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open access:
Cancer incidence attributable to the use of oral contraceptives and hormone therapy in Alberta in 2012
Background:
Hormonal contraceptives and hormone replacement therapies are
classified as carcinogenic to humans (group 1) by the International
Agency for Research on Cancer. We sought to estimate the proportion and
total number of cancers attributable to the use of oral contraceptives
and hormone therapy in Alberta in 2012.
Methods:
Population attributable risks were used to estimate the proportion of
attributable cases for each associated cancer site. Relative risk
estimates were obtained from the most relevant and recent epidemiologic
literature. Prevalences of the use of oral contraceptives and hormone
therapy in Alberta were collected from Alberta's Tomorrow Project.
Specific cancer incidence data were obtained from the Alberta Cancer
Registry for the year 2012.
Results:
Overall, 6.3% of breast cancers (n
= 135) diagnosed in Alberta in 2012 were estimated to be attributable
to the use of oral contraceptives, and the exposure potentially
prevented about 57.3% of endometrial cancers (n = 276) and 29.1% of ovarian cancers (n = 52). About 15.5% of breast cancers (n = 258) and 8.9% of ovarian cancers (n = 13) were estimated to be attributable to the use of hormone therapy, whereas 11.3% of endometrial cancers (n = 48) were possibly prevented by the exposure.
Interpretation:
Based on our estimates, oral contraceptive use resulted in a net
protective effect among the cancer sites studied, thus reducing the
cancer burden in Alberta in 2012. The use of hormone therapy was
estimated to increase the cancer burden in the province, therefore the
risk and benefit of hormone therapy should be carefully considered
before use.
Strengths and limitations
A
strength of our study was the inclusion of CIs around the population
attributable risk estimates, thereby providing the precision of the
estimates which was not done in the UK study. However, for estimates
associated with ever oral contraceptive use and current exposure to
hormone replacement therapies (Appendix 1, Supplementary Table 2), the
wide confidence intervals highlight the lack of precision for those
estimates. For example, although we estimated that 136 cases of breast
cancer are attributable to ever using oral contraceptives, this estimate
could range from 5 to 260 cases.
The
restricted prevalence data available on current oral contraceptive
exposure and cessation of hormone preparation use in Alberta created
some limitations in this study. Increased risk of breast cancer was
mostly found among current and recent users of oral contraceptives,1,2,25 and 10 years after cessation of use, the potential risk returned to baseline.1,2
Thus, the observed attributable risk for breast cancer related to ever
using oral contraceptives was likely overestimated for women who stopped
taking oral contraceptives more than 10 years ago. For endometrial and
ovarian cancer, the estimate should be accurate because the protective
effect of oral contraceptives on these cancers lasts for 20 years or
more.1
In addition, because of limited availability of data, conducting
sensitivity analyses to verify the impact of different latency periods
on population attributable risk estimates was not possible. In a
Canadian national study, where the population attributable risks of
hormone therapy use on breast cancer were estimated over a 12-year
period, the attributable risk decreased from 11.5% in 2000 to 5.2% in
2006 because hormone therapy use decreased after the Women's Health
Initiative Study was published in 2002.26
The same trend likely occurred in Alberta; however, because no
Alberta-specific data concerning hormone use with this level of detail
were available, we were unable to conduct these sensitivity analyses.
Conclusion
Although
oral contraceptives and hormone therapy are both classified as
carcinogens, the net effect of population attributable risks are
different when multiple cancer sites are considered. Our analyses showed
that the benefit of oral contraceptive use exceeds the potential risk
among the cancer sites investigated because the number of cancers
possibly reduced by oral contraceptive use was more than twice the
number potentially associated with the exposure. Oral contraceptive use
likely reduced the cancer burden in Alberta in 2012. In contrast,
hormone therapy was estimated to increase the cancer burden in the
province by about 200 excess cancer cases in 2012. The risks and
benefits of hormone therapies should be carefully considered before
their use.
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