Gilteritinib versus chemotherapy in Japanese patients with FLT3-mutated relapsed/refractory acute myeloid leukemia.


Journal

International journal of clinical oncology
ISSN: 1437-7772
Titre abrégé: Int J Clin Oncol
Pays: Japan
ID NLM: 9616295

Informations de publication

Date de publication:
Nov 2021
Historique:
received: 30 04 2021
accepted: 26 07 2021
pubmed: 8 8 2021
medline: 21 10 2021
entrez: 7 8 2021
Statut: ppublish

Résumé

Until recently, no effective targeted therapies for FLT3-mutated (FLT3 We evaluated the Japanese subgroup (n = 48) of the ADMIRAL trial, which included 33 patients randomized to 120-mg/day gilteritinib and 15 randomized to SC. Median OS was 14.3 months in the gilteritinib arm and 9.6 months in the SC arm. The complete remission/complete remission with partial hematologic recovery rate was higher in the gilteritinib arm (48.5%) than in the SC arm (13.3%). After adjustment for drug exposure, fewer adverse events (AEs) occurred in the gilteritinib arm than in the SC arm. Common grade ≥ 3 AEs related to gilteritinib were febrile neutropenia (36%), decreased platelet count (27%), and anemia (24%). Findings in Japanese patients are consistent with those of the overall ADMIRAL study population.

Sections du résumé

BACKGROUND BACKGROUND
Until recently, no effective targeted therapies for FLT3-mutated (FLT3
METHODS METHODS
We evaluated the Japanese subgroup (n = 48) of the ADMIRAL trial, which included 33 patients randomized to 120-mg/day gilteritinib and 15 randomized to SC.
RESULTS RESULTS
Median OS was 14.3 months in the gilteritinib arm and 9.6 months in the SC arm. The complete remission/complete remission with partial hematologic recovery rate was higher in the gilteritinib arm (48.5%) than in the SC arm (13.3%). After adjustment for drug exposure, fewer adverse events (AEs) occurred in the gilteritinib arm than in the SC arm. Common grade ≥ 3 AEs related to gilteritinib were febrile neutropenia (36%), decreased platelet count (27%), and anemia (24%).
CONCLUSION CONCLUSIONS
Findings in Japanese patients are consistent with those of the overall ADMIRAL study population.

Identifiants

pubmed: 34363558
doi: 10.1007/s10147-021-02006-7
pii: 10.1007/s10147-021-02006-7
pmc: PMC8522999
doi:

Substances chimiques

Aniline Compounds 0
Pyrazines 0
gilteritinib 0
FLT3 protein, human EC 2.7.10.1
fms-Like Tyrosine Kinase 3 EC 2.7.10.1

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

2131-2141

Informations de copyright

© 2021. The Author(s).

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Auteurs

Naoko Hosono (N)

Department of Hematology and Oncology, Faculty of Medical Sciences, University of Fukui, Fukui, 910-1193, Japan. hosono@u-fukui.ac.jp.

Hisayuki Yokoyama (H)

Sendai Medical Center, Sendai, Japan.
Tohoku University, Sendai, Japan.

Nobuyuki Aotsuka (N)

Japanese Red Cross Narita Hospital, Narita, Japan.

Kiyoshi Ando (K)

Tokai University School of Medicine, Isehara, Japan.

Hiroatsu Iida (H)

NHO Nagoya Medical Center, Nagoya, Japan.

Takayuki Ishikawa (T)

Kobe City Medical Center General Hospital, Hyogo, Japan.

Kensuke Usuki (K)

NTT Medical Center Tokyo, Tokyo, Japan.

Masahiro Onozawa (M)

Hokkaido University, Sapporo, Japan.

Masahiro Kizaki (M)

Saitama Medical Center, Saitama Medical University, Kawagoe, Japan.

Kohmei Kubo (K)

Aomori Prefectural Central Hospital, Aomori, Japan.

Junya Kuroda (J)

Kyoto Prefectural University of Medicine, Kyoto, Japan.

Yukio Kobayashi (Y)

International University of Health and Welfare (IUHW), Mita Hospital, Tokyo, Japan.

Takayuki Shimizu (T)

Keio University School of Medicine, Tokyo, Japan.

Shigeru Chiba (S)

University of Tsukuba, Tsukuba, Japan.

Miho Nara (M)

Akita University, Akita, Japan.

Tomoko Hata (T)

Nagasaki University, Nagasaki, Japan.

Michihiro Hidaka (M)

Kumamoto Medical Center, Kumamoto, Japan.

Shin-Ichiro Fujiwara (SI)

Jichi Medical University, Shimotsuke, Japan.

Yoshinobu Maeda (Y)

Okayama University Hospital, Okayama, Japan.

Yasuyoshi Morita (Y)

Kindai University, Osaka, Japan.

Mikiko Kusano (M)

Astellas Pharma, Inc., Tokyo, Japan.

Qiaoyang Lu (Q)

Astellas Pharma US, Inc., Northbrook, IL, USA.

Shuichi Miyawaki (S)

Tokyo Metropolitan Ohtsuka Hospital, Tokyo, Japan.

Erhan Berrak (E)

Astellas Pharma US, Inc., Northbrook, IL, USA.

Nahla Hasabou (N)

Astellas Pharma US, Inc., Northbrook, IL, USA.

Tomoki Naoe (T)

NHO Nagoya Medical Center, Nagoya, Japan.

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Classifications MeSH