Effect of (Neo)adjuvant zoledronic acid on disease-free and overall survival in clinical stage II/III breast cancer

被引:26
作者
Aft, R. L. [1 ,2 ,3 ]
Naughton, M. [2 ,4 ]
Trinkaus, K. [2 ,5 ]
Weilbaecher, K. [2 ,4 ]
机构
[1] Washington Univ, Dept Surg, Sch Med, St Louis, MO 63110 USA
[2] Washington Univ, Siteman Canc Ctr, St Louis, MO 63110 USA
[3] John Cochran Vet Adm Hosp, St Louis, MO 63106 USA
[4] Washington Univ, Dept Med, St Louis, MO 63110 USA
[5] Washington Univ, Div Biostat, St Louis, MO 63110 USA
关键词
bisphosphonate; breast cancer; chemotherapy; hormone receptor; neoadjuvant; zoledronic acid; NEOADJUVANT CHEMOTHERAPY; BONE; THERAPY; WOMEN;
D O I
10.1038/bjc.2012.210
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
BACKGROUND: Despite neoadjuvant/adjuvant chemotherapy, women with resectable stage II/III breast cancer (BC) have high risk of recurrent disease. Recent data suggest that zoledronic acid (ZOL) therapy concurrent with adjuvant treatments may improve cancer-related outcomes in patients with BC. METHODS: Disease-free survival (DFS; secondary end point) and overall survival (OS; tertiary end point) were evaluated in 119 women with stage II/III BC randomised to intravenous ZOL 4mg every 3 weeks for 1 year or no ZOL (control) starting with the first chemotherapy cycle. RESULTS: At 61.9 months' median follow-up, there was no significant difference in recurrence or survival between study arms. However, time to recurrence or death (DFS) was significantly different between subgroups defined by oestrogen receptor (ER) status (interaction P = 0.010 for DFS and 0.025 for OS). Hazard ratios (HRs) for disease recurrence and death were significantly less among patients with ER-negative (ER-) tumours who received ZOL vs no ZOL (DFS: HR = 0.361, 95% confidence interval (CI) 0.148, 0.880; OS: HR = 0.375, 95% CI 0.143, 0.985). CONCLUSION: ZOL administered with chemotherapy may improve DFS and OS in a subset of BC patients with ER- tumours. This study was not powered to compare subgroups of patients; thus, these findings should be considered hypothesis generating. British Journal of Cancer (2012) 107, 7-11. doi:10.1038/bjc.2012.210 www.bjcancer.com Published online 22 May 2012 (C) 2012 Cancer Research UK
引用
收藏
页码:7 / 11
页数:5
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