Trial Search Results

Chemotherapy With or Without Trastuzumab After Surgery in Treating Women With Invasive Breast Cancer

This randomized phase III clinical trial studies chemotherapy with or without trastuzumab after surgery to see how well they work in treating women with invasive breast cancer. Drugs used in chemotherapy work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving more than one drug (combination chemotherapy) and giving chemotherapy after surgery may kill more tumor cells. Monoclonal antibodies, such as trastuzumab, can block cancer growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. It is not yet known whether combination chemotherapy is more effective with trastuzumab in treating breast cancer.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

National Cancer Institute (NCI)

Intervention(s):

  • Drug: Cyclophosphamide
  • Drug: Docetaxel
  • Drug: Doxorubicin Hydrochloride
  • Other: Laboratory Biomarker Analysis
  • Drug: Paclitaxel
  • Other: Quality-of-Life Assessment
  • Biological: Trastuzumab

Phase:

Phase 3

Eligibility


Inclusion Criteria:

   - Patients should have a life expectancy of at least 10 years, excluding their diagnosis
   of breast cancer; (comorbid conditions should be taken into consideration, but not the
   diagnosis of breast cancer)

   - Women of reproductive potential must agree to use an effective non-hormonal method of
   contraception (for example condoms, some intrauterine devices, diaphragms, tubal
   ligation, vasectomized partner, or abstinence) during therapy and for at least 6
   months (Arm 1 patients) and for at least 7 months (Arm 2 patients) after the last dose
   of study therapy (chemotherapy or trastuzumab)

   - Submission of tumor samples from the breast surgery is required for all patients;
   therefore, the local pathology department policy regarding release of tumor samples
   must be considered in the screening process; patients whose tumor samples are located
   in a pathology department that by policy will not submit any samples for research
   purposes should not be approached for participation in the B-47 trial

   - The patient must have signed and dated an Institutional Review Board (IRB)-approved
   consent form that conforms to federal and institutional guidelines

   - Eastern Cooperation Oncology Group (ECOG) performance status of 0 or 1

   - The tumor must be unilateral invasive adenocarcinoma of the breast on histologic
   examination

   - All of the following staging criteria (according to the 7th edition of the American
   Joint Committee on Cancer [AJCC] Cancer Staging Manual) must be met:

      - By pathologic evaluation, primary tumor must be pT1-3

      - By pathologic evaluation, ipsilateral nodes must be pN0, pN1 (pN1mi, pN1a, pN1b,
      pN1c), pN2a, pN2b, pN3a, or pN3b

         - If pN0, one of the following criteria must be met:

            - pT2 and estrogen receptor (ER) negative and progesterone receptor (PgR)
            negative; or

            - pT2 and ER positive (PgR status may be positive or negative) and either
            grade 3 histology or Oncotype DX Recurrence Score of >= 25; or

            - pT3 regardless of hormone receptor status, histologic grade, and
            Oncotype DX Recurrence Score

   - HER2 status of the primary tumor must be evaluated prior to randomization; all testing
   performed must indicate that the tumor is HER2-low as defined below

      - IHC must be performed and the IHC staining results must indicate a score of 1+
      (in situ hybridization [ISH] testing is not required) or 2+ (ISH must also be
      performed and must indicate that the tumor is HER2-low as described below)

      - If ISH testing is performed, test results must be as follows and IHC must be 1+
      or 2+: the ratio of HER2 to chromosome enumeration probe 17 (CEP17) must be < 2.0
      or, if a ratio was not performed, the HER2 gene copy number must be < 4 per
      nucleus

      - Note: If the IHC staining intensity is reported as a range, e.g., 0 to 1+ or 1+
      to 2+, the higher intensity score in the range should be used to determine
      eligibility

   - The patient must have undergone either a total mastectomy or breast-conserving surgery
   (lumpectomy); (patients who have had a nipple-sparing mastectomy are eligible)

   - For patients who undergo lumpectomy, the margins of the resected specimen must be
   histologically free of invasive tumor and ductal carcinoma in situ (DCIS) as
   determined by the local pathologist; if pathologic examination demonstrates tumor at
   the line of resection, additional operative procedures may be performed to obtain
   clear margins; if tumor is still present at the resected margin after re-excision(s),
   the patient must undergo total mastectomy to be eligible; (patients with margins
   positive for lobular carcinoma in situ [LCIS] are eligible without additional
   resection)

   - For patients who undergo mastectomy, margins must be free of gross residual tumor;
   (patients with microscopic positive margins are eligible as long as post-mastectomy
   radiation therapy [RT] of the chest wall will be administered)

   - The patient must have completed one of the procedures for evaluation of pathologic
   nodal status listed below:

      - Sentinel lymphadenectomy alone:

         - If pathologic nodal staging based on sentinel lymphadenectomy is pN0 or pN1b

         - If pathologic nodal staging based on sentinel lymphadenectomy is pN1mi or
         pN1a, the primary tumor must be T1 or T2 by pathologic evaluation and the
         nodal involvement must be limited to 1 or 2 positive nodes

      - Sentinel lymphadenectomy followed by removal of additional non-sentinel lymph
      nodes if the sentinel node (SN) is positive; or

      - Axillary lymphadenectomy with or without SN isolation procedures

   - The interval between the last surgery for breast cancer (treatment or staging) and
   randomization must be no more than 84 days

   - The patient must have ER analysis performed on the primary tumor prior to
   randomization; if ER analysis is negative, then PgR analysis must also be performed
   (either the core biopsy or surgical resection specimen can be used for ER/PgR
   testing); patients with a primary tumor that is hormone receptor-positive or
   receptor-negative are eligible

   - Absolute neutrophil count (ANC) must be >= 1,200/mm^3

   - Platelet count must be >= 100,000/mm^3

   - Hemoglobin must be >= 10 g/dL

   - Total bilirubin must be =< upper limit of normal (ULN) for the lab unless the patient
   has a bilirubin elevation > ULN to 1.5 x ULN due to Gilbert disease or similar
   syndrome involving slow conjugation of bilirubin

   - Alkaline phosphatase must be =< 2.5 x ULN for the lab

   - Aspartate aminotransferase (AST) must be =< 1.5 x ULN for the lab (if alanine
   aminotransferase [ALT] is performed instead of AST [per institution's standard
   practice], the alanine aminotransferase [ALT] value must be =< 1.5 x ULN; if both were
   performed, the AST must be =< 1.5 x ULN)

   - Alkaline phosphatase and AST may not both be > the ULN

   - Patients with AST or alkaline phosphatase > ULN are eligible for inclusion in the
   study if liver imaging (computed tomography [CT], magnetic resonance imaging [MRI],
   positron emission tomography [PET]-CT, or PET scan) performed within 90 days prior to
   randomization does not demonstrate metastatic disease and the above requirements are
   met

   - Patients with alkaline phosphatase that is > ULN but =< 2.5 x ULN or unexplained bone
   pain are eligible for inclusion in the study if a bone scan, PET-CT scan, or PET scan
   performed within 90 days prior to randomization does not demonstrate metastatic
   disease

   - The most recent postoperative serum creatinine performed within 6 weeks prior to
   randomization must be =< ULN for the lab

   - Left ventricular ejection fraction (LVEF) assessment must be performed within 90 days
   prior to randomization; LVEF assessment performed by 2-dimensional (D) echocardiogram
   is preferred, however, multi-gated acquisition (MUGA) scan maybe substituted based on
   institutional preferences

      - For patients who will receive the TC chemotherapy regimen, the LVEF must be >=
      50% regardless of the cardiac imaging facility's lower limit of normal

      - For patients who will receive the AC-->WP chemotherapy regimen, the LVEF must be
      >= 55% regardless of the cardiac imaging facility's lower limit of normal

      - NOTE: Since the pre-entry LVEF serves as the baseline for comparing subsequent
      LVEF assessments, it is critical that this baseline study be an accurate
      assessment; if the baseline LVEF is > 70%, the investigator is encouraged to have
      the accuracy of the initial LVEF result confirmed and repeat the test if the
      accuracy is uncertain

Exclusion Criteria:

   - Primary tumor with any of the following HER2 testing results:

      - IHC staining intensity:

         - 0 on all evaluations of specimens

         - 3+ on evaluation of any specimen

      - ISH with a ratio of HER2 to CEP17 >= 2.0 on evaluation of any specimen

      - ISH result indicating HER2 gene copy number >= 4 per nucleus on evaluation of any
      specimen

   - T4 tumors including inflammatory breast cancer

   - Definitive clinical or radiologic evidence of metastatic disease

      - NOTE: Chest imaging (mandatory for all patients) and other imaging (if required)
      must have been performed within 90 days prior to randomization

   - Synchronous or previous contralateral invasive breast cancer (patients with
   synchronous and/or previous contralateral DCIS or LCIS are eligible)

   - Any previous history of ipsilateral invasive breast cancer or ipsilateral DCIS;
   (patients with synchronous or previous ipsilateral LCIS are eligible)

   - History of non-breast malignancies (except for in situ cancers treated only by local
   excision and basal cell and squamous cell carcinomas of the skin) within 5 years prior
   to randomization

   - Previous therapy with anthracyclines, taxanes, or trastuzumab for any malignancy

   - Chemotherapy or HER2-targeted therapy administered for the currently diagnosed breast
   cancer prior to randomization

   - Whole-breast RT prior to randomization or partial-breast RT that cannot be completed
   on or before the date of randomization

   - Continued endocrine therapy such as raloxifene or tamoxifen (or other selective
   estrogen receptor modulator [SERM]) or an aromatase inhibitor; patients are eligible
   if these medications are discontinued prior to randomization

   - Any continued use of sex hormonal therapy, e.g., birth control pills, ovarian hormone
   replacement therapy; patients are eligible if these medications are discontinued prior
   to randomization

   - Cardiac disease (history of and/or active disease) that would preclude the use of the
   drugs included in the treatment regimens; this includes but is not confined to:

      - Active cardiac disease:

         - Angina pectoris that requires the current use of anti-anginal medication

         - Ventricular arrhythmias except for benign premature ventricular contractions

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

         - Conduction abnormality requiring a pacemaker

         - Valvular disease with documented compromise in cardiac function

         - Symptomatic pericarditis

      - History of cardiac disease:

         - Myocardial infarction documented by elevated cardiac enzymes or persistent
         regional wall abnormalities on assessment of left ventricle (LV) function

         - History of documented congestive heart failure (CHF)

         - Documented cardiomyopathy

   - Hypertension defined according to the following ineligibility criteria:

      - For patients who will receive TC (regardless of the patient's age): uncontrolled
      hypertension defined as sustained systolic blood pressure (BP) > 150 mm Hg or
      diastolic BP > 90 mm Hg; (patients with initial BP elevations are eligible if
      initiation or adjustment of BP medication lowers pressure to meet entry criteria)

      - For patients < 50 years old who will receive AC-->WP: uncontrolled hypertension
      defined as sustained systolic BP > 150 mm Hg or diastolic BP > 90 mm Hg; patients
      with initial BP elevations are eligible if initiation or adjustment of BP
      medication lowers pressure to meet entry criteria

      - For patients >= 50 years old who will receive AC-->WP:

         - Uncontrolled hypertension defined as sustained systolic BP > 150 mm Hg or
         diastolic BP > 90 mm Hg

         - Controlled hypertension (systolic BP =< 150 mm Hg and diastolic BP =< 90
         mmHg), if anti-hypertensive medication(s) are needed

      - NOTE: Patients who are not eligible based on the AC-WP regimen BP criteria but
      who meet the TC regimen BP criteria are eligible for B-47, if the intended
      chemotherapy regimen is changed to TC

   - Active hepatitis B or hepatitis C with abnormal liver function tests

   - Intrinsic lung disease resulting in dyspnea

   - Poorly controlled diabetes mellitus

   - Active infection or chronic infection requiring chronic suppressive antibiotics

   - Nervous system disorder (paresthesia, peripheral motor neuropathy, or peripheral
   sensory neuropathy) >= grade 2, per the Common Terminology Criteria for Adverse Events
   (CTCAE) version (v)4.0

   - Conditions that would prohibit administration of corticosteroids

   - Chronic daily treatment with corticosteroids with a dose of >= 10 mg/day
   methylprednisol one equivalent (excluding inhaled steroids)

   - Known hypersensitivity to any of the study drugs or excipients, e.g., polysorbate 80
   and Cremophor EL

   - Pregnancy or lactation at the time of study entry; (Note: pregnancy testing must be
   performed within 2 weeks prior to randomization according to institutional standards
   for women of childbearing potential)

   - Other non-malignant systemic disease that would preclude the patient from receiving
   study treatment or would prevent required follow-up

   - Psychiatric or addictive disorders or other conditions that, in the opinion of the
   investigator, would preclude the patient from meeting the study requirements

   - Use of any investigational product within 30 days prior to randomization

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
CCTO
650-498-7061
Not Recruiting