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Safety and Efficacy of Irreversible Electroporation for Locally Advanced Pancreatic Cancer

Primary Purpose

Locally Advanced Pancreatic Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Irreversible electroporation
Sponsored by
Yonsei University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Locally Advanced Pancreatic Cancer

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Pathologically confirmed pancreatic cancer patients
  • Locally advanced pancreatic cancer patients. Vascular encasement by tumor was noted in radiological evaluation (CT, MRI or PET-CT)
  • Older than 19 years old and younger than 70 years old
  • Previously treated with systemic chemotherapy or chemoradiotherapy due to locally advanced pancreatic cancer.

Exclusion Criteria:

  • Patients with life-threatening systemic disease.
  • Metastatic or borderline-resectable pancreatic cancer patients
  • Patients with seizure history
  • Patients with arrythmia or heart failure
  • Recent history of myocardial infarction (within 1 year)
  • Patients who have implantable electronic devices. (e.g. pacemaker, defibrillator)
  • Patients who have metal devices (e.g. metal stent) around tumor.
  • Coagulopathy patients.

Sites / Locations

  • Yonsei university of medical centerRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

IRE

Arm Description

The intervention group

Outcomes

Primary Outcome Measures

Overall survival
Overall survival is calculated from the date of informed consent acquisition until the date of death.
Safety (frequency of procedure-related complication and death)
Safety is evaluated by the frequency of procedure-related complication and death.

Secondary Outcome Measures

Time to progression
Tumor control
Pain control
Change in CA 19-9

Full Information

First Posted
September 8, 2016
Last Updated
February 13, 2019
Sponsor
Yonsei University
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1. Study Identification

Unique Protocol Identification Number
NCT02898649
Brief Title
Safety and Efficacy of Irreversible Electroporation for Locally Advanced Pancreatic Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Unknown status
Study Start Date
December 2015 (undefined)
Primary Completion Date
August 2019 (Anticipated)
Study Completion Date
August 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yonsei University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Pancreatic cancer is 5th leading cause of cancer-related death in Korea. It has a dismal prognosis with very low 5-year survival rate, about 5%. Only 10% of pancreatic cancer patients is diagnosed in operable status. So, most of patients could not be treated with curative resection. Locally advanced pancreatic cancer (LAPC) is defined by defined as surgically unresectable due to vascular encasement (e.g. celiac trunk or superior mesenteric artery) by tumor, but have no evidence of distant metastases. In LAPC patients, systemic chemotherapy with/without radiotherapy was used as a standard therapy, but therapeutic response was very poor. Only less than 30% of patients showed treatment response, and median survival of LAPC patient was only 9 months. Thus, more effective treatment modality is needed for LAPC patients. Irreversible electroporation (IRE) is a soft tissue ablation technique using ultra short but strong electrical fields to create permanent and hence lethal nanopores in the cell membrane, to disrupt the cellular homeostasis. IRE does not cause thermally induced necrosis and has tissue selectivity, so adjacent tissue or vascular structures can be preserved. Several clinical trials using IRE were performed to liver, kidney or lung cancer patients. We will operate IRE procedure to LAPC patients who were previously received standard therapy but showed no response, using NanoKnife IRE device. We will investigate treatment response and safety of IRE.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Locally Advanced Pancreatic Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
IRE
Arm Type
Experimental
Arm Description
The intervention group
Intervention Type
Device
Intervention Name(s)
Irreversible electroporation
Intervention Description
IRE is operated to tumor under laparotomy or CT-guided percutaneous approach. Unipolar (19G) or bipolar (16G) electrode probe is inserted to around tumor. After insertion of probe, short duration (70-90㎲) of electric current (25~45A) is generated by IRE device (NanoKnife IRE device, AngioDynamics, Queens bury, New York). It is possible to obtain a three-dimensional ablation zone using multiple electrode. IRE can cause apoptosis of tumor cells, without adjacent tissue damage.
Primary Outcome Measure Information:
Title
Overall survival
Description
Overall survival is calculated from the date of informed consent acquisition until the date of death.
Time Frame
from 1 month to 3 month
Title
Safety (frequency of procedure-related complication and death)
Description
Safety is evaluated by the frequency of procedure-related complication and death.
Time Frame
from 1 month to 3 month
Secondary Outcome Measure Information:
Title
Time to progression
Time Frame
within 1 year
Title
Tumor control
Time Frame
within 1 year
Title
Pain control
Time Frame
within 1 year
Title
Change in CA 19-9
Time Frame
within 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pathologically confirmed pancreatic cancer patients Locally advanced pancreatic cancer patients. Vascular encasement by tumor was noted in radiological evaluation (CT, MRI or PET-CT) Older than 19 years old and younger than 70 years old Previously treated with systemic chemotherapy or chemoradiotherapy due to locally advanced pancreatic cancer. Exclusion Criteria: Patients with life-threatening systemic disease. Metastatic or borderline-resectable pancreatic cancer patients Patients with seizure history Patients with arrythmia or heart failure Recent history of myocardial infarction (within 1 year) Patients who have implantable electronic devices. (e.g. pacemaker, defibrillator) Patients who have metal devices (e.g. metal stent) around tumor. Coagulopathy patients.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Seung Min Bang, MD
Phone
+82 2 2228 1995
Email
BANG7028@yuhs.ac
Facility Information:
Facility Name
Yonsei university of medical center
City
Seoul
ZIP/Postal Code
03722
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Seung Min Bang, MD
Phone
+82 2 2228 1995
Email
BANG7028@yuhs.ac

12. IPD Sharing Statement

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Safety and Efficacy of Irreversible Electroporation for Locally Advanced Pancreatic Cancer

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