Zilembo N, Bajetta E, Noberasco C, Buzzoni R, Vicario G, Bono A, Laffranchi A, Biasi G, Dolci S, Bichisao E
Division of Medical Oncology B, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy.
J Cancer Res Clin Oncol. 1995;121(6):378-82. doi: 10.1007/BF01225692.
Formestane, a new selective aromatase inhibitor devoid of severe side-effects, has been shown to be active in patients with advanced breast cancer. To investigate the clinical activity and endocrinological effects of formestane as a first-line treatment, 52 patients were administered two different doses: 24 received 250 mg formestane and 28 received 500 mg formestane i.m. fortnightly. All of the patients had a performance status of 2 or less (ECOG scale), 34 (65%) had a disease-free interval of at least 2 years and 21 (40%) were both oestrogen-receptor- and progesterone-receptor-positive; 20 patients received hormone and 13, received chemotherapeutical adjuvant treatment. Objective responses were obtained in 8 patients in the 250-mg group (33%; 95% CI: 14%-52%) and in 13 patients in the 500-mg group (46%; 95% CI: 28%-64%). The median response duration in the two groups was respectively 11 and 12 months. E2 serum levels of oestradiol had significantly (P < 0.001) decreased to more than 40% below the baseline value in both groups after 15 days of treatment, and remained unchanged thereafter. Local and systemic tolerability was satisfactory. We conclude that formestane is an effective and well-tolerated agent in previously untreated patients, and that these results should be confirmed by further studies.
福美司坦是一种新型的选择性芳香化酶抑制剂,无严重副作用,已证明对晚期乳腺癌患者有活性。为研究福美司坦作为一线治疗的临床活性和内分泌效应,对52例患者给予两种不同剂量:24例接受250mg福美司坦,28例接受500mg福美司坦,均为每两周肌肉注射一次。所有患者的体能状态评分为2分或更低(东部肿瘤协作组量表),34例(65%)无病生存期至少2年,21例(40%)雌激素受体和孕激素受体均为阳性;20例患者接受过激素辅助治疗,13例接受过化疗辅助治疗。250mg组8例患者获得客观缓解(33%;95%置信区间:14%-52%),500mg组13例患者获得客观缓解(46%;95%置信区间:28%-64%)。两组的中位缓解持续时间分别为11个月和12个月。治疗15天后,两组雌二醇的血清E2水平均显著降低(P<0.001),降至基线值以下40%以上,此后保持不变。局部和全身耐受性良好。我们得出结论,福美司坦对既往未接受过治疗的患者是一种有效且耐受性良好的药物,这些结果应通过进一步研究予以证实。