Trial Search Results

A Study of AC Followed by a Combination of Paclitaxel Plus Trastuzumab or Lapatinib or Both Given Before Surgery to Patients With Operable HER2 Positive Invasive Breast Cancer

The primary purpose of this study is to determine whether breast cancer tumors respond (as measured by pathologic complete response: the absence of microscopic evidence of invasive tumor cells in the breast) to combined chemotherapy of AC(doxorubicin and cyclophosphamide) followed by paclitaxel plus trastuzumab or lapatinib or both given before surgery to patients with HER2-positive breast cancer. Trastuzumab will also be given to all patients after surgery. The study will also evaluate the toxic effects of the chemotherapy combination, including effects on the heart, and will determine survival and progression-free survival 5 years after treatment. Also, the study will look at whether there are gene expression profiles in the tumor tissue that can predict pathologic complete response.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

NSABP Foundation Inc

Collaborator: GlaxoSmithKline

Intervention(s):

  • Drug: doxorubicin
  • Drug: cyclophosphamide
  • Drug: paclitaxel
  • Drug: trastuzumab
  • Drug: lapatinib

Phase:

Phase 3

Eligibility


Inclusion criteria:

   - Female

   - 18 years or older

   - ECOG performance status of 0 or 1

   - Primary breast tumor palpable and measures greater than or equal to 2.0 cm by physical
   exam

   - Diagnosis of invasive adenocarcinoma made by core needle biopsy

   - Breast cancer determined to be HER2-positive

   - LVEF assessment by MUGA scan or ECG within 3 months prior to randomization

   - Blood counts must meet the following criteria:

      - ANC greater than or equal to 1200/mm3

      - Platelet count greater than or equal to 100,000/mm3

      - Hemoglobin greater than or equal to 10 g/dL

   - Serum creatinine less than or equal to ULN for the lab

   - Adequate hepatic function by these criteria:

      - Total bilirubin less than or equal to the ULN for the lab unless the patient has
      a bilirubin elevation greater than ULN to 1.5 x ULN resulting from Gilbert's
      disease or similar syndrome due to slow conjugation of bilirubin; and

      - Alkaline phosphatase less than or equal to 2.5 x ULN; and

      - AST less than or equal to 1.5 x ULN for the lab.

   - If skeletal pain present or alkaline phosphatase greater than ULN (but less than or
   equal to 2.5 x ULN), bone scan or PET scan must not demonstrate metastatic disease

   - If AST or alkaline phosphatase greater than ULN , liver imaging (CT, MRI or PET scan)
   must not demonstrate definitive metastatic disease and the requirements in criterion
   for hepatic function must be met

   - Able to swallow oral medications

Exclusion criteria:

   - FNA alone to diagnose the primary tumor

   - Excisional biopsy or lumpectomy was performed prior to randomization

   - Surgical axillary staging procedure prior to randomization. Exceptions: 1) FNA or core
   biopsy of an axillary node for any patient, and 2) although not recommended, a
   pre-neoadjuvant therapy SN biopsy for patients with clinically negative axillary
   nodes.

   - Tumors clinically staged as T4

   - Ipsilateral cN2b or cN3 disease (Patients with cN1 or cN2a disease are eligible)

   - Definitive clinical or radiologic evidence of metastatic disease

   - Synchronous bilateral invasive breast cancer

   - Requirement for chronic use of any of the medications or substances specified in the
   protocol

   - Treatment including RT, chemotherapy, and/or targeted therapy for the currently
   diagnosed breast cancer prior to randomization

   - Any sex hormonal therapy, e.g., birth control pills, ovarian hormone replacement
   therapy, etc. (These patients are eligible if therapy is discontinued prior to
   randomization)

   - Continued therapy with any hormonal agent such as raloxifene, tamoxifen, or other
   SERM. (Patients are eligible only if these medications are discontinued prior to
   randomization)

   - Prior history of breast cancer, including DCIS (Patients with a history of LCIS are
   eligible)

   - Prior therapy with anthracyclines, taxanes, trastuzumab, or lapatinib for any
   malignancy

   - Other malignancies unless the patient is considered to be disease-free for 5 or more
   years prior to randomization and is deemed by her physician to be at low risk for
   recurrence. Patients with the following cancers are eligible if diagnosed and treated
   within the past 5 years: carcinoma in situ of the cervix, carcinoma in situ of the
   colon, melanoma in situ, and basal cell and squamous cell carcinoma of the skin.

   - Cardiac disease that would preclude the use of the drugs included in the B-41
   treatment regimens. This includes but is not confined to:

      - Active cardiac disease:

         - angina pectoris requiring the use of anti-anginal medication;

         - ventricular arrhythmias except for benign premature ventricular contractions
         controlled by medication;

         - conduction abnormality requiring a pacemaker;

         - supraventricular and nodal arrhythmias requiring a pacemaker or not
         controlled with medication; and

         - clinically significant valvular disease.

      - History of cardiac disease:

         - myocardial infarction;

         - congestive heart failure; or

         - cardiomyopathy.

   - Uncontrolled hypertension, defined as blood pressure greater than 150/90 mm/Hg on
   antihypertensive therapy

   - History of or current symptomatic interstitial pneumonitis or pulmonary fibrosis or
   definitive evidence of interstitial pneumonitis or pulmonary fibrosis described on CT
   or chest x-ray in asymptomatic patients

   - Sensory/motor neuropathy greater than or equal to grade 2, as defined by the NCI's
   CTCAE v3.0

   - Malabsorption syndrome, ulcerative colitis, resection of the stomach or small bowel,
   or other disease significantly affecting gastrointestinal function

   - Other non-malignant systemic disease that would preclude treatment with any of the
   treatment regimens or would prevent required follow-up

   - Conditions that would prohibit administration of corticosteroids

   - Administration of any investigational agents within 30 days before randomization

   - Pregnancy or lactation

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

Female

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Cancer Clinical Trials Office
650-498-7061
Not Recruiting