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比卡鲁胺:一种用于晚期前列腺癌患者与去势联合使用的新型抗雄激素药物。

Bicalutamide: a new antiandrogen for use in combination with castration for patients with advanced prostate cancer.

作者信息

Blackledge G, Kolvenbag G, Nash A

机构信息

Medical Research Department, ZENECA Pharmaceuticals Ltd, Mereside, Macclesfield, UK.

出版信息

Anticancer Drugs. 1996 Jan;7(1):27-34.

PMID:8742095
Abstract

Maximum androgen blockade, a relatively recent development in the treatment of prostate cancer, combines medical or surgical castration with antiandrogen therapy. A large randomized study comparing the non-steroidal antiandrogen, bicalutamide, with flutamide, each in combination with luteinizing hormone-releasing hormone (LHRH) analogs, showed that after a median follow-up of 49 weeks, the time to treatment failure was significantly longer for the bicalutamide patients compared with the flutamide patients (p = 0.005). After a median follow up to 95 weeks, bicalutamide in combination with LHRH analog therapy produced at least equivalent efficacy with flutamide in combination with LHRH analog therapy in terms of time to treatment failure and equivalent efficacy in terms of survival. The tolerability profile of bicalutamide, as based on reported findings and a literature review, indicates a superior tolerability to that of currently available antiandrogens, particularly with respect to diarrhea with a low incidence of treatment-related withdrawals.

摘要

最大限度雄激素阻断是前列腺癌治疗领域一项相对较新的进展,它将药物或手术去势与抗雄激素治疗相结合。一项大型随机研究比较了非甾体抗雄激素药物比卡鲁胺与氟他胺,二者均与促黄体生成素释放激素(LHRH)类似物联合使用,结果显示,在中位随访49周后,与氟他胺组患者相比,比卡鲁胺组患者的治疗失败时间显著延长(p = 0.005)。在中位随访至95周后,就治疗失败时间而言,比卡鲁胺联合LHRH类似物治疗产生的疗效至少与氟他胺联合LHRH类似物治疗相当,就生存率而言疗效也相当。基于报告结果和文献综述,比卡鲁胺的耐受性表明其耐受性优于目前可用的抗雄激素药物,尤其是在腹泻方面,与治疗相关的停药发生率较低。

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