Health Care Resource Utilization and Costs for Metastatic Breast Cancer Patients Newly Treated with Human Epidermal Growth Factor Receptor 2 (HER2)-Targeted Agents.


Journal

Clinical breast cancer
ISSN: 1938-0666
Titre abrégé: Clin Breast Cancer
Pays: United States
ID NLM: 100898731

Informations de publication

Date de publication:
06 2022
Historique:
received: 26 08 2021
revised: 03 11 2021
accepted: 27 11 2021
pubmed: 25 1 2022
medline: 1 6 2022
entrez: 24 1 2022
Statut: ppublish

Résumé

HER2-positive metastatic breast cancer (mBC) is an incurable disease associated with years of chronic therapy and excess cost. HER2-targeted therapies have shown survival benefit for early-stage and mBC; however, the economic impact of these therapies has not been fully assessed. We evaluated health care resource use (HCRU) and costs of mBC patients treated with HER2-targeted therapy. This was a retrospective cohort study using the IQVIA Real-World Data Adjudicated Claims Database (July 1, 2014 to July 31, 2019). Female patients aged ≥18 years with mBC who initiated HER2-targeted therapy in the prior year were identified. The index date was the initiation date of the HER2-targeted agent, after which patients were required to have ≥12 months of follow-up. Annual and cumulative all-cause and BC-related costs (2019 USD) and annual BC-related HCRU were computed in years 1, 2, and 3 following the index date. Following the initiation of HER2-targeted therapy, the mean annual total all-cause costs per patient in years 1 (n = 423), 2 (n = 357), and 3 (n = 166) were $320,892 (SD: $224,343), $235,159 (SD: $185,287), and $226,254 (SD: $197,901), respectively. The mean annual total BC-related costs were $240,048 (SD: $151,230), $175,631 (SD: $148,058), and $165,506 (SD: $159,374) in years 1, 2, and 3, respectively. A major portion of BC-related costs were costs associated with HER2-targeted treatment. The 3-year cumulative all-cause and BC-related total costs were $769,573 (SD: $456,920) and $624,455 (SD: $401,319), respectively. Treatment of HER2-positive mBC is a substantial economic burden. A potential approach to minimizing cost and HCRU is to prevent recurrence.

Identifiants

pubmed: 35067467
pii: S1526-8209(21)00349-9
doi: 10.1016/j.clbc.2021.11.013
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e488-e496

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Reshma Mahtani (R)

Baptist Health South Florida, Plantation, Florida, United States. Electronic address: rmahtani@baptisthealth.net.

Nina Oestreicher (N)

Puma Biotechnology, Inc., University of California, Department of Clinical Pharmacy, San Francisco, CA.

Deepa Lalla (D)

Puma Biotechnology, Inc., Los Angeles, CA.

Augustina Ogbonnaya (A)

Xcenda, LLC, Carrollton, TX.

Vishal Saundankar (V)

Xcenda, LLC, Carrollton, TX.

Joanne Willey (J)

Xcenda, LLC, Carrollton, TX.

Anna D Coutinho (AD)

Xcenda, LLC, Carrollton, TX.

Kelly McCann (K)

University of California, Los Angeles, Los Angeles, CA.

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Classifications MeSH