Prognostic utility of pre-operative circulating osteopontin, carbonic anhydrase IX and CRP in renal cell carcinoma

被引:49
|
作者
Sim, S. H. [2 ]
Messenger, M. P. [1 ]
Gregory, W. M. [3 ]
Wind, T. C. [1 ]
Vasudev, N. S. [1 ]
Cartledge, J. [4 ]
Thompson, D. [1 ]
Selby, P. J. [1 ]
Banks, R. E. [1 ]
机构
[1] St James Univ Hosp, Canc Res UK Ctr, Leeds Inst Mol Med, Clin & Biomed Prote Grp, Leeds LS9 7TF, W Yorkshire, England
[2] St James Univ Hosp, St Jamess Inst Oncol, Leeds, W Yorkshire, England
[3] Univ Leeds, Clin Trials Res Unit, Leeds, W Yorkshire, England
[4] St James Univ Hosp, Dept Urol, Leeds LS9 7TF, W Yorkshire, England
基金
美国国家卫生研究院;
关键词
osteopontin; renal cancer; carbonic anhydrase IX; prognosis; RCC; CRP; LINKED-IMMUNOSORBENT-ASSAY; C-REACTIVE-PROTEIN; INDEPENDENT PREDICTOR; RADICAL NEPHRECTOMY; POOR SURVIVAL; EXPRESSION; SERUM; VALIDATION; RECURRENCE; NECROSIS;
D O I
10.1038/bjc.2012.360
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Objectively measured circulating biomarkers of prognosis complementing existing clinicopathological models are needed in renal cell carcinoma (RCC). METHODS: Blood samples collected from 216 RCC patients in Leeds before nephrectomy (median follow-up 7 years) were analysed for C-reactive protein (CRP), osteopontin (OPN) and carbonic anhydrase IX (CA9) and prognostic significance determined. RESULTS: CA9, OPN and CRP were univariately prognostic for overall survival (OS), cancer-specific survival (CSS) and disease-free survival (DFS) with CRP and CA9 being independently prognostic for OS/CSS and OS, respectively. Including CA9, OPN and CRP with other conventional prognostic factors gave a superior predictive capacity when compared with a previously published pre-operative clinical nomogram (Karakiewicz et al, 2009). Osteopontin outperformed this nomogram and the post-operative SSIGN score for OS but not for CSS, being significantly predictive for non-cancer deaths. Osteopontin, CRP and CA9 outperformed stage (c-index 76% compared with 70% for stage) and OPN or CA9 identified several subsets of poor prognosis patients including in T1 patients, who may benefit from adjuvant therapy and increased surveillance. CONCLUSION: Circulating CA9, OPN and CRP add value to existing clinicopathological prognostic factors/models and support further studies to investigate their potential use in improving the clinical management of RCC. British Journal of Cancer (2012) 107, 1131-1137. doi:10.1038/bjc.2012.360 www.bjcancer.com Published online 23 August 2012 (c) 2012 Cancer Research UK
引用
收藏
页码:1131 / 1137
页数:7
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