A real-world, retrospective, observational study examining treatment patterns and clinical outcomes in patients with FLT3m + AML in Japan.

FLT3i FLT3m + AML allogeneic HSCT anthracycline chemotherapy cytarabine

Journal

Current medical research and opinion
ISSN: 1473-4877
Titre abrégé: Curr Med Res Opin
Pays: England
ID NLM: 0351014

Informations de publication

Date de publication:
26 Oct 2023
Historique:
pubmed: 26 10 2023
medline: 26 10 2023
entrez: 26 10 2023
Statut: aheadofprint

Résumé

Acute myeloid leukemia (AML) is the most common form of leukemia among adults in Japan. This study aimed to understand the treatment patterns, health care resource utilization, and costs of FMS-like tyrosine kinase 3 mutation-positive (FLT3m+) AML patients in Japan. A retrospective cohort study of Japanese FLT3m + AML patients was conducted using data extracted from a national hospital-based claims database provided by Medical Data Vision Co. Ltd. (MDV; Tokyo, Japan). Patients were identified from the MDV database between April 2008 and April 2021 inclusive. A total of 360 patients were included in this study. The study results suggest that cytarabine + anthracyclines was the most common first-line (1 L) treatment, accounting for 41.3% of the patients. FLT3 inhibitors (FLT3i) was the most common treatment across the study period (95.7%). The mean age of patients was 62.4 years, and most were 65 years or older. The median overall survival (OS) after initiating FLT3i treatment was 394 days. The median treatment duration of FLT3i was 88.5 days, while it was 66.0 days for patients treated with FLT3i within 60 days after hematopoietic stem cell transplantation (HSCT). The overall mean monthly total treatment cost was JPY 2,009,531.7/per patient per month (PPPM) (USD 17,967.9/PPPM). The study found specific treatment patterns, trends and features in patients with FLT3m + AML. FLT3i was the most prescribed treatment across the study period and the overall median OS after initiating FLT3i treatment was over 1 year. The findings of this study could be helpful for clinicians to optimize treatment strategies for FLT3m + AML in Japan.

Identifiants

pubmed: 37881860
doi: 10.1080/03007995.2023.2271390
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-10

Auteurs

Toru Kiguchi (T)

Dokkyo Medical University Saitama Medical Center, Saitama, Japan.

Masaya Sakurai (M)

Astellas Pharma Inc., Tokyo, Japan.

Yusuke Tanaka (Y)

Astellas Pharma Inc., Tokyo, Japan.

Kazuyuki Kuramoto (K)

Astellas Pharma Inc., Tokyo, Japan.

Yuki Kado (Y)

IQVIA Solutions Japan K.K., Tokyo, Japan.

Sono Sawada (S)

IQVIA Solutions Japan K.K., Tokyo, Japan.

Takeshi Mitomi (T)

Astellas Pharma Inc., Tokyo, Japan.

Classifications MeSH