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Niraparib as maintenance therapy in Japan: a retrospective observational study using a Japanese claims database.
Motohashi, Takashi; Shimada, Muneaki; Tokunaga, Hideki; Kuwahara, Yuki; Kuwabara, Hiroyo; Kato, Ai; Tabata, Tsutomu.
Afiliación
  • Motohashi T; Department of Obstetrics and Gynecology, Tokyo Women's Medical University, Tokyo, Japan.
  • Shimada M; Department of Gynecology, Tohoku University Hospital, Sendai, Japan.
  • Tokunaga H; Department of Clinical Biobank, Tohoku University Advanced Research Center for Innovations in Next-Generation Medicine, Sendai, Japan. muneaki.shimada.b7@tohoku.ac.jp.
  • Kuwahara Y; Department of Gynecology, Graduate School of Medicine, Tohoku University, Sendai, Japan.
  • Kuwabara H; Division of Obstetrics and Gynecology, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan.
  • Kato A; Japan Medical Affairs, Japan Oncology Business Unit, Takeda Pharmaceutical Company Limited, Osaka, Japan.
  • Tabata T; Japan Medical Affairs, Japan Oncology Business Unit, Takeda Pharmaceutical Company Limited, Osaka, Japan.
J Gynecol Oncol ; 2024 Jul 04.
Article en En | MEDLINE | ID: mdl-39028152
ABSTRACT

OBJECTIVE:

Epithelial ovarian cancer (EOC) is the leading cause of female mortality in gynecologic malignancies, with a rising incidence in Japan. This study aimed to validate the treatment patterns and safety of niraparib as maintenance therapy for EOC following initial chemotherapy in clinical practice in Japan.

METHODS:

Leveraging claims data between April 2008 and December 2022, this descriptive study comprised EOC-diagnosed patients receiving initial platinum-based chemotherapy, debulking surgery, and niraparib as maintenance therapy. Patient characteristics, prescription status, transfusion details, and laboratory data were assessed and reported as summary statistics and frequencies.

RESULTS:

Among 291 patients, the median age was 64.0 years and 94.5% received a 200-mg daily dose of niraparib. At week 12, 78.7% (229/291) continued niraparib treatment, 21.3% (62/291) discontinued, and 52.2% (152/291) required treatment interruptions. Of the 62 patients who discontinued treatment, 27 patients initiated subsequent EOC treatment within 12 weeks following niraparib discontinuation. Blood transfusions were needed in 10.3% (30/291), and of 55 patients with available laboratory data, 61.8% (34/55) had decreased platelet count <100,000/µL, 25.5% (14/55) had decreased hemoglobin level <8 g/dL, and 22.7% (5/22) had decreased neutrophil count <1,000/µL, meeting the criteria for treatment interruption. Among those with thrombocytopenia, 88.2% (30/34) were able to either resume or continue treatment.

CONCLUSION:

Niraparib demonstrated favorable tolerability in Japanese patients with advanced EOC, with effective management of thrombocytopenia through dose adjustments and supportive care, supporting its viability as post-chemotherapy maintenance therapy.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Gynecol Oncol / J. gynecol. oncol. (Online) / Journal of gynecologic oncology (Online) Año: 2024 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Gynecol Oncol / J. gynecol. oncol. (Online) / Journal of gynecologic oncology (Online) Año: 2024 Tipo del documento: Article País de afiliación: Japón