Borgmann V, Nagel R, Al-Abadi H, Schmidt-Gollwitzer M
Prostate. 1983;4(6):553-68. doi: 10.1002/pros.2990040603.
Twenty-one of 32 patients with locally advanced prostatic cancer (stage C) were treated with the LH-RH analogue Buserelin for 7-19 months. After an initial sequence of subcutaneous injections, treatment was continued with intranasal spray application (three daily doses of 400 micrograms each) which ensured maintenance of serum testosterone within the range seen in castrated men. To evaluate the response of the primary tumor to Buserelin, cytological regression was established for all patients by fine-needle aspiration biopsy every 3 months. The cytological results corresponded with those of DNA analyses of single-cell cytophotometry showing a statistically significant drop of the grade of aneuploidy or polyploidy when the prostatic carcinoma responded positively to Buserelin therapy. Seventeen of 21 patients treated with the potent LH-RH analogue showed good therapy response. Four patients with no cytological signs of tumor regression received secondary treatment with estramustine phosphate because of hormone resistence. One patient had to be crossed over to cyclophosphamide, the third drug, for clinical progression after 15 months. Essential side effects have not been observed. Continuous treatment of locally advanced prostatic cancer with Buserelin, combined with close control of the patient, offers not only a real alternative to surgical castration--as the patient is spared the psychical stress of orchiectomy--but also to estrogen therapy with its risk of cardiovascular side effects.
32例局部晚期前列腺癌(C期)患者中有21例接受了促黄体生成素释放激素(LH-RH)类似物布舍瑞林治疗7至19个月。在最初一系列皮下注射后,改用鼻内喷雾给药(每日3次,每次400微克)继续治疗,以确保血清睾酮维持在去势男性的水平范围内。为了评估原发性肿瘤对布舍瑞林的反应,每3个月通过细针穿刺活检对所有患者进行细胞学消退评估。细胞学结果与单细胞细胞光度法的DNA分析结果一致,表明当前列腺癌对布舍瑞林治疗呈阳性反应时,非整倍体或多倍体等级有统计学意义的下降。21例接受强效LH-RH类似物治疗的患者中有17例显示出良好的治疗反应。4例无肿瘤消退细胞学迹象的患者因激素抵抗接受了磷酸雌莫司汀二线治疗。1例患者在15个月后因临床进展不得不改用第三种药物环磷酰胺。未观察到严重副作用。用布舍瑞林持续治疗局部晚期前列腺癌,并密切监测患者,不仅为手术去势提供了一种切实可行的替代方法(因为患者可避免睾丸切除术的心理压力),也为雌激素治疗提供了替代方法,后者存在心血管副作用风险。