The purpose of this study is to compare the incidence of cardiac dysfunction in subjects with human epidermal growth factor receptor 2 (HER2) positive breast cancer treated with either doxorubicin or pegylated liposomal doxorubicin (PLD), both in combination with trastuzumab.

Inclusion Criteria:

• Subjects with operable, node-positive or high-risk node-negative (see #3 below) HER2-positive breast carcinoma are eligible for the study, provided they satisfy the following criteria.

  • Subjects must demonstrate willingness to and be able to participate in the study and to adhere to dose and visit schedules

  • Subjects must be of female gender and >= 18 years of age

  • Subjects must have been diagnosed with operable, histologically confirmed adenocarcinoma of the breast with no clinical or radiological evidence of metastatic disease but with otherwise high or intermediate risk tumor characteristics:

    • node-positive: T1-3, N1-2, M0 (level of T [tumor involvement], N [lymph node involvement], & M [matastases]) OR

    • node-negative AND at least one of the following features:

      • Tumor >2 cm or

      • Tumor >1 cm and

        • Negative estrogen receptor/progesterone receptor (ER/PR) or
        • Malignancy Grade 2-3 or
        • Presence of peritumoral vascular invasion or
        • Age <35 years

  • HER2-positive by fluorescence in situ hybridization (FISH)(with gene amplification) or 3+ using

immunohistochemistry

• Subjects must have had complete resection (R0) of the primary tumor and axillary lymph nodes (or must have negative sentinel node[s])
• Baseline left ventricular ejection fraction (LVEF) by multiple gated acquisition (MUGA) scan or echocardiogram (ECHO) >=55%
• Easter Cooperative Oncology Group (ECOG)-performance status of 0-1
• Adequate postoperative bone marrow function with neutrophils >=1.5 x 10^9/l, platelets >=100 x 10^9/l and hemoglobin >= lower limit of normal (LLN)
• Adequate renal function: calculated creatinine clearance >=50 ml/min
• Adequate postoperative liver function with a total bilirubin < upper limit of normal (ULN), alkaline phosphatase <2.5 times the ULN and aspartate aminotransferase (AST) <1.5 times the ULN
• Subjects must be free of any clinically relevant disease that would, in the principal investigator's and/or sponsor's opinion, interfere with the conduct of the study or study evaluations
• Subjects of childbearing potential (including women who are less than one year postmenopausal and will be sexually active during the study) must agree to use a medically accepted method of contraception, while receiving protocol-specified medication and for 30 days (or as per local requirements) after stopping the medication or be surgically sterilized prior to screening
• Subjects must be able to provide written informed consent

Exclusion Criteria:

• Subject who meets any of the following exclusion criteria will be disqualified from participation in the study:

  • Clinical or radiological evidence of metastatic disease

  • Prior radiotherapy, chemotherapy or biotherapy for the currently diagnosed breast cancer prior to randomization

  • Clinically significant pericardial effusion

  • Serious cardiac illness including, but not confined to

    • history of documented congestive heart failure
    • history of any form of cardiomyopathy or active treatment for any form of cardiomyopathy
    • history of angina pectoris or documented transmural myocardial infarction, or active angina pectoris requiring medication
    • serious ventricular arrhythmias requiring medication or implantable cardioverter-defibrillator (ICD) therapy, uncontrolled supraventricular arrhythmias
    • clinically significant valvular disease
    • poorly controlled arterial hypertension (systolic blood pressure (BP) >180 mmHg, diastolic BP >100 mmHg)

  • Sensory/motor neuropathy > grade 2 as defined by National Cancer Institure - Common Toxicity Criteria (NCI-CTC)

  • Pregnancy, or intending to become pregnant during the study

  • Nursing (breastfeeding) or intending to be nursing during the study

  • Any of the following clinical conditions:

    • Chronic obstructive pulmonary disease, requiring chronic treatment
    • Clinically significant active infections
    • A history of a psychological illness of condition, preventing the subject to understand the requirements of the study
    • Unstable regulation of diabetes mellitus

  • A situation or condition that, in the opinion of the investigator, may interfere with optimal participation in the study

  • Is on staff, affiliated with, or a family member of the staff personnel directly involved with this study

  • Usage of any investigational product within 30 days prior to enrollment

  • Participation in any other interventional clinical study involving drug, device or biological. This would not prohibit the patient from participating in a quality of life (QOL), questionnaire, blood collection, or observational study.

  • Allergy to or sensitivity to the study drug or its excipients

http://www.merck.com/clinical-trials/pdf/Merck%20Procedure%20on%20Clinical%20Trial%20Data%20Access%20Final\_Updated%20July\_9\_2014.pdf

http://engagezone.msd.com/ds\_documentation.php

The principal investigators (PIs) agree not to publish/publicly present any interim study results without prior sponsor written consent. The PIs further agree to provide 45 days written notice to the sponsor, prior to submission for publication or presentation, to permit the sponsor to review abstracts/manuscripts, which report any study results. The sponsor has the right to review/comment. If the parties disagree, the PIs agree to meet with the sponsor, prior to submission, to discuss/resolve.