Stuart-Harris R, Dowsett M, Bozek T, McKinna J A, Gazet J C, Jeffcoate S L, Kurkure A, Carr L, Smith I E
Lancet. 1984 Sep 15;2(8403):604-7. doi: 10.1016/s0140-6736(84)90596-8.
The clinical and endocrine effects of low-dose aminoglutethimide without hydrocortisone in patients with advanced breast cancer were investigated. In a dose escalation study low-dose aminoglutethimide alone (62.5-125 mg twice daily) was as effective as conventional doses with hydrocortisone in lowering serum oestrone and oestradiol concentrations but caused minimum adrenal inhibition, as assessed by serum dehydroepiandrosterone sulphate. 11 of 57 (19%) evaluable patients had tumour regression by objective criteria on this treatment, but the frequency of side-effects was similar to that with conventional doses. Low-dose aminoglutethimide is active in the treatment of breast cancer. It appears to work by inhibition of the aromatase enzyme system in peripheral tissues rather than adrenal suppression.
研究了低剂量氨鲁米特(不联用氢化可的松)对晚期乳腺癌患者的临床及内分泌影响。在一项剂量递增研究中,单独使用低剂量氨鲁米特(每日两次,每次62.5 - 125毫克)在降低血清雌酮和雌二醇浓度方面与联用氢化可的松的常规剂量效果相当,但通过血清硫酸脱氢表雄酮评估,其对肾上腺的抑制作用最小。57例可评估患者中有11例(19%)在此治疗下依据客观标准出现肿瘤消退,但其副作用发生率与常规剂量相似。低剂量氨鲁米特在乳腺癌治疗中具有活性。它似乎是通过抑制外周组织中的芳香化酶系统而非抑制肾上腺起作用。