Overview

Preoperative Bevacizumab and Trastuzumab With ABI-007 and Carboplatin in HER2+ Breast Cancer

Status:
Completed
Trial end date:
2011-12-01
Target enrollment:
0
Participant gender:
Female
Summary
This trial combines trastuzumab and bevacizumab monoclonal antibodies, with ABI-007 and carboplatin, as neoadjuvant therapy in previously untreated locally advanced breast cancers demonstrating HER2 gene amplification. It is hoped that this novel combination will result in increased pathologic response rates that will translate into long term outcome improvements in HER2 positive patients with locally advanced breast cancer.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
SCRI Development Innovations, LLC
Collaborators:
Celgene Corporation
Genentech, Inc.
Treatments:
Albumin-Bound Paclitaxel
Bevacizumab
Carboplatin
Paclitaxel
Trastuzumab
Criteria
Inclusion Criteria:

- Female patients with histologically confirmed adenocarcinoma of the breast or
inflammatory breast cancer

- Clinical stage T 1-4, N 0-3, M0

- FISH+ HER2 gene amplified breast cancer

- 18 years or older

- Normal cardiac function

- Performance status 0-2

- Cannot have received any prior chemotherapy for this disease or cannot have received
chemotherapy for any other cancer in the past 5 years.

- Previous diagnosis of noninvasive breast cancer is OK.

- Must have adequate bone marrow, renal and liver function.

- Pregnant or lactating females not allowed.

- Preexisting peripheral neuropathy must be equal to or less than grade 1

- Must have archived tumor tissue for tissue testing.

Exclusion Criteria:

You cannot be in this study if you any of the following:

- History of cardiac disease, with New York Heart Association Class II or greater with
congestive heart failure

- Any heart attack, stroke or TIAs within the last 6 months or serious arrhythmias
needing medication; no bleeding diathesis or coagulopathy.

- No prior investigational drug within the last 30 days

- No prior trastuzumab or bevacizumab therapy

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.