Bajetta E, Zilembo N, Buzzoni R, Noberasco C, Martinetti A, Ferrari L, Bartoli C, Sacchini V, Attili A, Lepera P
Division of Medical Oncology B, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy.
Ann Oncol. 1994;5 Suppl 7:S15-7.
Aromatase inhibitors are a useful therapeutic option in the management of endocrine-dependent advanced breast cancer. Formestane (Lentaron) is the first irreversible aromatase inhibitor to be extensively investigated. In a phase II study to determine the effects of formestane on serum estradiol and urinary 17-hydroxycorticosteroid (17-OHCS) levels and to evaluate its clinical activity, 72 postmenopausal patients with advanced breast cancer were given formestane 250 mg intramuscularly every 2 weeks. Of 66 patients fully evaluable, 56 were estrogen receptor (ER) positive, and 43 had a disease-free interval > or = 2 years. Metastases were assessable in soft tissue (53%), bone (53%) and viscera (47%); 34 patients had 1, 32 had > or = 2 metastatic lesions. Serum estradiol levels fell significantly (p < 0.01) after 2 weeks and remained unchanged thereafter, whereas urinary 17-OHCS levels did not change during treatment. Objective responses were obtained in 19 patients (29%), of whom 8 had complete response. In relation to disease sites, similar responses were obtained in soft tissue (33%) and viscera (30%), whereas response in bone was 18%. The overall tolerability of formestane was satisfactory, and only two patients complained of local side effects. We conclude that formestane is an effective aromatase inhibitor in postmenopausal patients with hormone-dependent breast cancer, and does not interfere with adrenal steroidogenesis.
芳香化酶抑制剂是内分泌依赖性晚期乳腺癌治疗中的一种有用的治疗选择。福美司坦(兰特隆)是首个得到广泛研究的不可逆芳香化酶抑制剂。在一项旨在确定福美司坦对血清雌二醇和尿17-羟皮质类固醇(17-OHCS)水平的影响并评估其临床活性的II期研究中,72例绝经后晚期乳腺癌患者每2周接受250mg福美司坦肌肉注射。在66例可全面评估的患者中,56例雌激素受体(ER)阳性,43例无病间期≥2年。软组织(53%)、骨(53%)和内脏(47%)的转移灶可评估;34例患者有1处转移灶,32例有≥2处转移灶。2周后血清雌二醇水平显著下降(p<0.01),此后保持不变,而尿17-OHCS水平在治疗期间未发生变化。19例患者(29%)获得客观缓解,其中8例完全缓解。就疾病部位而言,软组织(33%)和内脏(30%)的缓解情况相似,而骨转移的缓解率为18%。福美司坦的总体耐受性良好,只有2例患者抱怨有局部副作用。我们得出结论,福美司坦对绝经后激素依赖性乳腺癌患者是一种有效的芳香化酶抑制剂,且不干扰肾上腺类固醇生成。