Safety of Biliary Intraductal Radiofrequency Ablation in Patients With Unresectable Extrahepatic Biliary Tract Cancer

Trial Title: Safety of Biliary Intraductal Radiofrequency Ablation in Patients With Unresectable Extrahepatic Biliary Tract Cancer

NCT ID: NCT06274879

Condition: Bile Duct Cancer

Conditions: Official terms:
Biliary Tract Neoplasms
Bile Duct Neoplasms
Cholangiocarcinoma
Durvalumab
Gemcitabine

Conditions: Keywords:
Durvalumab + chemotherapy
Radiofrequency ablation
Adverse events
Chemo-immune-checkpoint-inhibitor
Extra hepatic biliary tract cancer

Study type: Interventional

Study phase: Phase 2

Overall status: Not yet recruiting

Study design:

Allocation: Randomized

Intervention model: Parallel Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: Gemcitabin, Cisplatin and Durvalumab
Description: CICI (Gemcitabin d1 & d8 Cisplatin d1 & d8, Durvalumab d1) are administered repeating every 21 days for a total of 8 cycles.
Arm group label: Biliary radiofrequency ablation
Arm group label: Control arm

Intervention type: Procedure
Intervention name: Biliary Radiofrequency Ablation
Description: Biliary Radiofrequency Ablation is applied at baseline, 6 and 12 weeks
Arm group label: Biliary radiofrequency ablation

Intervention type: Procedure
Intervention name: Endoscopic Retrograde Cholangio-Pancreatography with stenting
Description: ERCP with stenting are applied at baseline and as clinically indicated
Arm group label: Biliary radiofrequency ablation
Arm group label: Control arm

Summary: The goal of this clinical trial is to provide evidence for the general tolerability of radiofrequency ablation (bRFA) in patients with unresectable bile duct cancer undergoing systemic palliative treatment consisting of chemotherapy (gemcitabine and cisplatin) plus durvalumab (immune-checkpoint-inhibitor, ICI). The main question it aims to answer is whether it is safe to combine chemotherapy (gemcitabine and cisplatin) and immunotherapy (durvalumab) - CICI therapy. Participants will be assigned to either the control group or the experimental group. In the control group, the standard of care consists of endoscopy with stent placement in the bile duct and CICI, whereas in the experimental group, bRFA will be performed in addition to the standard of care. Participants will be followed up for 6 months, during the follow-up, the stage of the tumor, blood examination, the duration of the stent from the insertion until its failure, adverse events and quality of life will be examined. Researchers will compare the standard of care alone to the experimental group to see if the additional bRFA procedure causes higher or no difference in adverse events rate.

Detailed description: Extrahepatic biliary tract cancer (EBTC) in most cases is diagnosed at an unresectable stage of disease. Standard-of-care systemic palliative treatment consists of chemotherapy (gemcitabine and cisplatin) plus durvalumab (immune-checkpoint-inhibitor, ICI). Nonetheless, overall survival remains limited at about 12.8 months. Moreover, severe adverse events can occur leading to treatment discontinuation increasing the risk of tumor progression and poor prognosis. Biliary obstruction is one of the most relevant factors for survival limiting eligibility and timing/dosing of chemo-immunotherapy. Endoscopic biliary stenting is standard to relieve jaundice, but tumor ingrowth can limit the rate and duration of success. Radiofrequency ablation (RFA) results from thermal damage created by a high-frequency alternating current released from an electrode into tissue. RFA has become a standard treatment modality in numerous indications, including the treatment of Barrett's oesophagus-related dysplasia and hepatocellular carcinoma. Intraductal biliary radiofrequency ablation (bRFA) is a relatively new method of inducing tumor necrosis via thermal energy. bRFA has been applied in patients suffering unresectable EBTC within randomized-controlled trials indicating improved stent patency as well as overall survival and progression-free survival. The primary objective of the study is to provide evidence for the general tolerability of bRFA in patients with unresectable extrahepatic biliary tract cholangiocarcinoma undergoing CICI. It is hypothesis that bRFA is generally safe and well tolerated by patients. Primary endpoint of the study is any grade 3 or 4 adverse events leading to chemo-immune checkpoint inhibitor-therapy discontinuation up to six months after enrolment. Eligible patients will be registered in the study database and randomized in 1:2 ratio to either the standard group (CICI with endoscopic biliary stenting) or the experimental bRFA group (CICI with endoscopic biliary stenting + bRFA). CICI with endoscopic biliary stenting are standard of care applied commonly in both the control and the experimental group: Endoscopic retrograde cholangiography (ERC) procedure stenting are applied at baseline and as clinically indicated. CICI cycle (Gemcitabin d1 & d8, Cisplatin d1 & d8, Durvalumab d1) are administered repeating every 21 days for a total of 8 cycles. bRFA will be applied only to the experimental group, it is standardized as for generator settings and protocol adapting to tumor morphology using the probe at baseline, 6 and 12 weeks after study start.

Criteria for eligibility:
Criteria:
Inclusion criteria 1. Male or female ≥18 years old. 2. Histologically or cytologically confirmed diagnosis of previously untreated and unresectable*, locally advanced and/or metastatic extrahepatic biliary tract cholangiocarcinoma with obstructive jaundice (increased serum level of total bilirubin). 3. ECOG performance status 0 to 1. 4. Adequate bone marrow function: Neutrophil count ≥1.0 x 109/L, platelet count ≥100 x 109/L. 5. Adequate renal function: Estimated Glomerular Filtration Rate (eGFR) ≥50mL/min/1.73m2. 6. Willing and able to provide written informed consent. *The reason for inoperability needs to be documented and categorized as follows: - Locally advanced or vascular invasion = surgically not removable. - Distant metastasis. - Severe comorbidities. - Other reasons. Exclusion criteria 1. Solely intrahepatic cholangiocarcinoma or mixed type liver tumors (cholangiocarcinoma with hepatocellular differentiation parts). 2. Multiple hepatic metastases with significant blockage of one or more liver segments and/or less than 50% of liver parenchyma potentially drainable on pre-intervention imaging. 3. Received prior systemic treatment for unresectable and/or metastatic Extrahepatic Biliary Tract Cancer (EBTC). 4. Any autoimmune diseases including inflammatory disorders such as Crohn's disease, ulcerative colitis, Wegener granulomatosis, systemic lupus erythematosus, rheumatoid arthritis, Graves' disease. Exceptions: - Hypothyroidism following Hashimoto thyroiditis stable on hormone replacement. - Patients with vitiligo. - Any chronic skin disorders that do not require systemic treatment. 5. Use of immunosuppressive medication within 3 weeks prior to the dose of durvalumab. Exceptions: - Topical or inhaled steroids. - Systemic corticosteroids at physiologic doses not exceeding >10mg/d of prednisone or equivalent. 6. Known history of Human Immunodeficiency Virus. 7. Prior Self-Expandable Metal Stent (SEMS) placement. 8. Biliary obstruction of non-tumoral etiology. 9. Liver cirrhosis Child-Pugh B or C. 10. Platelets <100 x 109/L or International Normalised Ratio (INR) >1.5. 11. History of organ transplantation. 12. Secondary tumor. Exceptions: - Tumor treated with curative intent without recurrence for more than 5 years. - Non-melanoma skin cancer treated carcinoma in situ without evidence of disease. 14. Other concomitant disease or condition likely to significantly decrease life expectancy i.e., life expectancy is less than 3 months according to investigator judgement. 15. Pregnancy or lactation. A negative blood or urine pregnancy test must be available before administration of CICI. 16. Known or suspected non-compliance, drug, or alcohol abuse. 17. Inability to follow the procedures of the study, e.g., due to language problems, psychological disorders, dementia, etc. of the candidate. 18. Participation in another interventional study within 30 days prior to enrollment. 19. Previous participation in the current study.

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Locations:

Facility:
Name: Inselspital Bern University Hospital

Address:
City: Bern
Zip: 3010
Country: Switzerland

Contact:
Last name: Reiner Prof. Dr. med. Wiest

Phone: +41 31 632 59 41
Email: reiner.wiest@insel.ch

Contact backup:
Last name: Martin Prof. Dr. med. Berger

Phone: +41 31 632 41 14
Email: martin.berger@insel.ch

Investigator:
Last name: Reiner Prof. Dr. med. Wiest
Email: Principal Investigator

Investigator:
Last name: Martin Prof. Dr. med. Berger
Email: Sub-Investigator

Start date: September 1, 2024

Completion date: December 30, 2028

Lead sponsor:
Agency: Insel Gruppe AG, University Hospital Bern
Agency class: Other

Collaborator:
Agency: Swiss Cancer League
Agency class: Other

Source: Insel Gruppe AG, University Hospital Bern

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06274879