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Immune Response After Pancreatic Cancer Treatment

Differential Immunologic Signature After Pancreatic Cancer Treatment: Does Irreversible Electroporation Lead to a Prolonged and Potent T-cell Mediated Immune Response Compared to Surgical Resection?

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03069599
Acronym
IRE Immuno
Enrollment
38
Registered
2017-03-03
Start date
2017-02-15
Completion date
2020-02-25
Last updated
2020-02-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic Cancer

Brief summary

The aim of this project is to describe the differential immunologic responses of patients who undergo in situ IRE, margin accentuation IRE with surgical resection of the primary tumor, and surgical resection of the primary tumor only. The primary hypothesis is that IRE induces a long and sustained activation of the cell-mediated immune system, which is distinct from the immune response after surgical resection only. The primary endpoint of this study is the comparison of the CD4+/CD8+ ratio as an indicator of antitumor immunity both longitudinally within a group after the intervention and over time between the three groups. CD4+/CD8+ ratio will be measured preoperatively and at postoperative days 1, 7, 42, and 180. As a secondary outcome, additional measurements will be taken to more specifically characterize the immune response based on peripheral blood samples. Flow cytometry will be used to quantify cell subsets, and ELISA will be used to measure cytokine levels , at the same time-points as for the primary outcome. Each group of patients as described above will consist of 10 consecutive pancreatic cancer patients. Patients aged 18 or older with resectable, borderline resectable, or locally advanced pancreatic cancer will be included. Patients with locally advanced disease will undergo 3 months of preoperative chemotherapy with monitoring to exclude metastatic disease. Main exclusion criteria are cardiac conduction abnormalities and signs of distant metastasis.

Interventions

PROCEDUREirreversible electroporation (IRE)

Irreversible electroporation is an emerging, mainly non-thermal ablative modality. It circumvents some downsides of thermal ablation and has the potential for broad application among patients with pancreatic cancer.

Sponsors

Insel Gruppe AG, University Hospital Bern
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * Able to undergo general anesthesia (ASA ≤ 4) * Performance status ECOG \<=2 (Eastern Cooperative Oncology Group) * Life expectancy of at least 6 months * Resectable, borderline resectable, or locally advanced pancreatic cancer * Patients who have locally advanced disease have to show no tumor progression after 3 month of neo-adjuvant chemotherapy+/-XRT before undergoing in situ IRE

Exclusion criteria

* Cardiac AV conduction abnormalities, ventricular fibrillation * History of epilepsy * Recent history of myocardial infarction (2 months) * Evidence of distant metastasis (e.g. liver, lung, peritoneum) * Informed consent cannot be given by the patient * Known hypersensitivity to the IRE electrodes (stainless steel 304L) * Women of childbearing potential who are pregnant, breast feeding, or not taking an adequate method of contraception at the time of procedure

Design outcomes

Primary

MeasureTime frameDescription
Immunological outcome42 daysflowcytometry

Secondary

MeasureTime frameDescription
Number of local tumor recurrences42 daysmeasured via CT
Number of distant tumor recurrences42 daysmeasured via CT
Overall survival42 dayssurvival of patient
Cancer specific survival42 dayssurvival of patient

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026