Safety and Efficacy of Irreversible Electroporation for Locally Advanced Pancreatic Cancer

NCT02898649 | Unknown DMC

• 1 other identifier: 4-2015-0150
• Study Type: interventional
• Target: 100
• Locations: 1 country
• Sites: 1

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.

Conditions

Locally Advanced Pancreatic Cancer

Outcome Measures

Primary Outcomes (2)

• Overall survival

  Overall survival is calculated from the date of informed consent acquisition until the date of death.

  from 1 month to 3 month

• Safety (frequency of procedure-related complication and death)

  Safety is evaluated by the frequency of procedure-related complication and death.

  from 1 month to 3 month

Secondary Outcomes (4)

• Time to progression

  within 1 year

• Tumor control

  within 1 year

• Pain control

  within 1 year

• Change in CA 19-9

  within 1 year

Study Arms (1)

IRE

EXPERIMENTAL

The intervention group

Device: Irreversible electroporation

Interventions

Irreversible electroporation DEVICE

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.

IRE

Eligibility Criteria

• Age: 19 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• 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.

You may not qualify if:

• 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.

Sponsors & Collaborators

• Yonsei University: lead

Study Sites (1)

Yonsei university of medical center

Seoul, 03722, South Korea

RECRUITING

MeSH Terms

Interventions

Electroporation

Intervention Hierarchy (Ancestors)

Cytological Techniques; Clinical Laboratory Techniques; Investigative Techniques; Electrochemical Techniques

Central Study Contacts

Seung Min Bang, MD

CONTACT

+82 2 2228 1995; BANG7028@yuhs.ac

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 8, 2016
• First Posted: September 13, 2016
• Study Start: December 1, 2015
• Primary Completion: August 1, 2019
• Study Completion: August 1, 2019
• Last Updated: February 15, 2019

Record last verified: 2019-02

Locations

KR (1)