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使用促黄体生成素释放激素类似物的长效剂型治疗前列腺癌。

Treatment of prostatic cancer with a depot form of a luteinizing hormone-releasing hormone analogue.

作者信息

Giuliani L, Barreca T, Giberti C, Franceschini R, Martorana G, Brancadoro M T, Salvemini M, Rolandi E

出版信息

Eur Urol. 1986;12(6):390-4. doi: 10.1159/000472664.

DOI:10.1159/000472664
PMID:2949979
Abstract

Chronic administration of a depot form of D-Trp6 luteinizing hormone-releasing hormone (LH-RH), an LH-RH analogue (3 mg i.m. every 28 days for a mean period of 9.1 months), to 14 patients with locally extended or metastatic cancer of the prostate provided a good degree of disease control. After a slight and transient increase in gonadotropin secretion, the peptide induced a sharp and long-lasting inhibition of both gonadotropin and testosterone secretion, contemporaneously with clinical improvement and without any important side effects. These results are comparable to those recorded by others after daily administration of LH-RH analogues.

摘要

对14例局部进展期或转移性前列腺癌患者长期给予一种长效剂型的D-色氨酸6促黄体生成激素释放激素(LH-RH),即一种LH-RH类似物(每28天肌肉注射3毫克,平均疗程9.1个月),可实现较好程度的疾病控制。在促性腺激素分泌出现轻微短暂增加后,该肽诱导了促性腺激素和睾酮分泌的急剧且持久的抑制,同时伴有临床改善,且无任何严重副作用。这些结果与其他人每日给予LH-RH类似物后所记录的结果相当。

相似文献

1
Treatment of prostatic cancer with a depot form of a luteinizing hormone-releasing hormone analogue.使用促黄体生成素释放激素类似物的长效剂型治疗前列腺癌。
Eur Urol. 1986;12(6):390-4. doi: 10.1159/000472664.
2
Persistent blockade of the pituitary-gonadal axis in patients with prostatic carcinoma during chronic administration of D-Trp-6-LH-RH.在慢性给予D-色氨酸-6-促黄体生成素释放激素期间,前列腺癌患者垂体-性腺轴的持续阻断。
Prostate. 1986;9(2):207-15. doi: 10.1002/pros.2990090211.
3
Long-term results with a long-acting formulation of D-TRP-6 LH-RH in patients with prostate cancer: an Italian prostatic cancer project (P.O.N.CA.P.) study.
Prostate. 1987;11(3):243-55. doi: 10.1002/pros.2990110305.
4
Inhibition of the pituitary-gonadal axis by a single intramuscular administration of D-Trp-6-LH-RH (decapeptyl) in a sustained-release formulation in patients with prostatic carcinoma.采用缓释制剂的 D-色氨酸-6-促黄体生成素释放激素(曲普瑞林)单次肌内注射对前列腺癌患者垂体-性腺轴的抑制作用。
Prostate. 1989;14(4):291-300. doi: 10.1002/pros.2990140402.
5
[Decapeptyl (D-Trp6-LH-RH) in the therapy of prostatic cancer with reference to the intramuscular administration of a depot preparation].[醋酸亮丙瑞林(D-色氨酸6-促黄体生成素释放激素)在前列腺癌治疗中关于长效制剂肌肉注射的应用]
Urologe A. 1986 Sep;25(5):298-301.
6
Combination of a long-acting delivery system for luteinizing hormone-releasing hormone agonist with Novantrone chemotherapy: increased efficacy in the rat prostate cancer model.长效促黄体生成素释放激素激动剂递送系统与米托蒽醌化疗联合应用:在大鼠前列腺癌模型中疗效增强。
Proc Natl Acad Sci U S A. 1986 Nov;83(22):8764-8. doi: 10.1073/pnas.83.22.8764.
7
Somatostatin analogs as adjuncts to agonists of luteinizing hormone-releasing hormone in the treatment of experimental prostate cancer.生长抑素类似物作为促黄体生成素释放激素激动剂的辅助药物用于实验性前列腺癌的治疗。
Proc Natl Acad Sci U S A. 1987 Oct;84(20):7275-9. doi: 10.1073/pnas.84.20.7275.
8
Inhibition of prostate tumor growth in two rat models by chronic administration of D-Trp6 analogue of luteinizing hormone-releasing hormone.通过长期给予促黄体生成素释放激素的D-色氨酸6类似物抑制两种大鼠模型中的前列腺肿瘤生长。
Proc Natl Acad Sci U S A. 1981 Oct;78(10):6509-12. doi: 10.1073/pnas.78.10.6509.
9
Sustained impairment of pituitary and testicular function in prostatic cancer patients treated with a depot form of a GnRH agonist.
Horm Res. 1988;30(1):22-5. doi: 10.1159/000181020.
10
[Treatment of prostatic cancer with slow-release formulation of luteinizing hormone releasing hormone (LH-RH) analog].
Hinyokika Kiyo. 1988 Mar;34(3):555-60.