...
首页> 外文期刊>CPT: Pharmacometrics & Systems Pharmacology >Parametric Time‐to‐Event Model for Acute Exacerbations in Idiopathic Pulmonary Fibrosis
【24h】

Parametric Time‐to‐Event Model for Acute Exacerbations in Idiopathic Pulmonary Fibrosis

机译:特发性肺纤维化急性加剧的参数对事件模型

获取原文
           

摘要

We describe a parametric time‐to‐event model for idiopathic pulmonary fibrosis (IPF) exacerbations and identify predictors of exacerbation risk using data obtained for the tyrosine‐kinase inhibitor nintedanib in two phase III studies (INPULSIS‐1/2). Parametric survival analysis was performed on time to first exacerbation (censoring on day 372), with univariate analysis to select statistically significant covariates (P?=?0.05). Multivariate covariate models were developed using stepwise covariate modeling with forward inclusion (P?=?0.05) and backward elimination (P?=?0.01). Sixty‐three first exacerbation events were reported across 1,061 subjects in the INPULSIS studies. Baseline and decline of forced vital capacity (FVC)/percent‐predicted FVC (%pFVC), supplemental oxygen use, baseline CO diffusing capacity and age were statistically significant in the univariate analysis. The final covariate model included decline in FVC to week 52, baseline %pFVC, supplemental oxygen use, and age. The developed model may be used to identify patients at high risk of IPF exacerbations and accelerate development of novel treatments.
机译:我们描述了用于特发性肺纤维化(IPF)加剧的参数 - 事件模型,并使用在两阶段III研究中获得酪氨酸激酶抑制剂尼林尼嗪(INPULSISIS-1/2)获得的数据鉴定加重风险的预测因子。参数存活分析是按时第一次加剧(第372天审查)进行的,单变量分析选择统计学显着的协变量(P?= 0.05)。使用逐步的调节模型开发多变量协变量模型(P?= 0.05)并向后消除(p?= 0.01)。在Inpulsis研究中,在1,061名受试者中报道了六十三个发热事件。基线和强制生命能力(FVC)/百分比 - 预测的FVC(%PFVC),补充氧气使用,基线CO扩散能力和年龄在单变量分析中具有统计学意义。最终的协变化模型包括FVC至第52周,基线%PFVC,补充氧气和年龄的下降。开发的模型可用于鉴定IPF加剧风险高风险的患者,并加速新型治疗的发展。

著录项

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