Repeated Endobiliary Radiofrequency Ablation Plus Durvalumab, Gemcitabine, and Cisplatin for Unresectable Extrahepatic Cholangiocarcinoma

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAichi Medical University

About this trial

This international, multicenter, open-label randomized controlled trial evaluates whether repeated endobiliary radiofrequency ablation (EB-RFA) improves overall survival in patients with unresectable extrahepatic cholangiocarcinoma undergoing first-line systemic therapy with durvalumab plus gemcitabine and cisplatin (GCD). Eligible patients will be randomized 1:1 to EB-RFA with plastic stent placement or standard plastic stenting alone. A scheduled second endoscopic session will be performed at 3 months in both groups (repeat EB-RFA only in the EB-RFA arm). The primary endpoint is overall survival. Secondary endpoints include time to recurrent biliary obstruction, progression-free survival, adverse events, and technical/clinical success.

Eligibility criteria

Qualifiers

None

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Endobiliary Radiofrequency Ablation (EB-RFA)
  • Plastic Biliary Stent

Treatment groups

120 Participants
are divided into 2 treatment groups

Locations

8
Japan
Aichi Medical University Aichi Japan
Nagoya City University Hospital Aichi Japan
Nagoya City University Midori Municipal Hospital Aichi Japan
Gifu University Hospital Gifu Japan

Sponsors and collaborators

Aichi Medical University

Lead sponsor