医学
卵巢癌
药代动力学
肿瘤科
内科学
人口
癌症
妇科
环境卫生
作者
Bradley J. Monk,Ignacio Romero,Whitney A. Spannuth Graybill,Cristina Churruca,David M. O’Malley,Anja Ør Knudsen,O.W. Stephanie Yap,Jean‐François Baurain,Peter G. Rose,Hannelore Denys,Sharad Ghamande,Carmela Pisano,Michel Fabbro,Elena Ioana Braicu,Paula Calvert,Amnon Amit,Emily Prendergast,Adekemi Taylor,Leila Kheibarshekan,Zhiyi Zhang
标识
DOI:10.1016/j.clinthera.2024.06.001
摘要
Niraparib is a poly(adenosine diphosphate [ADP]-ribose) polymerase inhibitor approved for the maintenance treatment of advanced ovarian cancer (OC). Niraparib was originally approved in recurrent OC at a fixed starting dose (FSD) of 300 mg once daily (QD). This analysis characterized the population pharmacokinetics (PK) of niraparib and evaluated the relationships between exposure, efficacy, and safety to support clinical use of an individualized dosing strategy, in which the starting dose of niraparib was adjusted based on patient characteristics to improve the benefit-risk profile.
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