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Improved survival prediction and comparison of prognostic models for patients with hepatocellular carcinoma treated with sorafenib

机译:改进索拉非尼治疗肝细胞癌患者的生存预测和预后模型比较

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Abstract Background The ‘Prediction Of Survival in Advanced Sorafenib‐treated HCC’ (PROSASH) model addressed the heterogeneous survival of patients with hepatocellular carcinoma (HCC) treated with sorafenib in clinical trials but requires validation in daily clinical practice. This study aimed to validate, compare and optimize this model for survival prediction. Methods Patients treated with sorafenib for HCC at five tertiary European centres were retrospectively staged according to the PROSASH model. In addition, the optimized PROSASH‐II model was developed using the data of four centres (training set) and tested in an independent dataset. These models for overall survival (OS) were then compared with existing prognostic models. Results The PROSASH model was validated in 445 patients, showing clear differences between the four risk groups (OS 16.9‐4.6?months). A total of 920 patients (n?=?615 in training set, n?=?305 in validation set) were available to develop PROSASH‐II. This optimized model incorporated fewer and less subjective parameters: the serum albumin, bilirubin and alpha‐foetoprotein, and macrovascular invasion, extrahepatic spread and largest tumour size on imaging. Both PROSASH and PROSASH‐II showed improved discrimination (C‐index 0.62 and 0.63, respectively) compared with existing prognostic scores (C‐index ≤0.59). Conclusions In HCC patients treated with sorafenib, individualized prediction of survival and risk group stratification using baseline prognostic and predictive parameters with the PROSASH model was validated. The refined PROSASH‐II model performed at least as good with fewer and more objective parameters. PROSASH‐II can be used as a tool for tailored treatment of HCC in daily practice and to define pre‐planned subgroups for future studies.
机译:摘要 背景 “晚期索拉非尼治疗的肝癌生存预测”(PROSASH)模型解决了在临床试验中接受索拉非尼治疗的肝细胞癌(HCC)患者的异质生存期,但需要在日常临床实践中进行验证。本研究旨在验证、比较和优化该模型的生存预测。方法 采用PROSASH模型回顾性分析欧洲5个三级中心接受索拉非尼治疗肝细胞癌的患者。此外,使用四个中心(训练集)的数据开发了优化的 PROSASH-II 模型,并在独立数据集中进行了测试。然后将这些总生存期 (OS) 模型与现有的预后模型进行比较。结果 PROSASH模型在445例患者中得到验证,4个风险组(OS 16.9-4.6?个月)之间存在明显差异。共有 920 名患者(训练组 n?=?615 名,验证组 n?=?305 名)可用于开发 PROSASH-II。该优化模型包含越来越少的主观参数:血清白蛋白、胆红素和甲胎蛋白,以及成像上大血管浸润、肝外扩散和最大肿瘤大小。与现有的预后评分(C指数≤0.59)相比,PROSASH 和 PROSASH-II 的鉴别力均有所提高(C 指数分别为 0.62 和 0.63)。结论 在接受索拉非尼治疗的HCC患者中,使用基线预后和预测参数以及PROSASH模型对生存率和风险组分层的个体化预测进行了验证。改进的 PROSASH-II 模型在更少和更客观的参数下至少表现同样好。PROSASH-II 可用作日常实践中定制 HCC 治疗的工具,并为未来的研究定义预先计划的亚组。

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