- IKEM RFA CCA PC
- Conditions
- Cholangiocarcinoma, Pancreas Cancer
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 140 participants (estimated)
- Lead sponsor
- Institute for Clinical and Experimental MedicineOther government
- Study start
- 8 Jun 2017 (estimated)
- Primary completion
- 8 May 2019 (estimated)
- Study completion
- 8 May 2020 (estimated)
- First posted
- 25 May 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
Cholangiocarcinoma and pancreatic cancer are by far the two most common causes of malignant bile duct obstruction. Cholangiocarcinoma is an adenocarcinoma originating in the bile duct whereas pancreatic cancer is an adenocarcinoma derived from pancreatic ductal cells. The incidence rates of both diseases have been rising over the past decades. Both diseases still have a very unfavorable prognosis with 5 year survival rates as low as 5-10%. Surgery represents the only therapeutic modality with a curative potential, however most patients are non-eligible for surgical treatment at the time of diagnosis. Patients present with either distant metastases, have a locally advanced disease or are unfit for surgery because of advanced age and/or co-morbidities. The prognosis of patients with unresectable bile duct or pancreatic cancer is poor with a median survival time of about 6 months. Chemotherapy and radiotherapy provide only a slight survival benefit and thus have only palliative intent.
Most patients with cholangiocarcinoma and pancreatic cancer present with bile duct obstruction in the course of their disease. Bile duct obstruction relief is an important part of palliation therapy. Endoscopic retrograde cholangiography with bile duct stenting is the method of choice with a high rate of technical success and a lower complication rate compared to surgery. Biliary stents are either plastic or metal (self-expandable metal stents, SEMS). SEMS can be covered, uncovered or partially covered. Plastic stents are cheaper and easier to exchange but have a shorter patency compared to metal stents. Metal stents have been shown to improve survival of patients with proximal malignant biliary obstruction. Both plastic and metal become occluded in a significant proportion of patients, especially in those with a longer life expectancy. Stent occlusion is often an acute event leading to sepsis and a prompt intervention is required. Failure of achieving adequate drainage may result in severe cholangitis and death.
Photodynamic therapy has been used for bile duct tumor ablation for more than a decade. It is a two stage process in which a photosensitizing agent is taken by the tumor tissue and is than activated by light of a specific wave length. Two randomized trials showed improved survival of patients treated with PDT plus stenting compared to stenting alone. However, side effects of photodynamic therapy such as phototoxicity, high costs and limited availability restrict the use of PDT.
Radiofrequency ablation (RFA), by means of alternating high-frequency current, generates heat that results in coagulation necrosis of tissue. It is widely used to treat liver tumors or dysplastic Barrett's esophagus. Endoluminal biliary RFA has become possible upon availability of narrow ERCP RFA catheters and represents a new modality of intraductal tumor ablation. The probe can be introduced over a 0.035-inch wire through a standard endoscope, thus allowing endoscopic ablation of malignant bile duct obstruction. The bipolar catheter has multiple circumferential electrodes at the distal tip. The coagulative effect is delivered in the area between the two electrodes.
A few human non-randomized case series investigating the safety and efficiency of RFA were reported. Steel at al reported their results in 22 patients with malignant bile duct obstruction (16 patients with pancreatic cancer and 6 patients with cholangiocarcinoma). Immediate, 30 day complication rates and 90 day stent patency were evaluated as primary parameters. Intraductal RFA was followed by a SEMS placement. One patient developed asymptomatic elevation of amylase, one patients developed rigors and two patients developed cholecystitis requiring cholecystectomy. All except 3 patients achieved 90 day stent patency.
In a recent study of Sharaiha et al, 26 patients with pancreatic or bile duct cancer underwent RFA followed by plastic or metal stent placement. They were compared to 40 matched controls who underwent only stenting. Technical success rate was 100%. Multivariable Cox proportional regression analysis showed RFA to be an independent predictor of survival [HR 0.29 (0.11-0.76), p = 0.012] together with age and receipt of chemotherapy [HR 1.04 (1.01-1.07), p = 0.011; HR 0.26 (0.10-0.70), p = 0.007]. Surprisingly, SEMS patency rates were the same across all groups.
In an Austrian national retrospective study, 84 ablations were performed in 58 patients in 11 centers. Cholangiocarcinoma was present in 45 patients. Technical feasibility was 100%, however multiple complications occurred (1 liver infarct, 5 cholangitis, 3 hemobilia, 2 sepsis, 1 gall-bladder empyema, 1 liver coma).
RFA was also investigated in pancreatic cancers only. In a retrospective comparison of 23 patients and 46 controls, the median survival was better in the RFA group (226 vs. 123 days, p=0,01). The median stent patency was not different.
The safety profile of RFA seems to be acceptable, however severe complications have occured. In the study of Tal et al, 3 cases of bleeding were reported, two of them resulted in death. In all of these patients, plastic stents were used.
Increasing evidence indicates that RFA might stimulate anti-tumor immunity. Active anti-cancer immune responses depend on efficient presentation of tumor antigens and cytokine-mediated stimulatory signaling. Tumor cells are generally regarded as poor stimulators of T-cells. In contrast, antigen-presenting cells (APCs) are highly specialized in this function and are therefore important in the process of stimulation of T-cell responses to tumors. RFA has been shown to stimulate anti-tumor immunity through the induction of heat shock proteins, especially HSP 70. HSPs have the capacity to affect the immunogenicity of tumor cells, to chaperone antigenic peptides and deliver them into APCs, thus activate and regulate innate and adaptive immunity.
Based on the available evidence, RFA seems to be a technically feasible technique of malignant bile duct stricture ablation with a favorable safety profile. Retrospective case series have reported improved stent patency and survival in cholangiocarcinoma and pancreatic cancer patients following RFA. Thus, endoluminal RFA may represent a novel treatment modality in patients with malignant biliary obstruction. For this to happen, however, prospectively obtained comparative data with established treatment, i.e. biliary stenting, regarding safety and efficiency are necessary.
The investigators aim to compare endoscopic radiofrequency ablation plus stenting vs. stenting alone for malignant bile duct obstruction not eligible for surgical resection in a randomized controlled trial.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Randomized controlled study
| Arm | Type | Receives |
|---|---|---|
| RFA plus stenting | Experimental | Procedure: Radiofrequency ablation, Procedure: Biliary stentingEndoluminal radiofrequency ablation followed by biliary stenting |
| Stenting alone | Active comparator | Procedure: Biliary stentingBiliary stenting alone |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- 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
Key exclusion criteria (6 listed)
- Unstable for ERC
- Inability to give informed consent
- Pregnancy
- Uncorrected coagulopathy
- Concomitant biliary oncological endoluminal therapy (photodynamic therapy, brachytherapy)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Radiofrequency ablationradiofrequency ablation | Procedure or surgery | RFA plus stenting |
| Biliary stentingbiliary stenting | Procedure or surgery | RFA plus stenting, Stenting alone |
Primary outcome
Survival
Time frame: 12 months
number of days/months of survival (being alive) post intervention
4 secondary outcomes
Stent patency
Time frame: 12 months
Complications
Time frame: 30 days
Quality of life
Time frame: 12 months
Augmentation of antitumor immunity
Time frame: 30 days
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 May 2017.
- Background: PubMed 24140396Ilyas SI, Gores GJ. Pathogenesis, diagnosis, and management of cholangiocarcinoma. Gastroenterology. 2013 Dec;145(6):1215-29. doi: 10.1053/j.gastro.2013.10.013. Epub 2013 Oct 15.
- Background: PubMed 22895392Khan SA, Davidson BR, Goldin RD, Heaton N, Karani J, Pereira SP, Rosenberg WM, Tait P, Taylor-Robinson SD, Thillainayagam AV, Thomas HC, Wasan H; British Society of Gastroenterology. Guidelines for the diagnosis and treatment of cholangiocarcinoma: an update. Gut. 2012 Dec;61(12):1657-69. doi: 10.1136/gutjnl-2011-301748. Epub 2012 Aug 15.
- Background: PubMed 23350673Rerknimitr R, Angsuwatcharakon P, Ratanachu-ek T, Khor CJ, Ponnudurai R, Moon JH, Seo DW, Pantongrag-Brown L, Sangchan A, Pisespongsa P, Akaraviputh T, Reddy ND, Maydeo A, Itoi T, Pausawasdi N, Punamiya S, Attasaranya S, Devereaux B, Ramchandani M, Goh KL; Asia-Pacific Working Group on Hepatobiliary Cancers. Asia-Pacific consensus recommendations for endoscopic and interventional management of hilar cholangiocarcinoma. J Gastroenterol Hepatol. 2013 Apr;28(4):593-607. doi: 10.1111/jgh.12128.
- Background: PubMed 21620466Vincent A, Herman J, Schulick R, Hruban RH, Goggins M. Pancreatic cancer. Lancet. 2011 Aug 13;378(9791):607-20. doi: 10.1016/S0140-6736(10)62307-0. Epub 2011 May 26.
- Background: PubMed 1281903Davids PH, Groen AK, Rauws EA, Tytgat GN, Huibregtse K. Randomised trial of self-expanding metal stents versus polyethylene stents for distal malignant biliary obstruction. Lancet. 1992 Dec 19-26;340(8834-8835):1488-92. doi: 10.1016/0140-6736(92)92752-2.
- Background: PubMed 22595446Sangchan A, Kongkasame W, Pugkhem A, Jenwitheesuk K, Mairiang P. Efficacy of metal and plastic stents in unresectable complex hilar cholangiocarcinoma: a randomized controlled trial. Gastrointest Endosc. 2012 Jul;76(1):93-9. doi: 10.1016/j.gie.2012.02.048. Epub 2012 May 15.
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- Background: PubMed 16279895Zoepf T, Jakobs R, Arnold JC, Apel D, Riemann JF. Palliation of nonresectable bile duct cancer: improved survival after photodynamic therapy. Am J Gastroenterol. 2005 Nov;100(11):2426-30. doi: 10.1111/j.1572-0241.2005.00318.x.
- Background: PubMed 12018113Curley SA, Izzo F. Radiofrequency ablation of primary and metastatic hepatic malignancies. Int J Clin Oncol. 2002 Apr;7(2):72-81. doi: 10.1007/s101470200010.
- Background: PubMed 21679712Shaheen NJ, Overholt BF, Sampliner RE, Wolfsen HC, Wang KK, Fleischer DE, Sharma VK, Eisen GM, Fennerty MB, Hunter JG, Bronner MP, Goldblum JR, Bennett AE, Mashimo H, Rothstein RI, Gordon SR, Edmundowicz SA, Madanick RD, Peery AF, Muthusamy VR, Chang KJ, Kimmey MB, Spechler SJ, Siddiqui AA, Souza RF, Infantolino A, Dumot JA, Falk GW, Galanko JA, Jobe BA, Hawes RH, Hoffman BJ, Sharma P, Chak A, Lightdale CJ. Durability of radiofrequency ablation in Barrett's esophagus with dysplasia. Gastroenterology. 2011 Aug;141(2):460-8. doi: 10.1053/j.gastro.2011.04.061. Epub 2011 May 6.
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- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Tomas Hucl, MD, PhD principal investigator
Institute for Clinical and Experimental Medicine
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Radiofrequency ablation and Biliary stenting in people with Cholangiocarcinoma and Pancreas Cancer, run by Institute for Clinical and Experimental Medicine at 1 site in Czechia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 30 May 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Czechia. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Tomas Hucl, MD, PhD (00420261362600, tomas.hucl@ikem.cz), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Survival (time frame: 12 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03166436, which also lists 20 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 May 2017.