Clinical and endocrine data for goserelin plus anastrozole as second-line endocrine therapy for premenopausal advanced breast cancer

被引:100
作者
Forward, DP [1 ]
Cheung, KL [1 ]
Jackson, L [1 ]
Robertson, JFR [1 ]
机构
[1] City Hosp, Surg Unit, Nottingham NG5 1PB, England
关键词
goserelin; tamoxifen; anastrozole; breast cancer; oestradiol; endocrine therapy;
D O I
10.1038/sj.bjc.6601557
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A total of 16 premenopausal women with metastatic breast cancer (N = 13) or locally advanced primary breast cancer (N = 3) were treated with a combination of a gonadotropin-releasing hormone agonist goserelin, and a selective aromatase inhibitor anastrozole. All had previously been treated with goserelin and tamoxifen. In all, 12 patients (75%) achieved objective response or durable stable disease at 6 months, with a median duration of remission of 17+ months (range 6-47 months). Four patients still have clinical benefit. Introduction of goserelin and tamoxifen resulted in an 89% reduction in mean oestradiol levels (pretreatment vs 6 months = 224 vs 24 pmol l(-1)) (P<0.0001). Substitution of tamoxifen by anastrozole on progression resulted in a further 76% fall (to 6 pmol l(-1) at 3 months) (P<0.0001). Treatment with goserelin and tamoxifen led to a 90% fall in the mean follicle-stimulating hormone (P<0.001). This was reversed once therapy was changed to goserelin and anastrozole. A similar initial reduction was seen in the mean luteinising hormone levels, but substitution of tamoxifen by anastrozole on progression resulted in no significant change. Goserelin and tamoxifen did not lead to any significant change in testosterone and androstenedione levels. The combined use of goserelin and anastrozole as second-line endocrine therapy produces a significant clinical response of worthwhile duration, with demonstrable endocrine changes, in premenopausal women with advanced breast cancer, and offers them another therapeutic option. Further studies involving more patients and longer follow-up are indicated.
引用
收藏
页码:590 / 594
页数:5
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