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CT Screening for Lung Cancer: Update 2007

机译:CT肺癌筛查:2007年更新

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I am writing about the article called "CT screening for lung cancer: Update 2007," which appeared in the January 2008 issue of The Oncologist . The article contains numerous problematic and unsubstantiated assertions, in many cases inappropriately coupled to references that are either unrelated to, or contradictory to the point made by the authors.1. The authors tell readers that the staging system for lung cancer "is based on differences in lung cancer survival." Their reference is to the update on lung cancer staging by Mountain, which states that the lung cancer staging system is based on identifying the intersection of similar treatment options and similar outcome expectations .2. The authors present the term "curability rate," although it has no concrete meaning in epidemiology. Their reference is to Martini and colleagues, where the concept of "curability rate" does not appear .3. The authors present, in Figure 1, estimates of "cure rates" a concept that is not found in conventional epidemiology. They cite as their source for the cure rate estimates the "American Cancer Society Facts and Figures: 2006." Yet, no cure rates appear in that report.4. The authors claim that there is a distinction between "baseline" and "subsequent" rounds of screening. They cite Morrison . In that article, no such distinction appears. In fact, Morrison focuses on a hypothetical scenario in which only a single round of screening (i.e., only the baseline round) has been performed.5. The authors assert that "length bias" only affects the firstround of screening, again referencing Morrison . Morrison's article explicitly contradicts the authors on this point, noting that length bias cannot be sequestered to certain patients in a single-arm noncomparative design (such as Early Lung Cancer Action Project [ELCAP]). The Morrison article more generally critiques the type of design pursued by ELCAP, while implicitly endorsing randomized trials such as the National Lung Screening Trial (NLST). He states that "the observed case-fatality (the ELCAP endpoint) is not an appropriate measure of the beneficial effect of screening. Outcome evaluation of a screening programme is best carried out by comparison of mortality rates in the screened population with those in another otherwise comparable unscreened population (i.e., the NLST design)."
机译:我写的是一篇名为“肺癌的CT筛查:2007年更新”的文章,该文章刊登在2008年1月的《肿瘤学家》上。本文包含许多有问题和没有根据的断言,在许多情况下,这些断言与与作者的观点无关或矛盾的参考文献不恰当地结合在一起。1。作者告诉读者,肺癌分期系统“基于肺癌生存率的差异”。他们参考的是Mountain的有关肺癌分期的最新资料,该研究指出,肺癌分期系统是基于确定相似治疗方案和相似结果预期的交叉点。2。尽管流行病学中没有具体含义,但作者提出了“可治愈率”一词。他们的参考对象是Martini及其同事,其中“可固化率”的概念没有出现。3。作者在图1中提出了“治愈率”的估计值,这是常规流行病学中没有的概念。他们援引《美国癌症协会事实与数字:2006》作为治愈率的来源。然而,该报告中没有治愈率4。作者声称,“基线”筛选和“后续”筛选之间存在区别。他们引用了莫里森。在该文章中,没有这种区别出现。实际上,莫里森专注于一个假设情景,在该情景中仅进行了单轮筛选(即仅基线轮次)5。作者断言“长度偏差”仅影响筛选的第一轮,再次引用了莫里森。 Morrison的文章在这一点上与作者明显矛盾,并指出在单臂非对比设计中(例如早期肺癌行动计划[ELCAP]),不能将长度偏倚隔离到某些患者。 Morrison的文章更普遍地批评了ELCAP追求的设计类型,同时暗中赞同诸如国家肺部筛查试验(NLST)之类的随机试验。他指出:“观察到的病死率(ELCAP终点)不是衡量筛查有益效果的适当方法。最好通过比较筛查人群的死亡率和其他人群的死亡率来对筛查计划进行结果评估。可比较的未筛选人群(即NLST设计)。”

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