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

HER2 IHC0 HER2 negative HER2-low metastatic breast cancer overall survival recurrent breast cancer

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
25 Jan 2024
Historique:
received: 27 11 2023
revised: 10 01 2024
accepted: 22 01 2024
medline: 10 2 2024
pubmed: 10 2 2024
entrez: 10 2 2024
Statut: epublish

Résumé

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.

Identifiants

pubmed: 38339269
pii: cancers16030518
doi: 10.3390/cancers16030518
pii:
doi:

Types de publication

Journal Article

Langues

eng

Auteurs

Eliya Farah (E)

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

Chantelle Carbonell (C)

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

Devon J Boyne (DJ)

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

Darren R Brenner (DR)

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

Jan-Willem Henning (JW)

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

Daniel Moldaver (D)

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

Simran Shokar (S)

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

Winson Y Cheung (WY)

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

Classifications MeSH