Basic Trial Information
Trial Description
     Summary
     Further Trial Information
     Eligibility Criteria
Trial Contact Information

Basic Trial Information

Trial Description

Summary

RATIONALE: Vaccines may make the body build an immune response and decrease the recurrence of breast cancer.

PURPOSE: Phase I trial to study the effectiveness of vaccine therapy in treating patients who are at high risk for breast cancer recurrence.

Further Study Information

OBJECTIVES:

• Determine whether immunization with multiple antigens comprising GM2, Globo-H, Lewis y, TF(c), sTn(c), Tn(c), and glycosylated MUC-1 32(aa) conjugated to keyhole limpet hemocyanin plus QS21 induces an antibody response against these individual antigens and breast cancer cells expressing these antigens in patients at high risk for breast cancer recurrence.

• Determine the toxic effects of this regimen in these patients.

OUTLINE: Patients receive Globo-H-GM2-Lewis-y-MUC1-32(aa)-sTn(c)-TF(c)-Tn(c)-KLH conjugate vaccine with QS21 adjuvant subcutaneously weekly on weeks 1, 2, 3, 7, and 19.

Patients are followed every 3 months.

PROJECTED ACCRUAL: A total of 30 patients will be accrued for this study within 2-3 months.

Eligibility Criteria

DISEASE CHARACTERISTICS:

• Diagnosis of breast cancer at high risk for recurrence, defined by one of the following:

• Stage IV that is free of all known disease after eradication by surgery, radiotherapy, or chemotherapy

• May or may not have elevated CA 15-3 or CEA levels

• Stage I, II, or III previously treated with adjuvant chemotherapy and clinically free of identifiable disease, but have rising CA 15-3 or CEA levels

• Rising CA 15-3 and CEA defined as a prior normal level increased on 2 consecutive occasions at least 2 weeks apart

• For patients with a significant history of smoking who have a chronically elevated CEA (less than 15), CEA must be increased at least 1.5 times the uppermost chronic value on 2 consecutive occasions at least 2 weeks apart

• Stage III and completed adjuvant therapy no more than 24 months ago

• Recurrence in the ipsilateral axilla after lumpectomy and/or axillary dissection or modified radical mastectomy

• Recurrence in the ipsilateral breast after lumpectomy and/or axillary dissection

• Stage II with at least 4 positive axillary nodes and completed adjuvant therapy no more than 24 months ago

• Stage IV that is stable on hormonal therapy

• Hormone receptor status:

• Not specified

PATIENT CHARACTERISTICS:

Age:

• 18 and over

Sex:

• Male or female

Menopausal status:

• Not specified

Performance status:

• Karnofsky 80-100%

Life expectancy:

• Not specified

Hematopoietic:

• Lymphocyte count at least 500/mm^3

• WBC at least 3,000/mm^3

Hepatic:

• AST no greater than 1.5 times upper limit of normal (ULN)

• Alkaline phosphatase no greater than 1.5 times ULN

Renal:

• Creatinine no greater than 1.5 times ULN

Cardiovascular:

• No clinically significant New York Heart Association class III or IV cardiac disease

Other:

• Not pregnant

• Negative pregnancy test

• Fertile patients must use effective contraception

• No prior seafood allergy

• No known prior immunodeficiency or autoimmune disease

• No other active cancer except basal cell or squamous cell skin cancer

PRIOR CONCURRENT THERAPY:

Biologic therapy:

• At least 6 weeks since prior immunotherapy

• No prior vaccine with any of the antigens in this study

Chemotherapy:

• See Disease Characteristics

• At least 4 weeks since prior chemotherapy

• No concurrent chemotherapy

Endocrine therapy:

• See Disease Characteristics

Radiotherapy:

• See Disease Characteristics

• At least 4 weeks since prior radiotherapy

• No concurrent radiotherapy

Surgery:

• See Disease Characteristics

• At least 4 weeks since prior surgery

• Concurrent surgery for local recurrence allowed if patient remains disease free

Trial Contact Information

Trial Lead Organizations/Sponsors

Memorial Sloan-Kettering Cancer Center

Teresa Ann Gilewski

Study Chair

Link to the current ClinicalTrials.gov record.
NLM Identifer NCT00030823
Information obtained from ClinicalTrials.gov on February 06, 2012

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