Vaccine Therapy in Treating Patients Receiving Trastuzumab For HER2-Positive Stage IIIB-IV Breast Cancer

NCT ID: NCT00343109

Last Updated: 2020-02-12

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 38 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-03-31

Brief Summary

This phase II trial is studying how well vaccine therapy works in treating patients receiving trastuzumab for HER2-positive stage IIIB- IV breast cancer. Vaccines made from peptides may help the body build an effective immune response to kill tumor cells

Detailed Description

PRIMARY OBJECTIVES:

1. To estimate the RFS in patients with HER2 positive locally advanced breast cancer vaccinated with a HER2 ICD peptide-based vaccine.

SECONDARY OBJECTIVES:

1. To assess the safety of a HER2 ICD peptide-based vaccine administered concurrently with trastuzumab.

2. To determine the immunogenicity of the HER2 ICD peptide based vaccine when given within one year of initiating standard treatment which includes trastuzumab.

1. To determine the incidence of the development of T cell immunity specific for the HER2 ICD.

2. To determine the incidence of the development of intramolecular epitope spreading.

3. To determine the magnitude of the HER2 ICD specific CD4+ and CD8+ immune response generated with immunization.

3. To assess whether there is an association between RFS and the development of an immune response (HER2 specific T cell immunity and/or the development of intramolecular epitope spreading).

OUTLINE:

Patients receive HER-2/neu intracellular domain peptide-based vaccine mixed with GM-CSF intradermally (ID) once monthly for 6 months in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up at 1, 4, 8, and 12 months and then annually thereafter for up to 5 years.

Conditions

HER2-positive Breast Cancer; Male Breast Cancer; Stage IIIB Breast Cancer; Stage IIIC Breast Cancer; Stage IV Breast Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Arm I

Patients receive HER-2/neu intracellular domain peptide-based vaccine mixed with GM-CSF intradermally once monthly for 6 months in the absence of disease progression or unacceptable toxicity.

Group Type: EXPERIMENTAL

HER-2/neu intracellular domain protein

Intervention Type: BIOLOGICAL

Given ID

leukapheresis

Intervention Type: PROCEDURE

Optional correlative studies

laboratory biomarker analysis

Intervention Type: OTHER

Correlative studies

sargramostim

Intervention Type: BIOLOGICAL

Given ID

immunologic technique

Intervention Type: OTHER

Correlative studies

synthetic tumor-associated peptide vaccine therapy

Intervention Type: BIOLOGICAL

Given ID

Interventions

HER-2/neu intracellular domain protein

Given ID

Intervention Type: BIOLOGICAL

leukapheresis

Optional correlative studies

Intervention Type: PROCEDURE

laboratory biomarker analysis

Correlative studies

Intervention Type: OTHER

sargramostim

Given ID

Intervention Type: BIOLOGICAL

immunologic technique

Correlative studies

Intervention Type: OTHER

synthetic tumor-associated peptide vaccine therapy

Given ID

Intervention Type: BIOLOGICAL

Other Intervention Names

HER-2 ICD Peptide; HER-2/neu ICD Protein; GM-CSF; Leukine; Prokine; immunological laboratory methods; laboratory methods, immunological

Eligibility Criteria

Inclusion Criteria

• Stage IIIB or Stage IIIC breast cancer who are within 1 year of diagnosis and initiating treatment with chemotherapy and trastuzumab; and are in complete remission
• Stage IV breast cancer in first complete remission and defined as NED (no evidence of disease) or with stable bone only disease who are within 6 months of initiating maintenance trastuzumab
• NED status should be documented by chest/abdominal CT, PET or PET/CT within the last 90 days
• Bone only disease documented as stable or healed by PET, PET/CT, or MRI within the last 90 days; stable bone-only disease must be documented with bone scan performed within the last 6 months
• HER2 overexpression by IHC of 2+ or 3+, in the primary tumor or metastasis or documented gene amplification by FISH analysis; if overexpression is 2+ by IHC, then patients must have HER2 gene amplification documented by FISH
• Eligible subjects must have been treated to NED or stable bone only disease status with trastuzumab and/or chemotherapy and be off cytotoxic chemotherapy or immunosuppressive agents (e.g. systemic steroids) for at least 30 days prior to enrollment (concurrent hormonal therapy allowed; concurrent bisphosphonate therapy allowed)
• Patients on trastuzumab should continue trastuzumab monotherapy per standard of care (the dosing and schedule of trastuzumab should follow standard guidelines as described below: trastuzumab 2mg/kg IV weekly or trastuzumab 6mg/kg IV every 3 weeks)
• Subjects must have an ECOG Performance Status Score =< 1
• Non-menopausal female subjects must agree to contraception for the remainder of their childbearing years
• Male subjects must use an acceptable form of contraception throughout the course of the study
• Hematocrit >= 30,000
• Platelet count >= 100,000
• WBC >= 3000/mcl
• Stable creatinine =< 2.0 mg/dl or a creatinine clearance greater than 60 ml/min
• Serum bilirubin < 1.5 mg/dl
• SGOT < 2x ULN
• Laboratory tests should be performed within 60 days of enrollment
• Subjects must have recovered from major infections and/or surgical procedures and, in the opinion of the investigator, not have any significant active concurrent medical illnesses precluding protocol treatment
• Patients on trastuzumab monotherapy must have adequate cardiac function as demonstrated by normal ejection fraction (EF) on MUGA scan or echocardiogram performed within last 6 months

Exclusion Criteria

• Subjects cannot be simultaneously enrolled in other treatment studies
• Patients cannot be receiving any other concurrent immunomodulators besides trastuzumab
• Any contraindication to receiving GM-CSF based vaccine products
• Cardiac disease, specifically restrictive cardiomyopathy, unstable angina within the last 6 months prior to enrollment, New York Heart Association functional class III-IV heart failure on active treatment with normalized LVEF on therapy, and symptomatic pericardial effusion
• Active autoimmune disease
• Subjects can not have active immunodeficiency disorder, e.g. HIV
• Cannot be pregnant or breast feeding

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: collaborator

University of Washington

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Mary Disis

Role: PRINCIPAL_INVESTIGATOR

Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium

Locations

Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium

Seattle, Washington, United States

Countries

United States

Other Identifiers

NCI-2010-00803

Identifier Type: REGISTRY

Identifier Source: secondary_id

BC 030289

Identifier Type: OTHER

Identifier Source: secondary_id

120

Identifier Type: OTHER

Identifier Source: secondary_id

6166 (FH/UWCC ID)

Identifier Type: -

Identifier Source: org_study_id

NCT00369525

Identifier Type: -

Identifier Source: nct_alias