HER2 quantitative continuous scoring for accurate patient selection in HER2-negative trastuzumab deruxtecan–treated breast cancer

Author:

Kapil Ansh1,Spitzmüller Andreas1,Brieu Nicolas1,Haneder Susanne1,Shumilov Anatoliy1,Meier Armin1,Cecchi Fabiola2,Barkell Alice2,Harder Nathalie1,Schneider Katrin1,Hidalgo-Sastre Ana1,Alleze Regina1,Schick Markus1,Schmidt Günter1,Sade Hadassah1,Tsuchihashi Zenta3,Suto Fumitaka3,Gustavson Mark2,Barrett J. Carl2,Carroll Danielle2

Affiliation:

1. Computational Pathology, Oncology R&D, AstraZeneca

2. Translational Medicine, Oncology R&D, AstraZeneca

3. Translational Science, Daiichi Sankyo, Inc.

Abstract

Abstract Many targeted cancer therapies rely on biomarkers assessed by scoring of immunohistochemically (IHC)-stained tissue, which is subjective, semiquantitative, and does not account for expression heterogeneity. We describe an image analysis-based method for quantitative continuous scoring (QCS) of digital whole-slide images acquired from baseline human epidermal growth factor receptor 2 (HER2) IHC-stained breast cancer tissue. Candidate signatures for patient stratification using QCS of HER2 expression on subcellular compartments were identified, addressing the spatial distribution of tumor cells and tumor-infiltrating lymphocytes. Using data from trastuzumab deruxtecan-treated patients with HER2-positive and HER2-negative breast cancer from a phase 1 study (NCT02564900; DS8201-A-J101; N = 151), QCS-based patient stratification showed longer progression-free survival (14.8 vs 8.6 months) with higher prevalence of patient selection (76.4 vs 56.9%) and a better cross-validated log-rank p value (0.026 vs 0.26) than manual scoring based on the American Society of Clinical Oncology / College of American Pathologists guidelines. QCS-based features enriched the HER2-negative subgroup by correctly predicting 20 of 26 responders.

Publisher

Research Square Platform LLC

Reference15 articles.

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