三叶曲烷:一种治疗晚期绝经后乳腺癌的新激素。

Cancer treatment reports Pub Date : 1987-12-01
C J Williams, V Barley, G Blackledge, A Hutcheon, S Kaye, D Smith, C Keen, D J Webster, C Rowland, C Tyrrell
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引用次数: 0

摘要

Trilostane是一种抑制肾上腺雌激素分泌的药物,与地塞米松一起应用于97名绝经后晚期乳腺癌妇女。74名接受trilostane治疗至少10周的患者或在此期间之前疾病进展的患者被评估肿瘤反应。18例患者(25%)有客观反应(2例完全,16例部分);另有21例患者病情稳定。所有97名患者(包括至少10周未接受治疗的患者)的缓解率为19%。97例患者中有32例报告不良反应,这些不良反应归因于trilostane和/或地塞米松。15名患者停止治疗,10名患者减少了trilostane的剂量。腹泻是最常见的副作用,有16例患者报告,其中9例停止治疗。Trilostane与皮质类固醇联合使用,是一种有效的替代激素,通过肾上腺阻断治疗绝经后晚期乳腺癌妇女。
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Multicenter study of trilostane: a new hormonal agent in advanced postmenopausal breast cancer.

Trilostane, an inhibitor of the production of adrenal estrogens, was administered, together with dexamethasone, to 97 eligible postmenopausal women with advanced breast cancer. Seventy-four patients who had either received trilostane for a minimum of 10 weeks or whose disease had progressed while on trilostane before this period were assessed for tumour response. Eighteen patients (25%) had objective responses (two complete, 16 partial); a further 21 patients had stable disease. The response rate among all 97 patients, including those not treated for a minimum 10-week period, was 19%. Thirty-two of 97 patients reported adverse reactions which were attributed to trilostane and/or dexamethasone. Therapy was stopped for 15 patients, and the dose of trilostane was reduced for ten. Diarrhea was the commonest side effect, being reported in 16 patients, of whom nine stopped treatment. Trilostane, given with a corticosteroid, is an effective alternative hormonal agent acting by adrenal blockade for postmenopausal women with advanced breast cancer.

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