The effects of adding zoledronic acid to neoadjuvant chemotherapy on tumour response: exploratory evidence for direct anti-tumour activity in breast cancer

被引:172
作者
Coleman, R. E. [1 ]
Winter, M. C.
Cameron, D. [2 ]
Bell, R. [3 ]
Dodwell, D. [4 ]
Keane, M. M. [5 ]
Gil, M. [6 ]
Ritchie, D. [7 ]
Passos-Coelho, J. L. [8 ]
Wheatley, D. [9 ]
Burkinshaw, R.
Marshall, S. J. [10 ]
Thorpe, H. [10 ]
机构
[1] Univ Sheffield, Weston Pk Hosp, Canc Res Ctr, Acad Unit Clin Oncol, Sheffield S10 2SJ, S Yorkshire, England
[2] Univ Leeds, St James Inst Oncol, Leeds, W Yorkshire, England
[3] Andrew Love Canc Ctr, Geelong, Vic, Australia
[4] Leeds Teaching Hosp NHS Trust, St James Inst Oncol, Leeds, W Yorkshire, England
[5] Univ Hosp Galway, Galway, Ireland
[6] IDIBELL, Inst Catala Oncol, Barcelona, Spain
[7] Western Infirm & Associated Hosp, Beatson Oncol Ctr, Glasgow G11 6NT, Lanark, Scotland
[8] Inst Portugues Oncol Francisco Gentil, Lisbon, Portugal
[9] Royal Cornwall Hosp, Cornwall, England
[10] Univ Leeds, Clin Trials Res Unit, Leeds, W Yorkshire, England
关键词
anti-tumour activity; breast cancer; chemotherapy; neoadjuvant; pathological response; ZOL; SURGICAL ADJUVANT BREAST; PREOPERATIVE CHEMOTHERAPY; PATHOLOGICAL ASSESSMENT; SYSTEMIC THERAPY; DOXORUBICIN; BISPHOSPHONATES; DISEASE; CARCINOMA; SURVIVAL; ISSUES;
D O I
10.1038/sj.bjc.6605604
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Pre-clinical studies have demonstrated synergistic anti-tumour effects of chemotherapy (CT) and zoledronic acid (ZOL). Within the AZURE trial, designed to determine whether the addition of ZOL to neoadjuvant therapy improves disease outcomes, a subgroup received neoadjuvant CT. We report a retrospective evaluation comparing pathological response in the primary tumour between treatment groups. METHODS: In total, 205 patients received neoadjuvant CT +/- ZOL (CT+ZOL, n=102; CT, n=103). The primary end point was pathologically assessed residual invasive tumour size (RITS) at surgery. Secondary end points were pathological complete response (pCR) rate and axillary nodal involvement. Following review of surgical pathology reports (n=195), outcome differences between groups were assessed adjusting for potential response modifiers. RESULTS: Baseline characteristics and CT treatments were similar. In multivariate analysis, allowing for biological and clinical factors known to influence tumour response, the adjusted mean RITS in CT and CT+ZOL groups were 27.4 and 15.5 mm, respectively, giving a difference in means of 12mm (95% confidence interval: 3.5-20.4 mm; P=0.006). The pCR rate was 6.9% in the CT group and 11.7% in the CT+ZOL group (P=0.146). There was no difference in axillary nodal involvement (P=0.6315). CONCLUSION: These data suggest a possible direct anti-tumour effect of ZOL in combination with CT, warranting formal evaluation in prospective studies. British Journal of Cancer (2010) 102, 1099-1105. doi:10.1038/sj.bjc.6605604 www.bjcancer.com Published online 16 March 2010 (C) 2010 Cancer Research UK
引用
收藏
页码:1099 / 1105
页数:7
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