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A Pilot Study, Evaluating the Efficacy of Regulatory T-cell Suppression by Ontak in Metastatic Pancreatic Cancer

Primary Purpose

Metastatic Pancreatic Cancer

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Ontak
Sponsored by
Loyola University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metastatic Pancreatic Cancer focused on measuring Denileukin diftitox, Metastatic Pancreatic Cancer, Ontak, Regulatory T-cell

Eligibility Criteria

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

Inclusion Criteria:

  • Male patients and nonpregnant, nonlactating female patient > 18 years old
  • Histologic diagnosis of pancreatic cancer with distant disease seen on CT or MRI with no prior chemotherapy or radiotherapy for a least 4 weeks
  • Karnofsky performance status equal to or greater than 70%
  • Life expectancy of at least 3 months.
  • No uncontrolled pain
  • No symptoms of bowel obstruction
  • Women with child bearing potential must agree to use adequate contraceptives. If she should become pregnant she needs to inform the treating physician
  • Ability to give informed consent

Exclusion Criteria:

  • Positive serologic testing for HIV, AIDS, human T-cell lymphotrophic virus type 1, hepatitis B, or hepatitis C.
  • Hemoglobin <9g/dL; hematocrit <27%; platelets <100,000/ U/L without transfusion support
  • Creatinine > 1.8 mg/dL
  • Serum albumin < 2.0 mg/dL
  • AST > 3X ULN; ALT > 3X ULN
  • Bilirubin > 1.8
  • Uncontrolled angina, arrhythmias, bronchospasm, hypertension, or hypercalcemia.
  • Corticosteroid use within 28 days
  • Chemotherapy or radiation within 28 days
  • Bacteremia or other signs of active systemic infection
  • History of autoimmune disease

Sites / Locations

  • Loyola Univeristy Medical Center, Cardinal Bernardin Cancer Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1

Arm Description

Three doses of Ontak 9 mcg/Kg IV over 30 minutes every other day for 1 week

Outcomes

Primary Outcome Measures

T-reg Suppression From a Fractionated Dose of Ontak in Patients With Metastatic Pancreatic Cancer
The duration of T reg suppression from a fractionated dose of Ontak in patients will be measured in patients with metastatic pancreatic cancer.

Secondary Outcome Measures

Optimal Time for Future Dendritic Cell Vaccine Administration
The goal is to define the optimal time with 95% sensitivity and 95% specificity for future dendritic cell vaccine administration

Full Information

First Posted
July 29, 2008
Last Updated
August 23, 2016
Sponsor
Loyola University
Collaborators
Riveria Country Club Organization, Eisai Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT00726037
Brief Title
A Pilot Study, Evaluating the Efficacy of Regulatory T-cell Suppression by Ontak in Metastatic Pancreatic Cancer
Official Title
A Pilot Study Evaluating the Efficacy of Regulatory T-cell (T-reg) Suppression by Denileukin Diftitox (Ontak) in Metastatic Pancreatic Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
August 2016
Overall Recruitment Status
Terminated
Why Stopped
Collaborator withdrew support due to a drug supply interruption.
Study Start Date
October 2008 (undefined)
Primary Completion Date
January 2012 (Actual)
Study Completion Date
January 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Loyola University
Collaborators
Riveria Country Club Organization, Eisai Inc.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study is designed to determine the duration of T reg suppression in patients with metastatic pancreatic cancer receiving Ontak. The goal is to define the optimal time for future dendritic cell vaccine administration.
Detailed Description
Despite improved insight into the epidemiology and biology, pancreatic cancer remains a significant health problem as evidenced by the disappointing survival rates associated with advanced disease. Because of its aggressive growth and early metastatic dissemination, only 20% of patients can be treated by surgery at the time of diagnosis. Furthermore, the overall 5-year survival rate of stage IV disease is < 5% [1-3] despite chemotherapy. With such a dismal outlook, it is obvious that novel treatment strategies are required. There is limited experience in the literature with the use of Ontak in the treatment of metastatic pancreatic cancer. Viehl, et al, demonstrated in a murine model of pancreatic cancer, that ontak combined with whole tumor vaccine led to a significantly increased T cell-dependent antitumor immune response, as well as an improved survival compared to controls. Our group has an active trial at Loyola evaluating the role of dendritic cell vaccine in patients with unresectable, not metastatic, pancreatic cancer. Preliminary data suggests a correlation with time to progression and restoration of Tregs following an initial decrease after the DC injection. The goal of the current proposal is to determine the time point at which the Tregs reach the nadir within four weeks of ontak injection. When this is determined, we will eventually propose administering ontak followed by DC vaccine at the nadir Treg time point for patients with unresectable pancreatic cancer

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic Pancreatic Cancer
Keywords
Denileukin diftitox, Metastatic Pancreatic Cancer, Ontak, Regulatory T-cell

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Three doses of Ontak 9 mcg/Kg IV over 30 minutes every other day for 1 week
Intervention Type
Drug
Intervention Name(s)
Ontak
Other Intervention Name(s)
Denileukin diftitox
Intervention Description
One dose of Ontak 9 mcg/Kg IV over 30 minutes times 3 doses. 1 dose every other day
Primary Outcome Measure Information:
Title
T-reg Suppression From a Fractionated Dose of Ontak in Patients With Metastatic Pancreatic Cancer
Description
The duration of T reg suppression from a fractionated dose of Ontak in patients will be measured in patients with metastatic pancreatic cancer.
Time Frame
days 8, 12 ,19,26 and 33 post administration
Secondary Outcome Measure Information:
Title
Optimal Time for Future Dendritic Cell Vaccine Administration
Description
The goal is to define the optimal time with 95% sensitivity and 95% specificity for future dendritic cell vaccine administration
Time Frame
33 Days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male patients and nonpregnant, nonlactating female patient > 18 years old Histologic diagnosis of pancreatic cancer with distant disease seen on CT or MRI with no prior chemotherapy or radiotherapy for a least 4 weeks Karnofsky performance status equal to or greater than 70% Life expectancy of at least 3 months. No uncontrolled pain No symptoms of bowel obstruction Women with child bearing potential must agree to use adequate contraceptives. If she should become pregnant she needs to inform the treating physician Ability to give informed consent Exclusion Criteria: Positive serologic testing for HIV, AIDS, human T-cell lymphotrophic virus type 1, hepatitis B, or hepatitis C. Hemoglobin <9g/dL; hematocrit <27%; platelets <100,000/ U/L without transfusion support Creatinine > 1.8 mg/dL Serum albumin < 2.0 mg/dL AST > 3X ULN; ALT > 3X ULN Bilirubin > 1.8 Uncontrolled angina, arrhythmias, bronchospasm, hypertension, or hypercalcemia. Corticosteroid use within 28 days Chemotherapy or radiation within 28 days Bacteremia or other signs of active systemic infection History of autoimmune disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Margo Shoup, MD
Organizational Affiliation
Loyola University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Loyola Univeristy Medical Center, Cardinal Bernardin Cancer Center
City
Maywood
State/Province
Illinois
ZIP/Postal Code
60153
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
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8604907
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A Pilot Study, Evaluating the Efficacy of Regulatory T-cell Suppression by Ontak in Metastatic Pancreatic Cancer

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