...
首页> 外文期刊>BMC Cancer >Safety and efficacy of Pazopanib in advanced soft tissue sarcoma: PALETTE (EORTC 62072) subgroup analyses
【24h】

Safety and efficacy of Pazopanib in advanced soft tissue sarcoma: PALETTE (EORTC 62072) subgroup analyses

机译:Pazopanib在晚期软组织肉瘤中的安全性和有效性:PALETTE(EORTC 62072)亚组分析

获取原文
   

获取外文期刊封面封底 >>

       

摘要

PALETTE is a phase 3 trial that demonstrated single-agent activity of pazopanib in advanced soft tissue sarcomas (aSTS). We performed retrospective subgroup analyses to explore potential relationships between patient characteristics, prior lines of therapy, dose intensity, and dose modifications on safety and efficacy of pazopanib in aSTS. PALETTE compared pazopanib with placebo in patients with aSTS (age?≥?18?years) whose disease had progressed during or following prior chemotherapy. In these subgroup analyses, median progression-free survival (mPFS) among patients receiving pazopanib was the efficacy outcome of interest. Adverse events (AEs) were also compared within subgroups. All analyses were descriptive and exploratory. A total of 246 patients received pazopanib in the PALETTE study. The mPFS was longer in patients who had only 1 prior line versus 2+ prior lines of therapy (24.7 vs 18.9?weeks, respectively); AE rates were similar regardless of number of prior lines of therapy. The mPFS was similar in patients aged ?65 and?≥?65 y (20.0 and 20.1?weeks, respectively). Although AEs leading to study discontinuation were higher in older patients (≥65 y, 30%; ?65 y, 17%), rates of dose reductions, dose interruptions, and serious AEs were similar between the 2 age groups. No reduction in mPFS was noted in patients requiring dose reductions or dose interruptions to manage toxicities. Longer mPFS was observed in patients receiving pazopanib following only 1 line of therapy. Additionally, mPFS with pazopanib was maintained regardless of patient age or dose modifications used to manage toxicity. NCT00753688 , first posted September 16, 2008 (registered prospectively).
机译:PALETTE是一项3期试验,证明了帕唑帕尼在晚期软组织肉瘤(aSTS)中的单药活性。我们进行了回顾性亚组分析,以探讨患者特征,以前的治疗方案,剂量强度以及剂量修改对aSTS中帕唑帕尼的安全性和有效性之间的潜在关系。 PALETTE将帕唑帕尼与安慰剂用于在既往化疗期间或之后发生疾病的aSTS(年龄≥18岁)患者中。在这些亚组分析中,接受帕唑帕尼治疗的患者中位无进展生存期(mPFS)是关注的疗效指标。还比较了亚组中的不良事件(AE)。所有分析均为描述性和探索性。在PALETTE研究中,共有246名患者接受了帕唑帕尼治疗。仅接受1线或2+线以上治疗的患者的mPFS更长(分别为24.7对18.9周)。无论先前治疗的数目如何,AE率均相似。 ≥65岁和≥65岁的患者的mPFS相似(分别为20.0周和20.1周)。尽管老年患者导致研究中断的不良事件较高(≥65岁,30%; <?65岁,17%),但在这两个年龄组之间,降低剂量,中断剂量和严重不良事件的发生率相似。需要降低剂量或中断剂量以控制毒性的患者中未发现mPFS降低。仅接受1线治疗后接受帕唑帕尼的患者观察到更长的mPFS。此外,无论患者年龄或用于管理毒性的剂量调整如何,均​​应维持含pazopanib的mPFS。 NCT00753688,首次发布于2008年9月16日(已预先注册)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号