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摘要
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卡米泽斯特(Etcamah®)是一种口服可用的强效选择性雌激素受体降解剂(SERD)和完全雌激素受体(ER)α拮抗剂,由阿斯利康公司开发用于治疗乳腺癌。该药物于2025年5月在阿联酋首次获得批准。截至本文撰写时,该药物已相继在沙特阿拉伯、日本、欧盟、加拿大、英国和美国获得批准。对于携带可检测ESR1突变的ER阳性、HER2阴性乳腺癌患者,在继续使用相同CDK4/6抑制剂的同时换用卡米泽斯特,与继续使用芳香化酶抑制剂联合CDK4/6抑制剂治疗相比,显著延长了无进展生存期。本文总结了卡米泽斯特在开发过程中的关键里程碑,这些里程碑促成了其首次批准用于治疗携带ESR1基因突变(该突变在一线激素治疗期间出现)的局部晚期或转移性激素受体阳性(HR+)、HER2阴性乳腺癌成人患者,联合CDK4/6抑制剂。
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14.4
论文数:
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被引数:
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引用论文
Metastatic breast cancer: ESMO Clinical Practice Guideline for diagnosis, treatment and follow-up†转移性乳腺癌: ESMO诊断、治疗和随访临床实践指南 †
Annals of Oncology
IF65.4
Heterogeneity and clinical significance of ESR1 mutations in ER-positive metastatic breast cancer patients receiving fulvestrant
NATURE COMMUNICATIONS
IF15.7
A phase I dose escalation and expansion trial of the next-generation oral SERD camizestrant in women with ER-positive, HER2-negative advanced breast cancer: SERENA-1 monotherapy results在ER阳性,HER2-negative晚期乳腺癌女性中,下一代口服SERD camizestrant的I期剂量递增和扩展试验: SERENA-1单药治疗结果
ANNALS OF ONCOLOGY
IF65.4
Abstract PS1-10-28: Phase 1/2a trial of new generation PARP1-selective inhibitor saruparib + next generation selective ER degrader (SERD) camizestrant in patients (pts) with advanced/relapsed ER+/HER2-negative or low (HER2−) breast cancer (PETRA Module 6)新一代PARP1选择性抑制剂saruparib与下一代选择性ER降解剂(SERD)camizestrant联合治疗晚期/复发性ER+/HER2阴性或低表达(HER2−)乳腺癌患者的1/2a期临床试验(PETRA Module 6)[摘要编号PS1-10-28]
Pharmacodynamics of Camizestrant Treatment in Postmenopausal Women With Estrogen Receptor–Positive, Human Epidermal Growth Factor Receptor 2–Negative Primary Breast Cancer: Results From the Randomized, Presurgical SERENA-3 Study在雌激素受体阳性、人表皮生长因子受体2阴性原发性乳腺癌的绝经后女性中卡米泽斯特抗治疗的药效学:来自随机、术前SERENA-3研究的结 果
Camizestrant, a next-generation oral SERD, versus fulvestrant in post-menopausal women with oestrogen receptor-positive, HER2-negative advanced breast cancer (SERENA-2): a multi-dose, open-label, randomised, phase 2 trialCamizestrant,一种下一代口服SERD,与fulvestrant对比用于绝经后雌激素受体阳性、HER2阴性晚期乳腺癌患者(SERENA-2):一项多剂量、开放标签、随机化、II期临床试验

