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Phase II trial with D-Trp-6-LH-RH in prostatic carcinoma: comparison with other hormonal agents.

作者信息

Mathé G, Schally A V, Comaru-Schally A M, Mauvernay R Y, Vovan M L, Machover D, Misset J L, Court B, Bouchard P, Duchier J

出版信息

Prostate. 1986;9(4):327-42. doi: 10.1002/pros.2990090404.

DOI:10.1002/pros.2990090404
PMID:2947053
Abstract

Various approaches to hormonal treatment of prostate carcinoma are discussed. Eighty-one patients with prostatic carcinoma, eight with stage B, nine with stage C, and 64 with stage D disease, were treated subcutaneously daily for 3 months with the LH-RH agonist D-Trp-6-LH-RH (Decapeptyl) in order to evaluate the incidence of remissions according to WHO recommendations for oncologic trials. The findings were compared to those obtained with other hormonal therapies of prostatic carcinoma according to the statistical method of "expected response rate" as adapted by Lee and Wesley for phase II trials. Treatment with D-Trp-6-LH-RH greatly reduced serum LH and testosterone levels without raising serum prolactin. After 1-2 weeks of therapy, there was relief of subjective symptoms and a reversal of the signs of prostatism as well as a marked decrease in bone pain. At 90 days 52 patients had complete relief of prostatism and 21 had only mild signs and symptoms. Seventy patients were experiencing no bone pain and an additional six had only mild pain. Prostatic size, evaluated by rectal examination and transabdominal ultrasonography, reverted to normal in 26.4% of patients (complete remission) and was reduced by more than 50% in an additional 17.6% (partial remission), the overall rate of complete plus partial regression of prostatic enlargement being 44%. Scans showed a major improvement of bone lesions in 14.8% of cases. This response increased to 37% after more than 6 months of follow-up. Prostatic acid phosphatase levels were decreased by more than 50% in 61% of the patients, but this test appears to be a less valid marker than the lipid-associated sialic acid (LASA). The increase in LASA before treatment and a reduction after treatment can frequently be correlated with the objective volume of the neoplasms. No flare-up of the disease was encountered, and there were no side effects except for impotence. Statistical analyses of results by the method of Lee and Wesley indicated that the incidence of complete and partial regression (CR and PR) observed with D-Trp-6-LH-RH was not significantly different from that recorded in previous studies for another LH-RH analog, Buserelin. However, CR and PR obtained with D-Trp-6-LH-RH (44%) were significantly higher than with subcapsular orchiectomy (22%). Hormonal effects and some other actions of D-Trp-6-LH-RH were compared and contrasted with those produced by castration, estrogens, antiandrogens, and progestogens.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

相似文献

1
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.
2
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.
3
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.
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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.
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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.
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Tumor growth inhibition in patients with prostatic carcinoma treated with luteinizing hormone-releasing hormone agonists.用促黄体生成素释放激素激动剂治疗的前列腺癌患者的肿瘤生长抑制
Proc Natl Acad Sci U S A. 1982 Mar;79(5):1658-62. doi: 10.1073/pnas.79.5.1658.
7
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.
8
[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.
9
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.
10
[Clinical phase I and phase II study on a sustained release formulation of leuprorelin acetate (TAP-144-SR), an LH-RH agonist, in patients with prostatic carcinoma. Collaborative++ Studies on Prostatic Carcinoma by the Study Group for TAP-144-SR].醋酸亮丙瑞林缓释制剂(TAP - 144 - SR),一种促性腺激素释放激素(LH - RH)激动剂,用于前列腺癌患者的临床I期和II期研究。TAP - 144 - SR研究组关于前列腺癌的协作++研究
Hinyokika Kiyo. 1990 Nov;36(11):1343-60.

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A 50-year journey in the development of treatment for benign prostatic hyperplasia.良性前列腺增生治疗发展的50年历程。
NPJ Aging. 2025 May 23;11(1):41. doi: 10.1038/s41514-025-00231-2.
2
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.
3
Active cell death in hormone-dependent tissues.激素依赖性组织中的细胞主动死亡。
Cancer Metastasis Rev. 1992 Sep;11(2):197-220. doi: 10.1007/BF00048064.