Preoperative Intratumor Dendritic Cells Injection Immunotherapy for Patients With Pancreatic Cancer
Primary Purpose
Pancreatic Cancer
Status
Unknown status
Phase
Phase 1
Locations
Japan
Study Type
Interventional
Intervention
dendritic cells, OK-432
Sponsored by
About this trial
This is an interventional treatment trial for Pancreatic Cancer focused on measuring preoperative, intratumor, dendritic cells, pancreatic cancer, OK-432
Eligibility Criteria
Inclusion Criteria:
Resectable pancreatic cancer without distant metastasis:
- ECOG performance status 0-2
- Laboratory values as follows 3,500/mm3 <WBC<12000/mm3 Platelet count>100,000/mm3 T-Bil<2.0mg/dl BUN<25mg/dl, Creatinin<1.5mg/dl, 24h Ccr>50ml/min Normal ECG
- Able and willing to give valid written informed consent
Exclusion Criteria:
- Pregnancy (women of childbearing potential: Refusal or inability to use effective means of contraception)
- Breast-feeder
- Active or uncontrolled infection
- Active or uncontrolled other malignancy
- Steroids or immunosuppressing agent dependant status
- Interstitial pneumonia
- Decision of unsuitableness by principal investigator or physician-in-charge
Sites / Locations
- Fukushima Medical University Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
dendritic cells
Arm Description
Outcomes
Primary Outcome Measures
To establish the maximally tolerated dose (MTD) and dose limiting toxicities (DLT) of intratumoral autologous dendritic cell vaccination in combination with OK-432
Secondary Outcome Measures
To determine the overall response rate for this regimen as determined by overall and disease-free survival.
To evaluate the immune response of patients treated with this regimen based on the presence and characterization of tumor-infiltrating white blood cells
Full Information
NCT ID
NCT00795977
First Posted
November 19, 2008
Last Updated
September 7, 2011
Sponsor
Fukushima Medical University
1. Study Identification
Unique Protocol Identification Number
NCT00795977
Brief Title
Preoperative Intratumor Dendritic Cells Injection Immunotherapy for Patients With Pancreatic Cancer
Official Title
Phase I/II Study on Intratumor Dendritic Cell Injection Immunotherapy Using Immature Dendritic Cells With S Pyogenes Preparation (OK-432) for Patients With Resectable Pancreatic Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
September 2011
Overall Recruitment Status
Unknown status
Study Start Date
November 2003 (undefined)
Primary Completion Date
November 2011 (Anticipated)
Study Completion Date
November 2012 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fukushima Medical University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to confirm safety and immunological responses of Preoperative intratumor dendritic cells injection immunotherapy using immature dendritic cells with S pyogenes Preparation (OK-432) for patients with resectable pancreatic cancer for pancreatic cancer patients.
Detailed Description
The prognosis of pancreatic cancer is extremely poor even with extensive surgery, and development of new treatment modalities is much-expected for cure of this disease. Dendritic cells (DCs) immunotherapy is expected favorable outcome when it is approached directly to the cancer tissue. To evaluate safety and immunological responses, we conducted a phase I/II study of intra-tumor DCs immunotherapy for pancreatic cancer patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Cancer
Keywords
preoperative, intratumor, dendritic cells, pancreatic cancer, OK-432
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
dendritic cells
Arm Type
Experimental
Intervention Type
Biological
Intervention Name(s)
dendritic cells, OK-432
Intervention Description
Single Group Assignment
Primary Outcome Measure Information:
Title
To establish the maximally tolerated dose (MTD) and dose limiting toxicities (DLT) of intratumoral autologous dendritic cell vaccination in combination with OK-432
Time Frame
2 years
Secondary Outcome Measure Information:
Title
To determine the overall response rate for this regimen as determined by overall and disease-free survival.
Time Frame
2 years
Title
To evaluate the immune response of patients treated with this regimen based on the presence and characterization of tumor-infiltrating white blood cells
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Resectable pancreatic cancer without distant metastasis:
ECOG performance status 0-2
Laboratory values as follows 3,500/mm3 <WBC<12000/mm3 Platelet count>100,000/mm3 T-Bil<2.0mg/dl BUN<25mg/dl, Creatinin<1.5mg/dl, 24h Ccr>50ml/min Normal ECG
Able and willing to give valid written informed consent
Exclusion Criteria:
Pregnancy (women of childbearing potential: Refusal or inability to use effective means of contraception)
Breast-feeder
Active or uncontrolled infection
Active or uncontrolled other malignancy
Steroids or immunosuppressing agent dependant status
Interstitial pneumonia
Decision of unsuitableness by principal investigator or physician-in-charge
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mitsukazu Gotoh, MD & PhD
Organizational Affiliation
Fukushima Medical University, Department of Surgery 1
Official's Role
Study Chair
Facility Information:
Facility Name
Fukushima Medical University Hospital
City
Fukushima
ZIP/Postal Code
960-1295
Country
Japan
12. IPD Sharing Statement
Citations:
PubMed Identifier
16309221
Citation
Kanzaki N, Terashima M, Kashimura S, Hoshino M, Ohtani S, Matsuyama S, Hoshino Y, Kogure M, Oshibe I, Endo H, Saito T, Yaginuma H, Gotoh M, Ohto H. Understanding the response of dendritic cells to activation by streptococcal preparation OK-432. Anticancer Res. 2005 Nov-Dec;25(6B):4231-8.
Results Reference
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PubMed Identifier
8854822
Citation
Takekuni K, Sakon M, Kishimoto S, Amano M, Sekimoto M, Aoki T, Oosato H, Dohno K, Umeshita K, Gotoh M, Monden T, Monden M. [A patient with unresectable cancer of pancreas head, effectively treated by a local injection of the mixture of OK-432, fibrinogen and thrombin]. Gan To Kagaku Ryoho. 1996 Sep;23(11):1621-3. Japanese.
Results Reference
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PubMed Identifier
15289356
Citation
Okamoto M, Furuichi S, Nishioka Y, Oshikawa T, Tano T, Ahmed SU, Takeda K, Akira S, Ryoma Y, Moriya Y, Saito M, Sone S, Sato M. Expression of toll-like receptor 4 on dendritic cells is significant for anticancer effect of dendritic cell-based immunotherapy in combination with an active component of OK-432, a streptococcal preparation. Cancer Res. 2004 Aug 1;64(15):5461-70. doi: 10.1158/0008-5472.CAN-03-4005.
Results Reference
background
PubMed Identifier
15553710
Citation
Oshikawa T, Okamoto M, Ahmed SU, Tano T, Yoshida H, Sato M. [Anti-cancer effect of an intratumoral injection of dendritic cells expressing TLR4 in combination with an active component of OK-432 in TLR4-deficient mice]. Gan To Kagaku Ryoho. 2004 Oct;31(11):1770-2. Japanese.
Results Reference
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Preoperative Intratumor Dendritic Cells Injection Immunotherapy for Patients With Pancreatic Cancer
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