Duffy Stephen W, Parmar Dharmishta
Breast Cancer Res. 2013 May 16;15(3):R41. doi: 10.1186/bcr3427.
Overdiagnosis in breast cancer screening is a controversial topic. One difficulty in estimation of overdiagnosis is the separation of overdiagnosis from lead time that is the advance in the time of diagnosis of cancers, which confers an artificial increase in incidence when a screening programme is introduced.
We postulated a female population aged 50-79 with a similar age structure and age-specific breast cancer incidence as in England and Wales before the screening programme. We then imposed a two-yearly screening programme; screening women aged 50-69, to run for twenty years, with exponentially distributed lead time with an average of 40 months in screen-detected cancers. We imposed no effect of the screening on incidence other than lead time.
Comparison of age- and time-specific incidence between the screened and unscreened populations showed a major effect of lead time, which could only be adjusted for by follow-up for more than two decades and including ten years after the last screen. From lead time alone, twenty-year observation at ages 50-69 would confer an observed excess incidence of 37%. The excess would only fall below 10% with 25 years or more follow-up. For the excess to be nullified, we would require 30 year follow-up including observation up to 10 years above the upper age limit for screening.
Studies using shorter observation periods will overestimate overdiagnosis by inclusion of cancers diagnosed early due to lead time among the nominally overdiagnosed tumours.
乳腺癌筛查中的过度诊断是一个有争议的话题。估计过度诊断的一个困难在于将过度诊断与领先时间区分开来,领先时间是癌症诊断时间的提前,当引入筛查计划时,这会人为地增加发病率。
我们假设了一个年龄在50 - 79岁之间的女性人群,其年龄结构和特定年龄的乳腺癌发病率与筛查计划实施前的英格兰和威尔士相似。然后我们实施了一项两年一次的筛查计划;对年龄在50 - 69岁的女性进行筛查,为期20年,筛查发现的癌症的领先时间呈指数分布,平均为40个月。除了领先时间外,我们假设筛查对发病率没有其他影响。
筛查人群和未筛查人群之间年龄和时间特异性发病率的比较显示了领先时间的主要影响,这只能通过超过二十年的随访并包括最后一次筛查后十年的随访来调整。仅考虑领先时间,在50 - 69岁进行20年观察会导致观察到的额外发病率为37%。随访25年或更长时间,额外发病率才会降至10%以下。要使额外发病率归零,我们需要30年的随访,包括观察超过筛查年龄上限10年的情况。
使用较短观察期的研究将通过把因领先时间而早期诊断的癌症纳入名义上的过度诊断肿瘤中,从而高估过度诊断。