Sydney Cancer Centre, Concord Repatriation General Hospital, Concord, Australia; Sydney Medical School, University of Sydney, Sydney, Australia.
Clin Genitourin Cancer. 2013 Dec;11(4):423-30. doi: 10.1016/j.clgc.2013.04.020. Epub 2013 Jun 28.
The modified Glasgow Prognostic Score (mGPS), derived from C-reactive protein (CRP) and albumin levels, and the neutrophil-lymphocyte ratio (NLR) have demonstrated prognostic significance in a number of malignancies.
Baseline mGPS and NLR were calculated in a prospective cohort of chemotherapy-naive patients with metastatic castration-resistant prostate cancer (mCRPC) (AT-101-CS-205 trial) who received docetaxel and prednisone ± AT101. Cox proportional hazards regression models estimated their effects on overall survival (OS).
Of 220 eligible patients, mGPS and neutrophil and lymphocyte counts were available for 184, 193, and 112 patients, respectively. Albumin (hazard ratio [HR], 0.28; 95% confidence interval [CI]: 0.14-0.56; P < .001) and CRP (HR, 1.22; 95% CI, 1.00-1.48; P = .048) were independently prognostic for OS. An association between mGPS and OS was found (HR, 1.87; 95% CI, 1.35-2.59; P < .001; median survival, 23.5 months at mGPS 0 vs. 9.8 months at mGPS 2). mGPS was significant after controlling for 3 previously published nomograms or NLR (P ≤ .001). NLR was not prognostic for OS (HR, 0.98; P = .91), and no association between mGPS and toxicity was noted.
Our results demonstrate the prognostic role of the mGPS in mCRPC over variables previously identified. mGPS is inexpensive, easily measured, and could be incorporated into routine clinical testing if our results are confirmed in a subsequent validation study. The utility of the NLR in mCRPC remains uncertain despite evidence in other malignancies.
改良格拉斯哥预后评分(mGPS)由 C 反应蛋白(CRP)和白蛋白水平推导而来,中性粒细胞与淋巴细胞比值(NLR)在多种恶性肿瘤中显示出预后意义。
在接受多西他赛和泼尼松±AT101 治疗的转移性去势抵抗性前列腺癌(mCRPC)(AT-101-CS-205 试验)的前瞻性队列研究中,计算了基线 mGPS 和 NLR。Cox 比例风险回归模型估计了它们对总生存(OS)的影响。
在 220 名符合条件的患者中,mGPS 和中性粒细胞及淋巴细胞计数分别可用于 184、193 和 112 名患者。白蛋白(危险比 [HR],0.28;95%置信区间 [CI]:0.14-0.56;P<0.001)和 CRP(HR,1.22;95%CI,1.00-1.48;P=0.048)独立预测 OS。mGPS 与 OS 之间存在相关性(HR,1.87;95%CI,1.35-2.59;P<0.001;mGPS 0 时中位生存 23.5 个月,mGPS 2 时 9.8 个月)。在控制了 3 个先前发表的列线图或 NLR 后,mGPS 仍然有意义(P≤0.001)。NLR 对 OS 无预后意义(HR,0.98;P=0.91),并且 mGPS 与毒性之间没有关联。
我们的结果表明 mGPS 在 mCRPC 中的预后作用超过了以前确定的变量。mGPS 价格低廉,易于测量,如果在后续验证研究中得到证实,它可以纳入常规临床检测。尽管在其他恶性肿瘤中有证据,但 NLR 在 mCRPC 中的应用仍不确定。