Suppr超能文献

奥那司酮,一种孕酮受体拮抗剂,作为原发性乳腺癌的一线治疗药物。

Onapristone, a progesterone receptor antagonist, as first-line therapy in primary breast cancer.

作者信息

Robertson J F, Willsher P C, Winterbottom L, Blamey R W, Thorpe S

机构信息

Professorial Unit of Surgery, City Hospital, Nottingham, U.K.

出版信息

Eur J Cancer. 1999 Feb;35(2):214-8. doi: 10.1016/s0959-8049(98)00388-8.

Abstract

The progesterone receptor antagonist, Onapristone, is an effective endocrine agent in experimental breast cancer models. This study aimed to investigate this agent as first-line endocrine therapy in patients with breast cancer. However, owing to the recognition in this and other clinical studies that some patients on Onapristone developed liver function test abnormalities, the development of this drug and recruitment to the study stopped in 1995. 19 patients either with locally advanced breast cancer (n = 12) or who were elderly, unfit patients with primary breast cancer (n = 7) received Onapristone 100 mg/day. Seventeen of the 19 tumours expressed oestrogen receptors (ER) whilst 12 of the 18 tumours tested expressed progesterone receptors (PgR). Tumour remission was categorised by International Union Against Cancer criteria. One patient was withdrawn after 4.5 months while her disease was static. Of the remaining 18 patients, 10 (56%) showed a partial response and 2 (11%) durable static disease (> or = 6 months), giving an overall tumour remission rate of 67%. The median duration of remission was 70 weeks. Transient liver function test abnormalities developed in a number of patients, mainly during the first 6 weeks of treatment. In conclusion Onapristone can induce tumour responses in human breast cancer.

摘要

孕酮受体拮抗剂奥那司酮在实验性乳腺癌模型中是一种有效的内分泌药物。本研究旨在探讨该药物作为乳腺癌患者一线内分泌治疗的效果。然而,鉴于本研究及其他临床研究发现,一些服用奥那司酮的患者出现肝功能检查异常,该药物的研发及本研究的受试者招募于1995年停止。19例局部晚期乳腺癌患者(n = 12)或老年、身体状况不佳的原发性乳腺癌患者(n = 7)接受了每日100 mg的奥那司酮治疗。19个肿瘤中有17个表达雌激素受体(ER),而在检测的18个肿瘤中有12个表达孕激素受体(PgR)。肿瘤缓解情况根据国际抗癌联盟标准进行分类。1例患者在疾病稳定4.5个月后退出研究。其余18例患者中,10例(56%)出现部分缓解,2例(11%)疾病持续稳定(≥6个月),总体肿瘤缓解率为67%。缓解的中位持续时间为70周。许多患者出现了短暂的肝功能检查异常,主要发生在治疗的前6周。总之,奥那司酮可诱导人类乳腺癌产生肿瘤反应。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验