NCT Number: NCT00482391
Doxorubicin and Cyclophosphamide Followed by Paclitaxel, Trastuzumab, and Lapatinib in Treating Patients With HER2/Neu-Overexpressed Breast Cancer
The purpose of this study is to study a new treatment for HER-2/neu (+) breast cancer.
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Conditions
Age range
18 year–120 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
Dana-Farber/Harvard Cancer Center at Dana Farber Cancer Institute, Boston, Massachusetts, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
DISEASE CHARACTERISTICS:
- Histologically confirmed adenocarcinoma of the breast
- Bilateral synchronous breast tumors allowed
- Any nodal status or tumor size allowed
- No stage IV disease
- HER2/neu-positive disease
- 3+ by IHC OR FISH-amplified
- Hormone receptor status not specified
PATIENT CHARACTERISTICS:
- Male or female
- Menopausal status not specified
- ECOG performance status 0-1
- Absolute neutrophil count ≥ 1,000/mm³
- Platelet count ≥ 100,000/mm³
- Bilirubin ≤ 1.1 mg/dL
- SGOT or SGPT ≤ 2.5 times upper limit of normal (ULN)
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective barrier contraception during and after completion of study therapy
- LVEF ≥ 50% by MUGA scan
- No peripheral neuropathy > grade 1
- No active second malignancy within the past 5 years except for adequately treated nonmelanoma skin cancer or in situ carcinoma of the cervix
- No known allergy or hypersensitivity to doxorubicin hydrochloride, cyclophosphamide, paclitaxel, or other drugs formulated in Cremophor EL
- No psychiatric illness or concurrent medical conditions that would preclude study treatment
- No other conditions, including any of the following:
- Unstable angina
- Congestive heart failure
- Myocardial infarction within the past 12 months
- High-risk uncontrolled arrhythmias (e.g., ventricular tachycardia, high-grade AV block, or supraventricular arrhythmias that are not adequately controlled)
- No QT prolongation (> 500 ms)
- No active unresolved infections
- No sensitivity to E. coli derived proteins
PRIOR CONCURRENT THERAPY:
- Prior hormonal therapy for chemoprevention allowed
- No prior trastuzumab (Herceptin®)
- No prior anthracyclines
- No concurrent hormonal therapy, including hormonal contraception (e.g., birth control pills or ovarian hormonal or replacement therapy)
- No other concurrent chemotherapy, radiotherapy, immunotherapy, or biotherapy for breast cancer
- No concurrent drugs that may prolong the QT
Treatment and study plan
Cyclophosphamide
DrugDoxorubicin hydrochloride
DrugLapatinib Ditosylate
Drugpaclitaxel
Druglaboratory biomarker analysis
OtherPrimary outcomes
-
Number of Patients Who Completed All Planned Therapy
Time frame: 2 years
The number of patients who completed all planned therapy (dose-dense adjuvant/ neoadjuvant chemotherapy regimen) in HER-2/neu-overexpressed/ amplified breast cancer patients.
Secondary outcomes
-
Number of Patients Who Were Evaluated for Toxicity
Time frame: 2 years
Please see adverse event section in the results. Toxicities were assessed by the National Cancer Institute Common Toxicity Criteria (NCI CTC) version 3.0.
Sponsors and collaborators
Lead sponsor
Memorial Sloan Kettering Cancer Center
Other
Collaborators
- Dana-Farber Cancer Institute
- GlaxoSmithKline
- National Cancer Institute (NCI)
Registry information
Official study title
Phase II Study of Dose-Dense Doxorubicin and Cyclophosphamide (AC) Followed by Weekly Paclitaxel With Trastuzumab and Lapatinib in HER2/NEU-Overexpressed/Amplified Breast Cancer: Feasibility
Important dates
- Study start
- 2007
- Primary completion
- 2011
- Study completion
- 2011
- First posted
- Jun 5, 2007
- Registry last updated
- May 12, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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