Department of Oncology, University Hospital in Motol, Charles University, Prague, Czech Republic,
Target Oncol. 2015 Sep;10(3):385-92. doi: 10.1007/s11523-014-0343-8. Epub 2014 Oct 12.
The aim of this study was to describe the characteristics and outcomes of a large cohort of patients treated with sorafenib in clinical practice and to identify predictive factors associated with prognosis. Patient data were obtained from the national Czech registry (RenIS). Data of virtually all Czech patients receiving targeted therapies are entered into this non-interventional post-registration database. Demographics and clinical data, as well as all treatment sequences and clinical outcomes, are reported in this registry. A total of 836 patients treated with sorafenib before March 2013 were included in the analysis. Median age was 63 years and 70% were men. Most patients had received prior treatment with cytokines, sunitinib or both. Sorafenib was the first-line treatment in 15% of patients. Median overall survival and progression-free survival were 21.7 months and 7.5 months, respectively. Median overall survival and progression-free survival was 26.3 and 8.3 months, respectively, in patients receiving sorafenib as first-line therapy. Cox proportional models identified several parameters associated with poor outcome including time ≤1 year from diagnosis to first-line systemic treatment, performance status ≥2, low hemoglobin, and LDH >1.5 times the upper limit of normal. Our data demonstrate that the outcomes of real-life patients are comparable to those enrolled in clinical trials. Prognostic factors identified in the present study were consistent with previously reported models.
本研究旨在描述接受索拉非尼治疗的大样本患者的特征和结局,并确定与预后相关的预测因素。患者数据来自捷克国家登记处(RenIS)。该非干预性上市后登记数据库记录了几乎所有接受靶向治疗的捷克患者的数据。该登记处报告了人口统计学和临床数据,以及所有的治疗序列和临床结局。在这项分析中,共纳入了 836 例于 2013 年 3 月前接受索拉非尼治疗的患者。中位年龄为 63 岁,70%为男性。大多数患者之前接受过细胞因子、舒尼替尼或两者联合治疗。15%的患者接受索拉非尼作为一线治疗。中位总生存期和无进展生存期分别为 21.7 个月和 7.5 个月。一线接受索拉非尼治疗的患者的中位总生存期和无进展生存期分别为 26.3 个月和 8.3 个月。Cox 比例风险模型确定了几个与不良结局相关的参数,包括从诊断到一线系统治疗的时间≤1 年、体能状态≥2、血红蛋白低和 LDH 高于正常值上限的 1.5 倍。我们的数据表明,真实世界患者的结局与临床试验中的患者相当。本研究中确定的预后因素与之前报道的模型一致。