Peters T G, Lewis J D, Wilkinson E J, Fuhrman T M
Cancer. 1977 Dec;40(6):2797-800. doi: 10.1002/1097-0142(197712)40:6<2797::aid-cncr2820400607>3.0.co;2-9.
The effect of Danazol, a synthetic gonadotropin inhibitor, on two groups of Sprague-Dawley rats with dimethylbenze (a) anthracine (DMBA) induced mammary carcinoma was studied. Twenty-four (83%) of 29 control animals developed mammary tumors. Forty-four rats in one treatment group received Danazol after tumor reached 0.5 cm in diameter. Twenty-nine (66%) demonstrated tumor regression (p less than 0.005) and in 16 (36%) tumor disappeared (p less than 0.005). In a second treatment group (given Danazol daily after administration of DMBA), only seven of 50 rats (14%) developed palpable mammary carcinoma (p less than 0.0005). Danazol therapy resulted in regression of established mammary carcinoma in rats, and produced a striking inhibition of carcinogenesis in those animals treated from the time DMBA was administered. Danazol is clinically safe; studies using it in the treatment of breast cancer in women who are candidates for hormonal ablative therapy seem warranted.
研究了合成促性腺激素抑制剂达那唑对两组经二甲基苯并(a)蒽(DMBA)诱导产生乳腺癌的斯普拉格-道利大鼠的影响。29只对照动物中有24只(83%)发生了乳腺肿瘤。在一个治疗组中,44只大鼠在肿瘤直径达到0.5厘米后接受达那唑治疗。其中29只(66%)肿瘤出现消退(p<0.005),16只(36%)肿瘤消失(p<0.005)。在第二个治疗组(在给予DMBA后每日给予达那唑)中,50只大鼠中只有7只(14%)出现可触及的乳腺癌(p<0.0005)。达那唑治疗可使大鼠已形成的乳腺癌消退,并对从给予DMBA时起就接受治疗的动物的致癌作用产生显著抑制。达那唑在临床上是安全的;在激素消融治疗候选女性中使用它治疗乳腺癌的研究似乎是有必要的。