IReversible Electroporation of Kidney Tumors Before Partial Nephrectomy. (IRENE)
Primary Purpose
Kidney Tumor, Renal Cell Cancer
Status
Unknown status
Phase
Phase 1
Locations
Germany
Study Type
Interventional
Intervention
Irreversible Electroporation (IRE)
Sponsored by
About this trial
This is an interventional treatment trial for Kidney Tumor focused on measuring kidney tumor, renal cell cancer, RCC, irreversible electroporation, IRE, partial kidney resection, percutaneous, ablation, IRENE
Eligibility Criteria
Inclusion Criteria:
- one or more localized, resectable kidney tumors (≤4 cm) suspicious of malignancy or histology -proven renal cell cancer (RCC)
- patients desire for therapy and surgical therapy
- Karnofsky-index >70%
- Age ≥ 18 years
- life expectancy ≥ 12 month
- compliance of the patient taking part in a study
- informed consent
Exclusion Criteria:
- violation against one or more inclusion criteria
- cardial pacemaker or other electrical implants
- QT-interval >550 ms or cardiac arrhythmias or condition after myocardial infarction, that make an ECG-synchronisation unfeasible
- known cardial ejection fraction < 30% or NYHA III or III-IV
- known epilepsy
- second malignancy (except basal-cell carcinoma and cervical carcinoma in situ)
- immunosuppression or HIV-positive patients
- active infection or severe health interference, that make taking part in a study unfeasible
- pregnancy, lactation period, no contraception
- metastatic disease
- palliative status
- running or executed RCC therapy
- taking part in another clinical study for RCC
- inoperable
- rejection of interventional or surgical therapy by the patient
- circulatory instability
- general contraindications for anesthesia, endotracheal anesthesia and muscle relaxation
- psychiatric disorders that make taking part in a study or giving informed consent unfeasible
- haemorrhage, impossible intermission of taking blood thinner, untreatable thrombophilia
- thromboplastin time ≤50 %, thrombocytes ≤50 Gpt/L; partial thromboplastin time >50
- MRI incompatibility
- metal implants <1 cm closed to the kidney / kidney tumor
- contraindication for biopsy and punction of the renal tumor under CT-guidance
- untreated urinary retention
- renal pelvis tumor, suspected transitional cell cancer
Sites / Locations
- Department of Pathology University Hospital Otto-von-Guericke-University MagdeburgRecruiting
- Department of Radiology University Hospital Otto-von-Guericke-University MagdeburgRecruiting
- Department of Urology University Hospital Otto-von-Guericke-University MagdeburgRecruiting
- MVZ Hanse Histologikum GmbH HamburgRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
renal tumor <4cm, suspected RCC
Arm Description
Intervention/ Time point: Irreversible Electroporation at day 0 of each patient.
Outcomes
Primary Outcome Measures
analysis of ablation effectiveness of non-metastatic renal tumors <4cm 28 days by after irreversible electroporation (NanoKnife, AngioDynamics Inc.) by histopathological examination of partial kidney resection specimens
onco-therapeutic effectiveness, measured against persistent active tumor / cancer cells by histopathological and magnet resonance imaging analysis
Secondary Outcome Measures
safety
adverse effects
Assessment of the procedural compliance
Assessment of the Quality of Life (QoL)
Full Information
NCT ID
NCT01967407
First Posted
October 15, 2013
Last Updated
November 18, 2014
Sponsor
University of Magdeburg
1. Study Identification
Unique Protocol Identification Number
NCT01967407
Brief Title
IReversible Electroporation of Kidney Tumors Before Partial Nephrectomy.
Acronym
IRENE
Official Title
Prospective, Monocentric, Clinical Phase-I/II Study of the Effectiveness of the Percutaneous Irreversible Electroporation (IRE) of Locally Confined Kidney Tumors (Renal Cell Carcinomas).
Study Type
Interventional
2. Study Status
Record Verification Date
November 2014
Overall Recruitment Status
Unknown status
Study Start Date
October 2013 (undefined)
Primary Completion Date
December 2015 (Anticipated)
Study Completion Date
January 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Magdeburg
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The aim of the study is the evaluation of the ablation efficiency of the percutaneous irreversible electroporation (IRE) as primary ablation therapy of locally confined renal cell carcinoma (≤4cm, see inclusion and exclusion criteria).
The ablation success will be proofed by magnet resonance imaging (MRI) and histologically after partial kidney resection or nephrectomy 4 weeks after IRE. Hypotheses: Kidney tumors ≤4cm can be ablated completely by percutaneous IRE. Surrounded structures and renal tissue can be preserved.
Detailed Description
Health Condition or Problem studied:
International Statistical Classification of Diseases and Related Health Problems, Tenth Revision (ICD10): C64 - Malignant neoplasm of kidney, except renal pelvis
ICD10: D41.0 - Neoplasm of uncertain or unknown behaviour: Kidney
Interventions/Observational Groups Arm 1:
Initial diagnostical examination of the renal mass.
If any extended diagnostical examination for treatment planning.
Day -29 to -1: Recruitment.
Day -1: MRI of the kidney, Karnofsky, physical examination, blood chemistry, urosonography, if any renal scintigraphy, life quality assessment.
Day 0: Percutaneous diagnostical biopsy with histopathological investigation and therapeutically, CT- and/or ultrasound-guided, ECG-synchronized irreversible electroporation (IRE) of the kidney tumor in endotracheal anaesthesia und muscle relaxation. Use of 1-6 IRE probes with 90-100 pulses of 1500-3000 volts und 20-50 amperes each.
Day 1-7: Postinterventional follow-up: MRI of the kidneys, Karnofsky, physical examination, blood chemistry, urosonography, life quality assessment.
Day 27: Postinterventional follow-up: MRI of the kidneys, Karnofsky, physical examination, blood chemistry, urosonography, if any renal scintigraphy, life quality assessment.
Day 28: Open surgery partial kidney resection or tumor nephrectomy of the IRE treated kidney resp. kidney tumor region with histopathological investigation.
Day 29-37: Postoperative follow-up: physical examination, blood chemistry, urosonography, life quality assessment.
Day 112: Study-Follow-up: MRI of the kidneys, Karnofsky, physical examination, blood chemistry, urosonography, if any renal scintigraphy, life quality assessment. Termination of the study.
Study closed, Individual follow-up due to the European Association of Urology guideline.
Recruitment:
(Anticipated or Actual) Date of First Enrollment: 2013/10/14
Planned/Actual: Opened
Target Sample Size: 20
Monocentric/Multicentric trial: Monocentric trial
National/International: National
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kidney Tumor, Renal Cell Cancer
Keywords
kidney tumor, renal cell cancer, RCC, irreversible electroporation, IRE, partial kidney resection, percutaneous, ablation, IRENE
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
renal tumor <4cm, suspected RCC
Arm Type
Experimental
Arm Description
Intervention/ Time point: Irreversible Electroporation at day 0 of each patient.
Intervention Type
Procedure
Intervention Name(s)
Irreversible Electroporation (IRE)
Other Intervention Name(s)
NanoKnife (Tissue Ablation) System, AngioDynamics Inc.
Intervention Description
Percutaneous CT-fluoroscopic-guided Irreversible Electroporation.
Primary Outcome Measure Information:
Title
analysis of ablation effectiveness of non-metastatic renal tumors <4cm 28 days by after irreversible electroporation (NanoKnife, AngioDynamics Inc.) by histopathological examination of partial kidney resection specimens
Description
onco-therapeutic effectiveness, measured against persistent active tumor / cancer cells by histopathological and magnet resonance imaging analysis
Time Frame
28 days
Secondary Outcome Measure Information:
Title
safety
Description
adverse effects
Assessment of the procedural compliance
Assessment of the Quality of Life (QoL)
Time Frame
4 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
one or more localized, resectable kidney tumors (≤4 cm) suspicious of malignancy or histology -proven renal cell cancer (RCC)
patients desire for therapy and surgical therapy
Karnofsky-index >70%
Age ≥ 18 years
life expectancy ≥ 12 month
compliance of the patient taking part in a study
informed consent
Exclusion Criteria:
violation against one or more inclusion criteria
cardial pacemaker or other electrical implants
QT-interval >550 ms or cardiac arrhythmias or condition after myocardial infarction, that make an ECG-synchronisation unfeasible
known cardial ejection fraction < 30% or NYHA III or III-IV
known epilepsy
second malignancy (except basal-cell carcinoma and cervical carcinoma in situ)
immunosuppression or HIV-positive patients
active infection or severe health interference, that make taking part in a study unfeasible
pregnancy, lactation period, no contraception
metastatic disease
palliative status
running or executed RCC therapy
taking part in another clinical study for RCC
inoperable
rejection of interventional or surgical therapy by the patient
circulatory instability
general contraindications for anesthesia, endotracheal anesthesia and muscle relaxation
psychiatric disorders that make taking part in a study or giving informed consent unfeasible
haemorrhage, impossible intermission of taking blood thinner, untreatable thrombophilia
thromboplastin time ≤50 %, thrombocytes ≤50 Gpt/L; partial thromboplastin time >50
MRI incompatibility
metal implants <1 cm closed to the kidney / kidney tumor
contraindication for biopsy and punction of the renal tumor under CT-guidance
untreated urinary retention
renal pelvis tumor, suspected transitional cell cancer
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Antje Wiede, Dr.
Phone
+493916721841
Email
antje.wiede@med.ovgu.de
First Name & Middle Initial & Last Name or Official Title & Degree
Johann J. Wendler, Dr. med.
Phone
+493916715036
Email
johann.wendler@med.ovgu.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Uwe- B. Liehr, Dr. med.
Organizational Affiliation
Department of Urology, University Magdeburg, Germany.
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Martin Schostak, Prof. Dr.
Organizational Affiliation
Department of Urology, University Magdeburg, Germany
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Johann J. Wendler, Dr. med.
Organizational Affiliation
Department of Urology, University Magdeburg, Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Pathology University Hospital Otto-von-Guericke-University Magdeburg
City
Magdeburg
State/Province
Sachsen-Anhalt
ZIP/Postal Code
39120
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sandra Böttcher, Dr.
First Name & Middle Initial & Last Name & Degree
Albert Roessner, Prof.
Facility Name
Department of Radiology University Hospital Otto-von-Guericke-University Magdeburg
City
Magdeburg
State/Province
Sachsen-Anhalt
ZIP/Postal Code
39120
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jens Ricke, Prof.
First Name & Middle Initial & Last Name & Degree
Frank Fischbach, Prof.
First Name & Middle Initial & Last Name & Degree
Maciej Pech, Prof.
First Name & Middle Initial & Last Name & Degree
Julian Jürgens
Facility Name
Department of Urology University Hospital Otto-von-Guericke-University Magdeburg
City
Magdeburg
State/Province
Sachsen-Anhalt
ZIP/Postal Code
39120
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Markus Porsch, Dr.
First Name & Middle Initial & Last Name & Degree
Andreas Janitzky, Dr.
First Name & Middle Initial & Last Name & Degree
Daniel Baumunk, Dr.
First Name & Middle Initial & Last Name & Degree
Daniel Schindele, Dr.
First Name & Middle Initial & Last Name & Degree
Simon Blaschke
Facility Name
MVZ Hanse Histologikum GmbH Hamburg
City
Hamburg
ZIP/Postal Code
22547
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jens Köllermann, PD Dr. med.
Phone
0049-40-707085200
Email
koellermann@pathologie-hh.de
First Name & Middle Initial & Last Name & Degree
Jens Köllermann, PD Dr. med
12. IPD Sharing Statement
Citations:
PubMed Identifier
23139026
Citation
Liehr UB, Wendler JJ, Blaschke S, Porsch M, Janitzky A, Baumunk D, Pech M, Fischbach F, Schindele D, Grube C, Ricke J, Schostak M. [Irreversible electroporation: the new generation of local ablation techniques for renal cell carcinoma]. Urologe A. 2012 Dec;51(12):1728-34. doi: 10.1007/s00120-012-3038-8. German.
Results Reference
background
PubMed Identifier
25389236
Citation
Jiang C, Davalos RV, Bischof JC. A review of basic to clinical studies of irreversible electroporation therapy. IEEE Trans Biomed Eng. 2015 Jan;62(1):4-20. doi: 10.1109/TBME.2014.2367543.
Results Reference
background
PubMed Identifier
25902855
Citation
Wendler JJ, Porsch M, Fischbach F, Pech M, Schostak M, Liehr UB. Letter to the Editor Concerning "Irreversible Electroporation (IRE) Fails to Demonstrate Efficacy in a Prospective Multicenter Phase II Trial on Lung Malignancies: The ALICE Trial" by Ricke et al. 2015 (doi:10.1007/s00270-014-1049-0). Cardiovasc Intervent Radiol. 2015 Aug;38(4):1064-5. doi: 10.1007/s00270-015-1096-1. Epub 2015 Apr 23. No abstract available.
Results Reference
derived
Links:
URL
http://urologie.med.uni-magdeburg.de/urologie.html
Description
Department of Urology, University Magdeburg
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IReversible Electroporation of Kidney Tumors Before Partial Nephrectomy.
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