A Phase III, Multicenter, Randomized, Placebo-controlled Trial Evaluating the Efficacy and Safety of Bevacizumab in Combination With Chemotherapy Regimens in Subjects With Previously Treated Metastatic Breast Cancer
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 684
- 主要终点
- Progression-free Survival
研究概览
简要总结
This phase III, multicenter, randomized, placebo-controlled, blinded trial is designed to evaluate the efficacy and safety of bevacizumab when combined with standard chemotherapy compared with chemotherapy alone in subjects with previously treated metastatic breast cancer.
详细描述
For all Outcome Measures except Overall Survival and One-year Survival, the Time Frame was from Baseline to data cut-off for analysis of the primary Outcome Measure (up to 3 years 2 months). For the Outcome Measures Overall Survival and One-year Survival, the Time Frame was from Baseline to the end of the study (up to 6 years, 7 months).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Signed informed consent form.
- •≥ 18 years of age.
- •Histologically confirmed carcinoma of the breast with measurable or non-measurable metastatic disease that has progressed (patients with a history of brain metastasis are eligible for study participation [USA only], as long as their brain metastases have been treated and they have no evidence of progression or hemorrhage after treatment and no ongoing requirement for dexamethasone).
- •Progression of disease during or following administration of one (non-investigational) chemotherapy regimen administered in the first-line setting.
- •Eastern Cooperative Oncology Group (ECOG) performance status of 0 or
- •For women of childbearing potential, use of an effective means of non-hormonal contraception.
- •Life expectancy ≥ 3 months.
- •Willingness and capacity to comply with study and follow-up procedures.
排除标准
- •Prior hormonal therapy only as treatment for metastatic disease without chemotherapy. Patients must have received chemotherapy for their metastatic disease in the first-line setting. Hormone therapy alone is not allowed.
- •For subjects who have received prior anthracycline-based therapy, documentation of left ventricular ejection fraction < 50% by either multiple gated acquisition (MUGA) or echocardiogram (ECHO).
- •Treatment with more than one prior cytotoxic regimen for metastatic breast cancer (MBC).
- •HER2-positive status (patients who have unknown HER2 status, and for whom determination of HER2 status is not possible, are eligible for this study).
- •Unknown estrogen receptor (ER) and progesterone receptor (PR) status.
- •Radiation therapy other than for palliation or brain metastasis, biologic therapy, or chemotherapy for MBC within 21 days prior to Day 0 (Day 1 of Cycle 1 of treatment).
- •Prior therapy with bevacizumab or other vascular endothelial growth factor (VEGF) pathway-targeted therapy.
- •Untreated brain metastasis.
- •Inadequately controlled hypertension.
- •Unstable angina.
- •New York Heart Association Grade II or greater congestive heart failure (CHF).
- •History of myocardial infarction within 6 months prior to Day 0 (the day of the first bevacizumab/placebo infusion).
- •History of stroke or transient ischemic attack within 6 months prior to Day
- •Clinically significant peripheral vascular disease.
- •Evidence of bleeding diathesis or coagulopathy.
- •Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to Day 0; anticipation of need for major elective surgical procedure during the study.
- •Minor surgical procedures, fine-needle aspirations, or core biopsies within 7 days prior to Day
- •History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 6 months prior to Day
- •Serious, non-healing wound, ulcer, or bone fracture.
- •History of anaphylactic reaction to monoclonal antibody therapy not controlled with treatment premedication.
- •History of other malignancies within 5 years of Day 0, except for tumors with a negligible risk for metastasis or death, such as adequately controlled basal cell carcinoma or squamous cell carcinoma of the skin or carcinoma in situ of the cervix.
- •inadequate organ function.
- •Pregnancy (positive serum pregnancy test) or lactation.
- •Any other diseases, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or that may affect the interpretation of the results or renders the subject at high risk from treatment complications.
研究组 & 干预措施
Standard chemotherapy + bevacizumab
Patients received one of several standard chemotherapies for metastatic breast cancer plus bevacizumab in a dose of either 10 mg/kg intravenously (IV) every 2 weeks or 15 mg/kg IV every 3 weeks depending upon the schedule of chemotherapy chosen.
干预措施: Bevacizumab (Drug)
Standard chemotherapy + bevacizumab
Patients received one of several standard chemotherapies for metastatic breast cancer plus bevacizumab in a dose of either 10 mg/kg intravenously (IV) every 2 weeks or 15 mg/kg IV every 3 weeks depending upon the schedule of chemotherapy chosen.
干预措施: Standard chemotherapy (Drug)
Standard chemotherapy + placebo
Patients received one of several standard chemotherapies for metastatic breast cancer plus placebo to bevacizumab administered IV either every 2 weeks or every 3 weeks depending upon the schedule of chemotherapy chosen.
干预措施: Placebo (Drug)
Standard chemotherapy + placebo
Patients received one of several standard chemotherapies for metastatic breast cancer plus placebo to bevacizumab administered IV either every 2 weeks or every 3 weeks depending upon the schedule of chemotherapy chosen.
干预措施: Standard chemotherapy (Drug)
结局指标
主要结局
Progression-free Survival
时间窗: Baseline to data cut-off for analysis of the primary Outcome Measure (up to 3 years, 2 months)
PFS was defined as the time from randomization to first documented disease progression (PD) as determined by the investigator using Response Evaluation Criteria in Solid Tumors (RECIST) or death due to any cause, whichever occurred first. For target lesions, PD was defined as at least a 20% increase in the sum of the longest diameter of target lesions, taking as reference the smallest sum of the longest diameter recorded since treatment started or the appearance of 1 or more new lesions. For non-target lesions, PD was defined as the appearance of 1 or more new lesions and/or unequivocal progression of existing non-target lesions. Target lesions should be selected on the basis of their size (those with the longest diameter) and their suitability for accurate repeated measurements by imaging techniques or clinically. All measurable lesions up to a maximum of 5 lesions per organ and 10 lesions in total, representative of all involved organs, should be identified as target lesions.
次要结局
- Progression-free Survival Within Individual Standard Chemotherapy Cohorts (Taxanes, Gemcitabine, Capecitabine, and Vinorelbine)(Baseline to data cut-off for analysis of the primary Outcome Measure (up to 3 years, 2 months))
- Overall Survival(Baseline to the end of the study (up to 6 years, 7 months))
- One-year Survival(Baseline to the end of the study (up to 6 years, 7 months))
- Objective Response(Baseline to data cut-off for analysis of the primary Outcome Measure (up to 3 years, 2 months))
- Duration of Objective Response(Baseline to data cut-off for analysis of the primary Outcome Measure (up to 3 years, 2 months))