Validation of serum C-reactive protein (CRP) as an independent prognostic factor for disease-free survival in patients with localised renal cell carcinoma (RCC)

被引:58
作者
de Martino, Michela [1 ]
Klatte, Tobias [1 ]
Seemann, Christoph [1 ]
Waldert, Matthias [1 ]
Haitel, Andrea [2 ]
Schatzl, Georg [1 ]
Remzi, Mesut [3 ]
Weibl, Peter [1 ]
机构
[1] Med Univ Vienna, Dept Urol, A-1090 Vienna, Austria
[2] Med Univ Vienna, Dept Clin Pathol, A-1090 Vienna, Austria
[3] LKH Weinviertel Korneuburg, Dept Urol, Korneuburg, Austria
关键词
CRP; inflammation; recurrence; accuracy; prognosis; kidney cancer;
D O I
10.1111/bju.12067
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objective To validate high-sensitivity C-reactive protein (hs-CRP) serum levels as an independent marker for disease-free survival (DFS) in clinically localised clear cell renal cell carcinoma (ccRCC). Patients and Methods In all, 403 consecutive patients with clinically localised (T1-3N0M0) ccRCC treated by radical or partial nephrectomy were enrolled. Preoperative serum levels of hs-CRP were evaluated as both a continuous and categorical variables. Associations with clinical (age, gender) and pathological variables (T classification, grade, tumour necrosis) were assessed with the chi-square and Kruskal-Wallis tests. Univariable and multivariable Cox proportional hazards models were fitted. The prognostic accuracy (PA) was assessed with Harrell's C-index. Results The mean hs-CRP level was 1.32mg/dL. The hs-CRP levels were associated with T classification (P = 0.05), high-grade disease (P < 0.001) and tumour necrosis (P = 0.003). After a median follow-up of 43 months, 41 patients (10.1%) had developed disease recurrence. With each unit increase in hs-CRP levels, the risk of recurrence increased by 10% (hazard ratio 1.10, P = 0.015). The thresholds of 0.5 and 0.75mg/dL showed the best discrimination for stratification of patients according to the probability of recurrence. These categorically coded hs-CRP levels were identified as independent prognostic factors in multivariable analyses (P < 0.001) and led to a significant increase in the PA of a multivariable base model containing the variables of the Stage, Size, Grade and Necrosis' (SSIGN) score. Conclusions This study validates preoperative serum hs-CRP levels as independent prognostic factor after surgery for localised ccRCC. Hs-CRP may be included in standard prognostic modelling after surgery and may guide surveillance and inclusion in adjuvant clinical trials.
引用
收藏
页码:E348 / E353
页数:6
相关论文
共 28 条
[1]  
Zisman A., Pantuck A.J., Wieder J., Chao D.H., Dorey F., Said J.W., DeKernion J.B., Figlin R.A., Belldegrun A.S., Risk group assessment and clinical outcome algorithm to predict the natural history of patients with surgically resected renal cell carcinoma, Journal of Clinical Oncology, 20, 23, pp. 4559-4566, (2002)
[2]  
Park Y.H., Baik K.D., Lee Y.J., Ku J.H., Kim H.H., Kwak C., Late recurrence of renal cell carcinoma >5 years after surgery: Clinicopathological characteristics and prognosis, BJU Int, 110, (2012)
[3]  
Kim S.P., Weight C.J., Leibovich B.C., Et al., Outcomes and clinicopathologic variables associated with late recurrence after nephrectomy for localized renal cell carcinoma, Urology, 78, pp. 1101-1106, (2011)
[4]  
Ljungberg B., Cowan N.C., Hanbury D.C., Et al., EAU guidelines on renal cell carcinoma: The 2010 update, Eur Urol, 58, pp. 398-406, (2010)
[5]  
Thillai K., Allan S., Powles T., Rudman S., Chowdhury S., Neoadjuvant and adjuvant treatment of renal cell carcinoma, Expert Rev Anticancer Ther, 12, pp. 765-776, (2012)
[6]  
Kenney P.A., Wood C.G., Integration of surgery and systemic therapy for renal cell carcinoma, Urol Clin North Am, 39, pp. 211-231, (2012)
[7]  
Klatte T., Lam J.S., Shuch B., Belldegrun A.S., Pantuck A.J., Surveillance for renal cell carcinoma: Why and how? When and how often?, Urol Oncol, 26, pp. 550-554, (2008)
[8]  
Leibovich B.C., Blute M.L., Cheville J.C., Lohse C.M., Frank I., Kwon E.D., Weaver A.L., Parker A.S., Zincke H., Prediction of progression after radical nephrectomy for patients with clear cell renal cell carcinoma: A stratification tool for prospective clinical trials, Cancer, 97, 7, pp. 1663-1671, (2003)
[9]  
Vakkila J., Lotze M.T., Inflammation and necrosis promote tumour growth, Nature Reviews Immunology, 4, 8, pp. 641-648, (2004)
[10]  
Karakiewicz P.I., Hutterer G.C., Trinh Q.-D., Jeldres C., Perrotte P., Gallina A., Tostain J., Patard J.-J., C-reactive protein is an informative predictor of renal cell carcinoma-specific mortality: A European study of 313 patients, Cancer, 110, 6, pp. 1241-1247, (2007)