Targeting HER2/HER3 co‐mutations in metastatic breast cancer: Case reports of exceptional responders to trastuzumab and pertuzumab therapy

Author:

Blas Page E.1ORCID,Rodriguez Esther San Roman1,Williams Heather L.1,Levin Maren K.1,Bell Joshua S. K.2,Pierobon Mariaelena3,Barrett Alexander S.2,Petricoin Emanuel F.3,O'Shaughnessy Joyce A.4

Affiliation:

1. Clinical Oncology Research Coordination Baylor Scott and White Research Institute Dallas Texas USA

2. Department of Translational Science Tempus Labs Inc. Chicago Illinois USA

3. Center for Applied Proteomics and Molecular Medicine George Mason University Manassas Virginia USA

4. Breast Cancer Research Program Baylor University Medical Center, Texas Oncology, US Oncology Dallas Texas USA

Abstract

AbstractBackgroundOverexpression of HER2 plays an important role in cancer progression and is the target of multiple therapies in HER2‐positive breast cancer. Recent studies have also highlighted the presence of activating mutations in HER2, and HER3 that are predicted to enhance HER2 downstream pathway activation in a HER2‐dependent manner.MethodsIn this report, we present two exceptional responses in hormone receptor‐positive, HER2‐nonamplified, HER2/HER3 co‐mutated metastatic breast cancer patients who were treated with the anti‐HER2‐directed monoclonal antibodies, trastuzumab and pertuzumab.ResultsBoth patients acheived exceptional responses to treatment, suggesting that combined trastuzumab, pertuzumab, and endocrine therapy could be a highly effective therapy for these patients and our observations could help prioritize trastuzumab deruxtecan as an early therapeutic choice for patients whose cancers have activating mutations in HER2.

Publisher

Wiley

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