Marcus Pamela M, Doria-Rose Vincent Paul, Gareen Ilana F, Brewer Brenda, Clingan Kathy, Keating Kristen, Rosenbaum Jennifer, Rozjabek Heather M, Rathmell Joshua, Sicks JoRean, Miller Anthony B
National Cancer Institute, Bethesda, MD, USA
National Cancer Institute, Bethesda, MD, USA.
Clin Trials. 2016 Aug;13(4):434-8. doi: 10.1177/1740774516638345. Epub 2016 Mar 22.
BACKGROUND/AIMS: Randomized controlled trials frequently use death review committees to assign a cause of death rather than relying on cause of death information from death certificates. The National Lung Screening Trial, a randomized controlled trial of lung cancer screening with low-dose computed tomography versus chest X-ray for heavy and/or long-term smokers ages 55-74 years at enrollment, used a committee blinded to arm assignment for a subset of deaths to determine whether cause of death was due to lung cancer.
Deaths were selected for review using a pre-determined computerized algorithm. The algorithm, which considered cancers diagnosed during the trial, causes and significant conditions listed on the death certificate, and the underlying cause of death derived from death certificate information by trained nosologists, selected deaths that were most likely to represent a death due to lung cancer (either directly or indirectly) and deaths that might have been erroneously assigned lung cancer as the cause of death. The algorithm also selected deaths that might be due to adverse events of diagnostic evaluation for lung cancer. Using the review cause of death as the gold standard and lung cancer cause of death as the outcome of interest (dichotomized as lung cancer versus not lung cancer), we calculated performance measures of the death certificate cause of death. We also recalculated the trial primary endpoint using the death certificate cause of death.
In all, 1642 deaths were reviewed and assigned a cause of death (42% of the 3877 National Lung Screening Trial deaths). Sensitivity of death certificate cause of death was 91%; specificity, 97%; positive predictive value, 98%; and negative predictive value, 89%. About 40% of the deaths reclassified to lung cancer cause of death had a death certificate cause of death of a neoplasm other than lung. Using the death certificate cause of death, the lung cancer mortality reduction was 18% (95% confidence interval: 4.2-25.0), as compared with the published finding of 20% (95% confidence interval: 6.7-26.7).
Death review may not be necessary for primary-outcome analyses in lung cancer screening trials. If deemed necessary, researchers should strive to streamline the death review process as much as possible.
背景/目的:随机对照试验经常使用死亡审查委员会来确定死亡原因,而不是依赖死亡证明上的死亡原因信息。国家肺癌筛查试验是一项针对年龄在55 - 74岁的重度和/或长期吸烟者进行的低剂量计算机断层扫描与胸部X光肺癌筛查的随机对照试验,该试验对一部分死亡病例使用了对分组情况不知情的委员会来确定死亡原因是否为肺癌。
使用预先确定的计算机算法选择进行审查的死亡病例。该算法考虑了试验期间诊断出的癌症、死亡证明上列出的病因和重要病症,以及由训练有素的疾病分类学家根据死亡证明信息得出的根本死因,选择了最有可能代表因肺癌直接或间接导致死亡的病例,以及可能被错误地将肺癌列为死因的病例。该算法还选择了可能因肺癌诊断评估的不良事件导致的死亡病例。以审查的死亡原因作为金标准,以肺癌死亡原因作为感兴趣的结果(分为肺癌与非肺癌),我们计算了死亡证明上死亡原因的性能指标。我们还使用死亡证明上的死亡原因重新计算了试验的主要终点。
总共审查了1642例死亡病例并确定了死因(占国家肺癌筛查试验3877例死亡病例的42%)。死亡证明上死亡原因的敏感性为91%;特异性为97%;阳性预测值为98%;阴性预测值为89%。重新分类为肺癌死亡原因的死亡病例中,约40%的死亡证明上的死因是除肺癌之外的肿瘤。使用死亡证明上的死亡原因,肺癌死亡率降低了18%(95%置信区间:4.2 - 25.0),而公布的结果为20%(95%置信区间:6.7 - 26.7)。
在肺癌筛查试验的主要结果分析中,可能无需进行死亡审查。如果认为有必要,研究人员应尽可能简化死亡审查过程。