Kung T T, Mingo G G, Siegel M I, Watnick A S
Research Division, Schering-Plough Corp., Bloomfield, New Jersey 07003.
Prostate. 1988;12(4):357-63. doi: 10.1002/pros.2990120409.
The R-3327 prostatic tumor implanted in the male Copenhagen x Fischer F1 rat continues to grow because androgen is being supplied from an endogenous source. It follows that regimens which decrease the availability of androgen will retard the growth rate of the tumor. These experiments showed that castration, the antiandrogen flutamide, and the luteinizing hormone-releasing hormone (LHRH) agonist leuprolide inhibited tumor growth. Adrenalectomy alone had no significant effect on tumor size and did not further retard the growth of the tumor in castrated rats. Further, under the conditions of this study, there was no significant difference in tumor growth rates between the groups of rats treated with either flutamide alone or flutamide combined with leuprolide. Total ablation of androgen may not be needed for maximal inhibition of tumor growth.
植入雄性哥本哈根×费舍尔F1大鼠体内的R - 3327前列腺肿瘤持续生长,因为雄激素由内源性来源供应。因此,降低雄激素可利用性的方案将延缓肿瘤的生长速度。这些实验表明,去势、抗雄激素氟他胺以及促黄体生成素释放激素(LHRH)激动剂亮丙瑞林可抑制肿瘤生长。单独肾上腺切除术对肿瘤大小无显著影响,且不会进一步延缓去势大鼠的肿瘤生长。此外,在本研究条件下,单独使用氟他胺或氟他胺与亮丙瑞林联合治疗的大鼠组之间,肿瘤生长速率无显著差异。最大程度抑制肿瘤生长可能不需要完全消除雄激素。