Nonsteroidal selective androgen receptor modulator Ostarine™ in cancer cachexia

被引:23
作者
Zilbermint, Mihail F. [2 ]
Dobs, Adrian S. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Div Endocrinol & Metab, Baltimore, MD 21287 USA
[2] St Agnes Hosp, Dept Med, Baltimore, MD 21229 USA
关键词
androgen receptor; aryl propionamide; cancer cachexia; GTx-024; MK-2866; muscle wasting; nonsteroidal androgen; Ostarine (TM); selective androgen receptor modulator; testosterone; PREVENTS BONE LOSS; MEGESTROL-ACETATE; DOUBLE-BLIND; WEIGHT-LOSS; LEAN TISSUE; ANOREXIA; PROSTATE; THERAPY; MASS; PHARMACOKINETICS;
D O I
10.2217/FON.09.106
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer cachexia is a complex syndrome, affecting up to 60% off he approximately 1.4 million patients diagnosed with cancer each year in the USA. This condition is characterized by progressive deterioration of a patient's nutritional status, weight loss, anorexia, diminished quality of life and increased mortality and morbidity. Current therapy with progestational, anti-inflammatory and anabolic agents is often ineffective and has a large number of undesirable effects. The newly developed nonsteroidal selective androgen receptor modulator Ostarine(TM) has demonstrated promising results in Phase I and II clinical trials, increasing total lean body mass, enhancing functional performance and decreasing total tissue percent fat. This selective androgen receptor modulator may have the ability to perform as a potent anabolic agent with minimal side effects on other organs (prostate and hair follicles), thus presenting a new strategy in managing cancer cachexia. However, more extensive data is required before its efficacy is confirmed.
引用
收藏
页码:1211 / 1220
页数:10
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