C-reactive protein is an informative predictor of renal cell carcinoma-specific mortality - A European study of 313 patients

被引:145
作者
Karakiewicz, Pierre I.
Hutterer, Georg C.
Trinh, Quoc-Dien
Jeldres, Claudio
Perrotte, Paul
Gallina, Andrea
Tostain, Jacques
Patard, Jean-Jacques
机构
[1] Univ Montreal, Ctr Hlth, Canc Prognost & Hlth Outcomes Unit, Montreal, PQ H2X 3J4, Canada
[2] Univ Montreal, Dept Urol, Montreal, PQ, Canada
[3] Graz Med Univ, Dept Urol, Graz, Austria
[4] Univ Vita Salute San Raffaele, Dept Urol, Milan, Italy
[5] St Etienne Univ Hosp, Dept Urol, St Etienne, France
[6] Rennes Univ Hosp, Dept Urol, Rennes, France
关键词
c-reactive protein; mortality; prognosis; renal cell carcinoma;
D O I
10.1002/cncr.22896
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
BACKGROUND. C-reactive protein (CRIP) represents a promising prognostic variable in patients with sporadic renal cell carcinoma (RCC). It was hypothesized that CRP can improve the prognostic ability of standard RCC-specific mortality (RCC-SM) predictors in patients treated with nephrectomy for all stages of RCC. METHODS. Radical nephrectomy was performed in 314 patients from 2 European centers. Life table, Kaplan-Meier, and Cox regression analyses addressed RCC-SM. Covariates included age, gender, TNM stage, tumor size, Fuhrman grade, and histologic Subtype. RESULTS. The median survival of the cohort was 19.9 years. Age ranged from 10 to 77 years. Most patients were male (69%). T-stages were distributed as follows: T1-121 (38.7%), T2-45 (14.4%), T3-140 (44.7%), T4-7 (2.2%). CRP values ranged from 1.0 to 358.0 mg/L (mean 40.9, median 11.0 mg/L). In multivariable analyses, CRP was an independent predictor of RCC-SM (P = .003). The consideration of CRP in the multivariable model increased the predictive accuracy by 3.7% (P < .001). Moreover, the model with CRP performed 2.4% and 4.6% better than the UCLA Integrated Staging System (UISS) at, respectively, 2 and 5 years. CONCLUSIONS. CRP represents an informative predictor of RCC-SM. Its routine use could allow better risk stratification and risk-adjusted follow-up of RCC patients.
引用
收藏
页码:1241 / 1247
页数:7
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