A Phase 2 interventional study of recombinant fowlpox-CEA(6D)/TRICOM vaccine and recombinant vaccinia-CEA(6D)-TRICOM vaccine in Breast Cancer, sponsored by National Cancer Institute (NCI). Completed at 2 sites in United States. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2013-06-19.
Sponsored by National Cancer Institute (NCI) · Phase 2, Interventional, and Treatment
RATIONALE: Vaccines made from a gene-modified virus may make the body build an immune response to kill tumor cells. Colony-stimulating factors such as sargramostim may increase the number of immune cells found in bone marrow or peripheral blood. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining vaccine therapy with sargramostim and chemotherapy may kill more tumor cells.
PURPOSE: Randomized clinical trial to study the effectiveness of vaccine therapy plus sargramostim and combination chemotherapy in treating women who have undergone surgery for stage II or stage III breast cancer that has spread to the lymph nodes.
OBJECTIVES:
OUTLINE: This is a randomized study. Patients are randomized to 1 of 2 treatment arms.
Fowlpox-CEA-TRICOM: Patients are treated on 1 of the following schedules:
Patients with hormone-receptor positive tumors receive oral tamoxifen for 5 years beginning on approximately week 32.
Patients are followed every 6 months for 5 years.
PROJECTED ACCRUAL: A total of 28 (14 per treatment arm) patients will be accrued for this study within 18 months.
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Of its 407 completed or terminated interventional studies of FDA-regulated products, 370 (91%) have results posted.
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DISEASE CHARACTERISTICS:
Histologically confirmed adenocarcinoma of the breast
Carcinoembryonic antigen (CEA) expression, as indicated by 1 of the following:
Must have received prior vaccinia for smallpox immunization with 1 of the following as evidence:
Hormone receptor status:
PATIENT CHARACTERISTICS:
Age
Sex
Menopausal status:
Performance status
Life expectancy
Hematopoietic
Hepatic
Renal
Cardiovascular
LVEF at least 45% by echocardiogram or MUGA if either of the following are true:
Immunologic
No autoimmune disease such as any of the following:
Other
Must be able to avoid close household contact with the following during and for 2 weeks after vaccinations:
PRIOR CONCURRENT THERAPY:
Biologic therapy
Chemotherapy
Endocrine therapy
No concurrent steroids except the following:
Radiotherapy
Surgery
Other
Drug page: Recombinant Fowlpox-CEA(6D)/TRICOM Vaccine
The record gives a start of Sep 2002 and a completion of Oct 2007. It does not say whether these dates are actual or estimated.
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This study is completed, as verified in May 2003. You cannot join it, but the record below documents what was studied.
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Studies of the drugs tested here: Recombinant Fowlpox-CEA(6D)/TRICOM Vaccine · Sargramostim
National Cancer Institute (NCI) →