PANFIRE-3 Trial: Assessing Safety and Efficacy of Irreversible Electroporation (IRE) + Nivolumab + CpG for Metastatic Pancreatic Cancer

• Status: Recruiting
• Trial end date: 2022-10-01
• Target enrollment: 0
• Participant gender: All

Summary

Irreversible electroporation is a local ablative technique used in the treatment of pancreatic cancer. In addition to its cytoreductive ability, IRE also induces a systemic immune response. However, this immune response is not potent enough to establish durable regression of the tumor. The immune response can be leveraged by combining IRE with immunotherapy. The primary aim of this study is to determine the safety of IRE + Nivolumab (arm B) and IRE + Nivolumab + CpG (arm C). The secondary aim is to assess efficacy of the experimental arms (B, C) and control arm A (Nivolumab monotherapy), based on overall and progression-free survival as well as locoregional and systemic immune modulation.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: VU University Medical Center
• Treatments: Nivolumab

Criteria

Inclusion Criteria:

• Radiological and histopathologically proven stage IV pancreatic cancer (according to the AJCC staging system for pancreatic cancer);

• Primary oligometastatic disease, defined as at least 1 hepatic metastasis but occurrence of other metastases is not necessarily restricted to the liver, maximum of metastases is to be determined on a case by case basis by the multidisciplinary tumor board.

• Primary tumor is in situ.

• A minimum of 4 cycles of FOLFIRINOX chemotherapy is required but with the explicit aim to strive for completion of 8 cycles of FOLFIRINOX before study inclusion, with at least stable disease on CTscan.

• Age ≥ 18 years.

• World Health Organisation scale (WHO) performance status 0 - 2;

• Adequate bile drainage in case of biliary obstruction.

Exclusion Criteria:

• Trans-mucosal tumor invasion into surrounding duodenum or stomach;

• Active epilepsy (last convulsion < 5 years);

• History of cardiac disease:

• Congestive heart failure > NYHA Class 2

• Active coronary artery disease (defined as myocardial infarction within 6 months prior to screening);

• Ventricular cardiac arrhythmias requiring anti-arrhythmic therapy or pacemaker (beta blockers for antihypertensive regimen are permitted; atrial fibrillation is not contra-indicated);

• Known hypersensitivity to any oligodeoxynucleotides.

• Compromised liver function defined as warning signs of portal hypertension, INR > 1,5 without use of anticoagulants, bilirubin > x 1.5 Upper limit of normal range (ULN) ASAT >3.0 x ULN, ALAT >3.0 x ULN.

• Compromised kidney function defined as eGFR <30 ml/min (using the Cockcroft Gault formula);

• Active autoimmune disease requiring disease-modifying therapy at the time of screening: i.e. > 10 mg prednisolone per day or equivalent to this regimen.

• 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); requiring antibiotics

• Pregnant or breast-feeding subjects; Women of childbearing potential must have a negative pregnancy test performed within 7 days of the start of treatment;

• Immunotherapy prior to the procedure for the treatment of cancer;

• Previous surgical therapy for pancreatic cancer;

• Second primary malignancy with median 5 year OS < 90%, this excludes adequately treated cancers like: non-melanoma skin cancer, in situ carcinoma of the cervix uteri, superficial bladder cancer or other malignancies treated previously without signs of recurrence.

• Allergy to contrast agent.

• Allergy to PET tracers 18F-FDG and 18F-BMS-986192 Zr-89-Nivolumab

• Any implanted stimulation device;

• Portal vein or VMS stenosis > 70% (relative contra-indication)

• Any condition that is unstable or that could jeopardize the safety of the subject and their compliance in the study.