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促黄体生成素释放激素激动剂布舍瑞林对晚期前列腺癌患者睾酮生成的持续抑制作用。一种新的治疗方法?

Sustained suppression of testosterone production by the luteinising-hormone releasing-hormone agonist buserelin in patients with advanced prostate carcinoma. A new therapeutic approach?

作者信息

Borgmann V, Hardt W, Schmidt-Gollwitzer M, Adenauer H, Nagel R

出版信息

Lancet. 1982 May 15;1(8281):1097-9. doi: 10.1016/s0140-6736(82)92279-6.

DOI:10.1016/s0140-6736(82)92279-6
PMID:6122893
Abstract

Nine patients with advanced carcinoma of the prostate were treated with the luteinising-hormone-releasing-hormone agonist buserelin (2 mg/day subcutaneously for 3 days then 0.4-1.2 mg/day intranasally for up to 24 weeks). There was a rise in luteinising-hormone levels during the first few days of treatment, but levels fell after 3 weeks and remained lower than normal after 24 weeks' treatment. In patients receiving 0.6-1.2 mg buserelin per day testosterone levels fell to less than 1 ng/ml within 3 weeks and were still as low as those found in surgically castrated men after 24 weeks. Histology showed regressive changes in some tumours after 3-6 months' buserelin treatment similar to those seen in surgically castrated men. Buserelin treatment may be an alternative to surgery in patients with advanced carcinoma of the prostate.

摘要

9例晚期前列腺癌患者接受了促黄体激素释放激素激动剂布舍瑞林治疗(皮下注射2毫克/天,共3天,然后鼻内给药0.4 - 1.2毫克/天,持续24周)。治疗开始的头几天促黄体激素水平升高,但3周后水平下降,24周治疗后仍低于正常水平。每日接受0.6 - 1.2毫克布舍瑞林治疗的患者,睾酮水平在3周内降至低于1纳克/毫升,24周后仍与手术去势男性的水平一样低。组织学检查显示,布舍瑞林治疗3 - 6个月后,部分肿瘤出现退行性变化,类似于手术去势男性所见。对于晚期前列腺癌患者,布舍瑞林治疗可能是手术的替代方案。

相似文献

1
Sustained suppression of testosterone production by the luteinising-hormone releasing-hormone agonist buserelin in patients with advanced prostate carcinoma. A new therapeutic approach?促黄体生成素释放激素激动剂布舍瑞林对晚期前列腺癌患者睾酮生成的持续抑制作用。一种新的治疗方法?
Lancet. 1982 May 15;1(8281):1097-9. doi: 10.1016/s0140-6736(82)92279-6.
2
Treatment with gonadotrophin releasing hormone analogue in advanced prostatic cancer.促性腺激素释放激素类似物治疗晚期前列腺癌。
Br Med J (Clin Res Ed). 1983 Apr 23;286(6374):1309-12. doi: 10.1136/bmj.286.6374.1309.
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Inhibition of serum androgen levels by chronic intranasal and subcutaneous administration of a potent luteinizing hormone-releasing hormone (LH-RH) agonist in adult men.成年男性长期经鼻内和皮下给予强效促黄体生成激素释放激素(LH-RH)激动剂对血清雄激素水平的抑制作用。
Fertil Steril. 1982 Mar;37(3):416-24. doi: 10.1016/s0015-0282(16)46107-8.
4
Suppression of testicular steroidogenesis by the GnRH agonistic analogue Buserelin (HOE-766) in patients with prostatic cancer: studies in relation to dose and route of administration.GnRH 激动剂类似物布舍瑞林(HOE-766)对前列腺癌患者睾丸类固醇生成的抑制作用:与剂量和给药途径相关的研究
J Steroid Biochem. 1983 Jul;19(1C):995-8. doi: 10.1016/0022-4731(83)90045-6.
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Treatment with a luteinising-hormone-releasing-hormone analogue (buserelin) in premenopausal patients with metastatic breast cancer.在绝经前转移性乳腺癌患者中使用促黄体生成素释放激素类似物(布舍瑞林)进行治疗。
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6
Endocrine studies with a gonadotropin-releasing hormone analogue to achieve withdrawal of testosterone in prostate carcinoma patients.使用促性腺激素释放激素类似物进行内分泌研究以促使前列腺癌患者体内睾酮撤退。
Eur Urol. 1982;8(6):343-7. doi: 10.1159/000473554.
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Results of a Dutch Phase II trial with the LHRH agonist buserelin in patients with metastatic prostatic cancer.
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Long term follow-up of patients with advanced prostatic cancer treated with nasal buserelin.鼻用布舍瑞林治疗晚期前列腺癌患者的长期随访
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Long term treatment with luteinising hormone releasing hormone agonists and maintenance of serum testosterone to castration concentrations.使用促黄体生成素释放激素激动剂进行长期治疗,并将血清睾酮维持在去势浓度。
Br Med J (Clin Res Ed). 1985 Aug 10;291(6492):369-70. doi: 10.1136/bmj.291.6492.369.

引用本文的文献

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Changing paradigms in management of metastatic Castration Resistant Prostate Cancer (mCRPC).转移性去势抵抗性前列腺癌(mCRPC)管理模式的转变
BMC Urol. 2014 Jul 25;14:55. doi: 10.1186/1471-2490-14-55.
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Abiraterone for the Treatment of Advanced Prostate Cancer.
阿比特龙用于治疗晚期前列腺癌。
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4
New prospects for luteinising hormone releasing hormone as a contraceptive and therapeutic agent.促黄体生成激素释放激素作为一种避孕和治疗药物的新前景。
Br Med J (Clin Res Ed). 1982 Oct 9;285(6347):990-1. doi: 10.1136/bmj.285.6347.990.
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Advanced prostatic adenocarcinoma: biological aspects and effects of androgen deprivation achieved by castration or agonistic analogues of LHRH.晚期前列腺腺癌:生物学特性以及去势或促黄体生成素释放激素(LHRH)激动剂类似物所致雄激素剥夺的影响
Med Oncol Tumor Pharmacother. 1984;1(2):129-36. doi: 10.1007/BF02934985.
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Long-term LHRH-agonist treatment in metastatic breast cancer as a single treatment and in combination with other additive endocrine treatments.在转移性乳腺癌中,长期使用促黄体激素释放激素(LHRH)激动剂进行单一治疗以及与其他辅助内分泌治疗联合使用。
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GnRH and its analogues. Current therapeutic applications and new prospects.促性腺激素释放激素及其类似物。当前的治疗应用与新前景。
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