Status:
COMPLETED
A Study of Trastuzumab-Mcc-DM1 Administered Intravenously to Patients With HER2-Positive Metastatic Breast Cancer
Lead Sponsor:
Genentech, Inc.
Conditions:
Metastatic Breast Cancer
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
Study of trastuzumab emtansine (T-DM1) administered to patients with human epidermal growth factor receptor 2 (HER2)-positive metastatic breast cancer.
Eligibility Criteria
Inclusion
- Signed study-specific Informed Consent Form(s)
- Age ≥ 18 years
- Histologically documented breast cancer
- HER2-positive disease
- Metastatic breast cancer
- Disease progression on the last chemotherapy regimen received in the metastatic setting
- Prior treatment with an anthracycline, trastuzumab, a taxane, lapatinib, and capecitabine in the neoadjuvant, adjuvant, locally advanced, or metastatic setting and prior treatment with at least two lines of therapy (a line of therapy can be a combination of two agents or single-agent chemotherapy) in the metastatic setting
- At least two lines of anti-HER2 therapy must have been given in the metastatic setting as monotherapy or combined with chemotherapy or hormonal therapy. The HER2-targeted agent can include trastuzumab, lapatinib, or an investigational agent with HER2-inhibitory activity.
- A minimum of 6 weeks of trastuzumab for the treatment of metastatic disease is required
- Patients must have had at least 14 days of exposure in the metastatic setting to lapatinib and capecitabine (given together or separately) unless they were intolerant of lapatinib and/or capecitabine
Exclusion
- Chemotherapy ≤ 21 days before enrollment
- Trastuzumab ≤ 21 days before enrollment
- Hormone therapy ≤ 7 days before enrollment
- Granulocyte-stimulating agent \< 14 days before enrollment
- Investigational therapy ≤ 28 days before enrollment
- Previous radiotherapy for treatment of metastatic breast cancer ≤ 21 days before enrollment
- Brain metastases that are untreated, symptomatic, or require therapy to control symptoms; or any radiation, surgery, or other therapy to control symptoms from brain metastases within 3 months of the first study treatment
- History of intolerance (including Grade 3-4 infusion reaction) or hypersensitivity to trastuzumab or murine proteins
- History of exposure to the following cumulative doses of anthracyclines: Doxorubicin or liposomal doxorubicin \> 500 mg/m\^2; Epirubicin \> 900 mg/m\^2; Mitoxantrone \> 120 mg/m\^2 and idarubicin \> 90 mg/m\^2
- Peripheral neuropathy of Grade ≥ 3 per National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE), v3.0
- History of other malignancy within the last 5 years, except for carcinoma in situ of the cervix or basal cell carcinoma
- Current unstable angina
- History of symptomatic congestive heart failure (CHF), or ventricular arrhythmia requiring treatment
- History of myocardial infarction within 6 months of enrollment
- Left ventricular ejection fraction (LVEF) \< 50% within 28 days of enrollment
- History of decreased LVEF to \< 50% or symptomatic CHF with previous adjuvant trastuzumab treatment
- Severe dyspnea at rest due to complications of advanced malignancy or requiring current continuous oxygen therapy
- Current severe, uncontrolled systemic disease (e.g., clinically significant cardiovascular, pulmonary, or metabolic disease)
- Major surgical procedure or significant traumatic injury within 28 days before enrollment or anticipation of the need for major surgery during the course of study treatment
- Current pregnancy or lactation
- Current known infection with human immunodeficiency virus (HIV), active hepatitis B, and/or hepatitis C virus
- Assessed by the investigator to be unable or unwilling to comply with the requirements of the protocol
Key Trial Info
Start Date :
August 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2011
Estimated Enrollment :
110 Patients enrolled
Trial Details
Trial ID
NCT00679211
Start Date
August 1 2008
End Date
April 1 2011
Last Update
March 31 2017
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