Breast Cancer Clinical Trial
Neoadjuvant Carboplatin, Weekly Abraxane and Trastuzumab in HER2+ Breast Cancer
Summary
Q3week carboplatin with weekly abraxane and trastuzumab as neoadjuvant therapy in resectable and unresectable HER2+ (stage IIa-IIIb) breast cancer
Full Description
Our goal is to develop an induction chemotherapy regimen that will have a pCR rate above 50% in HER2+ patients without exposing patients to the toxicity of an anthracycline-based regimen. A minimum of 60 evaluable patients will be accrued to the study. We are assuming an observed pCR (or near pCR) rate of 70%. Assuming no more than 10% of patients will be inevaluable for the primary endpoint (pCR), we will have at least 54 evaluable patients. With this number, we will have 90% power, with a 1-sided alpha error of 0.05, to demonstrate a pCR rate exceeding 50% for our novel regimen.
Eligibility Criteria
Inclusion Criteria:
Histologically documented adenocarcinoma of the breast
ANC > 1000 cells
Female; age > 18; Zubrod PS 0-1
Platelets > 100,000
Stage IIA-IIIB disease
Total bilirubin < or = ULN
No evidence of metastatic disease Not pregnant or lactating
No prior systemic therapy for this breast cancer
Serum Creatinine < 1.5 mg/dl or Creat Cl > 30 ml/min
Serum ALT < 2.5 x ULN
ER, PR and HER2 status required
LVEF (MUGA/echo)WNL
No baseline > 2 neuropathy
Hemoglobin > 9.0 gm/dl
HER2+, defined by IHC 3+ or FISH ratio > 2.0
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There are 5 Locations for this study
Duarte California, 91010, United States
New Haven Connecticut, 06437, United States
Providence Rhode Island, 02903, United States
Providence Rhode Island, 02908, United States
Providence Rhode Island, 02912, United States
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