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CompletedNCT00052351Updated Jun 19, 2013

Vaccine Therapy Plus Sargramostim and Chemotherapy in Treating Women With Stage II or Stage III Breast Cancer

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

Phase
Phase 2
Study type
Interventional
Allocation
Randomized
Ages
18 Years and older
Sex
Female
01

Study summary

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.

Read the detailed description

OBJECTIVES:

  • Compare the immunological effects of 2 different schedules of vaccinia-CEA-TRICOM vaccine, fowlpox-CEA-TRICOM vaccine, and sargramostim (GM-CSF) administered with standard adjuvant chemotherapy in women with high-risk stage II or III breast cancer.
  • Compare the safety of these regimens in these patients.
  • Determine the feasibility of obtaining determinations of CD4 response in patients treated with these regimens.
  • Compare disease-free survival of patients treated with these regimens.

OUTLINE: This is a randomized study. Patients are randomized to 1 of 2 treatment arms.

  • Vaccinia-CEA-TRICOM: Beginning 2-3 weeks after surgery and before initiation of standard adjuvant chemotherapy, all patients receive vaccinia-CEA-TRICOM vaccine subcutaneously (SC) on day 1 and sargramostim (GM-CSF) SC on days 1-4 of week 1.
  • Fowlpox-CEA-TRICOM: Patients are treated on 1 of the following schedules:

    • Arm I: During chemotherapy, patients receive fowlpox-CEA-TRICOM vaccine SC on day 1 and GM-CSF SC on days 1-4 of weeks 2, 5, 8, 11, 14, 17, 20, and 23. After chemotherapy, patients receive additional vaccinations on weeks 26, 38, and 50.
    • Arm II: Prior to chemotherapy, patients receive fowlpox-CEA-TRICOM vaccine SC on day 1 and GM-CSF SC on days 1-4 of week 2. After chemotherapy, patients receive additional vaccinations on weeks 26, 38, and 50.
  • Chemotherapy: Patients receive doxorubicin IV over 5-7 minutes and cyclophosphamide IV over 30 minutes on day 1 of weeks 3, 6, 9, and 12. Patients then receive paclitaxel IV over 3 hours on day 1 of weeks 15, 18, 21, and 24. Treatment continues in the absence of disease progression (after at least 1 course of chemotherapy) or unacceptable toxicity.
  • Radiotherapy: Patients undergo radiotherapy during weeks 26-32 in the absence of disease progression.

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.

02

Conditions studied

  • Breast Cancer

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Keywords

  • stage II breast cancer
  • stage IIIA breast cancer
  • stage IIIB breast cancer
03

In context

Breast Neoplasms

12,815 studies on the registry are indexed under Breast Neoplasms; 2,920 are open to participants now.

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Lead sponsor

National Cancer Institute (NCI) is the lead sponsor of 3,554 studies on the registry; 334 are open to participants now.

Of its 407 completed or terminated interventional studies of FDA-regulated products, 370 (91%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

Eligibility criteria

DISEASE CHARACTERISTICS:

  • Histologically confirmed adenocarcinoma of the breast

    • Stage II or III
    • At least 4 positive lymph nodes
    • No inflammatory ductal carcinoma
  • No positive lymph nodes by immunohistochemistry only
  • Carcinoembryonic antigen (CEA) expression, as indicated by 1 of the following:

    • At least 30% of tumor stains for CEA on immunohistochemistry
    • Elevated serum CEA (greater than 5 ng/mL) anytime during disease course
  • Must be HLA-A2 positive
  • Must have received prior vaccinia for smallpox immunization with 1 of the following as evidence:

    • If age 25 and under, physician certification of prior vaccination
    • If over age 25, patient recollection and vaccination-site scar
    • Any age, detectable anti-vaccinia antibodies
  • No metastases by CT scan of chest, abdomen, and pelvis and a bone scan
  • Hormone receptor status:

    • Estrogen receptor status and progesterone receptor status known

PATIENT CHARACTERISTICS:

Age

  • 18 and over

Sex

  • Female

Menopausal status:

  • Not specified

Performance status

  • ECOG 0-1

Life expectancy

  • Not specified

Hematopoietic

  • WBC at least 3,000/mm\^3
  • Absolute neutrophil count at least 1,500/mm\^3
  • Platelet count at least 100,000/mm\^3

Hepatic

  • Bilirubin no greater than 1.5 times upper limit of normal (ULN)
  • SGOT and SGPT no greater than 1.5 times ULN
  • Hepatitis B and C negative

Renal

  • Creatinine no greater than 1.5 mg/dL OR
  • Creatinine clearance greater than 60 mL/min
  • No proteinuria OR
  • Protein less than 1,000 mg per 24-hour urine collection
  • No hematuria
  • No abnormal sediment

Cardiovascular

  • LVEF at least 45% by echocardiogram or MUGA if either of the following are true:

    • History of cardiac disease
    • Received prior cardiotoxic chemotherapy

Immunologic

  • No evidence of immunocompromised status
  • No autoimmune disease such as any of the following:

    • Autoimmune neutropenia, thrombocytopenia, or hemolytic anemia
    • Systemic lupus erythematosus
    • Sjogren's syndrome
    • Scleroderma
    • Myasthenia gravis
    • Goodpasture syndrome
    • Addison's disease
    • Hashimoto's thyroiditis
    • Active Graves' disease
  • No active or prior eczema or other eczematoid skin disorders
  • No other acute, chronic, or exfoliative skin conditions (e.g., atopic dermatitis, burns, impetigo, varicella zoster, severe acne, or other open rashes or wounds)
  • HIV negative
  • No active infection within the past 3 days
  • No allergy to eggs
  • No history of allergy or untoward reaction to prior vaccination with vaccinia virus

Other

  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • No other serious illness
  • No other malignancy within the past 3 years except squamous cell or basal cell skin cancer
  • No history of seizures, encephalitis, or multiple sclerosis
  • No active inflammatory bowel disease
  • Must be able to avoid close household contact with the following during and for 2 weeks after vaccinations:

    • Persons with active or prior eczema or other eczematoid skin disorders
    • Persons with any other acute, chronic, or exfoliative skin conditions (e.g., atopic dermatitis, burns, impetigo, varicella zoster, severe acne, or other open rashes or wounds)
    • Pregnant or nursing women
    • Children under 5 years old
    • Immunodeficient or immunosuppressed persons (by disease or therapy), including those with HIV infection

PRIOR CONCURRENT THERAPY:

Biologic therapy

  • See Disease Characteristics

Chemotherapy

  • No prior doxorubicin, cyclophosphamide, or paclitaxel

Endocrine therapy

  • No concurrent steroids except the following:

    • Topical steroids
    • Inhaled steroids for moderate asthma
    • Dexamethasone prior to taxanes

Radiotherapy

  • No prior radiotherapy to more than 50% of the lymph nodes

Surgery

  • At least 2 weeks since prior surgery and recovered
  • No prior splenectomy

Other

  • No other concurrent anti-tumor therapies
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized

Interventions

06

Study locations

2 sites
  • Warren Grant Magnuson Clinical Center - NCI Clinical Studies Support
    Bethesda, Maryland 20892-1182, United States
  • Center for Cancer Research
    Bethesda, Maryland 20892, United States
07

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

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.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 24, 2003
First posted
Jan 27, 2003
Start
Sep 2002
CompletionActual
Oct 2007
Last update
Jun 19, 2013
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 19, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00052351
First posted
Jan 27, 2003
Start date
Sep 2002
Completion
Oct 2007
Last update
Jun 19, 2013

Study contacts

Philip M. Arlen, MD
study chair · National Cancer Institute (NCI)
View the source record on ClinicalTrials.gov ↗

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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

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