醋酸阿比特龙酯
医学
强的松
前列腺癌
阿比曲酮
肿瘤科
阉割
内科学
泌尿科
癌症
雄激素剥夺疗法
激素
雄激素受体
作者
Kim N.,Elena Castro,G. Attard,Matthew R. Smith,Shahneen Sandhu,Eleni Efstathiou,Guilhem Roubaud,Eric J. Small,A Gomes,Dana E. Rathkopf,Marniza Saad,Howard Gurney,Wonho Jung,Won Kim,Shiva Dibaj,Daphne Wu,Jenny Zhang,Angela Lopez‐Gitlitz,Peter Francis,David Olmos
标识
DOI:10.1016/j.euo.2025.04.012
摘要
BACKGROUND AND OBJECTIVE: ), particularly in BRCA1/2. METHODS: Patients were prospectively screened for HRR alterations and randomized 1:1 to niraparib + AAP (n = 212) or placebo + AAP (n = 211). We report results from the prespecified, event-driven, final analysis of secondary efficacy endpoints. KEY FINDINGS AND LIMITATIONS: population (HR 0.688, 95% CI 0.499-0.950; p = 0.022) and the BRCA1/2 subgroup (HR 0.598, 95% CI 0.387-0.924; nominal p = 0.019) in comparison to placebo + AAP. The niraparib + AAP safety profile remains unchanged at longer follow-up; adverse events were primarily hematologic and manageable. CONCLUSIONS AND CLINICAL IMPLICATIONS: mCRPC, including those with the approved indication of BRCA-altered mCRPC, generally continue to benefit from first-line treatment with niraparib + AAP in comparison to placebo + AAP.
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