Overdiagnosis and overtreatment of breast cancer: Overdiagnosis in randomised controlled trials of breast cancer screening
© BioMed Central Ltd 2005
Published: 25 August 2005
Data from randomised controlled trials of mammographic screening can be used to determine the extent of any overdiagnosis, as soon as either a time equivalent to the lead-time has elapsed after the final screen, or the control arm has been offered screening. This paper reviews those randomised trials for which breast cancer incidence data are available. In recent trials in which the control group has not been offered screening, an excess incidence of breast cancer remains after many years of follow-up. In those trials in which the control arm has been offered screening, although there is a possible shift from invasive to in situ disease, there is no evidence of overdiagnosis as a result of incident screens.
Overdiagnosis in mammographic screening is taken here to mean the diagnosis of invasive or in situ breast cancer that, in the absence of screening, would not have presented clinically during the woman's lifetime.
In studying overdiagnosis, randomised controlled trials have the advantage that data on the incidence of breast cancer in the intervention and control arms are usually available in detail at an individual level. Overdiagnosis of both ductal carcinoma in situ (DCIS) and invasive cancer may occur; however, it is not easy to determine to what extent an excess of DCIS is due to stage-shifting from invasive disease, although estimates can be made where sufficiently detailed information is available . Most trials have provided relatively little information on the treatment of breast cancer cases, so that the extent of overtreatment is difficult to quantify.
Overdiagnosis can be studied in randomised controlled trials by comparing the cumulative incidence of breast cancer in the intervention and control arms at different times from date of entry or randomisation. While screening is continuing in the intervention arm of a trial, incidence in that arm will be increased because of the advancement of diagnosis by the lead-time in screen-detected cancers, as well as by any overdiagnosis. This 'prevalence peak' will be followed by a corresponding decrease once screening ceases. Overdiagnosis can therefore be estimated only after a time equivalent to the lead-time has elapsed following the final screen. In several trials, women in the control arm have subsequently been offered screening. Once this has occurred, only overdiagnosis due to incident, not prevalent, screens would be observable, because women in both arms of the trial would be subject to any overdiagnosis occurring at prevalent screens.
The extent of any overdiagnosis in trials of breast screening may be affected by the 'intensity' of screening (one or two views, modalities employed, screening frequency and recall policy), and by the uptake of screening in the intervention arm. It may also depend on the age range of women included in the trial, both because of variation in the natural history of the disease with age and because of increased mortality from other causes in older women during the 'lead-time' before a screen-detected cancer would have presented clinically. The extent to which overdiagnosis is observed will also depend on the extent of 'contamination' in the control arm by opportunistic screening.
Randomised controlled trials of mammographic screening
Age range at entry (years)
Screening interval (months)
Number of views
Uptake rate (%) (prevalent screen)
Relative risk of breast cancer mortality
Randomised controlled trials of mammography screening: differences in breast cancer incidence between intervention and control arms in the follow-up period
Cumulative incidence of invasive breast cancer (per 1,000 women years)
Cumulative incidence of DCIS (per 1,000 women years)
Cumulative incidence of all breast cancer (invasive + DCIS) (per 1,000 women years)
Absolute excess in intervention arm
Absolute excess in intervention arm
Absolute excess in intervention arm
Control group screened
For studies in which rates have been published only per 1,000 women, rates per 1,000 women years have been calculated on the basis of estimated mean follow-up.
The randomised trials
The earliest of the randomised trials was the Health Insurance Plan (HIP) study performed in the United States in the 1960s, in which women in the intervention arm were offered annual screening by both mammography and clinical breast examination for four rounds. By the end of 5 years from date of entry (about 1.5 years after the last screen) the incidence of breast cancer in the two arms was similar (2.03 per 1,000 women years in the intervention arm, and 1.94 in the control arm ). An earlier report indicates that the percentages of in situ cancer were 13% and 8%, respectively, in the two arms . There have been considerable improvements in the sensitivity of mammography since this trial was conducted, and it therefore provides little indication of the potential for overdiagnosis with current techniques.
The four randomised trials conducted in Sweden all used screening by mammography alone, with screening intervals ranging from 18 to 33 months. In all except one of these the control group has subsequently been offered screening.
The Swedish Two County Study, which began in 1977/8, included 143,867 women aged 40 to 74 years at the date of randomisation . Women in the intervention arm were invited to screening at intervals of 24 to 33 months.
In 1985, after two to four rounds of screening in the intervention arm, women in the control arm were offered screening. After this screen had taken place, rates of invasive cancer have been reported as 16.90 and 17.79 per 1,000 women in the intervention and control arms, respectively; assuming an average of 7 years of follow-up, the estimated rates per 1,000 women years are 2.41 and 2.54, respectively, with rates of DCIS of 0.23 and 0.12 per 1,000 women years, respectively .
The Gothenberg trial invited women aged between 35 and 59 years, between 1982 and 1991. Again, women in the control arm were offered a single screen at approximately the same time as the final screen in the intervention arm.
The cumulative incidence of invasive breast cancer was greater in the intervention arm than in the control arm until year 6, at about the time of the first screen in the control arm. At the end of the 'screening phase' of the trial (that is, the period up to and including the first screen in the control arm), rates of DCIS were slightly higher in the intervention arm (about 0.22 versus 0.17 per 1,000 women years), with a slightly lower rate of invasive cancers (1.56 versus 1.73 per 1,000 women years) . The relative risk of overall breast cancer incidence in the intervention arm relative to the control arm at follow-up of up to 14 years is reported as 0.98 (95% confidence interval 0.88 to 1.09).
The first Malmö trial invited women between 45 and 69 years old to five rounds of screening between 1976 and 1978. Women in the control arm were not invited for screening (although those in the youngest cohort were eventually invited in 1992/3). At a mean follow-up of 8.8 years, when screening was still continuing, the rates of invasive breast cancers in the intervention and control arms were 2.62 and 2.12 per 1,000 women years, respectively. The rates of DCIS were 0.50 and 0.27 per 1,000 women years, respectively . It was estimated that 24% of the control arm had been screened, although most only once. No incidence data have been published on the subsequent (Malmö II) trial.
The Stockholm trial randomised about 60,000 women in 1981; there were two screening rounds using single-view mammography 28 months apart; during 1986 the control group was invited to a single screen. Uptake at first screen was 81% in the intervention arm and 77% in the control arm . At the end of 1986 there was no difference in overall cancer incidence between the two arms (0.90 versus 0.91 per 1,000 women years). There was a slightly higher rate of DCIS (0.09 versus 0.06) and lower rate of invasive cancers (0.81 versus 0.85) in the intervention arm, but the differences were not significant.
Two trials conducted in Canada both used volunteer populations, resulting in high uptake. The NBSS II trial was designed to compare mammography plus physical examination (MP), with physical examination alone (PO) in women aged 50 to 64 years . An initial excess of invasive cancers in the MP arm mainly disappeared with continued follow-up; at 13 years of follow-up, rates per 1,000 women years were 2.43 and 2.38 in the MP and PO arms, respectively . Rates of DCIS were 0.28 and 0.06 per 1,000 women years, respectively. The NBSS I trial was designed to compare breast cancer mortality in women aged 40 to 49 years randomised to either screening by annual mammography, physical examination and instruction on breast self-examination (BSE) or a single physical examination and BSE instruction . After 13 years of follow-up, the cumulative rates of DCIS were 0.22 and 0.09 per 1,000 women years in the screening and 'usual care' groups, respectively . The rates of invasive breast cancers were 1.81 and 1.68, respectively, per 1,000 women years.
The Edinburgh trial recruited women aged 45 to 64 years into the initial cohort during 1978 to 1981, with randomisation by general practice. Women in the intervention arm were offered annual screening for 7 years, by mammography and physical examination every 2 years, and physical examination only in the intervening years. At 10 years of follow-up the incidence rates of invasive breast cancer were 2.04 and 1.93 per 1,000 women years in the intervention and control arms, respectively; rates of DCIS were 0.19 and 0.05, respectively, per 1,000 women years .
However, the cluster randomisation in this trial led to an imbalance in socio-economic status, reflected in all-cause mortality, which is likely to have resulted in an increased risk of breast cancer in the intervention arm. Adjustment for this altered the rate ratio of breast cancer mortality at 14 years of follow-up from 0.87 to 0.79 .
Summary of the trials
In Table 2 the trials are grouped according to whether the control group had been offered screening. For the three trials in which this occurred the absolute excess of all breast cancers in the intervention arm ranged from -0.02 to -0.11 per 1,000 women years; the ratio of the incidence in the intervention arm to that in the control arm was 0.94 to 0.99. For DCIS the absolute excess ranged from 0.05 to 0.11, and for invasive cancer from -0.84 to -0.17.
By contrast, in those trials in which the control group had not been offered screening, there was an excess of both invasive cancers and DCIS in the intervention arm, although in the Malmö trial screening was still in progress at the time that rates were reported. The two Canadian trials are the most informative because they were conducted most recently and have 13 years of follow-up; these show an absolute excess of all breast cancers of 0.25 to 0.26 per 1,000 women years; the ratio of the incidence in the intervention arm to that in the control arm was 1.11 to 1.14.
UK trials of age and frequency
Two further trials in the UK have not yet reported mortality results. The 'age' trial is offering annual mammography from the age of 40 or 41 years to an intervention arm ; women in both arms will be invited as part of the national programme at ages 50 to 52 years. At the time of an interim analysis, when screening was still in progress, there was an 8% excess diagnosis of invasive breast cancers and a 17% excess of all breast cancers in the intervention arm in comparison with the control arm . Once all women in both arms have been invited for screening in the national programme, any excess diagnosis should be as a result of incident screens.
The 'frequency' trial has compared annual versus three-yearly screening in women aged 50 to 64 years within the UK National Health Service breast screening programme . Because all women had received a prevalent screen before randomisation, any excess diagnosis should be the result of more frequent screening (or difference in uptake). At 3 years of follow-up (that is, when both arms had been reinvited) a non-significant increase in breast cancers of 19% (13% invasive) was observed in the annual screening arm. Although the authors did not consider the difference to be real, they acknowledged a possible effect of increased diagnostic activity. The (31%) increase in DCIS was also non-significant.
This paper summarises the evidence for overdiagnosis in randomised trials of mammography, on the basis of comparisons of cumulative incidence, in the intervention and control arms of such trials. It is noted that differences in breast cancer incidence can also arise from bias in randomisation, and indeed equality of incidence has been used as evidence for a lack of such bias . No mathematical modelling of the extent of overdiagnosis has been attempted in the present paper, because this will be the subject of a later paper in this series.
In trials in which the control group has not been offered screening, only once sufficient time has elapsed since the end of screening can overdiagnosis be estimated. If screening in the intervention arm is still continuing at the time incidence is reported, an increase in the intervention arm would be expected owing to advanced diagnosis, as observed in the Malmö trials. In the Canadian trials there is an 11 to 14% excess of all cancers in the intervention arm at 13 years of follow-up, largely of DCIS, suggesting the existence of overdiagnosis. However, in those recent trials in which the control group have been invited for screening, although there is a possible shift from invasive disease to DCIS, there is no evidence of overdiagnosis of all breast cancers as a result of incident screens.
This article is part of a review series on Overdiagnosis and overtreatment of breast cancer, edited by Nick E Day, Stephen Duffy and Eugenio Paci.
Other articles in the series can be found online at http://breast-cancer-research.com/articles/review-series.asp?series=BCR_Overdiagnosis
ductal carcinoma in situ
Health Insurance Plan
mammography plus physical examination
National Breast Screening Study
physical examination alone.
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