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[晚期前列腺癌。使用促黄体生成素释放激素激动剂D-色氨酸-6-促黄体生成素释放激素进行治疗]

[Advanced cancer of the prostate. Treatment with an LH-RH agonist, D-Trp-6-LH-RH].

作者信息

Mathé G, Misset J L, Vovan M L, Machover D

出版信息

Bull Cancer. 1986;73(1):31-5.

PMID:2430652
Abstract

D-Trp-6-LH-RH, a long acting LH-RH agonist was given in a phase II trial to 85 patients aged 52 to 88 (mean 69) with advanced prostatic carcinoma, stage B (8 pts), C (9 pts) and D (68 pts). Twenty-five patients were previously untreated, 40 had received previous hormonal therapy but none was considered has having hormone resistant tumor; 20 patients had received surgery or radiotherapy or both. D-Trp-6-LH-RH was given s.c. at a daily dose of 500 micrograms during the first seven days, followed by 100 micrograms daily. Antitumor activity was assessed after 90 days and treatment was continued in responders. The results were the following: plasmatic levels of LH were sharply decreased and those of testosterone were in all cases under 1 ng/ml by the 90th day of treatment; urinary symptoms and bone pain disappeared or were greatly improved in almost all patients; the volume of the prostate measured by ultrasonography and/or computerized tomography regressed by more than 50% of initial volume in 44% of the 34 patients for which this parameter was evaluable; bone scintiscans were improved in 18% of evaluable patients; plasmatic levels of prostatic acid phosphatases determined by radio immuno-assay were elevated in 28 patients, 61% of which presented a decrease superior to 50% or normalisation of this parameter. No disease flare up was observed on initiation of therapy. Impotence was constant but reversible on discontinuation of therapy. No other side effect could be attributed to therapy.

摘要

D-色氨酸-6-促黄体激素释放激素(D-Trp-6-LH-RH)是一种长效促黄体激素释放激素激动剂,在一项II期试验中给予了85例年龄在52至88岁(平均69岁)的晚期前列腺癌患者,其中B期8例、C期9例、D期68例。25例患者此前未接受过治疗,40例曾接受过激素治疗,但均未被认为患有激素抵抗性肿瘤;20例患者接受过手术或放疗或两者皆有。D-Trp-6-LH-RH在前七天皮下注射,每日剂量为500微克,随后每日100微克。90天后评估抗肿瘤活性,有反应者继续治疗。结果如下:治疗至第90天时,促黄体生成素(LH)的血浆水平急剧下降,睾酮水平在所有病例中均低于1纳克/毫升;几乎所有患者的尿路症状和骨痛消失或大幅改善;在可评估该参数的34例患者中,44%通过超声和/或计算机断层扫描测量的前列腺体积缩小超过初始体积的50%;18%的可评估患者骨扫描得到改善;通过放射免疫测定法测定的前列腺酸性磷酸酶血浆水平在28例患者中升高,其中61%该参数下降超过50%或恢复正常。治疗开始时未观察到疾病突发。阳痿持续存在,但停药后可逆。未发现其他可归因于治疗的副作用。

相似文献

1
[Advanced cancer of the prostate. Treatment with an LH-RH agonist, D-Trp-6-LH-RH].[晚期前列腺癌。使用促黄体生成素释放激素激动剂D-色氨酸-6-促黄体生成素释放激素进行治疗]
Bull Cancer. 1986;73(1):31-5.
2
Phase II trial with D-Trp-6-LH-RH in prostatic carcinoma: comparison with other hormonal agents.
Prostate. 1986;9(4):327-42. doi: 10.1002/pros.2990090404.
3
Responses to the antagonistic analog of LH-RH (SB-75, Cetrorelix) in patients with benign prostatic hyperplasia and prostatic cancer.良性前列腺增生症和前列腺癌患者对促黄体生成素释放激素拮抗剂类似物(SB - 75,西曲瑞克)的反应。
Prostate. 1994;24(2):84-92. doi: 10.1002/pros.2990240206.
4
Treatment of advanced prostatic carcinoma with D-Trp-6-LH-RH.用D-色氨酸-6-促黄体生成素释放激素治疗晚期前列腺癌。
Prostate. 1985;7(1):21-30. doi: 10.1002/pros.2990070104.
5
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.
6
Investigation of the combination of the agonist D-Trp-6-LH-RH and the antiandrogen flutamide in the treatment of Dunning R-3327H prostate cancer model.激动剂D-色氨酸-6-促黄体生成素释放激素(D-Trp-6-LH-RH)与抗雄激素氟他胺联合用于治疗邓宁R-3327H前列腺癌模型的研究。
Prostate. 1985;6(3):219-32. doi: 10.1002/pros.2990060302.
7
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.
8
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.
9
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.
10
Long-acting (depot) D-TRP-6 LH-RH (Decapeptyl) in prostate cancer. An Italian multicentric trial.长效(缓释)D-色氨酸-6促黄体生成素释放激素(抑那通)治疗前列腺癌。一项意大利多中心试验。
Am J Clin Oncol. 1988;11 Suppl 2:S129-31. doi: 10.1097/00000421-198801102-00033.