A Study of the Efficacy and Safety of Trastuzumab Emtansine (Trastuzumab-MCC-DM1) vs. Trastuzumab (Herceptin®) and Docetaxel (Taxotere®) in Patients With Metastatic HER2-positive Breast Cancer Who Have Not Received Prior Chemotherapy for Metastati

• Status: Completed
• Trial end date: 2012-05-01
• Target enrollment: 0
• Participant gender: All

Summary

This was a Phase II, randomized, multicenter, international, 2-arm, open-label clinical trial designed to explore the efficacy and safety of trastuzumab emtansine (T-DM1) relative to the combination of trastuzumab and docetaxel in patients with human epidermal growth factor receptor 2 (HER2)-positive, unresectable, locally advanced breast cancer and/or metastatic breast cancer who have not received prior chemotherapy for metastatic disease.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Hoffmann-La Roche
• Treatments: Ado-Trastuzumab Emtansine; Docetaxel; Maytansine; Trastuzumab

Criteria

Inclusion Criteria:

• Histologically or cytologically confirmed adenocarcinoma of the breast with locally advanced or metastatic disease, and a candidate for chemotherapy.

• Human epidermal growth factor receptor 2 (HER2)-positive.

• No prior chemotherapy for their metastatic breast cancer (MBC).

• Measurable disease.

• Age ≥ 18 years.

• For women of childbearing potential and men with partners of childbearing potential, agreement to use a highly effective, non-hormonal form of contraception or 2 effective forms of non-hormonal contraception by the patient and/or partner. Contraception use must continue for the duration of study treatment and for at least 6 months after the last dose of study treatment. Male patients whose partners are pregnant should use condoms for the duration of the study.

Exclusion Criteria:

• History of any chemotherapy for MBC.

• An interval of < 6 months from the completion of cytotoxic chemotherapy in the neo-adjuvant or adjuvant setting until the time of metastatic diagnosis.

• Trastuzumab ≤ 21 days prior to randomization.

• Hormone therapy < 7 days prior to randomization.

• Current peripheral neuropathy of Grade ≥ 3.

• History of other malignancy within the last 5 years, except for appropriately treated carcinoma in situ of the cervix, non-melanoma skin carcinoma, Stage I uterine cancer, or other cancers with a similar outcome as those previously mentioned.

• Previous radiotherapy for the treatment of unresectable, locally advanced or metastatic breast cancer is not allowed if more than 25% of marrow-bearing bone has been irradiated or the last fraction of radiotherapy has been administered within approximately 3 weeks prior to randomization.

• 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 2 months prior to randomization.

• History of exposure to the following cumulative doses of anthracyclines: Doxorubicin or liposomal doxorubicin > 500 mg/m^2; epirubicin > 900 mg/m^2; mitoxantrone > 120mg/m^2 and idarubicin > 90 mg/m^2.

• Current unstable angina.

• History of symptomatic congestive heart failure, or ventricular arrhythmia requiring treatment.

• History of myocardial infarction within 6 months prior to randomization.

• Left ventricular ejection fraction (LVEF) below 50% within approximately 28 days prior to randomization.

• History of decreased LVEF or symptomatic congestive heart failure (CHF) with previous adjuvant trastuzumab treatment.

• Cardiac troponin I ≥ 0.2 ng/mL within 28 days of randomization.

• Severe dyspnea at rest because of complications of advanced malignancy or requiring current continuous oxygen therapy.

• Current severe, uncontrolled systemic disease (eg, clinically significant cardiovascular, pulmonary, or metabolic disease; wound healing disorders; ulcers; or bone fractures).

• Major surgical procedure or significant traumatic injury within approximately 28 days prior to randomization or anticipation of the need for major surgery during the course of study treatment.

• Current pregnancy or lactation.

• History of receiving any investigational treatment within approximately 28 days prior to randomization.

• Current known infection with human immunodeficiency virus (HIV), active hepatitis B and/or hepatitis C virus.

• History of intolerance (including Grade 3-4 infusion reaction) or hypersensitivity to trastuzumab, murine proteins, or docetaxel.

• Known hypersensitivity to any of the study drugs, including the excipients, or any drugs formulated in polysorbate 80.

• Assessed by the investigator to be unable or unwilling to comply with the requirements of the protocol.