首页> 美国卫生研究院文献>Springer Open Choice >Application of a decision analytic framework for adoption of clinical trial results: are the data regarding TARGIT-A IORT ready for prime time?
【2h】

Application of a decision analytic framework for adoption of clinical trial results: are the data regarding TARGIT-A IORT ready for prime time?

机译:应用决策分析框架来采用临床试验结果:有关TARGIT-A IORT的数据是否准备就绪?

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The results from randomized clinical trials are often adopted slowly. This practice potentially prevents many people from benefiting from more effective care. Provide a framework for analyzing clinical trial results to determine whether and when early adoption of novel interventions is appropriate. The framework includes the evaluation of three components: confidence in trial results, impact of early, and late adoption if trial results are reversed or sustained. The adverse impact of early adoption, and the opportunity cost of late adoption are determined using Markov modeling to simulate the impact of early and late adoption in terms of quality of life years and resources gained or lost. We applied the framework to the TARGIT-A randomized clinical trial comparing intraoperative radiation (IORT) to standard external beam radiation (EBRT) and considered these results in the context of trials comparing endocrine therapy with and without radiation therapy in postmenopausal women. Confidence in the TARGIT-A trial 4 year results is high because the peak hazard for local recurrence in the trial is between 2 and 3 years. This is consistent with most trials, and no second peak has been observed in similar patient populations, suggesting that the TARGIT-A trial results are stable. The interventions offer approximately equivalent life expectancy. If IORT local recurrences rate were as high as 10 % at 10 years (which is higher than expected), we would project only 0.002 fewer expected life years (less than 1 day) compared to EBRT if IORT is adopted early. However, there is a $1.7 billion opportunity cost of waiting an additional 5 years to adopt IORT in low risk, hormone-receptor-positive, postmenopausal women. EBRT costs an additional $1467 in indirect costs per patient. Applying an evaluative framework for the adoption of clinical trial results to the TARGIT-A IORT therapy trial results in the assessment that the trial results are stable, early adoption would lead to minimal adverse impact, and substantially less resource use. Both IORT and no radiation are reasonable strategies to adopt.
机译:随机临床试验的结果通常被缓慢采用。这种做法可能会阻止许多人从更有效的护理中受益。提供用于分析临床试验结果的框架,以确定是否以及何时适当采用新的干预措施。该框架包括对三个组成部分的评估:对试验结果的信心,如果试验结果被逆转或持续,则早期采用和延迟采用的影响。使用马尔可夫模型确定早期采用的不利影响以及后期采用的机会成本,以模拟寿命的高低和获得或损失的资源方面对早期采用和晚期采用的影响。我们将该框架应用于TARGIT-A随机临床试验,将术中放射线(IORT)与标准体外放射线(EBRT)进行了比较,并在比较绝经后妇女内分泌疗法与不接受放射疗法的试验中考虑了这些结果。 TARGIT-A试验4年结果的可信度很高,因为该试验中局部复发的最大危害在2至3年之间。这与大多数试验是一致的,并且在相似的患者人群中未观察到第二个高峰,表明TARGIT-A试验结果是稳定的。干预措施可提供大致相等的预期寿命。如果IORT的10年局部复发率高达10%(高于预期),则如果较早采用IORT,我们预计与EBRT相比,预期寿命仅减少0.002(少于1天)。但是,在低风险,激素受体阳性,绝经后的女性中,等待额外5年才能接受IORT的机会成本为17亿美元。 EBRT每位患者的间接费用额外需要$ 1467。将评估临床试验结果通过的评估框架应用于TARGIT-A IORT治疗试验结果,以评估试验结果是否稳定,尽早采用将带来最小的不良影响并大大减少资源使用。 IORT和无辐射都是采用的合理策略。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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