Springer Nature, Mairangi Bay, Private Bag 65901, Auckland, 0754, New Zealand.
Drugs. 2024 Mar;84(3):337-346. doi: 10.1007/s40265-024-01998-6.
Capivasertib (Truqap™) is an orally available, small-molecule pan-AKT inhibitor being developed by AstraZeneca for the treatment of various cancers, including breast and prostate cancers. Capivasertib received its first approval, in the USA, in November 2023 for use in combination with fulvestrant for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor 2 (HER2)-negative, locally advanced or metastatic breast cancer with one or more PIK3CA/AKT1/PTEN-alterations following progression on at least one endocrine-based regimen in the metastatic setting or recurrence on or within 12 months of completing adjuvant therapy. Capivasertib is also under regulatory review for HR-positive, HER2-negative breast cancer in the EU and several other countries, and in phase III clinical development for use (in combination with other anti-cancer agents) in the treatment of triple-negative breast cancer, castration-resistant prostate cancer, and hormone-sensitive prostate cancer. This article summarizes the milestones in the development of capivasertib leading to this first approval for HR-positive, HER2-negative, locally advanced or metastatic breast cancer.
卡匹维泮(Truqap)是一种口服小分子泛 AKT 抑制剂,由阿斯利康公司研发,用于治疗多种癌症,包括乳腺癌和前列腺癌。卡匹维泮于 2023 年 11 月在美国首次获得批准,与氟维司群联合用于治疗激素受体(HR)阳性、人表皮生长因子 2(HER2)阴性、局部晚期或转移性乳腺癌的成年患者,这些患者在转移性环境中至少接受过一种基于内分泌的方案治疗后进展,或在辅助治疗完成后 12 个月内复发,且存在一个或多个 PIK3CA/AKT1/PTEN 改变。卡匹维泮在欧盟和其他几个国家也正在接受 HR 阳性、HER2 阴性乳腺癌的监管审查,并且正在进行 III 期临床开发,用于联合其他抗癌药物治疗三阴性乳腺癌、去势抵抗性前列腺癌和激素敏感性前列腺癌。本文总结了卡匹维泮的开发里程碑,这些里程碑导致了其在 HR 阳性、HER2 阴性、局部晚期或转移性乳腺癌中的首次批准。