Pancreas Cancer
Conditions
Brief summary
Primary Objective(s) To collect clinical data related to the treatment outcomes of Pancreatic IRE in order to develop an evidence base such that physicians can provide the best possible care to patients with pancreatic cancer requiring surgical intervention. Secondary Objective(s) To collect data on adverse events and complications related to IRE treatment. The AHPBA (Americas Hepato-Pancreato-Biliary Association) will be responsible for data collection and will periodically audit the data for quality assurance purposes. The AHPBA will review outcomes reported by each participating Research Institution and if outcomes are in the lower percentile, the investigators will be offered support to analyze the reasons for the suboptimal outcomes and may seek support to improve outcomes. The participating Research Institutions will receive a certificate annually that acknowledges their participation in the Research Project.
Detailed description
This study is an international prospective, multi-center, registry study; collecting clinical data regarding standard-of-care use of the NanoKnife system intraoperatively (via laparotomy) to ablate the pancreatic tumors per the treating physicians discretion. NanoKnife System is a commercially available irreversible electroporation system. Since it is participants who are candidates for or undergo the NanoKnife procedure will be consented to participate in this prospective registry study. Clinical data from enrolled patients will be collected and patients will undergo clinical follow-up at the following time points post-procedure: 24-48 hours post-procedure, hospital discharge, 7 days post-procedure, 30 days, and 90 days. See Appendix 1: Schedule of Events Collected as Part of Study Registry. Participants will be followed for 4 years following the NanoKnife procedure. While in the hospital, they will be evaluated within 24-48 hours after the NanoKnife procedure. Additional assessments will be performed prior to being discharged from the hospital. Participants will be asked to return every 3 month follow up to 2 years and then every 6 months after 2 years from IRE. Each visit will last approximately two (2) to three (3) hours at the study doctor's clinic. During these visits, participants will also be asked to report any change in their medications. Except for the study visits, they will not need to visit the study doctor more often than their usual treatment unless they have other medical needs. However, if participants experience any significant change in their medical condition they may be asked to have additional tests such as CT scan, blood tests, etc. Participants will not receive any financial or other compensation for taking part in this study.
Interventions
OTHERNanoKnife procedure
clinical data regarding use of the NanoKnife system intraoperatively (via laparotomy) to ablate the pancreatic tumors per the treating physicians discretion will be collected.
Sponsors
Methodist Health System
Study design
Observational model
OTHER
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. more than 18 years of age 2. Diagnosed with pancreatic cancer and has consented to undergo the NanoKnife procedure per the treating physician 3. Willing and able to comply with the protocol requirements 4. Able to comprehend and sign the Informed Consent Form in English or Spanish
Exclusion criteria
* Patients who meet any of the following criteria will be excluded from the study: 1. Do not meet the Study Inclusion Criteria laid out above
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| CT scan finding new lymph nodes | pre-operatively and several timepoints post-operatively until 4 years | 15 mm short axis diameter or pathlology proven |
| CBC blood test | pre-operatively and several timepoints post-operatively until 4 years | Check participants blood counts |
| Clinical data collected prospectively and post-operatively at different timepoints | pre-operatively and several timepoints post-operatively until 4 years | The primary objective of the study is to collect clinical data related to treatment outcomes of Pancreatic Irreversible Electroporation in order to develop an evidence base such that physicians can provide the best possible care to patients with pancreatic cancer requiring surgical intervention. |
| Chemistry blood test | up to 4 years following operation | Check the elements and minerals in the blood |
| CA19-9 | pre-operatively and several timepoints post-operatively until 4 years | monitor the pancreas (74U/mL) |
| Physical exam-Height | pre-operatively and several timepoints post-operatively until 4 years | Review the height of the participant using the unit of measurement of feet and inches |
| Physical exam- Weight | pre-operatively and several timepoints post-operatively until 4 years | Review the weight of participant in lbs |
| CT scan of the tumor area-diameter | pre-operatively and several timepoints post-operatively until 4 years | Longest diameter in the axial plane of the soft tissue component of the primary tumor (mm) |
| CT scan of the tumor area- vessel narrowing | pre-operatively and several timepoints post-operatively until 4 years | measurement of of the vessels (mm) by comparison of diameter from first follow up scan |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Data on adverse events and complications related to Irreversible Electroporations. | It will be collected at different timepoints until 4 years postoperatively. | It supports the secondary objective of the study to collect data on adverse events and complications after IRE (Irreversible Electroporation). |
Countries
United States
Contacts
Primary ContactCrystee Cooper, DHEd
Backup ContactZaid Haddadin, MS
Outcome results
None listed