Experimental and epidemiological data suggest that vitamin D play a role in pathogenesis and progression of cancer, but prospective data on head and neck cancer (HNC) and oesophagus cancer are limited. The European Prospective Investigation into Cancer and Nutrition (EPIC) study recruited 385,747 participants with blood samples between 1992 and 2000. This analysis includes 497 case-control pairs of the head and neck and oesophagus, as well as 443 additional controls. Circulating 25(OH)D3 were measured in pre-diagnostic samples and evaluated in relation to HNC and oesophagus cancer risk and post-diagnosis all-cause mortality. After controlling for risk factors, a doubling of 25(OH)D3 was associated with 30% lower odds of HNC (OR 0.70, 95% confidence interval [95% CI] 0.56–0.88, Ptrend = 0.001). Subsequent analyses by anatomical sub-site indicated clear inverse associations with risk of larynx and hypopharynx cancer combined (OR 0.55, 95CI% 0.39–0.78) and oral cavity cancer (OR 0.60, 95CI% 0.42–0.87). Low 25(OH)D3 concentrations were also associated with higher risk of death from any cause among HNC cases. No clear association was seen with risk or survival for oesophageal cancer. Study participants with elevated circulating concentrations of 25(OH)D3 had decreased risk of HNC, as well as improved survival following diagnosis.
About 650,000 new cases of head and neck cancer (HNC) and 450,000 new cases of esophageal cancer occur worldwide each year1. This corresponds to approximately 11% of total cancer incidence. Global differences in incidence are primarily driven by its main risk factors tobacco and alcohol exposure2,3, but over the last decade infection by human papillomavirus has emerged as an important cause of HNC subsites, in particular oropharynx cancer4.
Vitamin D is a fat-soluble precursor to the steroid hormone calcitriol, primarily obtained via endogenous synthesis in the skin after exposure to sunlight5,6, and is fundamental for absorption of dietary calcium and maintaining bone health5,7. Vitamin D is also thought to have a protective role in cancer development and progression, and there is a large body of evidence from mechanistic studies supporting a role of vitamin D in multiple hallmarks of carcinogenesis7,8.
Vitamin D is metabolised in the liver to 25-hydroxyvitamin D [25(OH)D] and can be measured in the circulation to assess an individual’s vitamin D status8. In contrast to mechanistic studies, epidemiological studies of circulating 25(OH)D have not provided consistent evidence supporting a beneficial role of vitamin D in terms of cancer incidence, the exception being colorectal cancer for which the majority of studies support an inverse association between circulating vitamin D and risk9,10. Circulating 25(OH)D has not been frequently studied in relation to cancers of the head and neck and esophagus, and the literature is to date limited and typically total based on measures of total vitamin D (25(OH)D). One small Danish study based on 44 HNC cases from three cohorts found a nominal inverse association between circulating 25(OH)D and HNC risk11. From larger studies of circulating 25(OH)D and HNC risk, there is evidence both of an inverse association with risk, and of no association. The Copenhagen City Heart Study (CCHS) based on 122 HNC cases reported a 45% increase hazards of HNC for a 50% reduction in circulating vitamin D12 whereas the Alpha-Tocopherol Beta Carotene (ATBC) study based on 340 HNC cases did not observe any clear association between circulating vitamin D and HNC risk13. Furthermore, the Vitamin D Pooling Project (VDPP) combining 8 prospective cohorts and based on 267 esophageal cancer cases did not find any association with risk14. In addition, none of these studies have evaluated whether pre-diagnostic 25(OH)D is also related to risk of death after diagnosis.
While reverse causality is a principal concern in retrospective studies, the current study aimed to provide a comprehensive evaluation of pre-diagnostic circulating 25(OH)D and risk of cancers of the head and neck and oesophagus from a large case-control study nested within the European Prospective Investigation into Cancer and Nutrition (EPIC). In addition, we aimed to evaluate if pre-diagnostic circulating 25(OH)D is associated with survival following cancer diagnosis.
The final study population consisted of 497 cases, including 350 head and neck cancers and 147 oesophagus cancers, 497 individually matched controls and 443 subjects in control group 2. Approximately two thirds (68%) of the nested case-control population were men (Table 1), the median age at recruitment was 56.7 years (5th–95th percentile: 42–71) and the average time from blood draw to diagnosis for cases was 6.3 years. Control group 2 had similar demographic characteristics as the matched control group, but with a higher proportion of women.
Variations in circulating 25(OH)D3 by season and demographic characteristics
Predicted and observed concentrations in relation to season of blood draw are displayed in Fig. 1. Visual inspection suggests clear differences in circulating 25(OH)D3 that are consistent with sun exposure being the most important determinant of circulating vitamin D, 25(OH)D3 concentrations were lowest among those who had their blood drawn around February and March and highest among those who had their blood drawn around August.
The relation of nutrient intake, lifestyle factors, smoking, and alcohol intake with plasma 25(OH)D3 are presented in Supplementary Table 1. In comparison with control participants who reported being never smokers, current smokers had 7% lower 25(OH)D3 concentrations on average (95% CI: −14% to 0%), whereas former smokers had 9% higher 25(OH)D3 concentrations (95% CI: 2–16%). BMI was inversely associated with 25(OH)D3 concentrations. No differences in 25(OH)D3 were seen in relation to alcohol intake.
Circulating 25(OH)D3 in relation to head and neck and esophagus cancer risk
The risk analysis results for overall HNC overall are shown in Table 2. Participants with higher 25(OH)D3 concentrations had lower HNC risk, with a doubling in plasma 25(OH)D3 being associated with 45% lower risk (conditional ORlog2 0.55, 95% CI 0.42–0.72, Ptrend 1 × 10−5; unconditional ORlog2 0.54, 95% CI 0.44–0.68, Ptrend 3 × 10−8). Following adjustments for education, alcohol consumption, circulating cotinine, tobacco exposure, and BMI, the unconditional OR estimates were slightly attenuated but remained indicative of an inverse association between circulating 25(OH)D3 and risk (ORlog20.70, 95% CI 0.56–0.88, Ptrend 0.001). We also evaluated the association between concentrations of 25(OH)D3 and oesophageal cancer squamous cell carcinoma and adenocarcinoma, and whilst the OR estimates were consistent with that of overall HNC, the confidence intervals were wide (OR 0.69, 95% CI 0.44–1.10 for esophageal squamous cell carcinoma [ESCC], and OR 0.74, 95% CI 0.45–1.23 for esopheageal adenocarcinoma [EADC]). Because one of the key functions of vitamin D is to maintain calcium homoeostasis, we also included calcium intake in our models, but this did not affect the OR estimates (data not shown).
ORs of HNC across the observed range of 25(OH)D3 concentrations are depicted in Fig. 2. Compared to participants having 25(OH)D3 blood concentrations of 50 nmol/L, odds of HNC were 42% higher for those with 25(OH)D3 blood concentrations of 25 nmol/L, and 30% lower for those with 25(OH)D3 blood concentrations of 100 nmol/L.
Circulating 25(OH)D3 risk analysis stratified for head and neck cancer sub-sites demographic and lifestyle factors
Risk analyses stratified by HNC sub-sites are displayed in Table 3, and indicated that the association of 25(OH)D3 was particularly prominent for cancers of the larynx and hypopharynx (OR 0.55, 95% CI 0.39–0.78) and for cancers of the oral cavity (OR 0.60, 95% CI 0.42–0.87). No association was observed with risk of oropharynx cancer (OR 0.92, 95% CI 0.58–1.45), although the sample size was small.
Stratifications by demographic and lifestyle factors (Supplementary Figure 1) showed that the association between circulating 25(OH)D3 and HNC risk was solely driven by former (unadjusted ORlog2 0.65, 95% CI 0.42–1.01) and current smokers (unadjusted ORlog2 0.47, 95% CI 0.34–0.66), and was not seen in never smokers (ORlog2 1.21, 95% CI 0.72–2.03; (Pheterogeneity 0.02). In order to further evaluate if residual confounding by tobacco exposure might explain the association between circulating 25(OH)D3 and HNC risk in current smokers, we adjusted for circulating cotinine–a useful and objective indicator of recent tobacco exposure–which resulted in a small attenuation in OR estimates (cotinine adjusted ORlog2 0.55, 95% CI 0.39–0.80). Additional indicators of historical tobacco exposure, in particular duration and average number of cigarettes smoked per day (CPD), were incomplete and only available for 85% of the study population. Excluding subjects with missing data on these indicators yielded unadjusted OR estimates of 0.71 in former smokers (95% CI 0.44–1.14) and 0.46 (95% CI 0.31–0.66) in current smokers, with small attenuations in OR being observed when additionally adjusting for duration and CPD (former smokers ORlog2 0.77, 95% CI 0.45–1.24, current smoker ORlog2 0.55, 95% CI 0.36–0.81).
We also noted that the inverse association of circulating 25(OH)D3 with HNC risk was not affected after excluding cases within one year and 2 years after blood draw (ORlog2 0.69, 95% CI 0.54–0.88 and 0.69, 95% CI 0.54–0.89; respectively). Furthermore, the inverse association between circulating 25(OH)D3 and HNC risk was similar for cases diagnosed within three years after blood draw, as well as for those being diagnosed over 9 years after their blood draw (P for heterogeneity 0.79). Some indications of differences in strength of association between circulating 25(OH)D3 and HNC risk were also seen when stratifying for groups of alcohol intake at recruitment, where no association was seen among subject with 0 grams of alcohol intake per day, although OR estimates in the other drinking categories were compatible with that overall.
All-cause mortality for study participants diagnosed with HNC and oesophagus cancer
In total, 145 deaths occurred among the HNC cases during the follow-up. Median time between diagnosis and death for those cases who died during follow-up was 15 months (range: 0 months to 12 years), and median time between blood collection and death was 8.5 years (range: 7 months to 15 years).
Results of Cox proportional hazards regression for 25(OH)D3 of all-cause mortality are shown in Fig. 3A. Similarly to the analysis of incidence, an overall inverse association between pre-diagnostic circulating 25(OH)D3 and survival post HNC was observed; the HR for log2 25(OH)D3 [HRlog2] being 0.73 (95% CI 0.55–0.97). The hazard of death was 1.72 times higher (95% CI: 1.11–2.51) for participants with circulating concentrations of 25 nmol/L compared to those with 50 nmol/L. However, no further survival benefits were seen for cases with 25(OH)D3 concentrations above 50 nmol/L, and there was even an indication that higher 25(OH)D3 concentrations might be associated with elevated hazard of death, although very few participants had 25(OH)D3 greater than 75 nmol/L. For those deceased with HNC specifically indicated as underlying cause of death (87 deaths), HRlog2 was 0.68 (95% CI 0.51–0.91) and adjusting the cause-specific mortality analysis for potential confounders did not affect the HR estimates notably (HRlog2 0.71, 95% CI 0.53–0.96, Ptrend = 0.02). For comparison, 58 deaths occurred with other-than-HNC indicated as cause of death, and no association between circulating 25(OH)D3 and survival was observed, the HRlog2 being 0.88 (95% CI = 0.53–1.26, Ptrend = 0.29).
Model-based estimates of the survival function evaluated at 25, 50, and 75 nmol/L of 25(OH)D3 among HNC cases are presented Fig. 3B. The expected 5-year post diagnostic survival probabilities for cases with 25(OH)D3 concentrations of 25 nmol/L were 0.58 (95% CI 0.49, 0.65), and 0.71 (95% CI 0.64, 0.77) for those having 25(OH)D3 concentrations of 50 nmol/L. Estimated HRs did not vary notably when stratifying by sex, age, country, education, alcohol or tobacco exposure (Supplementary Figure 2). Of note, when stratifying the survival analysis by time from blood draw to diagnosis, the association of circulating 25(OH)D3 with all-cause mortality was apparent both among HNC cases diagnosed before 5 years (HRlog2 0.72, 95% CI 0.54–0.95) and those diagnosed over 5 years after blood draw (HRlog2 0.80, 95% CI 0.62–1.03). Regarding the 91 death that occurred among esophageal cancer, circulating concentrations of 25(OH)D3 did not display any clear association with all-cause mortality, nor with esophageal-specific cause mortality.
We had limited information on disease stage, and adjusting for stage in an analysis restricted to those 161 HNC cases (46%) for whom stage was available appeared to completely attenuate the association of circulating 25(OH)D3 with all-cause mortality (HRlog2 = 0.96 95% CI = 0.76–1.20, Ptrend = 0.64), suggesting that the inverse association with all-cause mortality noted in the unadjusted survival analysis was completely mediated by difference in disease stage.
To date, this is the largest prospective study investigating the relation between circulating vitamin D and head and neck cancer risk, and the first to also evaluate the relation with post-diagnosis survival. We report a notable risk decrease for participants with higher plasma vitamin D concentrations, as well as improved survival among cases having adequate pre-diagnostic vitamin D concentrations.
Vitamin D in cancer development and progression
The importance of vitamin D in maintaining bone health has long been recognized, and there is also an abundance of mechanistic studies supporting a beneficial role of vitamin D in carcinogenesis by inhibiting tumour initiation and progression. Specifically, circulating vitamin D (measured as 25(OH)D3 in the current study) is a precursor to its active hydroxylated form calcitriol (1,25(OH)D3). Calcitriol is a potent steroid hormone that has been implicated by in vitro and in vivo models as having a potential anti-cancer influence by affecting multiple cancer hallmarks, including reducing angiogenesis, metastasis, cell invasion, inflammation, and proliferation, as well as stimulating apoptosis7. Some studies have also demonstrated a beneficial role of calcitriol in tobacco-related cancers, including oral, lung and bladder cancer, where reductions in angiogenesis, metastasis, and cell-modulatory effects have been suggested7,8,15,16,17,18,19,20.
Prospective studies of 25(OH)D3 and head and neck cancer
Circulating vitamin D has been widely studied in relation to risk of multiple cancers in prospective studies, with the most consistent evidence accumulated to date being an inverse association of colorectal cancer9,10. The body of evidence on other cancers is contradictory and does not support a similar consistent inverse association of vitamin D with other common or rare cancers7. Head and neck cancer has been rarely studied in relation to circulating vitamin D, with only three prospective studies published to date; the CCHS based on 122 cases12, the ATBC study based on 340 cases13, and an additional small Danish study based on 44 cases from three cohorts11. The ATBC study did not observe any association between 25(OH)D and head and neck cancer risk, nor did the smaller Danish study, although the latter was underpowered to detect any notable association with risk. This contrasts to the results of the CCHS study which was a classical cohort study that assessed baseline 25(OH)D for a complete cohort of 9,791 participants at baseline, and then followed them for up to 28 years for a wide range of incident cancers. The CCHS study conducted their analysis by estimating the relative risk associated with a 50% reduction in circulating vitamin D (OR1/2), and whilst no association was noted for non-smoking related cancers overall (OR1/2: 0.95), the CCHS study reported a clear inverse association between 25(OH)D and smoking related cancers and circulating vitamin D (OR1/2: 1.20), with a particularly strong association for HNC (OR1/2: 1.44). The result was almost identical to that of the current EPIC study were we observed an OR of 0.70 for a doubling in 25(OH)D3, corresponding to an OR1/2 of 1.45. The VDPP study, a consortium of 8 prospective cohorts including 143 ESCC and 100 EADC, did not observe any clear relation with circulating vitamin D, an observation similar to our results.
We note that in the current study, the inverse association between vitamin D and HNC risk was solely observed in former and current smokers. In accordance with results from the vitamin D pooling project21, we observed 8% lower circulating vitamin D concentrations in current smokers compared to never smokers, but concurrently 8% higher circulating vitamin D in former smokers compare to never smokers (Supplementary Table 1). Residual confounding by tobacco exposure is therefore an important concern when interpreting the results, in particular among current smokers. In smoking stratified analyses we adjusted for several indicators of tobacco exposure, included circulating cotinine. Given that the inverse associations with risk in former and current smokers were largely unchanged after adjusting for these additional tobacco exposure indicators, residual confounding by tobacco exposure does not appear to explain the observed decreases in head and neck cancer risk among study participants with elevated circulating vitamin D.
Further, the observed association was very stable during the follow-up, and most notable for a follow-up time of 9 years after recruitment, suggesting that the findings are unlikely to be due to reverse causation (Supplementary Figure 1). Considering that we were able to carefully control for current tobacco exposure using circulating cotinine measures, as well as alcohol consumption, we therefore interpret these results to mean that the decrease in head and neck cancer risk observed with elevated circulating vitamin D cannot be readily explained by known risk factors.
Vitamin D and cancer progression
Head and neck cancer prognosis is generally poor with overall 5-year survival rates of 50% to 60%, an important reason being that a large fraction of cases are diagnosed at advanced disease stage22,23,24. It was therefore interesting to note that in our analysis of all-cause mortality, pre-diagnostic 25(OH)D3 was inversely associated with survival among head and neck cancer cases following their diagnosis. In contrast to the association noted with HNC risk, for which a log-linear trend was observed across the whole range of observed 25(OH)D3 concentrations, the association with survival was only evident in the lower 25(OH)D3 range. This manifested in 72% higher hazard of death for cases with 25(OH)D3 concentrations of 25 nmol/L compared with those with 50 nmol/L, with corresponding 5-year survival probabilities of 58% and 71%, respectively. Estimated HRs did not vary notably when stratifying by time from blood draw to diagnosis, suggesting that pre-clinical symptoms would not seem likely to explain the association with all-cause mortality. Furthermore, subsequent cause-specific survival indicated that the association of 25(OH)D3 was primarily driven by deaths caused by HNC, but not other causes of death. However, taking disease stage into account appeared to explain most of the survival association of vitamin D, indicating that any survival benefit of having adequate pre-diagnostic 25(OH)D levels for HNC cases is likely to be mediated through differences in disease stage at diagnosis. Furthermore, it would have been informative to attain blood samples at diagnosis to fully evaluate the importance of circulating vitamin D for HNC prognosis.
Advantages and limitations
Our study distinguished itself from most previous prospective studies on vitamin D in that we used a mass spectrometry-based platform (LC-MS/MS) to specifically assay 25(OH)D3, rather than the more commonly used enzyme-linked immunosorbent assay (ELISA) which measures 25(OH)D2 and 25(OH)D3 combined. Because the vast majority of total circulating vitamin D is in the form of 25(OH)D3, we would not expect this to explain any discrepant results with other studies, even though evaluating 25(OH)D3 would seem preferable as it precedes the most active form of vitamin D, calcitriol (1,25(OH)D3)7. Another distinguishing factor of our analysis was that we controlled for seasonal variations in vitamin D using trigonometric functions (Fig. 1), rather than discontinuous seasonal models, such as discrete variables indicating the four seasons. Using trigonometric functions has an advantage in providing a smooth seasonal model with minimum degrees of freedom, whilst providing a valid account of the inherent differences in vitamin D related to sun exposure. Still, given the prospective design of our study, we do not expect differential bias between cases and controls by season, and the most important distinguishing factors comparing ours and others studies on circulating vitamin D in relation to HNC risk are a) the large study population and b), the multicentre recruitment across multiple European countries which would make the results more generalizable to other populations.
The principal limitation of our study is that 25(OH)D3 was measured using a single blood sample drawn in adulthood and therefore it may be possible that a single measurement does not capture exposure to vitamin D in an etiologically relevant period. Furthermore, in risk analyses stratified by cancer site, as well as in analyses of oesophagus cancer subtypes, the resulting small sample size hampered the statistical power to provide accurate risk estimates of potential risk associations.
EPIC participants with adequate circulating concentrations of vitamin D had lower risk of head and neck cancer and improved survival following their diagnosis. Known risk factors could only partly explain these associations. Overall, our results are consistent with a beneficial role of vitamin D in head and neck cancer aetiology.
Materials and Methods
The study was conducted within the European Prospective Investigation into Cancer and nutrition (EPIC). EPIC recruitment procedures, collection of questionnaire data, anthropometric measurements, and blood samples have been described in detail elsewhere25. In brief, 521,330 individuals were recruited between 1992 and 2000 by 23 centres across 10 European countries, of which 385,747 contributed a blood sample. Blood fractions were aliquoted into 0.5 mL straws, which were heat-sealed and stored in liquid nitrogen tanks at −196 °C, except at the Umeå centre in Sweden where samples were stored in 1.8 mL plastic tubes in −80 °C freezers. Participants completed self-administered questionnaires on lifestyle factors and diet.
Follow-up for Cancer Incidence
Incident cancer cases were identified at regular intervals through population-based cancer registries (Denmark, Italy except Naples, the Netherlands, Norway, Spain, Sweden and United Kingdom) or by active follow-up (France, Germany, Greece and Naples), which involved a combination of methods, including review of health insurance records, cancer and pathology registries, as well as direct contact with participants and their next-of-kin.
Mortality data, including vital status, cause and date of death, were obtained from mortality registries at the regional or national level. Subjects were followed up from study entry until cancer diagnosis (except non-melanoma skin cancer), death, emigration, or the end of the follow-up period for the relevant study centre. End of follow-up was defined as the latest date of complete follow-up for both cancer incidence and vital status and varied between study centres from December 2004 to June 2010. Vital status at follow-up is over 98% complete.
Selection of Case and Control Participants
We initially identified 1,273 subjects diagnosed with incident head and neck or oesophagus cancer within the entire EPIC cohort by the end of the follow-up period for all centres. These cancer cases were defined on the basis of the International Classification of Diseases for Oncology, Second Edition (ICD-O-2), and included: oral cavity (ICD C02.0-C02.9, C04.0-C04.9, C03.0-C03.9, C05.0-C06.9, C14.0-C14.9), oropharynx (C01.9, C02.4, C09.0-C10.9), hypopharynx (C13.0-C13.9), larynx (C32.0-C32.9), and oesophagus (C15.0-C15.9). Cases who did not donate a blood sample (n = 152), did not have enough plasma available for biochemical analysis (n = 20), had a history of another cancer (n = 158, except non melanoma skin cancer), were not histologically confirmed, or did not have questionnaire information available (n = 22), were excluded, leaving 921 eligible cases. Because the aetiology of squamous cell carcinoma (SCC) and adenocarcinoma are thought to differ and the vast majority of HNC are SCC, we focused our analysis on SCC by excluding adenocarcinoma of the head and neck (n = 16). Also, we excluded esopheageal cases that were not classified as SCC or adenocarcinoma (n = 19). After further excluding cases from Denmark (n = 288) and the Malmö centre in Sweden (n = 101) who did not participate in this study, 497 eligible case participants with plasma samples were available for biochemical analyses. Data on histology were collected from each centre where possible.
For each case participant, one control was randomly chosen from appropriate risk sets consisting of all cohort members alive and free of cancer (except non-melanoma skin cancer) at the time (and hence age) of diagnosis of the index case. Matching criteria were country, sex, date of blood collection (±1 month, which was relaxed to ± 5 months for 22% of sets without available controls), and date of birth (±1 year, which was relaxed to ± 5 years for 1% of sets without available controls). In addition, we included 443 additional controls (control group 2) that were analysed in the context of a parallel study and individually matched to cases of another cancer site using identical matching criteria26.
The final dataset included 497 cancer cases and 497 individually matched controls, as well as 443 additional unmatched controls from control group 2 that contributed to unconditional and stratified risk analyses.
This research was conducted according to the principles expressed in the Declaration of Helsinki. This study was approved by the ethics review boards of the International Agency for Research on Cancer and individual EPIC centres. Informed consent was obtained from all EPIC participants at recruitment for use of their blood samples and data in future research.
All biochemical analyses were performed at Bevital A/S (http://www.bevital.no), Bergen, Norway. Liquid chromatography coupled to tandem mass spectrometry was used to measure plasma concentrations of 25-hydroxyvitamin D2 [25(OH)D2] and 25-hydroxyvitamin D3 [25(OH)D3]27, as well as cotinine27 (as indicator of recent nicotine exposure). We found that 25(OH)D2 was undetectable in the majority of the samples, thus our analyses focus on 25(OH)D3. We performed sensitivity analyses by using the sum of 25(OH)D3 and 25(OH)D2 (setting undetectable levels of 25(OH)D2 to 0) and we observed similar results.
Samples were analysed in batches of 86 and quality control included 6 calibration samples, 2 control samples, and 1 blank sample in each batch. The limit of detection for 25(OH)D3 was 6.3 nmol/L, and within- and between-day coefficients of variation were 4.4 to 8.2%. All plasma samples were kept at −80 °C and all HNC and oesophagus cancer cases and their individual matched controls were analysed together within the same batches in random order. Samples from control group 2 were evenly and randomly interspersed across the batches to ensure that no differential differences in 25(OH)D concentrations occurred. The laboratory staff was blinded to the case-control status of the blood samples.
We initially used conditional logistic regression, conditioning on matched case-sets, to evaluate the relation between circulating 25(OH)D3 and disease risk. Odds ratios (OR) and 95% confidence interval (CI) were calculated for the base 2 logarithm (log2) of 25(OH)D3 as estimates of the relative risk associated with a doubling in 25(OH)D3 concentrations. In order to increase the statistical power, we incorporated control group 2 in the risk analysis by use of unconditional logistic regression, adjusting for age at recruitment in years, sex and country of recruitment, as well as seasonality in 25(OH)D3 concentrations by fitting two pairs of sine and cosine functions of the day of blood draw (scaled to be between 0 and 1 through out any year). This method efficiently accounts for seasonal effects by providing smooth predictions without artificial discontinuities throughout the year. The logistic regression estimates were nearly identical with and without control group 2, and we therefore focused the result presentation of the risk analysis on the unconditional analyses with the matched controls and control group 2 combined. Additional adjustments were performed to account for possible confounding by known risk factors, including tobacco exposure (smoking status [never, former, current], and for cotinine concentrations [defined using quantiles of the distribution among current smokers]), alcohol consumption (self-reported intake in grams per day at recruitment [g/day]), as well as educational attainment (in five categories). Including additional smoking variables (duration of smoking, average cigarettes smoked per day) and body mass index did not alter the results notably and were not included in the final models. In order to the assess the statistical significance, log-linear trends (Ptrend) were calculated by including the base 2 logarithm (log2) of the biomarker concentration as a continuous variable in separate logistic regression models.
The relation between circulating pre-diagnostic 25(OH)D3 and post-diagnostic survival was assessed by calculating hazard ratios (HR) of all-cause mortality among incident head and neck and oesophagus cancer cases using a Cox proportional hazards model with time since diagnosis as the time-scale. We modelled 25(OH)D3 using restricted cubic splines with knots at its 10th, 33rd, 67th, and 90th percentiles, adjusting for the same covariates as in the unconditional logistic regression models, as well as age at diagnosis (years). Visual inspection of smoothed scaled Schoenfeld residuals revealed no notable departure from proportional hazards. In order to estimate the survival function at given concentrations of 25(OH)D3, we fitted a flexible parametric survival model28, modelling the baseline cumulative hazard with restricted cubic splines (knots at the 0th, 33rd, 67th, and 100th percentiles of the distribution of failure times).
The statistical uncertainty was evaluated by sampling from the asymptotic distribution of the regression coefficients (the multivariate normal distribution with location and scale given by the maximum likelihood estimates and their variance-covariance matrix respectively). 1000 samples were drawn for each model and used to generate plausible predicted OR and HR. We plotted predictions that fall within the 95% CI to provide a visual impression of the 95% highest posterior density for the estimates under uniform prior distributions. All P-values were two-sided and statistical analyses were conducted using SAS version 9.2 (Cary, NC) and R version 3.0.229.
This study was approved by the ethics review boards of the International Agency for Research on Cancer and individual EPIC centres. All EPIC participants provided written consent at recruitment for use of their blood samples and data in future research.
How to cite this article: Fanidi, A. et al. Circulating vitamin D in relation to cancer incidence and survival of the head and neck and oesophagus in the EPIC cohort. Sci. Rep. 6, 36017; doi: 10.1038/srep36017 (2016).
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World Cancer Research Fund (UK) funded the biochemical analyses for the current study. The funding organization had no role in design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript. Dr Ueland reports that he is a member of the steering board of the nonprofit Foundation to Promote Research Into Functional Vitamin B12 Deficiency. No other disclosures were reported. The EPIC study has been supported by the Europe Against Cancer Program of the European Commission (SANCO); Deutsche Krebshilfe; Deutsches Krebsforschungszentrum; German Federal Ministry of Education and Research; Danish Cancer Society; Health Research Fund (FIS) of the Spanish Ministry of Health; Spanish Regional Governments of Andalucia, Asturias, Basque Country, Murcia and Navarra; Catalan Institute of Oncology, Spain; the ISCIII of the Spanish Ministry of Health (RETICC DR06/0020); Cancer Research UK; Medical Research Council, United Kingdom; Greek Ministry of Health; Stavros Niarchos Foundation; Hellenic Health Foundation; Italian Association for Research on Cancer (AIRC); Italian National Research Council; Fondazione-Istituto Banco Napoli, Italy; Associazione Italiana per la Ricerca sul Cancro-AIRC-Milan; Compagnia di San Paolo; Dutch Ministry of Public Health, Welfare and Sports; World Cancer Research Fund; Swedish Cancer Society; Swedish Scientific Council; Regional Government of Västerbotten, Sweden; NordForsk (Centre of excellence programme HELGA), Norway; French League against Cancer (LNCC), France; National Institute for Health and Medical Research (INSERM), France; Mutuelle Générale de l’Education Nationale (MGEN), France; 3M Co, France; Gustave Roussy Institute (IGR), France; and General Councils of France.
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