Herceptin and GM-CSF for Metastatic Breast Cancer

M.D. Anderson Cancer Center18 enrolled

Overview

Primary Objectives: 1. To determine the patient's tumor response rate that this protocol will produce. 2. To determine the 1 year progression-free survival that this protocol will produce. Secondary Objective: 1\. To determine whether antibody-dependent cell-mediated cytotoxicity (ADCC) is the mechanism of overcoming Herceptin-resistance by use of Granulocyte-Macrophage Colony Stimulating Factor (GM-CSF).

GM-CSF stimulates the immune system and may increase the effectiveness of Herceptin. Before you can start treatment on this study, you will have what are called "screening tests." These tests will help the doctor decide if you are eligible to take part in this study. You will have a complete medical history and physical exam. This includes blood tests (about 2 tea spoons), and x-rays. Women who are able to have children must have a negative blood or urine pregnancy test. If you are found to be eligible to take part in this study, you will receive trastuzumab through a vein (IV) every week until the disease gets worse. GM-CSF will be injected under the skin at least once a day until the white blood cell count is stable. GM-CSF will also continue during the course of study until the disease progresses. You will have further evaluation of your disease by computed tomography-CT scan, bone scan, chest X-ray, etc. at 2, 4, 6, 9, 12, 18, and 24 months after the start of treatment. You will have blood tests (about 2 tea spoons) at least twice a week until the appropriate dose of GM-CSF is found. The dose may increase or decrease depending on the blood test. You will have blood (about 2 tablespoons) drawn before treatment at the 2nd and 4th month, and if the disease gets worse. You will be removed from the study if the disease is progressing or severe side effects occur. This is an investigational study. The FDA has approved trastuzumab and GM-CSF, but their use in this study is experimental. A total of 36 patients will take part in this study. All will be enrolled at UT MD Anderson Cancer Center.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Breast Cancer

Interventions

HerceptinDRUG

4 mg/kg IV Over 90 Minutes

GM-CSFDRUG

250 mcg/m\^2 Subcutaneously

Eligibility

Sex: FEMALE

Medical Language ↔ Plain English

Inclusion Criteria: 1. Histological confirmation of invasive carcinoma of the breast. 2. HER-2/neu overexpression: 3+ by immunohistochemical staining or Fluorescence in situ hybridization (FISH) (+). 3. Stage IV breast cancer with measurable disease. 4. Patient receiving progressive disease after Herceptin plus chemotherapy or Herceptin alone. No more than two Herceptin containing regimens. 5. Zubrod performance status 0 or 1. 6. Adequate hematological parameters (White Blood cells-WBC \> 3,000/mm3, platelet count \> 100,000/mm3), adequate renal function (serum creatinine \< 2.0 mg/dl), adequate liver function (total bilirubin, aspartate aminotransferase (AST or SGOT) or alanine aminotransferase (ALT or SGPT) \< 3 x normal). Exclusion Criteria: 1. Active Brain metastasis. 2. No measurable disease at the time of registration (e.g. bone only, leptomeningeal disease alone or pleural effusion alone). 3. More than 2 Herceptin containing regimens in metastatic breast cancer. 4. Known history of HIV positive. 5. Chronic active hepatitis or cirrhosis. 6. Symptomatic pulmonary disease. 7. Use of steroid of non-steroidal anti-inflammatory analgesic or Cox-2 inhibitor 1 week prior to registration.

Locations (1)

U.T.M.D. Anderson Cancer Center

Houston, Texas, United States

Outcomes

Primary Outcomes

Number of Participants With Tumor Response (Stable Disease)

Number of participants with response defined as stable disease or better using Response Evaluation Criteria In Solid Tumors (RECIST) at the month 2 evaluation.

Time frame: 2 months

Secondary Outcomes

Duration of Stable Disease

Stable disease is measured from the start of the treatment until the RECIST criteria for disease progression is met.

Time frame: 6 Years

Data from ClinicalTrials.gov

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