Trends in molecular subtypes of breast cancer: description of incidence rates between 2007 and 2012 from three French registries

Breast cancer is the most frequent cancer in women in France [1]. Trends in incidence are well described [1], although explanations for these trends are lacking. Epidemiological studies have failed to propose explanations for observed trends in breast cancer incidence. However, help may be at hand from biological researchers. Indeed, breast cancer is now defined according to molecular subtypes [2], which can be roughly identified by routine immunohistochemical exams, namely hormonal receptors (HR) and Human epidermal growth factor receptor (HER2) [3]. The molecular subtypes identified correspond to different disease profiles within the overall heading of breast cancer. Their epidemiological features are not the same, with different risk factors, recurrence patterns, recurrence rates and survival curves. Additionally, management is not the same, and treatment now depends on the molecular subtype.

There is still few population-based epidemiological studies on this subject, since immunohistochemical characteristics are rarely available at a population level. HER2 status is available in the Surveillance, Epidemiology and End Result program (SEER) registries since 2010, and HR status since slightly earlier. Descriptions of incidence according to molecular subtypes were reported by the SEER [4, 5] for two years (2010, 2011), corresponding to the first years with available HER2 status. One study was conducted in Norway, with estimation of secular trends, with imputation for unknown molecular subtypes [6]. However, to the best of our knowledge, no study exists to date reporting trends in the incidence of breast cancer according to molecular subtype from a population perspective.

French cancer registries systematically record precise information about each case. HR and HER2 status have been recorded since 2007 in three French cancer registries, namely th registries of the Manche, Loire-Atlantique and Côte d’Or Departments of France.

Therefore, this study aimed to describe the trends in breast cancer incidence according to molecular subtype at a population level.

Overall, 12,040 incident cases of breast cancer were included in the three French departments between 2007 and 2012 (Table 1). Among all cancer cases, 4.5% were diagnosed before the age of 40, and 30.5% after 70 years of age.

The proportion of ER positive tumours was high (78.8%). All PR-positive tumours were ER positive; 10.3% of tumours were positive for HER2.

Estimated incidence rates are presented in Table 2. HR+/ HER2-cancers were the most frequent. The lowest standardized incidence rate (SIR) was in 2009, and the highest in 2010 for the overall population.

Figure 1 presents the proportion of each molecular subtype among cancers for each year. Figure 2 presents the proportion of each molecular subtype, by age class. The frequency of cancers with unknown subtype decreased with year of diagnosis. There were more unknown types among elderly patients. The proportion of triple negative cancers was higher in younger patients than in elderly patients, while the proportion of HER2+ tumours decreased with age.

Using Poisson models, we analysed the incidence rates by age class, molecular subtype and year of diagnosis. The final model is adjusted for year of diagnosis, molecular subtype and patient age. It also includes a term for the interaction of the year of diagnosis with molecular subtype (p < 0.001), as well as a term for the interaction of age class with molecular subtype (p < 0.001), since these interactions were significant using likelihood ratio tests. The trend in incidence was therefore different among age classes according to molecular subtype. The course of incidence from 2007 to 2012 also significantly differed depending on the molecular subtype according to this model. The incidence rates obtained by Poisson modelisation by by year, according to the different molecular subtypes and for each age class are described in Fig. 3. Only four age classes are described. The other age class are available in Appendix 1. HR+/HER2- tumours incidence does not seem to change except for 60–64 age class, where it seems to increase with time. The other molecular subtypes tend to decrease in incidence, except for the 60–64 age class. This decreasement is not confirmed in 2012 diagnosis year.

Our study is based on population data from established and exhaustive cancer registries. For this study, molecular information about breast tumours was recorded, and these data about molecular subtype are now recognized as useful for predicting prognosis and therefore, for making treatment decisions. The results show different evolution of molecular profile incidence among age class and among the studied years of diagnosis.

The strength of this study is the report of valid population data, with a good registration of incident cases. Nevertheless, the immunohistochemical data were not available for all incident cases. This missing data were more frequent in early years and for old patients. The SEER reports [4, 5] had missing data about immunohistochemical analyses for 12% of patients in 2010. The report from Norway [6] produced imputed estimation. Here, missing data were described by age class and by year of diagnosis, to show that they were not missing at random. Missing data were more frequent in first year of immunohistochemical data registration and for elderly patients.

The spread of the different molecular subtypes is similar to that described by Howlader and Kohler [4, 5] in the SEER study. In their article, Howlader et al. found 73% Luminal A tumours, defined as HR+/HER2- tumours (versus 77.6% in our study), 12% triple-negative tumours (versus 10.7% in our study), 5% HER 2 positive tumours with negative hormone receptors (versus 4.3%) and 10% HR+/HER2 + tumours (versus 7.3% in our study). These two studies, both conducted on population databases, thus reported coherent results, and both reported a different spread in molecular subtypes than that described in clinical trials, where HER2 positive tumours are described as being much more frequent than in population databases (15–30% vs 11.8%) [9]. Indeed, HER2 positive tumours are probably more exposed to inclusion in clinical trial since they are probably more frequently managed in cancer comprehensive cancer.

The profile of incidence by age class and by molecular subtype also differed compared to that described in the United States, where the age class with the maximal incidence is around 65–75 [4], compared to age 50–60 in France. This may be due to nationwide implementation of mass screening for breast cancer from age 50 onwards in France. For the administrative areas described here, the participation rate to the national screening programme is between 52% and 55%. This national program is for women aged between 50 and 75 years-old.

The course of the trends in breast cancer incidence may be at least partially explained by the incidence of each molecular subtype. Indeed, several studies have shown that the distribution of molecular subtypes depends on ethnicity as well as environmental risk factors [10] even if a recent French study found no significant association between socioeconomic status and molecular subtype [11] . Ethnicity and environmental risk factors were not studied here but the differences in incidence trends between the molecular subtypes may be explained by changes in environmental factors.

Treatment of breast cancer is now adapted according to the molecular subtype, and recurrence-free survival differs among the different subtypes, both in terms of time to recurrence, and type of recurrence [12]. The analysis of incidence and prognosis at a population level should take into account these molecular subtypes to evaluate and compare patient survival and to plan ressources needed for treatment.

These different molecular subtypes have different risk factors, and a different distribution across age classes. Some studies showed that the proportion of luminal A subtype increased with age class [13], whereas triple negative tumours decreased with age. In absolute incidence rates, these findings were not observed in our study.

This study aimed to describe the trends in incidence and distribution among age classes of breast cancers by molecular subtypes. The models used show an increasing proportion of luminal non HER2 cancers between 2007 and 2012, the one targeted by the screening program since they progress slowly. The effect of age class was also significantly different depending on the molecular subtype in our study. First, the overall trends show a decrease in breast cancer incidence in 2009. This decrease corresponds to a decreasing proportion of cancers diagnosed in the screening program.

The overall trends in incidence of breast cancer may be explained by the trends in incidence of molecular subtypes. This study shows significant differences in the age distribution by molecular subtype, and in year-on-year trends between molecular subtypes. Further studies are needed to understand the differences observed here. This analysis is crucial for the planning of screening, diagnosis and treatment resources for breast cancer at a population level.