Phase 2
N=29
Preoperative Bevacizumab and Trastuzumab With ABI-007 and Carboplatin in HER2+ Breast Cancer
Breast Cancer
Bottom Line
View on ClinicalTrials.gov: NCT00392392 ↗Enrolled (actual)
29
Serious AEs
27.6%
Results posted
Feb 2013
Primary outcome: Primary: Pathologic Complete Response Rate (PCRR), the Percentage of Patients Who Have No Evidence of Cancer in the Breast or Lymph Nodes Following Surgery — 56 percentage of participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- nab-paclitaxel (Drug); Bevacizumab (Drug); Trastuzumab (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- Female
- Sponsor
- SCRI Development Innovations, LLC
- Primary completion
- Apr 2008
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Pathologic Complete Response Rate (PCRR), the Percentage of Patients Who Have No Evidence of Cancer in the Breast or Lymph Nodes Following Surgery |
56 | — |
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.
Eligibility 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.
Data sourced from ClinicalTrials.gov (NCT00392392). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.