search
Back to results

Thalidomide and Doxil® in Patients With Androgen Independent Prostate Cancer (AIPC)

Primary Purpose

Prostate Cancer

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Thalidomide
Doxil
Sponsored by
University of Pittsburgh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring Prostate, Androgen, AIPC, Doxil

Eligibility Criteria

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

Inclusion Criteria: Histologically or cytologically confirmed adenocarcinoma of the prostate. Confirmed androgen independent prostate cancer with evidence of rising PSA (two successive increases in PSA, at least 4 weeks apart) while on chemotherapy. If the PSA is less than 5, the increase in PSA must be at least 50%. Must also have castrate testosterone levels (<50 ng/ml) Patients could not have received more than 2 previous chemotherapy regimens. No anthracyclines within the past 6 months. No prior single agent thalidomide in the last 12 months. No prior cytotoxic chemotherapy + thalidomide given in conjunction Age > 18 years of age Performance status ECOG 0-2 Peripheral neuropathy must be < grade 1 Must have adequate hematologic, hepatic and renal function Men of reproductive potential must be willing to consent to using effective contraception while on treatment and for at least 4 weeks thereafter Patients must have left ventricular ejection fraction of > 50% within 42 days prior to first dose of study drug. The method used at baseline must be used for later monitoring Must have been off an anti-androgen for at least 4-6 weeks (Flutamide and Bicalutamide respectively) and documented as having a rising PSA Measurable or evaluable disease (PSA elevation will constitute evaluable disease). Measurable disease is defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded) as >20 mm with conventional techniques CT scan or as >10 mm with spiral CT scan. See section 6.B for the evaluation of measurable disease Life expectancy of greater than 3 months Patients must be willing and able to comply with the FDA-mandated S.T.E.P.S.® program Ability to understand and sign written informed consent approved by the Institutional Review Board [IRB/Ethics Committee], which will be obtained prior to study entry. Exclusion Criteria: Patients with unstable angina, uncompensated CHF, a history of an MI, PE or DVT within the last 3 months

Sites / Locations

  • Hillman Cancer Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

thalidomide and doxil

Arm Description

Combination of Thalidomide and Doxil

Outcomes

Primary Outcome Measures

Response Rate
The number of patients experiencing a response to treatment, per RECIST criteria / total number of patients evaluable for response.

Secondary Outcome Measures

Best Overall PSA Response
PSA response as stable disease or progressive disease, per Prostate-Specific Antigen Working Group criteria.
Overall Survival
Time to Progression
Time from start of treatment until the disease progression per RECIST criteria.

Full Information

First Posted
March 24, 2006
Last Updated
October 20, 2017
Sponsor
University of Pittsburgh
Collaborators
Ortho Biotech, Inc.
search

1. Study Identification

Unique Protocol Identification Number
NCT00307294
Brief Title
Thalidomide and Doxil® in Patients With Androgen Independent Prostate Cancer (AIPC)
Official Title
Phase II Trial of Thalidomide and Doxil® (Doxorubicin HCL Liposome Injection) in Patients With Androgen Independent Prostate Cancer (AIPC) With a Rising PSA While on Chemotherapy
Study Type
Interventional

2. Study Status

Record Verification Date
January 2016
Overall Recruitment Status
Completed
Study Start Date
March 2006 (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
University of Pittsburgh
Collaborators
Ortho Biotech, Inc.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The primary objective of this study is to evaluate PSA response rates of the combination of Doxil and Thalidomide in patients with AIPC who have failed chemotherapy. Secondary objectives include: 1) To evaluate the clinical response rate of this combination on measurable disease 2) To evaluate overall survival for this combination.
Detailed Description
This is an open label, Phase II trial of thalidomide and Doxil in patients with androgen independent prostate cancer whom have a rising PSA while on chemotherapy. The primary objective of this study is to evaluate PSA response rates of the combination of Doxil and Thalidomide in patients with AIPC who have failed chemotherapy. Secondary objectives include: 1) To evaluate the clinical response rate of this combination on measurable disease (If measurable soft tissue lesions are present on radiological or clinical exam) ; 2) To evaluate overall survival for this combination. There will be between 18 and 35 subjects at least 18 years of age enrolled on this single site study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Prostate, Androgen, AIPC, Doxil

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
thalidomide and doxil
Arm Type
Experimental
Arm Description
Combination of Thalidomide and Doxil
Intervention Type
Drug
Intervention Name(s)
Thalidomide
Other Intervention Name(s)
Thalomid
Intervention Description
100 mg PO q day and escalation will occur bt 50 mg every 4 weeks to a maximum of 200mg
Intervention Type
Drug
Intervention Name(s)
Doxil
Other Intervention Name(s)
doxorubicin liposome
Intervention Description
On day 1 of each cycle 40 mg/m2 IV over 1 hr every 28 days
Primary Outcome Measure Information:
Title
Response Rate
Description
The number of patients experiencing a response to treatment, per RECIST criteria / total number of patients evaluable for response.
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
Best Overall PSA Response
Description
PSA response as stable disease or progressive disease, per Prostate-Specific Antigen Working Group criteria.
Time Frame
4 weeks
Title
Overall Survival
Time Frame
36 months
Title
Time to Progression
Description
Time from start of treatment until the disease progression per RECIST criteria.
Time Frame
Up to 18 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically or cytologically confirmed adenocarcinoma of the prostate. Confirmed androgen independent prostate cancer with evidence of rising PSA (two successive increases in PSA, at least 4 weeks apart) while on chemotherapy. If the PSA is less than 5, the increase in PSA must be at least 50%. Must also have castrate testosterone levels (<50 ng/ml) Patients could not have received more than 2 previous chemotherapy regimens. No anthracyclines within the past 6 months. No prior single agent thalidomide in the last 12 months. No prior cytotoxic chemotherapy + thalidomide given in conjunction Age > 18 years of age Performance status ECOG 0-2 Peripheral neuropathy must be < grade 1 Must have adequate hematologic, hepatic and renal function Men of reproductive potential must be willing to consent to using effective contraception while on treatment and for at least 4 weeks thereafter Patients must have left ventricular ejection fraction of > 50% within 42 days prior to first dose of study drug. The method used at baseline must be used for later monitoring Must have been off an anti-androgen for at least 4-6 weeks (Flutamide and Bicalutamide respectively) and documented as having a rising PSA Measurable or evaluable disease (PSA elevation will constitute evaluable disease). Measurable disease is defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded) as >20 mm with conventional techniques CT scan or as >10 mm with spiral CT scan. See section 6.B for the evaluation of measurable disease Life expectancy of greater than 3 months Patients must be willing and able to comply with the FDA-mandated S.T.E.P.S.® program Ability to understand and sign written informed consent approved by the Institutional Review Board [IRB/Ethics Committee], which will be obtained prior to study entry. Exclusion Criteria: Patients with unstable angina, uncompensated CHF, a history of an MI, PE or DVT within the last 3 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gurkamal S Chatta, MD
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hillman Cancer Center
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15232
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Thalidomide and Doxil® in Patients With Androgen Independent Prostate Cancer (AIPC)

We'll reach out to this number within 24 hrs