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Multipeptide Vaccine for Advanced Breast Cancer

Primary Purpose

Breast Neoplasm, Breast Cancer, Cancer of the Breast

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
hTERT/Survivin Multi-Peptide Vaccine
Sponsored by
University of Pennsylvania
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Neoplasm focused on measuring Advanced breast cancer

Eligibility Criteria

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

Inclusion Criteria:

  • Stage IV breast cancer that has failed at least one conventional therapy for metastatic disease
  • HLA-A2 positive
  • Measurable or evaluable disease
  • ECOG performance status 0-1
  • Negative contrast CT or MRI scan of the brain within 30 days of treatment
  • Negative pregnancy test within 14 days of treatment for women of childbearing potential

Exclusion Criteria:

  • History of brain metastases within the last 4 years
  • The use of chemotherapy, radiation therapy, immunosuppressive drugs, systemic glucocorticoids, growth factors, or experimental therapy, and anti-coagulants within 14 days prior to treatment
  • Initiation of hormonal agent in the 30 days before treatment
  • Initiation of Herceptin in the 30 days prior to treatment.
  • History of bone marrow or stem cell transplantation
  • Pregnant or lactating

Sites / Locations

  • University of Pennsylvania Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

hTERT/Survivin Multi-Peptide Vaccine

Arm Description

Outcomes

Primary Outcome Measures

Safety

Secondary Outcome Measures

Immunologic response

Full Information

First Posted
December 12, 2007
Last Updated
September 27, 2016
Sponsor
University of Pennsylvania
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1. Study Identification

Unique Protocol Identification Number
NCT00573495
Brief Title
Multipeptide Vaccine for Advanced Breast Cancer
Official Title
A Study of hTERT/Survivin Multi-peptide Vaccine With Daclizumab and Prevnar for Patients With Metastatic Breast Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
September 2016
Overall Recruitment Status
Completed
Study Start Date
November 2007 (undefined)
Primary Completion Date
July 2011 (Actual)
Study Completion Date
February 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Pennsylvania

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a study on how to activate the immune system with a vaccine. The vaccine is made up of two proteins found in breast cancer: telomerase and survivin. The vaccine is given in combination with other drugs that may also have an effect on the immune system and attack the cancer. The goals of the study are: to test the safety of the combination of agents to find out what effects the treatment has on advanced breast cancer
Detailed Description
Patients with advanced breast cancer may often fail standard of care treatments for metastatic disease. This research is studying a combinations of agents that impact the immune system. About >85% of all human cancers, including breast cancer, express telomerase (hTERT) activity. Targeting hTERT immunologically may also minimize immune escape due to antigen loss because mutation or deletion of hTERT may be incompatible with sustained tumor growth. hTERT Multi-Peptide Vaccine is made up of 1540 hTERT peptide and cryptic peptides selected for "low-affinity" binding to HLA-A2 in order to increase the likelihood that the host immune system would ignore them, and then they have been modified by changing the first amino acid of the peptides to tyrosine in order to increase HLA - A2 affinity. The two "heteroclitic" peptides are R572Y (YLFFYRKSV) and D988Y (YLQVNSLQTV), which bind HLA-A2 with high avidity and elicit specific CTL (cytotoxic T lymphocyte) responses using healthy donor mononuclear cells in vitro. In addition, in mouse models, these peptide vaccines elicit lytic CTL responses which are protective against tumor challenges using a TERT-expressing murine tumor. Subjects will also be immunized with a peptide vaccine derived from survivin, an important anti-apoptotic protein which is overexpressed in a broad range of malignancies including breast cancer. Survivin may be an ideal and "universal" tumor antigen since it is overexpressed in a wide variety of cancers yet terminally differentiated adult cells do not express the protein. CMV derived CTL epitopes will be used as positive control peptides. Daclizumab is a humanized anti-human CD25 monoclonal antibody that binds specifically to CD25 expressing cells, including Treg cells, and inhibits its proliferation. Prevnar is designed to augment T-helper cell immunity.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Neoplasm, Breast Cancer, Cancer of the Breast, Carcinoma, Ductal
Keywords
Advanced breast cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
11 (Actual)

8. Arms, Groups, and Interventions

Arm Title
hTERT/Survivin Multi-Peptide Vaccine
Arm Type
Experimental
Intervention Type
Biological
Intervention Name(s)
hTERT/Survivin Multi-Peptide Vaccine
Other Intervention Name(s)
hTERT, Telomerase
Intervention Description
100 mcg subcutaneous every 2 weeks four times, then monthly up to 28 vaccinations
Primary Outcome Measure Information:
Title
Safety
Time Frame
Up to 30 days after the last vaccination
Secondary Outcome Measure Information:
Title
Immunologic response
Time Frame
After 4th vaccination, then after every 3-4 vaccinations, and then every 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Stage IV breast cancer that has failed at least one conventional therapy for metastatic disease HLA-A2 positive Measurable or evaluable disease ECOG performance status 0-1 Negative contrast CT or MRI scan of the brain within 30 days of treatment Negative pregnancy test within 14 days of treatment for women of childbearing potential Exclusion Criteria: History of brain metastases within the last 4 years The use of chemotherapy, radiation therapy, immunosuppressive drugs, systemic glucocorticoids, growth factors, or experimental therapy, and anti-coagulants within 14 days prior to treatment Initiation of hormonal agent in the 30 days before treatment Initiation of Herceptin in the 30 days prior to treatment. History of bone marrow or stem cell transplantation Pregnant or lactating
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kevin Fox, MD
Organizational Affiliation
University of Pennsylvania
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Pennsylvania Medical Center
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19341
Country
United States

12. IPD Sharing Statement

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Multipeptide Vaccine for Advanced Breast Cancer

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