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Safety Study of Radiofrequency Ablation of Locally Advanced Pancreatic Cancer (RFA of LAPC)

Primary Purpose

Locally Advanced Pancreatic Cancer

Status
Completed
Phase
Phase 2
Locations
Netherlands
Study Type
Interventional
Intervention
radiofrequency ablation (RFA)
Sponsored by
UMC Utrecht
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Locally Advanced Pancreatic Cancer focused on measuring Pancreatic cancer, locally advanced, irresectable, Radiofrequency, RFA

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients with irresectable locally advanced pancreatic cancer found at laparotomy with histologic diagnosis before start of RFA
  2. Patient considered eligible to undergo pancreatic surgery as assessed by the general criteria of the departments of anaesthesiology and surgery of the UMC Utrecht
  3. Fully informed written consent given

Exclusion Criteria:

  1. Patients younger than 18 years
  2. Pregnancy
  3. Patients with distant metastases
  4. Portal vein thrombosis seen on CT preoperatively

Sites / Locations

  • University Medical Center Utrecht

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

radiofrequency ablation

Arm Description

Outcomes

Primary Outcome Measures

Safety
The safety will be specified as the percentage of patients with complications directly related to RFA and the routinely performed double-bypass procedure, requiring re-intervention (i.e. endoscopy, radiology, or surgery). This is also known as a complication of grade III or higher in the Clavien-Dindo classification (internationally accepted classification for surgical complications). Moreover all in-hospital complications or complications developed within 30 days after the RFA procedure will be evaluated according to the Clavien-Dindo classification.

Secondary Outcome Measures

survival
VAS pain score
length hospital stay
progression free survival
CA19-9 response
Chemotherapy
Type, frequency, dosage and duration of chemotherapy will be registered.

Full Information

First Posted
June 20, 2012
Last Updated
January 29, 2015
Sponsor
UMC Utrecht
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1. Study Identification

Unique Protocol Identification Number
NCT01628458
Brief Title
Safety Study of Radiofrequency Ablation of Locally Advanced Pancreatic Cancer
Acronym
RFA of LAPC
Official Title
Phase II Study: Radiofrequency Ablation of Locally Advanced Pancreatic Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
January 2015
Overall Recruitment Status
Completed
Study Start Date
September 2012 (undefined)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
November 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
UMC Utrecht

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the study is to determine the safety of radiofrequency ablation of locally advanced pancreatic cancer that can not be surgically removed with the current standard procedures. Complications after the operation will be registered. Moreover a pain score will be determined, length of hospital stay, chemotherapy, survival, progression free survival and a tumour marker.
Detailed Description
Pancreatic cancer is the fourth leading cause of cancer related death in the Western world. At time of diagnosis, 20% of patients present with a resectable tumour, 40% with an irresectable locally advanced tumour (without metastases) and 40% with metastatic disease. The median survival of patients with irresectable locally advanced pancreatic cancer is only 6 months. Currently, there is no effective treatment for these patients. Therefore, there is an urgent need for new therapies. Radiofrequency ablation (RFA) is a technique that has been demonstrated to be effective in the treatment of several irresectable tumours. RFA produces local tumour destruction through high frequency alternating current flowing from an electrode implanted directly into the tumour and causing frictional heating. The purpose of this study is to determine the safety of RFA-pancreas in patients with non-metastasized, irresectable, locally advanced pancreatic cancer.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Locally Advanced Pancreatic Cancer
Keywords
Pancreatic cancer, locally advanced, irresectable, Radiofrequency, RFA

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
17 (Actual)

8. Arms, Groups, and Interventions

Arm Title
radiofrequency ablation
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
radiofrequency ablation (RFA)
Other Intervention Name(s)
CELON Power System, CE mark 0197
Intervention Description
RFA with CELON bipolar probes. Settings: Power 30 watts, total energy 15 KJ.
Primary Outcome Measure Information:
Title
Safety
Description
The safety will be specified as the percentage of patients with complications directly related to RFA and the routinely performed double-bypass procedure, requiring re-intervention (i.e. endoscopy, radiology, or surgery). This is also known as a complication of grade III or higher in the Clavien-Dindo classification (internationally accepted classification for surgical complications). Moreover all in-hospital complications or complications developed within 30 days after the RFA procedure will be evaluated according to the Clavien-Dindo classification.
Time Frame
Within 30 days after the RFA procedure
Secondary Outcome Measure Information:
Title
survival
Time Frame
2 years after RFA procedure
Title
VAS pain score
Time Frame
3 months
Title
length hospital stay
Time Frame
3 months
Title
progression free survival
Time Frame
2 years after RFA procedure
Title
CA19-9 response
Time Frame
2 years after RFA procedure
Title
Chemotherapy
Description
Type, frequency, dosage and duration of chemotherapy will be registered.
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with irresectable locally advanced pancreatic cancer found at laparotomy with histologic diagnosis before start of RFA Patient considered eligible to undergo pancreatic surgery as assessed by the general criteria of the departments of anaesthesiology and surgery of the UMC Utrecht Fully informed written consent given Exclusion Criteria: Patients younger than 18 years Pregnancy Patients with distant metastases Portal vein thrombosis seen on CT preoperatively
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richard van Hillegersberg, Professor
Organizational Affiliation
UMC Utrecht
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Medical Center Utrecht
City
Utrecht
ZIP/Postal Code
3584 CX
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
22648697
Citation
Cantore M, Girelli R, Mambrini A, Frigerio I, Boz G, Salvia R, Giardino A, Orlandi M, Auriemma A, Bassi C. Combined modality treatment for patients with locally advanced pancreatic adenocarcinoma. Br J Surg. 2012 Aug;99(8):1083-8. doi: 10.1002/bjs.8789. Epub 2012 May 30.
Results Reference
background
PubMed Identifier
20069610
Citation
Girelli R, Frigerio I, Salvia R, Barbi E, Tinazzi Martini P, Bassi C. Feasibility and safety of radiofrequency ablation for locally advanced pancreatic cancer. Br J Surg. 2010 Feb;97(2):220-5. doi: 10.1002/bjs.6800.
Results Reference
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Safety Study of Radiofrequency Ablation of Locally Advanced Pancreatic Cancer

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