Ovarian function suppression and fulvestrant as endocrine therapy in premenopausal women with metastatic breast cancer

被引:42
|
作者
Bartsch, Rupert
Bago-Horvath, Zsuzsanna [2 ]
Berghoff, Anna
DeVries, Catharina
Pluschnig, Ursula
Dubsky, Peter [3 ]
Rudas, Margaretha [2 ]
Mader, Robert M.
Rottenfusser, Andrea [4 ]
Fitzal, Florian [3 ]
Gnant, Michael [3 ]
Zielinski, Christoph C.
Steger, Guenther G. [1 ]
机构
[1] Med Univ Vienna, Comprehens Canc Ctr Vienna, Div Clin Oncol, Dept Med 1, A-1090 Vienna, Austria
[2] Med Univ Vienna, Dept Pathol, A-1090 Vienna, Austria
[3] Med Univ Vienna, Dept Surg, A-1090 Vienna, Austria
[4] Med Univ Vienna, Dept Radiotherapy, A-1090 Vienna, Austria
关键词
Endocrine therapy; Fulvestrant; Goserelin; Metastatic breast cancer; Premenopausal patients; POSTMENOPAUSAL WOMEN; ESTROGEN-RECEPTOR; AROMATASE INHIBITOR; RANDOMIZED TRIALS; DOUBLE-BLIND; ANASTROZOLE; MULTICENTER; CARCINOMA; TAMOXIFEN; GOSERELIN;
D O I
10.1016/j.ejca.2012.03.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Endocrine therapy is the preferred treatment for hormone-receptor (HR) positive metastatic breast cancer. In premenopausal patients, ovarian function suppression with goserelin in combination with anastrozole yielded promising results in phase II studies. Fulvestrant, a pure antioestrogen, yields high rates of disease stabilisation in postmenopausal women. Therefore, we investigated the feasibility and safety of fulvestrant plus goserelin in premenopausal women with HR-positive metastatic breast cancer. Methods: Premenopausal patients with metastatic breast cancer eligible for endocrine treatment received fulvestrant 250 mg and goserelin 3.6 mg every four weeks as first- to fourth-line therapy. Clinical benefit rate (CBR; response rate plus disease stabilisation >= 6 months) was defined as the primary study end-point. Time to progression (TTP) and overall survival (OS) were estimated using the Kaplan-Meier product limit method. Findings: Twenty-six patients received treatment as scheduled. 81% were pre-treated with tamoxifen and 69% had received prior aromatase inhibitors in combination with goserelin. The majority of patients (69%) presented with visceral metastases. Complete response was observed in a single patient, partial response in three and disease stabilisation >= 6 months in eleven patients, resulting in a CBR of 58%. Median TTP was 6 months (95% confidence interval (CI), 2.4-9.6) and OS 32 months (95% CI, 14.28-49.72), respectively. Interpretation: Results suggest that the combination of fulvestrant and goserelin offers promising activity in premenopausal patients and further investigation is warranted. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1932 / 1938
页数:7
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