About this trial

This study gathers information from the blood cells and tumor tissue during treatment with anti-HER2 therapies, such as trastuzumab, pertuzumab, lapatinib, or neratinib, in patients with HER2 positive stage I-IV breast cancer who are scheduled to start anti-HER2 therapy. The information gained from this study may help researchers better understand the relation between cell response and anti-HER2 therapies.

Eligibility criteria

Qualifiers

Age >= 18 years

Histological confirmed adenocarcinoma of the breast stage I-IV from the American Joint Committee on Cancer staging 8th edition

Any estrogen receptor (ER) or progesterone receptor (PR) but HER2 positive defined as per the most current American Society of Clinical Oncology (ASCO)/College of American Pathologists (CAP) guideline

Provide written informed consent

Disqualifiers

Immunocompromised patients including patients known to be human immunodeficiency virus (HIV) positive

Receiving systemic steroid therapy or any other immunosuppressive therapy =< 30 days prior to registration. NOTE: Inhaled steroids, low-dose corticosteroids (e.g. equivalent to or less than oral prednisone 10 mg daily), and steroid use for primary prevention of nausea per institutional guidelines are allowed.

Trial design

Treatments tested in this trial

  • Biospecimen Collection

Treatment groups

230 Participants
are divided into 2 treatment groups

Locations

1
Mayo Clinic in Florida32224-9980, JacksonvilleFlorida, United States

Sponsors and collaborators

Mayo Clinic

Lead sponsor