A Study Of PF-05280014 [Trastuzumab-Pfizer] Or Herceptin® [Trastuzumab-EU] Plus Paclitaxel In HER2 Positive First Line Metastatic Breast Cancer Treatment (REFLECTIONS B327-02)
Status: | Active, not recruiting |
---|---|
Conditions: | Breast Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/7/2019 |
Start Date: | February 24, 2014 |
End Date: | June 30, 2020 |
A PHASE 3 RANDOMIZED, DOUBLE-BLIND STUDY OF PF-05280014 PLUS PACLITAXEL VERSUS TRASTUZUMAB PLUS PACLITAXEL FOR THE FIRST-LINE TREATMENT OF PATIENTS WITH HER2-POSITIVE METASTATIC BREAST CANCER
The current study will compare the efficacy, safety, pharmacokinetics and immunogenicity of
PF-05280014 in combination with paclitaxel versus trastuzumab sourced from the European Union
(trastuzumab-EU) with paclitaxel in female patients with HER2-positive, metastatic breast
cancer in the first-line treatment setting. The hypothesis to be tested in this study is that
the efficacy (ORR) of PF-05280014 is similar to trastuzumab-EU.
PF-05280014 in combination with paclitaxel versus trastuzumab sourced from the European Union
(trastuzumab-EU) with paclitaxel in female patients with HER2-positive, metastatic breast
cancer in the first-line treatment setting. The hypothesis to be tested in this study is that
the efficacy (ORR) of PF-05280014 is similar to trastuzumab-EU.
Inclusion Criteria:
- Histologically confirmed diagnosis of breast cancer.
- Presence of metastatic disease.
- Documentation of HER2 gene amplification or overexpression.
- Available tumor tissue for central review of HER2 status.
- At least 1 measurable lesion as defined by RECIST 1.1.
- Eastern Cooperative Oncology Group status of 0 to 2.
- Left ventricular ejection fraction within institutional range of normal, measured by
either two dimensional echocardiogram or multigated acquisition scan.
Exclusion Criteria:
- Relapse within 1 year of last dose of previous adjuvant (including neoadjuvant)
treatment (except endocrine therapy) and within 1 year before randomization.
- Prior systemic therapy for metastatic disease (except endocrine therapy).
- Prior cumulative dose of doxorubicin of >400 mg/m2, epirubicin dose >800 mg/m^2, or
the equivalent dose for other anthracyclines or derivatives (eg, 72 mg/m^2 of
mitoxantrone). If the patient has received more than one anthracycline, then the
cumulative dose must not exceed the equivalent of 400 mg/m^2 of doxorubicin.
- Inflammatory breast cancer.
- Active uncontrolled or symptomatic central nervous system metastases.
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