Real-World Treatment Patterns and Outcomes of Palbociclib Plus an Aromatase Inhibitor for Metastatic Breast Cancer: Flatiron Database Analysis.


Journal

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

Informations de publication

Date de publication:
08 2022
Historique:
received: 21 12 2021
revised: 11 03 2022
accepted: 01 05 2022
pubmed: 2 6 2022
medline: 2 8 2022
entrez: 1 6 2022
Statut: ppublish

Résumé

To describe real-world treatment patterns and effectiveness of first-line palbociclib plus an aromatase inhibitor (PAL+AI) and examine the association between PAL initial dose and effectiveness among patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative metastatic/advanced breast cancer (HR+/HER2- MBC) in routine clinical practice. This retrospective analysis used Flatiron Health's database of electronic health records from >280 cancer clinics representing >2.4 million actively treated cancer patients in the United States. Women with HR+/HER2- MBC who received first-line PAL+AI were included. Real-world progression-free survival (rwPFS) was defined as the time from starting PAL+AI to death or disease progression. Real-world best tumor response (rwBTR) was assessed based on the treating clinician's assessment of radiologic evidence for change in disease burden. Of 813 eligible patients, median age was 65.0 years, and median follow-up was 21.0 months. PAL was initiated at 125 mg/d and 75/100 mg/d in 86.5% and 13.5% of patients, respectively. Median duration of PAL+AI was 16.3 months. 43.0% of patients discontinued PAL+ AI; 11.0% discontinued because of toxicity. Median time to subsequent therapy and chemotherapy was 24.6 and 36.6 months, respectively. Median rwPFS was 20.0 months, and best rwBTR rate was 51.9%. Patients starting PAL at 125 versus 75/100 mg/d had longer median rwPFS (27.8 vs. 18.6 months) and higher rwBTR rate (54.0% vs. 40.4%). These data demonstrate the benefit of PAL+AI in routine clinical practice and may support the initiation of palbociclib at the recommended dose of 125 mg/d for HR+/HER2- MBC. NCT04176354, November 25, 2019.

Identifiants

pubmed: 35643624
pii: S1526-8209(22)00081-7
doi: 10.1016/j.clbc.2022.05.002
pii:
doi:

Substances chimiques

Aromatase Inhibitors 0
Piperazines 0
Pyridines 0
Receptors, Estrogen 0
Receptor, ErbB-2 EC 2.7.10.1
palbociclib G9ZF61LE7G

Banques de données

ClinicalTrials.gov
['NCT04176354']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

601-610

Informations de copyright

Copyright © 2022. Published by Elsevier Inc.

Auteurs

Debra Patt (D)

Texas Oncology-Austin Central, Austin, TX. Electronic address: Debra.Patt@Usoncology.Com.

Xianchen Liu (X)

Pfizer Inc, New York, NY. Electronic address: Jasonxc.Liu@pfizer.com.

Benjamin Li (B)

Pfizer Inc, New York, NY.

Lynn McRoy (L)

Pfizer Inc, New York, NY.

Rachel M Layman (RM)

The University of Texas MD Anderson Cancer Center, Houston, TX.

Adam Brufsky (A)

UPMC Hillman Cancer Center, University of Pittsburgh Medical Center, College of Medicine, Pittsburgh, PA.

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Classifications MeSH