Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Genentech, Inc.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Signed Informed Consent Form
Histologically or cytologically confirmed adenocarcinoma of the breast with measurable or non-measurable locally recurrent or metastatic disease
Age ≥ 18 years
Adequate left ventricular function at study entry, defined as an Left Ventricular Ejection Fraction (LVEF) \> 50% by either Multi Gated Acquisition(MUGA) scan or Electrocardiogram (ECHO)
Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
Ability and willingness to comply with study and follow-up procedures
You may not be if
Unknown HER2 status or known HER2-positive status
Prior chemotherapy for locally recurrent or metastatic disease
Prior hormonal therapy within 2 weeks prior to Day 1
Prior adjuvant or neoadjuvant taxane chemotherapy within 12 months prior to Day 1
Prior adjuvant or neoadjuvant non-taxane chemotherapy within 6 months prior to Day 1
For patients who have received recent radiotherapy, ongoing Grade ≥ 3 acute toxicity
Patients with brain metastasis on full dose anticoagulation therapy
Life expectancy of \< 12 weeks
Current, recent (within 4 weeks of Day 1), or planned participation in an experimental drug study
Inadequate organ function within 28 days prior to Day 1
Untreated abnormal thyroid function tests
Uncontrolled serious medical or psychiatric illness
Active infection requiring IV antibiotics at enrollment or randomization
History of other malignancies within 5 years prior to Day 1 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
Inadequately controlled hypertension
Prior history of hypertensive crisis or hypertensive encephalopathy
New York Heart Association (NYHA) Class II or greater CHF
History of myocardial infarction or unstable angina within 12 months prior to Day 1
History of stroke or transient ischemic attack within 12 months prior to Day 1
Known central nervous system (CNS) disease except for treated brain metastasis
Significant vascular disease (e.g., aortic aneurysm, aortic dissection) or recent peripheral arterial thrombosis within 6 months prior to Day 1
History of hemoptysis within 1 month prior to Day 1
Evidence of bleeding diathesis or significant coagulopathy (in the absence of therapeutic anticoagulation)
Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to Day 1 or anticipation of need for major surgical procedure during the course of the study
Core biopsy or other minor surgical procedure, excluding placement of a vascular access device, within 7 days prior to Day 1
History of abdominal fistula or gastrointestinal perforation within 6 months prior to Day 1
Serious, non-healing wound, active ulcer, or untreated bone fracture
Proteinuria at screening, as demonstrated by a urine protein/creatinine ratio of ≥ 1.0 at screening
Known hypersensitivity to any component of bevacizumab or sunitinib
Pregnancy (positive pregnancy test) or lactation
Clareo Health | A Study of Sunitinib in Combination With Bevacizumab and Paclitaxel in Previously Untreated Patients With Metastatic Breast Cancer (SABRE-B)
