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激素疗法对局限性前列腺癌有重大影响——死亡已可能是个例外情况。

Major impact of hormonal therapy in localized prostate cancer--death can already be an exception.

作者信息

Labrie Fernand, Cusan Leonello, Gomez José, Luu-The Van, Candas Bernard, Bélanger Alain, Labrie Claude

机构信息

Oncology and Molecular Endocrinology Research Center, Le Centre Hospitalier de l'Université Laval (CHUL) and Laval University, 2705 Laurier Boulevard, Quebec City, Quebec, Canada G1V 4G2.

出版信息

J Steroid Biochem Mol Biol. 2004 Dec;92(5):327-44. doi: 10.1016/j.jsbmb.2004.10.011. Epub 2004 Dec 21.

Abstract

For about 50 years, androgen blockade in prostate cancer has been limited to monotherapy (surgical castration) or high doses of estrogens in patients with advanced disease and bone metastases. The discovery of medical castration with LHRH agonists has led to fundamental changes in the endocrine therapy of prostate cancer. In 1979, the first prostate cancer patient treated with an LHRH agonist received such treatment at the Laval University Medical Center. A long series of studies have clearly demonstrated that medical castration with an LHRH agonist has inhibitory effects on prostate cancer equivalent to those of surgical castration. The much higher acceptability of LHRH agonists has been essential to permit a series of studies in localized disease. Based upon the finding that the testicles and adrenals contribute approximately equal amounts of androgens in the human prostate, the combination of medical (LHRH agonist) or surgical castration associated with a pure antiandrogen (flutamide, nilutamide or bicalutamide) has led to the first demonstration of a prolongation of life in prostate cancer, namely a 10-20% decreased risk of death according to the various metaanalyses of all the studies performed in advanced disease. In analogy with the other types of advanced cancers, the success of combined androgen blockade in metastatic disease is limited by the development of resistance to treatment. To avoid the problem of resistance to treatment while taking advantage of the relative ease of diagnosis of prostate cancer at an "early" stage, the much higher acceptability of LHRH agonists has permitted a series of studies which have demonstrated a major reduction in deaths from prostate cancer ranging from 31% to 87% at 5 years of follow-up in patients with localized or locally advanced prostate cancer. Most importantly, recent data show that the addition of a pure antiandrogen to an LHRH agonist in order to block the androgens made locally in the prostate leads to a 90% long-term control or probable cure of prostate cancer.

摘要

在大约50年的时间里,前列腺癌的雄激素阻断治疗仅限于晚期疾病和骨转移患者的单一疗法(手术去势)或高剂量雌激素治疗。促性腺激素释放激素(LHRH)激动剂药物去势的发现引发了前列腺癌内分泌治疗的根本性变革。1979年,首位接受LHRH激动剂治疗的前列腺癌患者在拉瓦尔大学医学中心接受了该治疗。一系列长期研究清楚地表明,LHRH激动剂药物去势对前列腺癌的抑制作用与手术去势相当。LHRH激动剂更高的可接受性对于开展一系列局限性疾病研究至关重要。基于睾丸和肾上腺对人体前列腺雄激素贡献量大致相等这一发现,药物(LHRH激动剂)或手术去势联合一种纯抗雄激素药物(氟他胺、尼鲁米特或比卡鲁胺)首次证明可延长前列腺癌患者的生命,即在对所有晚期疾病研究进行的各种荟萃分析中,死亡风险降低了10%至20%。与其他类型的晚期癌症类似,转移性疾病联合雄激素阻断治疗的成功受到治疗耐药性发展的限制。为了在利用前列腺癌“早期”相对容易诊断这一优势的同时避免治疗耐药性问题,LHRH激动剂更高的可接受性使得一系列研究得以开展,这些研究表明,在局限性或局部晚期前列腺癌患者中,随访5年时前列腺癌死亡人数大幅减少,降幅在31%至87%之间。最重要的是,最近的数据显示,在LHRH激动剂基础上加用一种纯抗雄激素药物以阻断前列腺局部产生的雄激素,可使前列腺癌实现90%的长期控制或可能治愈。

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