Treatment Patterns and Health Outcomes among Patients with HER2 IHC0/-Low Metastatic or Recurrent Breast Cancer

Author:

Farah Eliya12,Carbonell Chantelle12ORCID,Boyne Devon J.12ORCID,Brenner Darren R.12,Henning Jan-Willem1ORCID,Moldaver Daniel3,Shokar Simran3,Cheung Winson Y.12

Affiliation:

1. Department of Oncology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 1N4, Canada

2. Department of Community Health Sciences, University of Calgary, Calgary, AB T2N 1N4, Canada

3. AstraZeneca Canada Inc., Mississauga, ON L4Y 1M4, Canada

Abstract

Improved understanding of the biological heterogeneity of breast cancer (BC) has facilitated the development of more effective and personalized approaches to treatment. This study describes real-world evidence on treatment patterns and outcomes for a population-based cohort of patients with human epidermal growth factor receptor (HER2) IHC0 and -low BC with de novo or recurrent disease from Alberta, Canada. Patients 18+ years old diagnosed with HER2 IHC0/-low, de novo/recurrent BC from 2010 to 2019 were identified using Alberta’s cancer registry. Analyses of these patients’ existing electronic medical records and administrative claims data were conducted to examine patient characteristics, treatment patterns, and survival outcomes. A total of 3413 patients were included in the study, of which 72.10% initiated first line hormonal and non-hormonal systemic therapy. The 1-year overall survival (OS) was 81.09% [95% CI, 79.52–82.69]. Recurrent patients had a higher OS compared to de novo patients: 54.30 months [95% CI, 47.80–61.90] vs. 31.5 months [95% CI, 28.40–35.90], respectively. Median OS was 43.4 months [95% CI, 40.70–47.10] and 35.80 months [95% CI, 29.00–41.70] among patients with HER2-low and HER2 IHC0 cancer, respectively. The study results provide real-world evidence regarding the clinical outcomes of HER2 IHC0/-low and de novo/recurrent disease.

Funder

AstraZeneca Canada Inc.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

Reference32 articles.

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3. Biological subtypes of breast cancer: Prognostic and therapeutic implications;Yersal;World J. Clin. Oncol.,2014

4. Performance of Three-Biomarker Immunohistochemistry for Intrinsic Breast Cancer Subtyping in the AMBER Consortium;Allott;Cancer Epidemiol. Biomark. Prev.,2016

5. Treatment Landscape for Patients with HER2-Positive Metastatic Breast Cancer: A Review on Emerging Treatment Options;Gampenrieder;Cancer Manag. Res.,2020

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