This study used published mortality data and regression techniques to look at time trends in cervical cancer mortality between 1970 and 2000 in the UK and the Republic of Ireland. Mortality from cancer of the cervix has been declining in the UK for at least the past 30 years. The rate of decrease has been greatest in England, Wales and Scotland and has accelerated in these countries since the reorganisation of screening services in the late 1980s. Mortality in Northern Ireland is also decreasing, but at a lesser rate and without significant change over the same period. In contrast, cervical cancer mortality in the Irish Republic, which, unlike the UK, does not have comprehensive population-based screening, has been increasing by an average of 1.5% per year since 1978. The mortality rate, which was half of that in the UK in the late 1970s, now exceeds that in any of the region of the UK. The absence of population-based screening for cervical cancer in the Republic of Ireland is the most plausible explanation for these differences in trend.
Population-based cervical screening programmes have been shown to be effective in reducing morbidity and mortality from cervical cancer (Laara et al, 1987; Anderson et al, 1988; Hakama and Louhivuori, 1988). Different mortality trends in Nordic countries have been ascribed to the ways in which cervical screening was delivered (Laara et al, 1987; Hakama and Louhivuori, 1988). While Iceland, Finland, Sweden and parts of Denmark achieved almost complete coverage of the target populations, resulting in sharp falls in incidence and mortality, Norway did not have an organised screening programme and the risk of invasive cancer continued to rise into the late 1970s.
Opportunistic screening, with recall of those who previously had a smear, began in Britain in 1964 (Cancer Research UK, 2003). However, in England prior to 1988, at least two-thirds of patients with invasive cancer had never been screened and in those aged over 40 years (70% of cases), 90% had never been screened (Cancer Research UK, 1994). In the UK, the 1987 recommendation of the Intercollegiate Working Party (Intercollegiate Working Party on Cervical Cytology Screening, 1987) recommended population screening and by 1991 all District Health Authorities operated population screening on either a 3 or 5 yearly basis. Coverage of women in the target age range had increased from 43% in 1988/9 to 83% in 1992/3 (Cervical Screening Programme England 2001–02, 2002). In contrast, in the Republic of Ireland, although there is a high level of opportunistic screening (Department of Health and Children, 2003), the only population-based screening is a small pilot project in the MidWestern Health Board, covering 9% of the national population (Irish Cervical Screening Project, 2003).
This study compares trends in cervical cancer mortality between 1970 and 2001 in Ireland, Northern Ireland, Scotland, England and Wales, and investigates differences in rates and trends, which might be attributable to population-based screening.
Materials and methods
Official mortality statistics were examined for all the regions from 1971 to the most recent available date. The JoinPoint Regression Programme, developed at the National Cancer Institute (JoinPoint Regression Program, 2000), was used to fit linear regression lines to the age-standardised (World population) mortality rates and to identify points of inflection. Variances for each point were calculated from the number of observed deaths.
In 1971, mortality from cancer of the cervix in Britain was much higher than in Ireland and slightly higher in Northern Ireland than in the Republic (Table 1). However, between 1971 and 2000, mortality in Britain dropped dramatically, especially after 1989, and that in Northern Ireland more slowly, while that in Ireland did not. As a result, by 2000, cervical cancer mortality in the Republic of Ireland exceeded that in all the other regions. In England, Wales and Scotland, the mortality rate for women age 20–34 years halved between 1986 and 2000–2001. No trend was apparent in Ireland, and the numbers were too small to draw any conclusion concerning Northern Ireland. However, the numbers in this age group were too small to have any effect on overall trends.
JoinPoint modelling (Figure 1) showed the trends for England, Wales and Scotland to be almost identical. In England and Wales, mortality rates fell slowly before 1988, with an estimated annual percentage decrease of 1.0% with 95% confidence intervals (CI) of 0.7–1.2%, but after 1988 the rate of decrease was much greater, 4.6% per annum (95% CI 4.2–5.0%). In Scotland, the rate of decrease went from 1.0% per annum (95% CI 0.4–1.6%) before 1989 to 4.2% (2.9–5.5%) after that date. In Northern Ireland, there was a small but steady decrease in mortality over the period 1971–2000, with an annual rate of decrease of 1.8% (95% CI 1.0–2.6%), but no observable point of inflection.
In the Republic of Ireland, the pattern was quite different. Prior to 1978, cervical cancer mortality fell by an estimated 3.9% per year (95% CI 1.0–8.7%), but this trend reversed to give a steady increase of 1.5% per annum (95% CI 0.6–2.3%) up to 2001. The model suggests that this trend will continue into the near future.
In England, Scotland and Wales, mortality from cancer of the cervix has been declining since 1970, as reported previously (Quinn et al, 1999). These long-term trends in death rates have brought mortality in England, Scotland and Wales below that in the Republic of Ireland for the first time. If current trends continue, mortality rates in Northern Ireland also look likely to exceed those in the rest of the UK in the near future. The reduction in deaths up to 1997 in England due to screening has been estimated at 800 (Quinn et al, 1999), 1300 (Sasieni and Adams, 1999) or 2000 (Quinn et al, 1999; Peto et al, 2004).
Cervical cancer mortality in Northern Ireland has historically been lower than in Britain. The impact of population-based screening in the past two decades seems lower than that in Britain and, although mortality is steadily falling, the more rapid rate of decrease seen in the rest of the UK in the 1990s has not happened in Northern Ireland. However, the data for Northern Ireland are sparse and an acceleration in the decline of mortality in the late 1980s may be concealed within the random variation. On the other hand, cervical cancer mortality in the Republic of Ireland has increased steadily throughout the 1980 and 1990s and looks like continuing this trend into this decade. As the number of deaths registered as due to cancer of the uterus (part unspecified) has remained low throughout this period (Central Statistics Office, 1974, 2002), changes in death registration practice seem an unlikely explanation for the trend. Assuming that the trend is real, there are two possible, but not mutually exclusive, explanations for the increase – the incidence of cervical cancer may be increasing or survival may be worsening. Data from the National Cancer Registry (National Cancer Registry, 2003) show that the incidence of invasive cervical cancer decreased by 1.1% annually between 1994 and 1999, but no incidence information is available for the period before 1994. It is possible, although unlikely, that the trend may have been in the opposite direction in the 1980s and 1990s. Major changes in sexual behaviour seem to have occurred during that time, as evidenced by an increase in the percentage of births outside marriage from 5% (1980) to 30% (Central Statistics Office, 2002) and in sexually transmitted infection, including a ten-fold increase in the incidence of anogenital warts between 1989 and 2000 (National Disease Surveillance Centre, 2001). However, similar changes have occurred in the UK without a corresponding increase in cervical cancer mortality (Peto et al, 2004).
The second possibility is of a decrease in survival, although this seems unlikely in view of the general increase in cervical cancer survival throughout Europe during this period (Coleman et al, 2003). The most probable explanation is that in Ireland, unlike the UK, an increase in cervical cancer incidence has not been offset by the improvement in detection of precancerous lesions, and so survival, brought about by screening (Peto et al, 2004). Early detection through effective screening is a major factor in improving survival. Screening activity in Ireland can be measured only through the number of smears processed in public laboratories, which was over 180 000 in 2000 (Department of Health and Children, 2003). If all women in the target group were having regular screening, this volume of activity would equate, over a 3-year period, to 61% coverage of the female population aged 25–59 years. However, no information is available on the ages of women screened, nor on their screening history, so women of the wrong age, or those with recent negative tests, may make up a significant proportion of the total.
The experience of the Nordic countries and of British Columbia (Laara et al, 1987; Anderson et al, 1988; Hakama and Louhivuori, 1988) suggests that only those with an organised population-based programme show significant decreases in mortality. Although deaths from cervical cancer are relatively infrequent in Ireland (76 per year on average; 2.2% of all cancer deaths), they are largely preventable through screening. The opportunistic screening at present carried out in Ireland appears to be having little impact on the overall rate of mortality from cervical cancer. A move from the current system to a population-based programme would not greatly increase the volume of screening while probably bringing about the type of mortality reduction seen elsewhere.
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The National Cancer Registry is funded by the Department of Health and Children and the Northern Ireland Cancer Registry by the Department of Health, Social Services and Public Safety. We would like to thank Dr Linda Caughley for her comments.
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Comber, H., Gavin, A. Recent trends in cervical cancer mortality in Britain and Ireland: the case for population-based cervical cancer screening. Br J Cancer 91, 1902–1904 (2004). https://doi.org/10.1038/sj.bjc.6602236
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