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巴多昔芬:一种用于治疗绝经后骨质疏松症的第三代选择性雌激素受体调节剂。

Bazedoxifene: a third-generation selective estrogen receptor modulator for treatment of postmenopausal osteoporosis.

作者信息

Stump Amy L, Kelley Kristi W, Wensel Terri M

机构信息

Division of Pharmacy Practice, School of Pharmacy, University of Wyoming, Cheyenne, WY 82001, USA.

出版信息

Ann Pharmacother. 2007 May;41(5):833-9. doi: 10.1345/aph.1H428. Epub 2007 Apr 10.

Abstract

OBJECTIVE

To review clinical studies and other available literature regarding the development, pharmacology, toxicology, pharmacokinetics/pharmacodynamics, adverse effects, and place in therapy of bazedoxifene, a selective estrogen receptor modulator (SERM), currently in Phase III clinical trials for the treatment and prevention of postmenopausal osteoporosis.

DATA SOURCES

A literature search was performed of PubMed (1966-February 2007), International Pharmaceutical Abstracts (1970-February 2007), Web of Science (1975-February 2007), Biological Abstracts (1926-2007), and Google Scholar (2001-February 2007) databases, using the search terms bazedoxifene, TSE-424, Indole-33, WAY-140424, selective estrogen receptor modulator, and SERM. In addition, product information was requested from the manufacturer, and www.clinicaltrials.gov was searched for unpublished Phase III clinical trials in progress.

STUDY SELECTION AND DATA EXTRACTION

Articles on Phase I and II trials were selected for review, as well as articles discussing preclinical development of bazedoxifene. At the time of writing, no articles on Phase III trials were available for review. Abstracts of unpublished data were reviewed, as was information provided by the manufacturer.

DATA SYNTHESIS

Bazedoxifene is a third-generation SERM currently in Phase III clinical trials. It has been found to act as an agonist on skeletal tissue, with bone turnover reduced by 20-25% with doses of 20 or 40 mg daily. In addition, bazedoxifene has been found to be an antagonist on breast tissue and uterine tissue, demonstrating inhibition of breast tissue proliferation and decreased endometrial stimulation as the dose is increased.

CONCLUSIONS

Current literature suggests that bazedoxifene will likely be safe and effective when used in the treatment of postmenopausal osteoporosis. Completion of Phase III clinical trials will more fully elucidate the safety and efficacy profile of bazedoxifene, as well as more clearly define its place in therapy.

摘要

目的

回顾有关巴多昔芬(一种选择性雌激素受体调节剂(SERM),目前正处于治疗和预防绝经后骨质疏松症的III期临床试验阶段)的研发、药理学、毒理学、药代动力学/药效学、不良反应及治疗地位的临床研究和其他现有文献。

数据来源

使用搜索词“巴多昔芬”“TSE - 424”“吲哚 - 33”“WAY - 140424”“选择性雌激素受体调节剂”和“SERM”,对PubMed(1966年 - 2007年2月)、国际药学文摘(1970年 - 2007年2月)、科学引文索引(1975年 - 2007年2月)、生物学文摘(1926年 - 2007年)和谷歌学术(2001年 - 2007年2月)数据库进行文献检索。此外,向制造商索取了产品信息,并在www.clinicaltrials.gov上搜索正在进行的未发表的III期临床试验。

研究选择与数据提取

选择了关于I期和II期试验的文章,以及讨论巴多昔芬临床前研发的文章。在撰写本文时,尚无关于III期试验的文章可供审查。对未发表数据的摘要以及制造商提供的信息进行了审查。

数据综合

巴多昔芬是一种第三代SERM,目前正处于III期临床试验阶段。已发现它在骨骼组织上起激动剂作用,每日剂量为20或40毫克时,骨转换率降低20 - 25%。此外,已发现巴多昔芬在乳腺组织和子宫组织上起拮抗剂作用,随着剂量增加,显示出对乳腺组织增殖的抑制作用以及对子宫内膜刺激的减少。

结论

当前文献表明,巴多昔芬用于治疗绝经后骨质疏松症可能是安全有效的。III期临床试验的完成将更全面地阐明巴多昔芬的安全性和有效性概况,并更清楚地确定其在治疗中的地位。

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