• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

芳香化酶抑制剂治疗晚期乳腺癌的经验。

Experience with aromatase inhibitors in the treatment of advanced breast cancer.

作者信息

Höffken K

机构信息

Klinik für Innere Medizin II, Friedrich-Schiller-Universität Jena, Germany.

出版信息

Cancer Treat Rev. 1993 Apr;19 Suppl B:37-44. doi: 10.1016/0305-7372(93)90006-d.

DOI:10.1016/0305-7372(93)90006-d
PMID:8481933
Abstract

Inhibition of the aromatase enzyme system has become an established means of hormonal treatment for hormone-responsive advanced breast cancer. The widest clinical experience is with aminoglutethimide, which achieves around 30% objective remissions of metastatic disease for up to 1 year. Due to the sometimes serious side-effects of this drug, preclinical and clinical investigations have been undertaken and have yielded a number of steroidal and non-steroidal aromatase inhibitors that have been shown in early or mature clinical trials to give objective disease remissions similar to those with aminoglutethimide but with less toxicity. There is thus good reason to believe that newer aromatase inhibiting drugs will soon be available for routine use in patients with breast cancer. This paper summarizes our experience and reviews data from other groups.

摘要

抑制芳香化酶系统已成为激素反应性晚期乳腺癌激素治疗的既定方法。临床经验最丰富的是氨鲁米特,它能使转移性疾病的客观缓解率达到约30%,持续长达1年。由于该药物有时会产生严重的副作用,因此已经开展了临床前和临床研究,并产生了一些甾体和非甾体芳香化酶抑制剂,这些抑制剂在早期或成熟的临床试验中已显示出能产生与氨鲁米特相似的客观疾病缓解,但毒性较小。因此,有充分的理由相信,新型芳香化酶抑制药物很快将可用于乳腺癌患者的常规治疗。本文总结了我们的经验并回顾了其他研究组的数据。

相似文献

1
Experience with aromatase inhibitors in the treatment of advanced breast cancer.芳香化酶抑制剂治疗晚期乳腺癌的经验。
Cancer Treat Rev. 1993 Apr;19 Suppl B:37-44. doi: 10.1016/0305-7372(93)90006-d.
2
Aromatase inhibitors: clinical pharmacology and therapeutic implications in breast cancer.
J Int Med Res. 1992 Aug;20(4):303-12. doi: 10.1177/030006059202000401.
3
Survival with aromatase inhibitors and inactivators versus standard hormonal therapy in advanced breast cancer: meta-analysis.芳香化酶抑制剂和失活剂与标准激素疗法治疗晚期乳腺癌的生存情况:荟萃分析
J Natl Cancer Inst. 2006 Sep 20;98(18):1285-91. doi: 10.1093/jnci/djj357.
4
Aromatase inhibitors in the treatment of advanced breast cancer.芳香化酶抑制剂在晚期乳腺癌治疗中的应用
Cancer Treat Rev. 1989 Jun;16(2):83-93. doi: 10.1016/0305-7372(89)90012-1.
5
Recent progress in development of aromatase inhibitors.
J Steroid Biochem Mol Biol. 1990 Dec 20;37(6):1029-35. doi: 10.1016/0960-0760(90)90461-s.
6
Aromatase in breast cancer and the role of aminoglutethimide and other aromatase inhibitors.芳香化酶在乳腺癌中的作用以及氨鲁米特和其他芳香化酶抑制剂的作用。
Crit Rev Oncol Hematol. 1986;5(4):361-96. doi: 10.1016/s1040-8428(86)80003-8.
7
Aromatase inhibition with 4-OHAndrostenedione after prior aromatase inhibition with aminoglutethimide in women with advanced breast cancer.在晚期乳腺癌女性中,先用氨鲁米特抑制芳香化酶后,再用4-羟基雄烯二酮抑制芳香化酶。
Breast Cancer Res Treat. 1995 Sep;35(3):249-53. doi: 10.1007/BF00665976.
8
Clinical use of aromatase inhibitors in the treatment of breast cancers.芳香化酶抑制剂在乳腺癌治疗中的临床应用。
J Cell Biochem Suppl. 1993;17G:242-6. doi: 10.1002/jcb.240531144.
9
Aromatase, its inhibitors and their use in breast cancer treatment.
Pharmacol Ther. 1993 Dec;60(3):501-15. doi: 10.1016/0163-7258(93)90033-a.
10
[Preclinical evaluation of aromatase inhibitors antitumor activity].[芳香化酶抑制剂抗肿瘤活性的临床前评估]
Bull Cancer. 2000 Dec;87 Spec No:7-22.

引用本文的文献

1
Breast cancer therapies in development. A review of their pharmacology and clinical potential.正在研发的乳腺癌治疗方法。对其药理学及临床潜力的综述。
Drugs. 1997 Sep;54(3):385-413. doi: 10.2165/00003495-199754030-00003.
2
Arimidex (ZD1033): a selective, potent inhibitor of aromatase in postmenopausal female volunteers.瑞宁得(ZD1033):绝经后女性志愿者体内芳香化酶的一种选择性强效抑制剂。
Br J Cancer. 1996 Feb;73(4):543-8. doi: 10.1038/bjc.1996.94.