Bevacizumab Given With Either Anastrozole or Fulvestrant With Trastuzumab for Postmenopausal Metastatic Breast Cancer

Completed · Phase 2

Conditions studied: Breast Cancer, Breast Neoplasms

In brief

This is a phase II trial combining bevacizumab with either fulvestrant or anastrozole with trastuzumab in the treatment of metastatic breast cancer in postmenopausal women. It is hoped that these combinations will keep the cancer from growing and spreading further.

Key facts

Study ID

NCT00405938

Run by

SCRI Development Innovations, LLC

People needed

79

Starts

2006-11-01

Expected to finish

2011-06-01

Last updated by the study team

2021-11-18

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Postmenopausal breast cancer (adenocarcinoma) estrogen (ER)and/or progesterone (PR) receptor positive that is locally advanced or locally recurrent and not able to be surgically removed OR with measurable and/or disease that is able to be assessed including isolated bone metastasis
• Female patients 18 years or older
• Documentation of ER+ and/or PR+
• No prior chemotherapy or hormone therapy for metastatic breast cancer or inoperable breast cancer that is locally recurrent or locally advanced
• Measurable or evaluable disease
• Radiation therapy to painful bone lesions or impending fractures is allowed as long as there is measurable or evaluable disease outside the radiated area.
• Must have adequate bone marrow, renal and liver function
• Patients receiving prior treatment with an anthracycline based chemotherapy must have a normal left ventricle ejection fraction

You may not qualify if…

• No metastatic disease to the Central Nervous System
• No history of myocardial infarction (MI), stroke or transient ischemic attacks in the last 6 months
• No symptoms of peripheral vascular disease
• No history of abdominal fistula, gastrointestinal perforation or intrabdominal abscess in the past 6 months
• No known hypersensitivity to phosphate, trehalose or polysorbate
• No serious non-healing wound, ulcer or bone fracture
• No uncontrolled high blood pressure or history of hypertensive crisis
• No New York Hear Association class II congestive heart failure
• No extensive cancer involvement of the liver or lungs
• No history of significant psychiatric disorders
• No significant vascular disease
• There are additional inclusion/exclusion criteria. The study center will determine if you meet all of the criteria. If you do not qualify for the trial, study personnel will explain the reasons. If you do qualify, study personnel will explain the trial in detail and answer any questions you may have. You can then decide if you wish to participate.

Where it is running

• Florida Cancer Specialists — Fort Myers, Florida, United States
• Integrated Community Oncology Network — Jacksonville, Florida, United States
• Florida Hospital Cancer Institute — Orlando, Florida, United States
• Northeast Georgia Medical Center — Gainesville, Georgia, United States
• Wellstar Cancer Research — Marietta, Georgia, United States
• Graves-Gilbert Clinic — Bowling Green, Kentucky, United States
• Baton Rouge General Medical Center — Baton Rouge, Louisiana, United States
• St. Louis Cancer Care — Chesterfield, Missouri, United States
• Sletten Cancer Institute — Great Falls, Montana, United States
• Chattanooga Oncology & Hematology Associates — Chattanooga, Tennessee, United States
• Tennessee Oncology, PLLC — Nashville, Tennessee, United States

Full record on ClinicalTrials.gov

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