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氨鲁米特治疗绝经后晚期乳腺癌妇女。

Aminoglutethimide as treatment of postmenopausal women with advanced breast carcinoma.

作者信息

Santen R J, Worgul T J, Lipton A, Harvey H, Boucher A, Samojlik E, Wells S A

出版信息

Ann Intern Med. 1982 Jan;96(1):94-101. doi: 10.7326/0003-4819-96-1-94.

Abstract

Hormone-dependent breast carcinomas respond to deprivation of biologically active estrogens with objectively quantifiable tumor regression. Aminoglutethimide, a known inhibitor of steroid synthesis, is also a potent blocker of the aromatase enzyme and, thus, of estrogen production. We developed an effective regimen to inhibit estrogen production in postmenopausal women using aminoglutethimide and replacement glucocorticoid. One hundred forty-seven women initially received aminoglutethimide and replacement glucocorticoid as treatment of metastatic breast carcinoma. One hundred twenty-nine women are currently evaluable for assessment of clinical and hormonal responses. Thirty-seven percent of unselected women and 49% of estrogen receptor-positive patients experienced objective tumor regression. Responses occurred predominantly in soft tissue (47%) and bone (35%) and lasted 30 +/- 9.1 months for complete and 14 +/- 1.5 months for partial regressions. Plasma and urinary estrogen levels fell equally in responder versus nonresponder groups whereas androgen levels declined less in patients with progressive disease.

摘要

激素依赖性乳腺癌对生物活性雌激素的剥夺会产生客观可量化的肿瘤消退反应。氨鲁米特是一种已知的类固醇合成抑制剂,也是芳香化酶的有效阻断剂,因此可抑制雌激素生成。我们研发了一种使用氨鲁米特和替代糖皮质激素来抑制绝经后女性雌激素生成的有效方案。147名女性最初接受氨鲁米特和替代糖皮质激素治疗转移性乳腺癌。目前有129名女性可进行临床和激素反应评估。未筛选女性中有37%以及雌激素受体阳性患者中有49%出现了客观肿瘤消退。反应主要发生在软组织(47%)和骨骼(35%),完全消退持续30±9.1个月,部分消退持续14±1.5个月。反应组与无反应组的血浆和尿液雌激素水平下降程度相同,而疾病进展患者的雄激素水平下降较少。

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