Real-world treatment patterns and outcomes of abemaciclib for the treatment of HR + , HER2- metastatic breast cancer patients in Japan.


Journal

Breast cancer (Tokyo, Japan)
ISSN: 1880-4233
Titre abrégé: Breast Cancer
Pays: Japan
ID NLM: 100888201

Informations de publication

Date de publication:
Jul 2023
Historique:
received: 13 01 2023
accepted: 08 04 2023
medline: 23 6 2023
pubmed: 23 5 2023
entrez: 22 5 2023
Statut: ppublish

Résumé

This study described, in routine clinical practice in Japan, the patient characteristics, treatment patterns, and outcomes of female patients with HR + /HER2- metastatic breast cancer (MBC) who started abemaciclib treatment. Clinical charts were reviewed for patients starting abemaciclib in 12/2018-08/2021 with a minimum of 3 months follow-up data post-abemaciclib initiation regardless of abemaciclib discontinuation. Patient characteristics, treatment patterns, and tumor response were descriptively summarized. Kaplan-Meier curves estimated progression-free survival (PFS). 200 patients from 14 institutions were included. At abemaciclib initiation, median age was 59 years, and the Eastern Cooperative Oncology Group performance status score was 0/1/2 for 102/68/5 patients (58.3/38.9/2.9%), respectively. Most had an abemaciclib starting dose of 150 mg (92.5%). The percentage of patients receiving abemaciclib as 1st, 2nd, or 3rd line treatment was 31.5%, 25.8%, and 25.2%, respectively. The most frequent endocrine therapy drugs used with abemaciclib were fulvestrant (59%) and aromatase inhibitors (40%). Evaluation of tumor response was available for 171 patients, 30.4% of whom had complete/partial response. Median PFS was 13.0 months (95% CI 10.1-15.8 months). In a routine clinical practice setting in Japan, patients with HR + , HER2- MBC appear to benefit from abemaciclib treatment in terms of treatment response and median PFS, with the results broadly reflecting the evidence demonstrated in clinical trials.

Identifiants

pubmed: 37217763
doi: 10.1007/s12282-023-01461-6
pii: 10.1007/s12282-023-01461-6
pmc: PMC10284953
doi:

Substances chimiques

abemaciclib 60UAB198HK
Aminopyridines 0
Fulvestrant 22X328QOC4
Receptor, ErbB-2 EC 2.7.10.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

657-665

Informations de copyright

© 2023. The Author(s).

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Auteurs

K Nozawa (K)

Department of Breast Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.

M Terada (M)

Department of Breast Surgery, Graduate School of Medical Sciences, Nagoya City University, Nagoya, Japan.

M Onishi (M)

Department of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.

Y Ozaki (Y)

Department of Breast Medical Oncology, Breast Oncology Center, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.

T Takano (T)

Department of Breast Medical Oncology, Breast Oncology Center, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.

W Fakhouri (W)

Eli Lilly and Company, Indianapolis, IN, USA.

D Novick (D)

Eli Lilly and Company, Indianapolis, IN, USA.

J M Haro (JM)

Parc Sanitari Sant Joan de Déu, Universitat de Barcelona, Sant Boi de Llobregat, Barcelona, Spain.

L H Faris (LH)

Parc Sanitari Sant Joan de Déu, Universitat de Barcelona, Sant Boi de Llobregat, Barcelona, Spain.

T Kawaguchi (T)

Eli Lilly and Company, Indianapolis, IN, USA.

Y Tanizawa (Y)

Eli Lilly and Company, Indianapolis, IN, USA.

Junji Tsurutani (J)

Advanced Cancer Translational Research Institute, Showa University, Tokyo, Japan. tsurutaj@med.showa-u.ac.jp.

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