Department of Urology, Gartnavel General Hospital, Glasgow G12 0YN, UK.
Br J Cancer. 2012 Jan 17;106(2):279-83. doi: 10.1038/bjc.2011.556. Epub 2011 Dec 13.
Measurement of the systemic inflammatory response in malignancy has been recently refined using a selective combination of C-reactive protein and albumin (modified Glasgow Prognostic Score, mGPS). This has prognostic value in patients with metastatic kidney cancer. This study examines the prognostic value of the mGPS in patients undergoing curative nephrectomy for clear cell cancer.
Patients with localised renal cell carcinoma undergoing potentially curative resection between March 1997 and July 2007 in a single institution were prospectively studied. The mGPS, University of California Los Angeles Integrated Staging System (UISS), 'Stage Size Grade Necrosis' (SSIGN), Kattan and Leibovich scores were constructed.
A total of 169 patients were studied. The minimum follow-up was 49 months; the median follow-up of the survivors was 98 months. During this period, 35 patients died of their cancer; a further 24 patients died of intercurrent disease. On univariate survival analysis of the scoring systems, Kattan (P<0.05), UISS (P<0.001), SSIGN (P<0.001) and Leibovich (P<0.001) were significantly associated with cancer-specific survival. Using cancer-specific mortality at 4 years as an endpoint, the area under the receiver operator curve was 0.726 (95% CI 0.629-0.822; P=0.001) for Kattan, 0.776 (95% CI 0.671-0.880; P<0.001) for UISS, 0.812 (95% CI 0.733-0.892; P<0.001) for SSIGN, 0.778 (95% CI 0.666-0.889; P<0.001) for Leibovich and 0.800 (95% CI 0.687-0.912; P<0.001) for the mGPS scoring system. On multivariate analysis of significant independent scoring systems and mGPS, UISS (HR 3.08, 95% CI 1.54-6.19, P=0.002) and mGPS (HR 5.13, 95% CI 2.89-9.11, P<0.001) were significant independent predictors of cancer-specific survival.
The present prospective study shows that the mGPS, an inflammation-based prognostic score, is at least equivalent to and independent of other current validated prognostic scoring systems for patients undergoing curative nephrectomy for renal clear cell cancer. The mGPS is simple, measured preoperatively, based on well-standardised, widely available protein assays, and therefore provides an objective and rational basis before treatment for future staging systems in patients with operable renal cancer.
最近,使用 C 反应蛋白和白蛋白(改良格拉斯哥预后评分,mGPS)的选择性组合来精确测量恶性肿瘤的全身炎症反应,这在转移性肾癌患者中具有预后价值。本研究检查了 mGPS 在接受根治性肾切除术治疗透明细胞癌的患者中的预后价值。
1997 年 3 月至 2007 年 7 月在一个机构中前瞻性研究接受潜在根治性切除的局限性肾细胞癌患者。构建 mGPS、加利福尼亚大学洛杉矶分校综合分期系统(UISS)、“分期大小分级坏死”(SSIGN)、卡坦和莱博维奇评分。
共研究了 169 例患者。最小随访时间为 49 个月;幸存者的中位随访时间为 98 个月。在此期间,35 例患者死于癌症;另有 24 例患者死于并发疾病。在单变量生存分析中,卡坦(P<0.05)、UISS(P<0.001)、SSIGN(P<0.001)和莱博维奇(P<0.001)与癌症特异性生存显著相关。使用 4 年癌症特异性死亡率作为终点,卡坦的受试者工作特征曲线下面积为 0.726(95%CI 0.629-0.822;P=0.001),UISS 为 0.776(95%CI 0.671-0.880;P<0.001),SSIGN 为 0.812(95%CI 0.733-0.892;P<0.001),莱博维奇为 0.778(95%CI 0.666-0.889;P<0.001),mGPS 为 0.800(95%CI 0.687-0.912;P<0.001)。在对显著独立评分系统和 mGPS 的多变量分析中,UISS(HR 3.08,95%CI 1.54-6.19,P=0.002)和 mGPS(HR 5.13,95%CI 2.89-9.11,P<0.001)是癌症特异性生存的独立显著预测因素。
本前瞻性研究表明,mGPS,一种基于炎症的预后评分,与目前用于接受根治性肾切除术治疗肾透明细胞癌的其他经证实的预后评分系统至少相当且独立。mGPS 简单,术前测量,基于经过良好标准化、广泛可用的蛋白质检测,因此为可手术性肾癌患者的未来分期系统提供了治疗前的客观和合理依据。