Coombes R C, Hughes S W, Dowsett M
Department of Medical Oncology, Charing Cross Hospital, London, U.K.
Eur J Cancer. 1992;28A(12):1941-5. doi: 10.1016/0959-8049(92)90232-q.
We have evaluated 4-hydroxyandrostenedione, a specific inhibitor of aromatase, as treatment for breast cancer in a phase I dose-ranging study and a phase II study of the best-tolerated dose. 168 postmenopausal patients with locally advanced and metastatic breast cancer were treated intramuscularly. 19% of patients attained a complete or partial response but 26% of those who completed at least 4 weeks treatment responded. Side-effects were least in the group receiving 250 mg every 2 weeks. 13% of patients experienced local discomfort due to the injection and 5% had other side-effects. Serum oestradiol fell to 42.4 and 26.5% of baseline at 7 days after the start of treatment with the 250 mg and 500 mg dose, respectively. We conclude that 4-hydroxyandrostenedione at 250 mg every 2 weeks is a safe and effective form of treatment for postmenopausal patients with metastatic breast cancer.
我们在一项I期剂量范围研究和一项关于最佳耐受剂量的II期研究中,评估了芳香化酶的特异性抑制剂4-羟基雄烯二酮对乳腺癌的治疗效果。168例局部晚期和转移性绝经后乳腺癌患者接受了肌肉注射治疗。19%的患者获得了完全或部分缓解,但在至少完成4周治疗的患者中,有26%出现了缓解。副作用在每2周接受250mg治疗的组中最少。13%的患者因注射出现局部不适,5%有其他副作用。分别在开始使用250mg和500mg剂量治疗7天后,血清雌二醇降至基线的42.4%和26.5%。我们得出结论,每2周250mg的4-羟基雄烯二酮是治疗转移性绝经后乳腺癌患者的一种安全有效的治疗方式。