A Study of the Use of Irreversible Electroporation in Pancreatic Ductal Cancer

University Health Network, Toronto

Status

Completed

Conditions

Pancreatic Ductal Adenocarcinoma

Treatments

Procedure: Irreversible Electroporation

Device: NanoKnife System

Study type

Interventional

Funder types

Other

Identifiers

NCT03257150

LEAP

Details and patient eligibility

About

This I/II study will evaluate to see how safe and useful irreversible electroporation (also called NanoKnife) is in patients with locally advanced pancreatic cancer.

Full description

In this phase I/II trial, patients with locally advanced pancreatic ductal carcinoma will be assigned to receive interventional treatment of irreversible electroporation (IRE).

IRE will be performed by laparotomy under general anesthesia in the operating room.

All patients enrolled in the study will have a biopsy at the time of laparotomy. Blood will be collected for regular blood tests and correlative studies at baseline and during the study. Computed tomography (CT) scans will be done at baseline, 4 weeks post treatment, 12 weeks, 24 weeks, and 36 weeks follow up. Quality of Life (QOL) questionnaires will be completed at baseline and during the study. Patients will be given optional consent for storage of any leftover tissue and blood samples for future analysis. Patients will be followed up 4 weeks post treatment, then every 12 weeks until death.

Enrollment

12 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Histologically proven pancreatic ductal adenocarcinoma (PDAC)
Age ≥ 18 years
Locally advanced unresectable primary tumor
Tumors ≤5 cm in largest dimension at the time of enrollment that is technically amenable to treatment with irreversible electroporation (IRE)
At least 4 months of combination chemotherapy
Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 2
Acceptable organ and bone marrow function
Life expectancy estimated ≥6 months
Ability and willingness to sign informed consent form
Have a measurable primary tumor at the time of study enrollment
Suitable and fit to undergo general anesthetic and laparotomy
Women of child-producing potential must agree to use effective contraceptive methods prior to study entry, during study participation, and for at least 30 days after the last administration of study medication.

Exclusion criteria

Stage IV (i.e. metastatic) PDAC
Have a cystic subtype PDAC of the pancreas
Previous local treatments for locally advanced PDAC including IRE or radiotherapy
Recent or concurrent cancer, that is distinct from PDAC in primary site/histology, except cervical carcinoma in situ, localized prostate cancer, treated basal cell carcinoma, superficial bladder tumours (Ta, Tis & T1) and those that can be permitted with sufficient clinical justification confirming patient safety to undergo the procedure per Principle Investigator and is in the best interest of the patient. Cancer curatively treated ≥3 years prior to entry is permitted.
Prior chemotherapy within 3 years of diagnosis of PDAC. Chemotherapy for PDAC is permitted
Direct invasion of locally advanced PDAC into the stomach or duodenum
Metallic biliary stent that cannot be substituted with a plastic stent
Allergy to computed tomography (CT) or magnetic resonance imaging (MRI) contrast that cannot be safely managed with premedication which preclude assessment and/or surveillance of PDAC
History of cardiac disease (including, but not limited to: congestive heart failure, active coronary artery disease, uncontrolled hypertension)
Any active major medical illnesses of the respiratory or immune system, or other conditions that may affect patient's ability to tolerate general anesthesia and IRE therapy on this trial
History of solid organ transplantation or collagen vascular disease
Medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of the study results
Pregnant or breast feeding women
Pre-menopausal women unwilling to take a pregnancy test
Any other condition that would, in the Investigator's judgment, contraindicate the patient's participation in the clinical study due to safety concerns or compliance with clinical study procedures (e.g.: infection/inflammation, intestinal obstruction, unable to swallow medication, social/ psychological issues, etc.)
History of human immunodeficiency virus (HIV) infection
Progression of the primary lesion as judged by the Investigator
Working knowledge of English is a must in order to complete the quality of life questionnaires being administered in this study. Patients who do not meet this requirement will be exempt from the quality of life assessments but remain eligible for all other components of the study.