Multipeptide Vaccine for Advanced Breast Cancer

This study has been completed.
Sponsor:
Information provided by:
Abramson Cancer Center of the University of Pennsylvania
ClinicalTrials.gov Identifier:
NCT00573495
First received: December 12, 2007
Last updated: May 2, 2013
Last verified: May 2013

December 12, 2007
May 2, 2013
November 2007
July 2011   (final data collection date for primary outcome measure)
Safety [ Time Frame: Up to 30 days after the last vaccination ] [ Designated as safety issue: Yes ]
Same as current
Complete list of historical versions of study NCT00573495 on ClinicalTrials.gov Archive Site
Immunologic response [ Time Frame: After 4th vaccination, then after every 3-4 vaccinations, and then every 6 months ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Multipeptide Vaccine for Advanced Breast Cancer
A Study of hTERT/Survivin Multi-peptide Vaccine With Daclizumab and Prevnar for Patients With Metastatic Breast Cancer

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:

  1. to test the safety of the combination of agents
  2. to find out what effects the treatment has on advanced breast cancer

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.

Interventional
Phase 1
Allocation: Non-Randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Breast Neoplasm
  • Breast Cancer
  • Cancer of the Breast
  • Carcinoma, Ductal
Biological: hTERT/Survivin Multi-Peptide Vaccine
100 mcg subcutaneous every 2 weeks four times, then monthly up to 28 vaccinations
Other Names:
  • hTERT
  • Telomerase
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
10
July 2011
July 2011   (final data collection date for primary outcome measure)

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
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00573495
UPCC 08107
Yes
Robert H. Vonderheide, M.D., D.Phil, University of Pennsylvania
Abramson Cancer Center of the University of Pennsylvania
Not Provided
Principal Investigator: Kevin Fox, MD University of Pennsylvania
Abramson Cancer Center of the University of Pennsylvania
May 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP