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Evaluation of exposure-response-safety relationship of model-informed low-dose 500 mg abiraterone acetate inprostate cancer patients
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作者 Edmund Chiong Ziteng Wang +13 位作者 Eleanor Jing Yi Cheong Yi Chen Yao Sin Mun Tham Revathi Periaswami Poh Choo Toh Ziting Wang Qing Hui Wu Woon Chau Tsang Arshvin Kesavan Alvin Seng Cheong Wong Patrick Thomas Wong felicia lim Shuaibing Liu Eric Chun Yong Chan 《Cancer Communications》 2025年第8期971-975,共5页
Prostate cancer is a common cancer among men world-wide.Large-scale clinicalstudies of the 1,000 mg daily dos-ing of abiraterone acetate(AA)have confirmed its antitu-mor efficacy in patients with metastatic hormone-se... Prostate cancer is a common cancer among men world-wide.Large-scale clinicalstudies of the 1,000 mg daily dos-ing of abiraterone acetate(AA)have confirmed its antitu-mor efficacy in patients with metastatic hormone-sensitiveprostate cancer(mHSPC)or metastatic castration-resistantprostate cancer(mCRPC),regardless of their cancer’sresponse to androgen deprivation therapy(ADT)or treat-ment duration.However,this dosage was indirectly jus-tified based on the absence of dose-limiting toxicities(DLTs)in prior phase I dose-escalation trials,where aplateau in the increase of upstream steroids relating tosecondary mineralocorticoid excess was observed at dosesgreater than 750 mg and up to 2,000 mg daily[1,2].Notably,prostate specific antigen(PSA)levels declined atall investigated doses(250 to 1,000 mg)[1,2]. 展开更多
关键词 androgen deprivation therapy adt prostate cancer abiraterone acetate aa SAFETY model informed low dose exposure response abiraterone acetate
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