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Original Research ARTICLE

Front. Oncol., 30 June 2015 | https://doi.org/10.3389/fonc.2015.00139

Socioeconomic status and childhood leukemia incidence in Switzerland

imageMartin Adam1,2,3*, imageClaudia E. Kuehni3†, imageAdrian Spoerri3, imageKurt Schmidlin3, imageFabienne Gumy-Pause4, imagePierluigi Brazzola5, imageNicole Probst-Hensch1,2 and imageMarcel Zwahlen3
  • 1Swiss Tropical and Public Health Institute, Basel, Switzerland
  • 2University of Basel, Basel, Switzerland
  • 3Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland
  • 4Haematology/Oncology Unit, Department of Paediatrics, University Hospital of Geneva, Geneva, Switzerland
  • 5Department of Paediatrics, Ospedale San Giovanni, Bellinzona, Switzerland

Socioeconomic status (SES) discrepancies exist for child and adult cancer morbidity and are a major public health concern. In this Swiss population-based matched case–control study on the etiology of childhood leukemia, we selected the cases from the Swiss Childhood Cancer Registry diagnosed since 1991 and the controls randomly from census. We assigned eight controls per case from the 1990 and 2000 census and matched them by the year of birth and gender. SES information for both cases and controls was obtained from census records by probabilistic record linkage. We investigated the association of SES with childhood leukemia in Switzerland, and explored whether it varied with different definitions of socioeconomic status (parental education, living condition, area-based SES), time period, and age. In conditional logistic regression analyses of 565 leukemia cases and 4433 controls, we found no consistent evidence for an association between SES and childhood leukemia. The odds ratio comparing the highest with the lowest SES category ranged from 0.95 (95% CI: 0.71–1.26; Ptrend = 0.73) for paternal education to 1.37 (1.00–1.89; Ptrend = 0.064) for maternal education. No effect modification was found for time period and age at diagnosis. Based on this population-based study, which avoided participation and reporting bias, we assume the potential association of socioeconomic status and childhood leukemia if existing to be small. This study did not find evidence that socioeconomic status, of Switzerland or comparable countries, is a relevant risk factor or strong confounder in etiological investigations on childhood leukemia.

Introduction

In Switzerland and other western countries, childhood cancer is the second leading cause of death in children (1, 2). About 200 new diagnoses of cancer in children younger than 15 years are annually registered in the Swiss Childhood Cancer Registry (SCCR) with leukemia accounting for about one-third of all diagnoses (35). Incidence numbers all over Europe show some evidence for an increase of leukemia during the past decades (6, 7). Risk factors for childhood leukemia are poorly understood, most likely involving the interplay of environmental and genetic factors (812). Inequalities in health between socioeconomic groups are a major public health concern. Epidemiological studies found higher rates of all-cause mortality and morbidity among infants, children, and adults of lower socioeconomic status (SES), defined at an individual or area-level (1315). Childhood leukemia and similarly acute lymphoblastic leukemia (ALL), the most common subtype, have been reported to be one of the rare exceptions, being more common among children of high SES (1618). This led to speculations about a large range of potential etiological factors linked with affluence and modern lifestyle, which could act in part via altered host susceptibility (1618). Two reviews, summarizing the evidence on SES and childhood leukemia until August 2002 (19) and April 2008 (20), concluded that the results of these studies were heterogeneous and varied by place, time, study design, leukemia subgroup, age at diagnosis, and measures of SES used. They advised future studies to minimize bias in selecting cases and controls, to distinguish between different SES measures, and between leukemia subtypes.

In Switzerland, the existence of the population-based SCCR (5, 21) and the Swiss National Cohort (SNC) (5, 22) provided an ideal opportunity to study these questions. We linked childhood leukemia cases from SCCR to SNC and conducted a matched case–control study to investigate the association between socioeconomic status and incidence of childhood leukemia. We explored whether this association varied with different definitions of SES (parental education, living condition, area-based SES), with time period and with age at diagnosis.

Materials and Methods

Study Population and Data Sources

The Swiss Childhood Cancer Registry (SCCR)1 started in 1976 to register all patients treated in one of the nine pediatric cancer centers in Switzerland located in the tertiary care pediatric hospitals in Aarau, Basel, Bern, Geneva, Lausanne, Locarno, Lucerne, St. Gallen, and Zurich (5, 21). Physicians treating these children are members of the Swiss Paediatric Oncology Group (SPOG). The registry includes children and adolescents up to the age of 20 years and aims to be complete for Switzerland in those aged 0–15 years as this age range should be treated in pediatric cancer centers (23). The database contains clinical information on past medical history, cancer diagnosis, treatment, follow-up, as well as cause and date of death. The Swiss National Cohort (SNC)2 is a long-term, census-based, cohort study of the Swiss-resident population (22). It is based on individual data from the census 1990 and the census 2000 in Switzerland. Mortality records from 1991 up to 2008 have been linked to this cohort using probabilistic record linkage procedures.

To investigate the association between socioeconomic status and risk of leukemia in Switzerland, we used a case–control study design. Data on cases, with the exception of the SES information, was obtained through the SCCR. Controls were selected from the census 1990 and 2000. Using a probabilistic linkage procedure, cases were linked to the census 1990 and census 2000 datasets, to obtain SES information for the cases (24). By design, we wanted SES information to be available from before the date of diagnosis. Cases therefore needed to be born before one of the censuses (1990 or 2000), and the disease had to be diagnosed after the census (Figure 1). This circumvented the problem of including cases with a diagnosis before the census that had died prior to the census. Subject to this restriction, the study included as cases all children in the SCCR who were resident in Switzerland, aged <16 years at diagnosis (the age group for which the registry achieves highest coverage) and had been diagnosed with leukemia [Diagnostic group I of the International Classification of Childhood Cancer, third revision (ICCC3)] (25). For the probabilistic linkage with the census, the childhood cancer patients from the SCCR were divided into two subgroups. All cases born before census 1990 and diagnosed between January 1991 and December 2000 were assigned to the “census 1990 case subset” (situation 1 in Figure 1); all cases born before census 2000 and diagnosed between January 2001 and December 2006 (reported to the SCCR by December 2007 when this study was initiated) were assigned to the “census 2000 case subset” (situations 2 and 3 in Figure 1). For every case, we randomly selected eight control children from the two census rounds (census 1990 and census 2000) and matched them individually to the cases by gender and birth year. Our study was designed as a case cohort study (26, 27). We did not attempt to exclude diseased children from the control set, as the theoretical foundation of case–control studies allows to include as controls a representative sample from the source population from which the cases arise, thus providing an unbiased estimate of the exposure–disease risk ratio (26).

FIGURE 1
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Figure 1. Schematic description of the included cases and controls and the linkage with census information. Only childhood cancer cases born before a census and diagnosed after a census were eligible to be included as cases; controls were matched for year of birth and gender.

Linkage with the Swiss National Cohort

The probabilistic record linkage was done based on variables available both in the census records and in the SCCR: sex, date of birth, place of residence (Data Sheet 1 in Supplementary Material). In some instances, several possible matches per records with different probability weights were found and we therefore prepared three different data sets for sensitivity analyses: (1) best links data set, (2) second best links data set, and (3) third best links data set.

Assignment of Socioeconomic Status and Operational Definitions of SES

To assign a child meaningful SES information, the child had to live in a family household. We restricted our study to cases and controls living in a family household for which a reference adult person could be assigned by the Swiss Federal Statistical Office. The reference person of a household (i.e., the householder) being responsible for the socioeconomic position of the household is assigned in the census according to the following criteria: job position, role in the household, age (named “mother” if female reference person or partner of the reference person, respectively “father” if male). Based on previous publications, which had shown conflicting results with varying SES definitions, we had decided to use several variables available in the census as indicators of SES, including individual-based SES information (education of the mother or the father in the household), household-based information (number of rooms per person excluding kitchen and bathrooms, square meter living space per person), and a publicly available area-based SES index (SES index) as developed by the Department of Geography at the University of Zurich3. The area-based SES index is constructed to reflect the social status of the population-based information about net income, education level, and job position in the respective area (community or quarter) (28). We created categories for the SES information as follows. We created three levels for the living space per person and for the area-based SES index based on tertiles with lower values representing the lower SES and the higher values higher SES. For additional analyses, we also created five levels based on quintiles. Parental education was grouped into three categories: “compulsory schooling or less” (up to 9 years of education), “secondary education” (10–16 years, high school, teachers training colleges, technical colleges, and upper vocational education), and “tertiary education” (16 years or more). Number of habitable rooms per person was grouped into three categories based on cut-offs, which can easily be interpreted: <1 room per person [=more than 1 person per room (ppr >1 = overcrowded), 1–1.25 room per person, >1.25 room per person (29)].

Statistical Analyses

We described the characteristics of the children and their parents for leukemia cases and controls. We fitted conditional logistic regressions models that account for the matched case–control study design, to assess the association of SES with the odds of having leukemia. We report odds ratios with 95% confidence intervals and statistical significance based on Wald tests. To account for possible confounding factors, we fitted multivariable conditional logistic regression models adjusting for mother’s age, father’s age, nationality, language region, and number of older children in household. To calculate a P-value for trend over the SES levels, we included SES as a continuous variable coded from 1 to 3. In additional analysis, incorporating appropriately constructed terms for effect modification in the conditional logistic regression models, we examined whether the association with SES measures differed by time period (census 1990 versus census 2000) or by age at diagnosis (0–4 years versus 5–15 years). All the analyses were repeated including only acute lymphoblastic leukemia (ALL) cases and their matched controls. Because it had been suggested that associations with SES might only be seen in the most extreme groups (highest or lowest 10–20%) (16, 20, 30, 31), we also performed an analysis comparing only the highest 20% (highest quintile) to the lowest 20% (lowest quintile) for the SES measures living space and area-based SES index. Finally, we performed a sensitivity analysis with regard to linkage probability, by repeating the conditional logistic regressions for the second best links and third best links datasets (Tables S1 and S2 in Supplementary Material).

All P-values are two sided and a P-value ≤0.05 indicated statistical significance. All statistical analyses were performed using STATA, version 10 (StataCorp., 2005. Stata Statistical Software: Release 10.1. College Station, TX, USA: StataCorp LP).

Consent and Approval

The SCCR has national approval to collect information on children with childhood cancer. Parents are granted the right to demand that the data on their children in the SCCR is anonymized. The data of the Swiss National Cohort are fully anonymous, and approval for the design and conduct of the SES project was given by the Swiss Federal Statistical Office via a specific legal contract. The project data are fully anonymous and kept separate from both SNC and SCCR. By design, this purely observational and anonymous study could not obtain individual informed consent.

Results

Demographic and Clinical Characteristics of the Patients

Almost 100% (565 of 566) of leukemia cases registered in the SCCR and meeting the inclusion criteria of this study could be linked to the census 1990 or to the census 2000. To 559 of 565 leukemia cases (98.9%) and to 4433 of the 4520 controls (98.1%), a householder could be assigned to the household of the child by the Swiss Federal Statistical Office. Therefore, the leukemia case–control study file for analyzing the association with SES levels consisted of 559 cases and 4433 matched controls with an average control to case ratio of 7.9 (in some instances, <8 matching controls were available). Of the 559 leukemia patients, 425 (76%) were diagnosed with an acute lymphoblastic leukemia (ALL) and 60% (334/559) were male (Table 1). Roughly 28% of all leukemia patients and about 32% of the ALL patients were younger than 5 years of age at time of diagnosis. The distortion of the usual age distribution of leukemia/ALL is explained by the linkage design (born before census, diagnosed after census), giving older children a higher likelihood of inclusion into the study. At the time of birth, the mother was on average 29.2 (±5.3 years) years of age and the father 32.3 (±6.0). Half of the cases had older children in the household. Similar to the distribution in the general population, 78.4% (438/559) leukemia cases were Swiss and 76.4% (427/559) were from the German speaking part of Switzerland.

TABLE 1
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Table 1. Demographic and clinical characteristics of leukemia (and ALL) patients.

Socioeconomic Characteristics of the Patients

The distribution according to the available SES information for cases and controls is given in Table 2. Over 90% (504/559) of the assigned householders were males and married. In 42% of the households (234/559), both father and mother were working, and in 55% of the households (310/559) only one of the parents worked. The large majority [97.2% (512/527)] of the fathers was employed and 78.9% (413/527) had at least a secondary education. Of the mothers, 47.8% (266/557) were employed and 71.7% (399/557) had at least a secondary education. About 27% (149/559) of the households of cases had <1 room per person and a third had <23 m2 living space per person.

TABLE 2
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Table 2. Socioeconomic characteristics of leukemia (and ALL) patients.

Association between SES Measures and Childhood Leukemia

We used conditional logistic regression analyses to estimate the strength of the association between various SES measures and the risk of childhood leukemia (Table 3), analyzing all leukemia patients (left columns) or ALL patients only (right columns). Results were very similar for the unadjusted analysis, including only the SES characteristic, and for the adjusted analysis additionally including mother’s age, father’s age, nationality, language region, and older children in household as additional exposures. Analyses using the individual-based (education of the mother, education of the father), the household-based SES measures (rooms per person and square meter of living space per person), and the area-based SES index showed no consistent association. Only for maternal education, there was a weak trend for an increased risk of leukemia in children of mothers with tertiary education compared to mothers with compulsory schooling (OR1.37, 95% CI 1.00–1.89; Ptrend = 0.064). This association was less pronounced for ALL cases (OR 1.19, 95% CI 0.82–1.73; Ptrend = 0.39). For a higher educational level of the father (OR 0.95, 95% CI 0.71–1.26; Ptrend = 0.73) and square meter per person (OR 0.96, 95% CI 0.74–1.25; Ptrend = 0.78), the risk of childhood leukemia was slightly decreased in the highest SES group. Both, living space in square meter (OR 1.18, 95% CI 0.90–1.54; Ptrend = 0.22) and the area-based SES index (OR 1.21, 95% CI 0.94–1.55; Ptrend = 0.34), showed an increased leukemia risk of about a factor 1.2 for the upper SES tertile group compared to the lower tertile group but showing no clear incremental trend. Comparing highest with lowest 20% (instead of tertiles) for living space and for area-based SES index, the ORs for the highest 20% showed weak elevated risks with imprecise confidence intervals.

TABLE 3
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Table 3. Risk association (odds ratio and 95% confidence intervals) of socioeconomic status with leukemia (and ALL), by type of SES characteristic.

When repeating the analyses with the second and third best links datasets, we found similar results (Tables S1 and S2 in Supplementary Material). In further analyses, we investigated whether the strength of the SES association varied by time period (census 1990 versus census 2000) or by age at diagnosis (0–4 years versus 5–15 years). We did these analyses separately for all leukemia cases and for cases with acute lymphoblastic leukemia only. No effect modification between these two factors and any of the socioeconomic status measures was found (Table 4).

TABLE 4
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Table 4. Interaction of P-valuesa when assessing effect modification between SES measures and census (period of diagnosis) and SES measures and age at diagnosis, for leukemia (and ALL) respectively.

Discussion

Summary

In this Swiss population-based matched case (N = 559) -control (N = 4433) study, we found no consistent evidence for an association between socioeconomic status and risk of childhood leukemia or ALL. The associations did not change substantially with the operational definition of SES (individual-based, household-based, or area-based SES), time (comparing the periods 1990–2000 and 2000–2006), or age at diagnosis. Our results show that the included measures of socioeconomic status did not act as considerable risk factors or strong confounders in the etiology of childhood leukemia.

Comparison with Other Studies

The results on the association between SES and incidence of leukemia published in the last years remain inconsistent (17, 20, 32). Researchers who had found a potential association had usually reported it only from the most extreme SES groups (the highest or lowest 10–20%) (16, 17, 30, 31). Therefore, we analyzed our continuous exposure measures (living space, area-based SES index) in two ways: comparing tertiles and comparing the two most extreme quintiles. Both analyses did not result in a significant association. The trend for a higher risk in the least deprived group (most living space, highest area-based index) was far from being statistically significant. Any true and causal association would be too small to explain an appreciable proportion of leukemia cases in childhood. Similarly, any of the included SES indicators would unlikely act as a strong confounder in other childhood leukemia incidence studies. Last, we did not find evidence that the association might have changed over time, as suggested in a review by Poole et al. (19). Our results are in line with the findings presented in a large population-based study of the Haematological Malignancy Research Network, in which the researchers questioned the benefit of future etiological investigations that focus solely on socioeconomic factors (33).

Strengths and Limitations

The chosen study design allowed us to overcome most limitations of earlier studies on SES and incidence of childhood leukemia. First, the study was nationwide and could largely avoid case and control participation bias, as active participation for cases and controls was not required. The sample included all leukemia cases of the childhood cancer registry fulfilling the criteria for linkage with the census datasets. Controls were drawn from the census, which are virtually complete datasets of the Swiss population. Participation bias was a major issue in many preceding studies (19, 20), as illustrated by Smith and co-authors, who simulated effects of control and case participation bias in their analysis (34). Second, by obtaining the information on socioeconomic status for both cases and controls from the census, we avoided reporting bias. Third, due to the linkage design (the children had to be born before the census and diagnosed after the census), the information on socioeconomic status was always collected before the cancer diagnosis. We can therefore be sure that the exposure preceded the outcome (e.g., SES did not change as a consequence of the diagnosis, for instance, if one of the parents had stopped working in order to care for the child). Fourth, the availability of different operational definitions of socioeconomic status with data on individual-based information (education), household-based information (number of rooms per person, square meter of living space per person), and area-based SES index is an important strength of our study. This allowed assessing the robustness of the association between SES and leukemia, and analyzing potential differences between these measures as previously suggested (19, 30). Last, information on potential leukemia risk factors associated with SES (maternal and paternal age; nationality; language region; number of children in household) minimized the potential for confounding.

This study has its limitations. First, the probabilistic linkage might have incorrectly linked some of the childhood cancer cases to a census child creating measurement error in the information of socioeconomic status. We addressed this issue by repeating the analyses with different linkage probability datasets. The results did not materially change. Second, the assignment of father and mother status in the same household might be incorrect, since male and female adults living in the same household are not necessarily biological fathers or mothers of the child. However, if there was a true SES leukemia association, one might argue that the socioeconomic status of the child is determined by the householder(s) it lives with. Third, the householders represent a relatively affluent and homogeneous population (Swiss nationals, well educated, employed, male head of household). Fourth, to have SES information preceding the diagnosis of leukemia, we excluded by design all children with leukemia born after census 1990 and diagnosed before census 2000, which leads to an underrepresentation of younger leukemia cases. This selection could lead to biased results if the association of SES is non-zero but varies with age. However, we did not find strong evidence against a common effect over age groups when testing for effect modification by age. If we had, in contrary, included these children, we would possibly have introduced survivor bias, because survival might be linked to SES and cases dying before 2000 were not linkable and would have missing SES information. Additionally, case registration in the childhood cancer registry was not complete during the first years. Completeness of the SCCR, estimated by the proportion of patients that first came to the registries attention via death certificate notification, was 85% in 1985–1989, 90% from 1990 to 1994, and ≥95% since 1995 (data not shown). Fifth, as we could only use information on socioeconomic status available in the census, we could not include any measure reflecting directly income or wealth. Sixth, as our sample size, although nationwide, was reduced by the inclusion criteria for our linkage design, statistical power was limited. This reduces particularly the ability to find small non-zero effects and to assess effects in subgroups, such as age groups (e.g., 1- to 4-year olds) or in rare leukemia subtypes (e.g., acute myeloid leukemia). Seventh, we were only able to include information available in the SCCR or the SNC and did hence not dispose of information on lifestyle-related risk factors, such as exposure to infections (e.g., nursery care) or to environmental tobacco smoke. Eight, the transferability of our results to other countries might be restricted. Evidence on the association of childhood leukemia with SES has been inconsistent across nations (20). An explanation for these inconsistencies might be the difficulties in the measurement of SES, possibly to a varying degree across studies and nations. Furthermore, SES might actually not be causally associated with childhood leukemia but merely be a marker for a varying degree of exposure to a true risk factor, again possibly varying between studies and countries. In the latter situation, results from one country would not be transferable to other countries. A last limitation concerns the timing of the SES information in the life course of the child. For a child born in 1990, the 1990 census information reflects SES at birth. For a child born in 1984 and diagnosed with leukemia in 1992, the census 1990 reflects SES at age 6. By individually matching controls to cases by year of birth, we guaranteed that the variability of timing in the life course was the same for cases and controls. However, if socioeconomic status particularly matters during a specific age period, as suggested by Raaschou-Nielsen and co-authors (30), we might have diluted such an association.

Implications of Our Results

Given the various analyses performed, we concluded that the results show no consistent evidence for an effect of the included socioeconomic status indicators and the risk of childhood leukemia. The strongest association found with maternal but not paternal education might imply the involvement of intrauterine or postnatal factors, such as smoking behavior, occupational exposures, or dietary habits of the mother. As families with a mother of higher education usually exhibit lower prevalence of indoor cigarette smoking, higher health consciousness including attention to dietary habits, and lower occupational exposures to solvents, the observed association is unexpected (3537). Future studies should take a life-course approach (38, 39) by assessing measures of SES at different developmental stages in order to distinguish the potential influence of SES during the separate stages of intrauterine development, infancy, and early childhood. SES per se is not a direct cause of leukemia, but rather a proxy measure indicating unequal distribution of a number of environmental and familial factors, which could influence the likelihood of a child to develop leukemia. To understand the chain of causation, it will be inevitable to study the relation of specific SES indicators with potential leukemia risk factors in great detail, as the risk factors for childhood leukemia remain poorly understood (4045). Some potential SES-associated risk factors, for instance, paternal and maternal age, and number of older and younger siblings, have directly been considered in this study. A further, much discussed potential cause of leukemia is early or delayed exposure to infectious diseases during pregnancy and early childhood, with an influence on the development of the immune system of the child (18). By adjusting the numbers of older siblings, we have partly accounted for this, but had no information on nursery care, another risk factor for exposure to infections. Similarly, unhealthy lifestyle and higher exposure to a number of environmental factors (e.g., environmental tobacco smoke, different household chemical compounds, or radiation) are socially patterned and usually more prevalent in the lower SES groups being associated with a higher leukemia incidence risk. However, with the exception of parental smoking (46), none of these factors have been consistently and strongly associated with leukemia risk in children.

In conclusion, this carefully designed study did not find consistent evidence for an association between different SES definitions (parental education, living condition, area-based SES) and incidence of childhood leukemia. The included SES indicators are unlikely to be strong risk factors or confounding factors for leukemia incidence in children, in Switzerland or comparable countries. Future studies should therefore carefully define socioeconomic indicators and critically interpret their role when investigating the etiology of childhood leukemia.

Author Contributions

CK and MZ designed the study. AS and KS contributed and interpreted the data from the Swiss National Cohort. FGP and PB contributed data to the Swiss Childhood Cancer Registry and interpreted the data from the perspective of the Swiss Paediatric Oncology Group. NPH interpreted the data as an expert in cancer epidemiology. MA and MZ analyzed the data. MA, CK, and MZ wrote the first draft of the manuscript. All authors of this research paper have directly participated in the planning, execution, or analysis of the study and revised the manuscript.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We thank all pediatric cancer centers organized in the SPOG for the data collection within the Swiss Childhood Cancer Registry and Swiss Federal Statistical Office for providing the data necessary to build the Swiss National Cohort. Swiss Pediatric Oncology Group (SPOG) Scientific Committee: Prof. Dr. med. R. Ammann, Bern; Dr. med. R. Angst, Aarau; Prof. Dr. med. A. Ansari, Geneva; PD Dr. med. M. Beck Popovic, Lausanne; Dr. med. E. Bergstraesser, Zurich; Dr. med. P. Brazzola, Bellinzona; Dr. med. J. Greiner, St. Gallen; Prof. Dr. med. M. Grotzer, Zurich; Dr. med. H. Hengartner, St. Gallen; Prof. Dr. med. T. Kuehne, Basel; Prof. Dr. med. C. Kuehni, Bern; Prof. Dr. med. K. Leibundgut, Bern; Prof. Dr. med. F. Niggli, Zurich; PD Dr. med. J. Rischewski, Lucerne; Prof. Dr. med. N. von der Weid, Basel. Swiss National Cohort Study Group (SNC): Matthias Egger (Chairman of the Executive Board), Adrian Spoerri and Marcel Zwahlen (all Bern), Milo Puhan (Chairman of the Scientific Board), Matthias Bopp (both Zurich), Nino Künzli (Basel), Fred Paccaud (Lausanne) and Michel Oris (Geneva). Funding: This work was supported by Oncosuisse (OCS – 01869 – 02 – 2006, KLS 01869-02-2006) and the Swiss National Science Foundation (Prosper 3233-069348 to CK, and SNC (3347CO-108806, 33CS30_134273 and 33CS30_148415)). The work of the Swiss Childhood Cancer Registry is supported by the Swiss Paediatric Oncology Group (www.spog.ch), Schweizerische Konferenz der kantonalen Gesundheitsdirektorinnen und -direktoren (www.gdk-cds.ch), Swiss Cancer Research (www.krebsforschung.ch), Kinderkrebshilfe Schweiz (www.kinderkrebshilfe.ch), Ernst-Göhner Stiftung, Stiftung Domarena, and National Institute of Cancer Epidemiology and Registration (www.nicer.ch).

Supplementary Material

The Supplementary Material for this article can be found online at https://www.frontiersin.org/article/10.3389/fonc.2015.00139

Footnotes

References

1. Bouchardy C, Lutz J-M, Kühni C. Cancer in Switzerland: Situation and Development from 1983 up to 2007. Neuchâtel: Federal Statistical Office (FSO), National Institute for Cancer Epidemiology and Registration (NICER), Swiss Childhood Cancer Registry (SCCR). (2011).

Google Scholar

2. Gatta G, Corazziari I, Magnani C, Peris-Bonet R, Roazzi P, Stiller C. Childhood cancer survival in Europe. Ann Oncol (2003) 14(Suppl 5):v119–27. doi:10.1093/annonc/mdg755

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Kuehni C, Michel G, Egger M, Zwahlen M, Beck Popovic M, Niggli F, et al. Das Schweizer Kinderkrebsregister: Erfahrungen als nationales Register. Schweiz Ärzteztg (2013) 94(9):327–31.

Google Scholar

4. Kuehni CE, Rueegg CS, Michel G, Rebholz CE, Strippoli MP, Niggli FK, et al. Cohort profile: the Swiss childhood cancer survivor study. Int J Epidemiol (2012) 41(6):1553–64. doi:10.1093/ije/dyr142

CrossRef Full Text | Google Scholar

5. Michel G, von der Weid NX, Zwahlen M, Adam M, Rebholz CE, Kuehni CE. The Swiss Childhood Cancer Registry: rationale, organisation and results for the years 2001–2005. Swiss Med Wkly (2007) 137(35–36):502–9.

PubMed Abstract | Google Scholar

6. Shah A, Coleman MP. Increasing incidence of childhood leukaemia: a controversy re-examined. Br J Cancer (2007) 97(7):1009–12. doi:10.1038/sj.bjc.6603946

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Steliarova-Foucher E, Stiller C, Kaatsch P, Berrino F, Coebergh J-W, Lacour B, et al. Geographical patterns and time trends of cancer incidence and survival among children and adolescents in Europe since the 1970s (the ACCIS project): an epidemiological study. Lancet (2004) 364(9451):2097–105. doi:10.1016/S0140-6736(04)17550-8

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Bailey HD, Fritschi L, Infante-Rivard C, Glass DC, Miligi L, Dockerty JD, et al. Parental occupational pesticide exposure and the risk of childhood leukemia in the offspring: findings from the childhood leukemia international consortium. Int J Cancer (2014) 135(9):2157–72. doi:10.1002/ijc.28854

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Buffler PA, Kwan ML, Reynolds P, Urayama KY. Environmental and genetic risk factors for childhood leukemia: appraising the evidence. Cancer Invest (2005) 23(1):60–75. doi:10.1081/CNV-46402

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Crosignani P, Tittarelli A, Borgini A, Codazzi T, Rovelli A, Porro E, et al. Childhood leukemia and road traffic: a population-based case-control study. Int J Cancer (2004) 108(4):596–9. doi:10.1002/ijc.11597

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Stiller CA. Epidemiology and genetics of childhood cancer. Oncogene (2004) 23(38):6429–44. doi:10.1038/sj.onc.1207717

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Wiemels J. Perspectives on the causes of childhood leukemia. Chem Biol Interact (2012) 196(3):59–67. doi:10.1016/j.cbi.2012.01.007

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Arntzen A, Samuelsen SO, Bakketeig LS, Stoltenberg C. Socioeconomic status and risk of infant death. A population-based study of trends in Norway, 1967–1998. Int J Epidemiol (2004) 33(2):279–88. doi:10.1093/ije/dyh054

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Huisman M, Kunst AE, Bopp M, Borgan JK, Borrell C, Costa G, et al. Educational inequalities in cause-specific mortality in middle-aged and older men and women in eight western European populations. Lancet (2005) 365(9458):493–500. doi:10.1016/S0140-6736(05)17867-2

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Phelan JC, Link BG, Tehranifar P. Social conditions as fundamental causes of health inequalities: theory, evidence, and policy implications. J Health Soc Behav (2010) 51:S28–40. doi:10.1177/0022146510383498

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Borugian MJ, Spinelli JJ, Mezei G, Wilkins R, Abanto Z, McBride ML. Childhood leukemia and socioeconomic status in Canada. Epidemiology (2005) 16(4):526–31. doi:10.1097/01.ede.0000164813.46859.63

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Kroll ME, Stiller CA, Murphy MF, Carpenter LM. Childhood leukaemia and socioeconomic status in England and Wales 1976–2005: evidence of higher incidence in relatively affluent communities persists over time. Br J Cancer (2011) 105(11):1783–7. doi:10.1038/bjc.2011.415

CrossRef Full Text | Google Scholar

18. Ribeiro KB, Buffler PA, Metayer C. Socioeconomic status and childhood acute lymphocytic leukemia incidence in Sao Paulo, Brazil. Int J Cancer (2008) 123(8):1907–12. doi:10.1002/ijc.23738

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Poole C, Greenland S, Luetters C, Kelsey JL, Mezei G. Socioeconomic status and childhood leukaemia: a review. Int J Epidemiol (2006) 35(2):370–84. doi:10.1093/ije/dyi248

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Adam M, Rebholz CE, Egger M, Zwahlen M, Kuehni CE. Childhood leukaemia and socioeconomic status: what is the evidence? Radiat Prot Dosimetry (2008) 132(2):246–54. doi:10.1093/rpd/ncn261

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Michel G, von der Weid NX, Zwahlen M, Redmond S, Strippoli MP, Kuehni CE. Incidence of childhood cancer in Switzerland: the Swiss Childhood Cancer Registry. Pediatr Blood Cancer (2008) 50(1):46–51. doi:10.1002/pbc.21129

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Bopp M, Spoerri A, Zwahlen M, Gutzwiller F, Paccaud F, Braun-Fahrlander C, et al. Cohort profile: the Swiss national cohort – a longitudinal study of 6.8 million people. Int J Epidemiol (2009) 38(2):379–84. doi:10.1093/ije/dyn042

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Mitter V, Michel G, Wölfli P, Gianinazzi M, Rüegg C, Sommer G. Swiss Childhood Cancer Registry: Annual Report 2011/2012. Bern: Swiss Childhood Cancer Registry (2012).

Google Scholar

24. Furukawa T, Yamasaki M, Hiraga Y, Fukasawa E, Soejima S. [Pharmacological action of triazolam]. Igaku Kenkyu (1975) 45(5):285–302.

PubMed Abstract | Google Scholar

25. Steliarova-Foucher E, Stiller C, Lacour B, Kaatsch P. International classification of childhood cancer, third edition. Cancer (2005) 103(7):1457–67. doi:10.1002/cncr.20910

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Knol MJ, Vandenbroucke JP, Scott P, Egger M. What do case-control studies estimate? Survey of methods and assumptions in published case-control research. Am J Epidemiol (2008) 168(9):1073–81. doi:10.1093/aje/kwn217

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Wacholder S. Practical considerations in choosing between the case-cohort and nested case-control designs. Epidemiology (1991) 2(2):155–8. doi:10.1097/00001648-199103000-00013

CrossRef Full Text | Google Scholar

28. Hermann M, Heye C, Leuthold H. Soziokulturelle Unterschiede in der Schweiz. Vier Indizes zu räumlichen Disparitäten, 1990–2000. Neuchâtel: Swiss Federal Statistical Office (SFSO) (2005). p. 1–72.

Google Scholar

29. Myers D, Baer WC, Choi SY. The changing problem of overcrowded housing. J Am Plan Assoc (1996) 62(1):66–84. doi:10.1080/01944369608975671

CrossRef Full Text | Google Scholar

30. Raaschou-Nielsen O, Obel J, Dalton S, TjOnneland A, Hansen J. Socioeconomic status and risk of childhood leukaemia in Denmark. Scand J Public Health (2004) 32(4):279–86. doi:10.1080/14034940310022214

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Stiller CA, Kroll ME, Boyle PJ, Feng Z. Population mixing, socioeconomic status and incidence of childhood acute lymphoblastic leukaemia in England and Wales: analysis by census ward. Br J Cancer (2008) 98(5):1006–11. doi:10.1038/sj.bjc.6604237

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Pan IJ, Daniels JL, Zhu K. Poverty and childhood cancer incidence in the United States. Cancer Causes Control (2010) 21(7):1139–45. doi:10.1007/s10552-010-9528-3

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Smith A, Howell D, Patmore R, Jack A, Roman E. Incidence of haematological malignancy by sub-type: a report from the Haematological Malignancy Research Network. Br J Cancer (2011) 105(11):1684–92. doi:10.1038/bjc.2011.450

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Smith A, Roman E, Simpson J, Ansell P, Fear NT, Eden T. Childhood leukaemia and socioeconomic status: fact or artefact? A report from the United Kingdom childhood cancer study (UKCCS). Int J Epidemiol (2006) 35(6):1504–13. doi:10.1093/ije/dyl193

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Ferreira JD, Couto AC, Pombo-de-Oliveira MS, Koifman S. Brazilian Collaborative Study Group of Infant Acute L. Pregnancy, maternal tobacco smoking, and early age leukemia in Brazil. Front Oncol (2012) 2:151. doi:10.3389/fonc.2012.00151

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Kwan ML, Jensen CD, Block G, Hudes ML, Chu LW, Buffler PA. Maternal diet and risk of childhood acute lymphoblastic leukemia. Public Health Rep (2009) 124(4):503–14.

PubMed Abstract | Google Scholar

37. McKinney PA, Raji OY, van Tongeren M, Feltbower RG. The UK Childhood Cancer Study: maternal occupational exposures and childhood leukaemia and lymphoma. Radiat Prot Dosimetry (2008) 132(2):232–40. doi:10.1093/rpd/ncn265

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Ben-Shlomo Y, Kuh D. A life course approach to chronic disease epidemiology: conceptual models, empirical challenges and interdisciplinary perspectives. Int J Epidemiol (2002) 31(2):285–93. doi:10.1093/ije/31.2.285

CrossRef Full Text | Google Scholar

39. Kuh D, Ben-Shlomo Y, Lynch J, Hallqvist J, Power C. Life course epidemiology. J Epidemiol Community Health (2003) 57(10):778–83. doi:10.1136/jech.57.10.778

CrossRef Full Text | Google Scholar

40. Chokkalingam AP, Buffler PA. Genetic susceptibility to childhood leukaemia. Radiat Prot Dosimetry (2008) 132(2):119–29. doi:10.1093/rpd/ncn255

PubMed Abstract | CrossRef Full Text | Google Scholar

41. de Klerk N, Milne E. Overview of recent studies on childhood leukaemia, intra-uterine growth and diet. Radiat Prot Dosimetry (2008) 132(2):255–8. doi:10.1093/rpd/ncn303

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Infante-Rivard C. Chemical risk factors and childhood leukaemia: a review of recent studies. Radiat Prot Dosimetry (2008) 132(2):220–7. doi:10.1093/rpd/ncn292

PubMed Abstract | CrossRef Full Text | Google Scholar

43. McNally RJ, Eden TO. An infectious aetiology for childhood acute leukaemia: a review of the evidence. Br J Haematol (2004) 127(3):243–63. doi:10.1111/j.1365-2141.2004.05166.x

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Raaschou-Nielsen O. Indoor radon and childhood leukaemia. Radiat Prot Dosimetry (2008) 132(2):175–81. doi:10.1093/rpd/ncn288

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Schuz J, Ahlbom A. Exposure to electromagnetic fields and the risk of childhood leukaemia: a review. Radiat Prot Dosimetry (2008) 132(2):202–11. doi:10.1093/rpd/ncn270

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Liu R, Zhang L, McHale CM, Hammond SK. Paternal smoking and risk of childhood acute lymphoblastic leukemia: systematic review and meta-analysis. J Oncol (2011) 2011:854584. doi:10.1155/2011/854584

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: childhood cancer, leukemia, socioeconomic status, risk factor, case–control study

Citation: Adam M, Kuehni CE, Spoerri A, Schmidlin K, Gumy-Pause F, Brazzola P, Probst-Hensch N and Zwahlen M (2015) Socioeconomic status and childhood leukemia incidence in Switzerland. Front. Oncol. 5:139. doi: 10.3389/fonc.2015.00139

Received: 07 April 2015; Accepted: 02 June 2015;
Published: 30 June 2015

Edited by:

Karina Braga Ribeiro, Hospital AC Camargo, Brazil

Reviewed by:

Julia Heck, University of California Los Angeles, USA
Paola Friedrich, Dana-Farber Cancer Institute, USA

Copyright: © 2015 Adam, Kuehni, Spoerri, Schmidlin, Gumy-Pause, Brazzola, Probst-Hensch and Zwahlen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Martin Adam, Swiss Tropical and Public Health Institute, Socinstrasse 57, Basel 4002, Switzerland, martin.adam@unibas.ch

Martin Adam and Claudia E. Kuehni have contributed equally to this work.