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Predictive Markers of First Line Pazopanib Treatment in Kidney Cancer

机译:第一线Pazopanib治疗在肾癌中的预测标志

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Real-world evidence from clinical practices is fundamental for understanding the efficacy and tolerability of medicinal products. Patients with renal cell cancer were studied to gain data not represented by analyses conducted on highly selected patients participating in clinical trials. Our goal was to retrospectively collect data from patients with advanced renal tumours treated with pazopanib (PZ) to investigate the efficacy, frequency of side effects, and searching for predictive markers. Eighty-one patients who had received PZ therapy as first-line treatment were retrospectively evaluated. Overall survival (OS), progression-free survival (PFS) were assessed as endpoints. Median PFS and OS were 11.8months (95% CI: 8.8 22.4); and 30.2months (95% CI: 20.3 41.7) respectively. Severe side effects were only encountered in 11 (14%) patients. The presence of liver metastasis shortened the median PFS (5.5 vs. 14.8months, p= 0.003). Median PFS for patients with or without side effects was 25.6 vs. 7.3months, respectively (p= 0.0001). Patients younger than 65years had a median OS of 41.7months vs. 25.2months for those over 65years of age (p= 0.008). According to our results absence of liver metastases, younger age (65years) and presence of side effects proved to be independent predictive markers of better PFS and OS.
机译:来自临床实践的现实证据是了解药品的疗效和耐受性的基础。研究了肾细胞癌的患者,以获得在参与临床试验的高度选定患者上进行的分析不代表的数据。我们的目标是回顾用Pazopanib(PZ)治疗的晚期肾肿瘤患者的患者进行患者来研究副作用的功效,频率,以及寻找预测标志物的疗效。回顾性评估了作为第一线治疗的八十一名接受PZ治疗的患者。总存活(OS),无进展存活(PFS)被评估为终点。中位数PFS和OS是11.8个月(95%CI:8.8 22.4); 30.2个月(95%CI:20.3 41.7)。仅在11例(14%)患者中遇到严重的副作用。肝转移的存在缩短了中值PFS(5.5 vs.14.8months,P = 0.003)。具有或不具有副作用的患者的中位数PFS分别为25.6 vs.3month(P = 0.0001)。比65年龄小的患者有41.7个月的中位数,65岁以上的年龄超过25.2个月(P = 0.008)。根据我们的结果,缺乏肝转移,年龄较小(<65年)和存在的副作用的存在被证明是更好的PFS和OS的独立预测标记。

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