Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan.
Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan.
Urol Oncol. 2020 Jan;38(1):6.e9-6.e16. doi: 10.1016/j.urolonc.2019.07.013. Epub 2019 Aug 8.
To develop a novel model to predict outcomes in patients with previously treated metastatic renal cell carcinoma.
This study included 78 consecutive metastatic renal cell carcinoma patients receiving first- and second-line targeted therapies at our institution. Predictive factors of overall survival (OS) at the second-line setting in these patients were investigated, and a novel prognostic model was developed.
Median OS from the initiation of second-line therapy was 21.9 months. A multivariate analysis of several parameters identified the following independent predictors associated with poor OS: albumin (Alb, ≤3.5 g/dl), C-reactive protein (CRP, >0.5 mg/dl), and lactate dehydrogenase (LDH, >1.5 × upper limit of normal). When patients were divided into 3 groups based on the positive numbers of these 3 independent risk factors, named the ACL (Alb, CRP, and LDH) model, median OS durations were 50 months in the favorable risk group without risk factors (n = 26), 25 months in the intermediate-risk group with a single risk factor (n = 24), and 8 months in the poor risk group (n = 28) with multiple risk factors. The superiority of the ACL model as a prognostic tool to the Memorial Sloan Kettering Cancer Center model for previously treated patients and the International Metastatic Renal Cell Carcinoma Database Consortium model was demonstrated by Harrell's concordance index and a decision curve analysis.
The ACL model in the second-line targeted therapy setting may predict outcomes more accurately than the Memorial Sloan Kettering Cancer Center and International Metastatic Renal Cell Carcinoma Database Consortium models.
开发一种新的模型来预测接受过一线和二线靶向治疗的转移性肾细胞癌患者的结局。
本研究纳入了 78 例在我院接受一线和二线靶向治疗的转移性肾细胞癌患者。研究了这些患者二线治疗总体生存(OS)的预测因素,并建立了一个新的预后模型。
二线治疗开始后的中位 OS 为 21.9 个月。对多个参数的多变量分析确定了以下与不良 OS 相关的独立预测因素:白蛋白(Alb,≤3.5g/dl)、C 反应蛋白(CRP,>0.5mg/dl)和乳酸脱氢酶(LDH,>1.5×正常上限)。当根据这 3 个独立危险因素的阳性数量将患者分为 3 组,命名为 ACL(Alb、CRP 和 LDH)模型时,无危险因素的有利风险组(n=26)中位 OS 持续时间为 50 个月,单一危险因素的中危组(n=24)为 25 个月,多个危险因素的不良风险组(n=28)为 8 个月。通过 Harrell 一致性指数和决策曲线分析,证明了 ACL 模型作为预测工具优于 Memorial Sloan Kettering 癌症中心模型和国际转移性肾细胞癌数据库联盟模型。
在二线靶向治疗环境中,ACL 模型可能比 Memorial Sloan Kettering 癌症中心和国际转移性肾细胞癌数据库联盟模型更能准确预测结局。