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Immunotherapy in Treating Patients With Metastatic Breast Cancer

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Kiungo kimehifadhiwa kwenye clipboard
HaliKuachishwa
Wadhamini
Duke University
Washirika
National Cancer Institute (NCI)

Maneno muhimu

Kikemikali

RATIONALE: Immunotherapy using CEA-treated white blood cells may help a person's body build an immune response to and kill their tumor cells.
PURPOSE: Phase I/II trial to study the effectiveness of immunotherapy with CEA-treated white blood cells in treating patients with metastatic breast cancer who have achieved a partial or complete response after chemotherapy and peripheral stem cell transplantation.

Maelezo

OBJECTIVES:

- Evaluate the ability of active immunotherapy with carcinoembryonic antigen (CEA) RNA pulsed dendritic cells to induce CEA specific T cells in patients with metastatic breast cancer in complete remission following peripheral blood stem cell transplant.

- Determine the clinical efficacy in terms of overall and recurrence free survival of immunotherapy with CEA RNA pulsed dendritic cells in this patients population.

OUTLINE: Dendritic cells are taken from the leukapheresis product obtained during the peripheral blood stem cell transplant procedure performed prior to treatment on this study. The dendritic cells are pulsed with carcinoembryonic antigen (CEA) RNA. Approximately 60-90 days after the peripheral blood stem cell transplant, patients receive CEA RNA pulsed dendritic cells IV every 3 weeks for a total of 4 doses. Patients undergo a second leukopheresis after the last dose of immunotherapy to obtain specimens for immunologic tests.

Patients are followed every 3 months for the first year and annually thereafter.

PROJECTED ACCRUAL: A total of 14-26 patients will be accrued for this study within 2 years.

Tarehe

Imethibitishwa Mwisho: 10/31/2013
Iliyowasilishwa Kwanza: 10/31/1999
Uandikishaji uliokadiriwa Uliwasilishwa: 04/23/2003
Iliyotumwa Kwanza: 04/24/2003
Sasisho la Mwisho Liliwasilishwa: 11/04/2013
Sasisho la Mwisho Lilichapishwa: 11/05/2013
Tarehe halisi ya kuanza kwa masomo: 05/31/1998
Tarehe ya Kukamilisha Msingi iliyokadiriwa: 10/31/2002
Tarehe ya Kukamilisha Utafiti: 10/31/2002

Hali au ugonjwa

Breast Cancer

Uingiliaji / matibabu

Biological: carcinoembryonic antigen RNA-pulsed DC cancer vaccine

Awamu

Awamu 1/Awamu 2

Vikundi vya Arm

MkonoUingiliaji / matibabu
Experimental: carcinoembryonic antigen RNA-pulsed DC cancer vaccine
carcinoembryonic antigen RNA-pulsed DC cancer vaccine
Biological: carcinoembryonic antigen RNA-pulsed DC cancer vaccine
Approximately 60-90 days after the peripheral blood stem cell transplant, patients receive CEA RNA pulsed dendritic cells IV every 3 weeks for a total of 4 doses.

Vigezo vya Kustahiki

Zama zinazostahiki Kujifunza 18 Years Kwa 18 Years
Jinsia Inastahiki KujifunzaAll
Hupokea Wajitolea wa AfyaNdio
Vigezo

DISEASE CHARACTERISTICS:

- Histologically confirmed metastatic breast cancer that expresses carcinoembryonic antigen (CEA)

- At least 25% of the tumor cells must stain positive for CEA with at least moderate intensity

- Must have achieved either partial response or complete response after high dose chemotherapy and peripheral blood stem cell transplant

- Hormone receptor status:

- Not specified

PATIENT CHARACTERISTICS:

Age:

- 18 and over

Menopausal status:

- Not specified

Performance status:

- Karnofsky 70-100%

Life expectancy:

- Greater than 6 months

Hematopoietic:

- Absolute neutrophil count at least 1000/mm^3

- Absolute lymphocyte count at least 1000/mm^3

- Hemoglobin at least 9 mg/dL

- Platelet count at least 100,000/mm^3

Hepatic:

- Bilirubin less than 2.0 mg/dL

- No serious ongoing chronic or acute hepatic disease

Renal:

- Creatinine less than 2.5 mg/dL

Cardiovascular:

- No serious ongoing chronic or acute cardiac disease (New York Heart Association class III or IV)

Pulmonary:

- No serious ongoing chronic or acute pulmonary illness such as asthma, chronic obstructive pulmonary disease, or radiation or drug induced pneumonitis

Other:

- No other prior or concurrent malignancy except nonmelanoma skin cancer or controlled superficial bladder cancer within the past 5 years

- No history of autoimmune disease such as inflammatory bowel disease, systemic lupus erythematosus, rheumatoid arthritis, ankylosing spondylitis, scleroderma, or multiple sclerosis

- No inflammatory bowel condition such as active infectious enteritis or eosinophilic enteritis

- No active acute or chronic infection such as urinary tract infection, HIV, or viral hepatitis

- Not pregnant or nursing

PRIOR CONCURRENT THERAPY:

Biologic therapy:

- See Disease Characteristics

- No concurrent immunotherapy

Chemotherapy:

- See Disease Characteristics

- No concurrent chemotherapy

Endocrine therapy:

- At least 4 weeks since steroids

- No concurrent steroid therapy

Radiotherapy:

- No concurrent radiotherapy

Surgery:

- Not specified

Other:

- No concurrent immunosuppressive agents such as azathioprine or cyclosporine A

Matokeo

Hatua za Matokeo ya Msingi

1. Evaluate the ability of active immunotherapy with carcinoembryonic antigen (CEA) RNA pulsed dendritic cells to induce CEA specific T cells in patients with metastatic breast cancer in complete remission following peripheral blood stem cell transplant. [Following administration of 4 IV vaccine doses (1 vaccine administered every 3 weeks)]

Hatua za Matokeo ya Sekondari

1. Determine the clinical efficacy in terms of overall and recurrence free survival of immunotherapy with CEA RNA pulsed dendritic cells in this patients population. [Following administration of 4 IV vaccine doses (1 vaccine administered every 3 weeks)]

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