Vaccine for the prevention of breast cancer relapse
View Patent ↗The invention features methods to induce and maintain a protective cytotoxic T-lymphocyte response to a peptide of the HER2/neu oncogene, E75, with the effect of inducing and maintaining protective or therapeutic immunity against breast cancer in a patient in clinical remission. The methods comprise administering to the patient an effective amount of a vaccine composition comprising a pharmaceutically acceptable carrier, an adjuvant such as recombinant human GM-CSF, and the E75 peptide at an optimized dose and schedule. The methods further comprise administering an annual or semi-annual booster vaccine dose due to declining E75-specific T cell immunity. The invention also features vaccine compositions for use in the methods.
1. A method of inducing and maintaining an immune response to HER2/neu expressing tumor cells in a subject who is in clinical remission from a HER2/neu expressing tumor characterized as having a fluorescence in situ hybridization (FISH) rating of less than about 2.0 for HER2/neu gene expression, the method comprising:
(a) inducing immunity to HER2/neu expressing tumor cells by administering to the subject a vaccine composition at least 1 time per month for three to six months, the vaccine composition comprising a peptide having the amino acid sequence of SEQ ID NO: 2 or variant thereof, wherein immunity is established by a statistically significant increase in the presence of CD8+ cells specific for the peptide in peripheral blood mononuclear cells of the patient when compared to pre-vaccine levels; and
(b) maintaining immunity to HER2/neu expressing tumor cells by administering a vaccine booster composition to the subject about 6 months after the primary immunization schedule is completed, the booster composition comprising a peptide having the amino acid sequence of SEQ ID NO: 2 or variant thereof.
2. A method of inducing and sustaining a cytotoxic T lymphocyte (CTL) response to HER2/neu in a subject in clinical remission from a tumor characterized as having a fluorescence in situ hybridization (FISH) rating of less than about 2.0 for HER2/neu gene expression, the method comprising:
(a) inducing a CTL response to HER2/neu by administering to the subject a vaccine composition comprising a peptide having the amino acid sequence of SEQ ID NO: 2 or variant thereof in an amount effective to establish a statistically significant increase in the presence of CD8+ cells specific for the peptide in peripheral blood mononuclear cells of the subject when compared to pre-vaccine levels; and
(b) sustaining a CTL response to HER2/neu by administering a vaccine booster composition to the subject about 6 months after administration of the vaccine composition is completed, the booster composition comprising a peptide having the amino acid sequence of SEQ ID NO: 2 or variant thereof.
3. A method of reducing the risk of cancer recurrence in a subject who is in clinical remission from a HER2/neu expressing tumor characterized as having a fluorescence in situ hybridization (FISH) rating of less than about 2.0 for HER2/neu gene expression, the method comprising:
(a) administering to the subject a vaccine composition at least 1 time per month for three to six months, the vaccine composition comprising a peptide having the amino acid sequence of SEQ ID NO: 2; and
(b) administering a vaccine booster composition to the subject about 6 months after the primary immunization schedule is completed, the booster composition comprising a peptide having the amino acid sequence of SEQ ID NO: 2.
4. A method of preventing bone only recurrence of a HER2/neu expressing cancer in a subject who is in clinical remission from a HER2/neu expressing cancer, the method comprising:
(a) administering to the subject a primary vaccination series of four to six monthly intradermal injections of a vaccine composition comprising a peptide having the amino acid sequence of SEQ ID NO: 2; and,
(b) administering to the subject a booster composition comprising a peptide having the amino acid sequence of SEQ ID NO: 2 about 6 months after completion of the primary vaccination series.
5. The method of any one of claims 1 - 4 , wherein the vaccine composition comprises about 0.1 mg to about 10 mg of the peptide.
6. The method of claim 5 , wherein the vaccine composition comprises about 0.5-2.0 mg of the peptide.
7. The method of any one of claims 1 - 4 , wherein the vaccine composition further comprises an adjuvant.
8. The method of any one of claims 1 - 4 , wherein the booster composition further comprises an adjuvant.
9. The method of claim 7 , wherein the adjuvant is GM-CSF.
10. The method of claim 9 , wherein vaccine composition comprises about 0.01 to 0.5 mg GM-CSF.
11. The method of claim 10 , wherein the vaccine composition comprises about 0.125 mg or about 0.250 mg GM-CSF.
12. The method of claim 8 , wherein the adjuvant is GM-CSF.
13. The method of claim 12 , wherein the booster composition comprises about 0.01 to 0.5 mg GM-CSF.
14. The method of claim 13 , wherein the booster composition comprises about 0.125 mg or about 0.250 mg GM-CSF.
15. The method of any one of claims 1 - 4 , wherein the vaccine booster composition is administered every 6 months for 3 or more years.
16. The method of any one of claims 1 - 4 , wherein the vaccine composition comprises about 0.5-2.0 mg of the peptide.
17. The method of any one of claims 1 - 4 , wherein the vaccine composition and the booster composition comprise and adjuvant.
18. The method of claim 17 , wherein adjuvant is GM-CSF.
19. The method of claim 18 , wherein the vaccine composition and the booster composition each comprise about 0.125 mg or about 0.250 mg GM-CSF.