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Fostamatinib for the treatment of Japanese patients with primary immune thrombocytopenia: A phase 3, placebo-controlled, double-blind, parallel-group study.
Kuwana, Masataka; Ito, Tomoki; Kowata, Shugo; Hatta, Yoshihiro; Fujimaki, Katsumichi; Naito, Kensuke; Kurahashi, Shingo; Kagoo, Toshiya; Tanimoto, Kazuki; Saotome, So; Tomiyama, Yoshiaki.
Afiliação
  • Kuwana M; Department of Allergy and Rheumatology, Nippon Medical School Graduate School of Medicine, Tokyo, Japan.
  • Ito T; First Department of Internal Medicine, Kansai Medical University, Osaka, Japan.
  • Kowata S; Division of Hematology and Oncology, Department of Internal Medicine, Iwate Medical University, Iwate, Japan.
  • Hatta Y; Department of Hematology and Rheumatology, Nihon University School of Medicine, Tokyo, Japan.
  • Fujimaki K; Department of Hematology, Fujisawa City Hospital, Kanagawa, Japan.
  • Naito K; Department of Hematology, Hamamatsu Medical Center, Shizuoka, Japan.
  • Kurahashi S; Department of Hematology and Oncology, Toyohashi Municipal Hospital, Aichi, Japan.
  • Kagoo T; Division of Hematology, Department of Internal Medicine, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
  • Tanimoto K; Hematology and Oncology Division, Japanese Red Cross Fukuoka Hospital, Fukuoka, Japan.
  • Saotome S; Kissei Pharmaceutical Co., Ltd., Tokyo, Japan.
  • Tomiyama Y; Department of Blood Transfusion, Osaka University Hospital, Osaka, Japan.
Br J Haematol ; 200(6): 802-811, 2023 03.
Article em En | MEDLINE | ID: mdl-36470677
ABSTRACT
Fostamatinib, a spleen tyrosine kinase inhibitor, has been approved for the treatment of chronic primary immune thrombocytopenia (ITP) in the United States, Canada and some European countries. We conducted a phase 3, placebo-controlled, double-blind, parallel-group study to evaluate the efficacy and safety of fostamatinib in Japanese patients with primary ITP. Thirty-four patients were randomised to fostamatinib (n = 22) or placebo (n = 12) at 100-150 mg twice a day for 24 weeks. Stable responses (platelet ≥50 000/µl at ≥4 of the 6 visits from weeks 14 to 24) were observed in eight (36%) patients on fostamatinib and in none of the patients on placebo (p = 0.030). Overall responses (platelet ≥50 000/µl at ≥1 of the 6 visits from weeks 2 to 12) were seen in 10 (45%) patients on fostamatinib and in none of the patients on placebo (p = 0.006). Patients on fostamatinib required rescue medication less often and experienced fewer bleeding symptoms than patients on placebo. Adverse events observed were mild or moderate and were manageable. No new safety signals were identified in Japanese patients with ITP.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Púrpura Trombocitopênica Idiopática Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Púrpura Trombocitopênica Idiopática Idioma: En Ano de publicação: 2023 Tipo de documento: Article