IRE Immuno: Immune Response After Pancreatic Cancer Treatment

Sponsor
University Hospital Inselspital, Berne (Other)
Overall Status
Terminated
CT.gov ID
NCT03069599
Collaborator
(none)
38
1
36.3
1

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: irreversible electroporation (IRE)

Study Design

Study Type:
Observational
Actual Enrollment :
38 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
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?
Actual Study Start Date :
Feb 15, 2017
Actual Primary Completion Date :
Feb 25, 2020
Actual Study Completion Date :
Feb 25, 2020

Arms and Interventions

Arm Intervention/Treatment
10 IRE locally advanced

patients undergoing in situ IRE for locally advanced pancreatic

Procedure: irreversible 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.

10 IRE borderline resection

patients undergoing margin accentuation IRE for borderline resectable disease

Procedure: irreversible 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.

10 resection only

patients undergoing surgical resection only

Outcome Measures

Primary Outcome Measures

  1. Immunological outcome [42 days]

    flowcytometry

  2. Immunological outcome [6 months]

    Flowcytometry

  3. Immunological outcome [9 months]

    Flowcytometry

  4. Immunological outcome [42 days]

    ELISA

  5. Immunological outcome [6 months]

    ELISA

  6. Immunological outcome [9 months]

    ELISA

Secondary Outcome Measures

  1. Number of local tumor recurrences [42 days]

    measured via CT

  2. Number of local tumor recurrences [3 months]

    measured via CT

  3. Number of local tumor recurrences [6 months]

    measured via CT

  4. Number of local tumor recurrences [9 months]

    measured via CT

  5. Number of distant tumor recurrences [42 days]

    measured via CT

  6. Number of distant tumor recurrences [3 months]

    measured via CT

  7. Number of distant tumor recurrences [6 months]

    measured via CT

  8. Number of distant tumor recurrences [9 months]

    measured via CT

  9. Overall survival [42 days]

    survival of patient

  10. Overall survival [3 months]

    survival of patient

  11. Overall survival [6 months]

    survival of patient

  12. Overall survival [9 months]

    survival of patient

  13. Cancer specific survival [42 days]

    survival of patient

  14. Cancer specific survival [3 months]

    survival of patient

  15. Cancer specific survival [6 months]

    survival of patient

  16. Cancer specific survival [9 months]

    survival of patient

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Inselhospital Bern Switzerland

Sponsors and Collaborators

  • University Hospital Inselspital, Berne

Investigators

  • Principal Investigator: Mathias Worni, MD, Inselspital Berne

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital Inselspital, Berne
ClinicalTrials.gov Identifier:
NCT03069599
Other Study ID Numbers:
  • 2016-02037
First Posted:
Mar 3, 2017
Last Update Posted:
Feb 26, 2020
Last Verified:
Feb 1, 2020
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 26, 2020