Lønning P E, Dowsett M, Jones A, Ekse D, Jacobs S, McNeil F, Johannessen D C, Powles T J
Department of Oncology, Haukeland University Hospital, Bergen, Norway.
Breast Cancer Res Treat. 1992;23(1-2):57-62. doi: 10.1007/BF01831476.
The clinical and biochemical effects of combined treatment with the two aromatase inhibitors aminoglutethimide and 4-hydroxyandrostenedione were evaluated in 10 patients suffering from advanced breast cancer. All patients had become resistant to treatment with one of the drugs before having combined treatment. Seven patients progressing on 4-hydroxyandrostenedione who had aminoglutethimide added to their treatment and achieved a further suppression of plasma oestradiol by a mean of 40.0% (p < 0.05). Plasma oestrone was suppressed by a mean of 40.6% (p < 0.025) and plasma oestrone sulphate was suppressed by a mean of 63.6% (p < 0.025). Two of the patients, neither of whom had responded to 4-hydroxyandrostenedione alone, experienced objective tumour regression when aminoglutethimide was given in concert. Three patients progressing on aminoglutethimide who had 4-hydroxyandrostenedione added showed no further suppression of their plasma oestrogen levels, and no tumour regression was observed. These findings suggest a dose-response relationship between plasma oestrogen suppression at low postmenopausal levels and objective tumour response in breast cancer.
对10例晚期乳腺癌患者评估了两种芳香化酶抑制剂氨鲁米特和4-羟基雄烯二酮联合治疗的临床和生化效果。所有患者在接受联合治疗前均已对其中一种药物产生耐药性。7例在接受4-羟基雄烯二酮治疗过程中病情进展的患者,在治疗中加用氨鲁米特后,血浆雌二醇进一步平均抑制40.0%(p<0.05)。血浆雌酮平均抑制40.6%(p<0.025),血浆硫酸雌酮平均抑制63.6%(p<0.025)。2例单独使用4-羟基雄烯二酮均无反应的患者,在联合使用氨鲁米特后出现客观肿瘤退缩。3例在接受氨鲁米特治疗过程中病情进展的患者,加用4-羟基雄烯二酮后血浆雌激素水平未进一步抑制,未观察到肿瘤退缩。这些发现提示绝经后低水平血浆雌激素抑制与乳腺癌客观肿瘤反应之间存在剂量反应关系。