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Phase 2 N=8 Treatment

Trial of IRE in Cholangiocarcinoma

Cholangiocarcinoma

Enrolled (actual)
8
Serious AEs
0.0%
Results posted
Sep 2022
Primary outcome: Primary: Number of Patients Experiencing a Clinically Relevant Complications — 1; 7 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
IRE Device (Device)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Memorial Sloan Kettering Cancer Center
Primary completion
Aug 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Patients Experiencing a Clinically Relevant Complications
1; 7

Summary

The purpose of this study is to test any good and bad side effects of surgery using IRE to treat cancer of the bile duct.

Eligibility Criteria

Inclusion Criteria

  • Age 18 years or older
  • Capable of providing written and oral informed consent in English
  • Locally advanced disease based on preoperative work-up demonstrating that the tumor is unresectable due to portal vein, hepatic artery, and/or bile duct involvement, insufficient hypertrophy response of the future liver remnant after portal vein embolization, or patients not able to tolerate major liver surgery
  • Found to be unresectable intraoperatively based on vascular, biliary, or lymph node (N2) involvement upon exploratory laparotomy
  • Patients will be assessed for chemotherapy prior to treatment with IRE, but given the common problem of recurrent cholangitis, some patients will not be candidates for chemotherapy until after IRE is performed.

Exclusion Criteria

  • Locally advanced PHC eligible and accepted for liver transplantation evaluation
  • PHC with > 5 cm extension along the common hepatic duct or common bile duct on preoperative imaging or intraoperative ultrasound
  • Metastases to peritoneum, liver or other organs confirmed by percutaneous biopsy, staging laparoscopy or intraoperative frozen section
  • Lymph node metastases beyond N2 stations, confirmed by intraoperative frozen sections or radiographic diagnosis
  • History of cardiac disease:
  • Congestive heart failure (NYHA class >2)
  • Active Coronary Artery Disease (defined as myocardial infarction within 6 months prior to screening)
  • Cardiac arrhythmias requiring anti-arrhythmic therapy or pacemaker (beta blockers are permitted)
  • Any implanted stimulation device (defined as implantable cardiac device and a pacemaker)
  • Uncontrolled hypertension (blood pressure must be ≤160/95 mmHg at the time of screening on a stable antihypertensive regimen)
  • Uncontrolled infections (> grade 2 NCI-CTC, version 3.0)
  • Epilepsy
  • Both narrowing (sclerosis) of the main portal vein and a reduced diameter of either the common hepatic artery, celiac trunk or superior mesenteric artery of >50%
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03769753). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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