Regional Versus Systemic Chemotherapy in the Treatment of Unresectable Pancreatic Cancer
Primary Purpose
Unresectable Pancreatic Cancer
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
regional interventional chemotherapy group
Sponsored by
About this trial
This is an interventional treatment trial for Unresectable Pancreatic Cancer focused on measuring Pancreatic cancer, Intra-arterial infusion, Gemcitabine
Eligibility Criteria
Inclusion Criteria:
- Signed written informed consent
- Karnofsky score > 60,
- Expected survival > 3 months,
- Liver, kidney function and routine blood test within normal range
- No serious cardiopulmonary dysfunction
- No acute infection
Exclusion Criteria:
- Pregnant or lactating women
- Uncontrolled internal diseases
- Past or the presence of other malignancy
- Those who had received immunosuppressive therapy
Sites / Locations
- Xijing Hospital of Digestive Diseases, Fourth Military Medical University
- Xijing Hospital of Digestive Diseases, Fourth Military Medical University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
regional interventional chemotherapy group
systemic chemotherapy
Arm Description
Outcomes
Primary Outcome Measures
overall surviva
Secondary Outcome Measures
Clinical Benefit Rate
The median progression-free survival PFS
Drug Toxicity
The grading standards of the World Health Organization for acute and subacute toxicity of anticancer drugs will be used to grade toxicity.
surgical complications
Major surgical complications included allergic reaction to the contrast agent, local hematoma, pneumothorax, puncture site bleeding, wound infection, delayed healing or cracking, port-catheter blockage, and necrosis of the tissue surrounding the port-catheter.
Full Information
NCT ID
NCT01665625
First Posted
July 15, 2012
Last Updated
August 10, 2012
Sponsor
Air Force Military Medical University, China
1. Study Identification
Unique Protocol Identification Number
NCT01665625
Brief Title
Regional Versus Systemic Chemotherapy in the Treatment of Unresectable Pancreatic Cancer
Official Title
A Prospective Randomized Trial of Regional Versus Systemic Continuous Gemcitabine Chemotherapy in the Treatment of Unresectable Pancreatic Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
August 2012
Overall Recruitment Status
Unknown status
Study Start Date
August 2012 (undefined)
Primary Completion Date
August 2015 (Anticipated)
Study Completion Date
February 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Air Force Military Medical University, China
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Systemic chemotherapy with cytotoxic drug is of limited effectiveness in advanced pancreatic cancer patients. Gemcitabine has been used as the first-line drug for advance pancreatic cancer for over two decades and combinations of gemcitabine with different chemotherapeutic drugs have been investigated to improve the outcomes of pancreatic cancer. However, no substantial improvement in patient survival has been achieved. Locoregional chemotherapy via intra-arterial perfusion or chemoemoblization takes advantage of the increasing local drug concentrations and reducing systemic toxicities. In this study, the investigators hypothesis that artery infusion chemotherapy had a better antitumor effect than systemic chemotherapy. The investigators will analyze and evaluate the effect and safety of an implanted percutaneous left subclavian artery port-catheter drug delivery system for regional chemotherapy of inoperable pancreatic carcinoma.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Unresectable Pancreatic Cancer
Keywords
Pancreatic cancer, Intra-arterial infusion, Gemcitabine
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
regional interventional chemotherapy group
Arm Type
Experimental
Arm Title
systemic chemotherapy
Arm Type
No Intervention
Intervention Type
Procedure
Intervention Name(s)
regional interventional chemotherapy group
Intervention Description
The patients in experimental group were monitored by X-ray imaging. A 0.038 super-sliding guide wire was inserted after successful puncture, and when site of the pancreatic carcinoma was reconfirmed by conventional angiography, a 5F cobra catheter was used to place the port-catheter drug delivery system in the celiac artery (pancreatic head) or the hepatic artery (pancreatic body and tail). Finally, the port-catheter was embedded under the left upper chest.
Primary Outcome Measure Information:
Title
overall surviva
Time Frame
36 months
Secondary Outcome Measure Information:
Title
Clinical Benefit Rate
Time Frame
12 months
Title
The median progression-free survival PFS
Time Frame
12 months
Title
Drug Toxicity
Description
The grading standards of the World Health Organization for acute and subacute toxicity of anticancer drugs will be used to grade toxicity.
Time Frame
18 months
Title
surgical complications
Description
Major surgical complications included allergic reaction to the contrast agent, local hematoma, pneumothorax, puncture site bleeding, wound infection, delayed healing or cracking, port-catheter blockage, and necrosis of the tissue surrounding the port-catheter.
Time Frame
18 months
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:
Signed written informed consent
Karnofsky score > 60,
Expected survival > 3 months,
Liver, kidney function and routine blood test within normal range
No serious cardiopulmonary dysfunction
No acute infection
Exclusion Criteria:
Pregnant or lactating women
Uncontrolled internal diseases
Past or the presence of other malignancy
Those who had received immunosuppressive therapy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jun Tie, PH.D., MD
Phone
+86-29-84771528
Email
tiejun7776@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Guohong Han, MD
Organizational Affiliation
Xijing Hospital of Digestive Diseases, Fourth Military Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Xijing Hospital of Digestive Diseases, Fourth Military Medical University
City
Xi'an
State/Province
Shaanxi
ZIP/Postal Code
710032
Country
China
Facility Name
Xijing Hospital of Digestive Diseases, Fourth Military Medical University
City
Xi'an
State/Province
Shaanxi
ZIP/Postal Code
710032
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
GuoHong Han, MD
Phone
86-29-84775221
Email
hangh@fmmu.edu.cn
First Name & Middle Initial & Last Name & Degree
Jun Tie, PH.D.,MD
12. IPD Sharing Statement
Citations:
PubMed Identifier
16412037
Citation
Han GH, Yin ZX, Meng XJ, He CY, Zhang HB, Sun AH, Wu KC, Ding J, Fan DM. Prospective randomized clinical trial of two drug delivery pathway in the treatment of inoperable advanced pancreatic carcinoma. Chin J Dig Dis. 2006;7(1):45-8. doi: 10.1111/j.1443-9573.2006.00243.x.
Results Reference
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Regional Versus Systemic Chemotherapy in the Treatment of Unresectable Pancreatic Cancer
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