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. 2015 Mar 27;123(9):860–866. doi: 10.1289/ehp.1408762

Long-Term Ambient Residential Traffic–Related Exposures and Measurement Error–Adjusted Risk of Incident Lung Cancer in the Netherlands Cohort Study on Diet and Cancer

Jaime E Hart 1,2,✉, Donna Spiegelman 3,4,5, Rob Beelen 6, Gerard Hoek 6, Bert Brunekreef 6,7, Leo J Schouten 8, Piet van den Brandt 8,9
PMCID: PMC4559954  PMID: 25816363

Abstract

Background

The International Agency for Research on Cancer (IARC) recently declared air pollution carcinogenic to humans. However, no study of air pollution and lung cancer to date has incorporated adjustment for exposure measurement error, and few have examined specific histological subtypes.

Objectives

Our aim was to assess the association of air pollution and incident lung cancer in the Netherlands Cohort Study on Diet and Cancer and the impact of measurement error on these associations.

Methods

The cohort was followed from 1986 through 2003, and 3,355 incident cases were identified. Cox proportional hazards models were used to estimate hazard ratios and 95% confidence intervals, for long-term exposures to nitrogen dioxide (NO2), black smoke (BS), PM2.5 (particulate matter with diameter ≤ 2.5 μm), and measures of roadway proximity and traffic volume, adjusted for potential confounders. Information from a previous validation study was used to correct the effect estimates for measurement error.

Results

We observed elevated risks of incident lung cancer with exposure to BS [hazard ratio (HR) = 1.16; 95% CI: 1.02, 1.32, per 10 μg/m3], NO2 (HR = 1.29; 95% CI: 1.08, 1.54, per 30 μg/m3), PM2.5 (HR = 1.17; 95% CI: 0.93, 1.47, per 10 μg/m3), and with measures of traffic at the baseline address. The exposures were positively associated with all lung cancer subtypes. After adjustment for measurement error, the HRs increased and the 95% CIs widened [HR = 1.19 (95% CI: 1.02, 1.39) for BS and HR = 1.37 (95% CI: 0.86, 2.17) for PM2.5].

Conclusions

These findings add support to a growing body of literature on the effects of air pollution on lung cancer. In addition, they highlight variation in measurement error by pollutant and support the implementation of measurement error corrections when possible.

Citation

Hart JE, Spiegelman D, Beelen R, Hoek G, Brunekreef B, Schouten LJ, van den Brandt P. 2015. Long-term ambient residential traffic–related exposures and measurement error–adjusted risk of incident lung cancer in the Netherlands Cohort Study on Diet and Cancer. Environ Health Perspect 123:860–866; http://dx.doi.org/10.1289/ehp.1408762

Introduction

A growing literature has demonstrated positive associations between long-term exposures to ambient air pollution and an increased risk of lung cancer. Most studies have focused on particulate matter (PM); in a recent meta-analysis including 18 studies, each 10-μg/m3 increase in PM ≤ 2.5 μm in diameter (PM2.5) was associated with a meta-relative risk of 1.09 [95% confidence interval (CI): 1.01, 1.14] (Hamra et al. 2014). However, increases in lung cancer risk have also been observed with roadway proximity and exposures to traffic-related pollutants including oxides of nitrogen (NO2 and NOx), polycyclic aromatic hydrocarbons (PAHs), and volatile organic compounds (VOCs) (Abbey et al. 1999; Beelen et al. 2008; Carey et al. 2013; Cesaroni et al. 2013; Filleul et al. 2005; Hart et al. 2011; Heinrich et al. 2013; Hystad et al. 2013; Jerrett et al. 2013; Katanoda et al. 2011; Krewski et al. 2009; Lipsett et al. 2011; Nyberg et al. 2000; Puett et al. 2014; Raaschou-Nielsen et al. 2010, 2013; Villeneuve et al. 2013, 2014; Vineis et al. 2006; Yorifuji et al. 2013). Therefore, the International Agency for Research on Cancer (IARC) recently declared ambient air pollution generally, and particulate matter specifically, carcinogenic to humans (Loomis et al. 2013).

Empirical adjustment for bias due to exposure measurement error has been applied in occupational, nutritional, and environmental epidemiology studies (Allodji et al. 2012; Armstrong 1990, 2004; Fearn et al. 2008; Heid et al. 2004; Horick et al. 2006; Keshaviah et al. 2003; Li et al. 2006; Rosner et al. 1990; Spiegelman 2010; Van Roosbroeck et al. 2008b; Zhukovsky et al. 2011). Using regression calibration, bias due to exposure measurement can be adjusted for when a validation study is available that contains information on both the standard exposure collected for the participants in the main study, as well as the “gold standard” exposure collected only in the validation study. To date, however, no study of the chronic effects of air pollution on the risk of lung cancer has incorporated adjustment for exposure measurement error.

We previously examined the associations of long-term exposures to traffic-related exposures and the risk of incident lung cancer from the Netherlands Cohort Study on Diet and Cancer (NLCS); we observed no elevations with specific pollutants, but small elevations in risk with measures of roadway proximity and traffic density (Beelen et al. 2008). Our present objective is to extend these analyses with an additional 7 years of follow-up, to determine the association of air pollution with specific histological subtypes, and to perform analyses incorporating adjustment for measurement error, using information from an exposure validation study (Van Roosbroeck et al. 2008a).

Methods

Study population. Details of the NLCS population have been reported previously (Beelen et al. 2008; van den Brandt et al. 1990). Briefly, the cohort was initiated in September 1986 with 120,852 subjects 55–69 years of age living in 204 municipalities throughout the Netherlands who had not previously had cancer (other than skin cancer). All participants provided detailed information on diet, lifestyle factors, and personal characteristics at baseline. The study was designed as a case-cohort study, where cases arise over follow-up from the full cohort, but the characteristics of person-years at risk were estimated from a randomly selected subcohort of 5,000 participants. We excluded any participants from the present analysis with missing data on the exposures of interest, or on current cigarette, pipe, or cigar smoking status, resulting in a final subcohort of 4,666 members. The study was approved by the Maastricht University and the Netherlands Organization for Applied Scientific Research Institutional Review Boards and the Human Subjects Committee of the Harvard T.H. Chan School of Public Health. All cohort members consented to participate in the study by completing and returning the self-administered questionnaire.

Outcome assessment. Participants were followed through 31 December 2003, for a total of 17.3 years of follow-up. Incident cases of the first occurrence of primary lung cancer [International Classification of Diseases for Oncology (ICD-O-3) code C34] were identified by linkage of the full cohort to the Netherlands Cancer Registry and to the nationwide network and registry of histopathology and cytopathology (PALGA). A total of 3,355 incident cases of lung cancer [1,298 squamous-cell carcinomas (ICD-O-3 8050–8076), 573 small-cell carcinomas (ICD-O-3 8040–8045), 498 large-cell carcinomas (ICD-O-3 8012–8031, 8310), 737 adenocarcinomas (ICD-O-3 8140, 8211, 8230–8231, 8250–8260, 8323, 8480–8490), and 249 with other or unknown histological subtypes] were identified.

Exposure assessment. Each exposure metric was calculated based on only the baseline (1986) home address of each participant. The methods for calculating long-term average (1987–1996) exposures of NO2, black smoke (BS), and PM2.5 have been described in detail (Beelen et al. 2007, 2008). In brief, the regional, urban, and local contributions of each pollutant were determined and summed to obtain background concentrations (the sum of regional and urban contributions) or overall concentrations (the sum of the background and local contributions) for each participant. The regional contribution was predicted using inverse distance weighting of monitoring at regional background locations from the National Air Quality Monitoring Network (http://www.rivm.nl/en/Documents_and_publications/Scientific/Reports/1999/maart/The_Dutch_National_Air_Quality_Monitoring_Network_monitoring_program_in_1999?sp=cml2bXE9ZmFsc2U7c2VhcmNoYmFzZT01OTAxMDtyaXZtcT1mYWxzZTs=&pagenr=5902), whereas urban predictions were estimated using a land-use regression model including data from all regional and urban background monitoring sites and variables for population density and residential or industrial land use. The local contribution was estimated from land-use regressions incorporating monitoring data from field monitoring campaigns and a variety of traffic variables as predictors. Three measures of exposure to traffic were defined using a geographic information system (GIS) using a digital road network and traffic intensity information from 1986: a) an indicator for living near a major road, defined as within 100 m of a motorway or within 50 m of a local road with ≥ 10,000 vehicles per 24 hr, b) the traffic intensity in vehicles per 24 hr (mvh/24 hr) on the nearest road, and c) the sum of traffic intensity times road length within a 100-m buffer around the residential address in vehicles per 24 hr. We have previously shown that although the traffic intensities have increased during the follow-up period, data from different years were highly correlated, even over periods as long as 10 years (Beelen et al. 2007, 2008).

Exposure validation data. Details of the validation study have also been published previously (Van Roosbroeck et al. 2008a). Briefly, personal and near-home outdoor exposures to PM2.5 absorbance, NO2, and PM2.5 were collected for 48 hr up to five times from 47 adult nonsmoking participants living in Utrecht between November 2004 and July 2005. PM2.5 absorbance and BS are both surrogates of black carbon obtained by filter reflectance measurement but from different types of filters (Roorda-Knape et al. 1998). Approximately 50% lived near roads with a traffic intensity ≥ 10,000 mvh/24 hr, and 50% lived on on streets with < 5,000 mvh/24 hr, > 50 m from a road ≥ 10,000 mvh/24 hr, and > 400 m away from freeways with traffic intensities higher than 70,000 mvh/24 hr. We explored the utility of this validation study to correct our health effect estimates for the difference between personal and ambient measures of BS, NO2, and PM2.5.

Statistical analysis. Cox proportional hazards models were used to determine the associations of each measure of exposure to traffic or air pollution with risk of incident lung cancer overall or specific histological subtype. For continuous exposures, after assessing linearity using restricted cubic splines (Durrleman and Simon 1989; Govindarajulu et al. 2007) and performing log-likelihood tests to determine the best-fitting model, we calculated hazard ratios (HRs) and 95% CIs for an interquartile range increase (10 μg/m3 for BS and PM2.5, 30 μg/m3 for NO2, 10,000 mvh/24 hr for traffic intensity on the nearest road, and 335,000 mvh/24 hr for traffic intensity in a 100-m buffer). To account for the additional variance introduced by the case-cohort design, standard errors were estimated using the robust sandwich estimator (Lin and Wei 1989). We adjusted for a number of a priori potential confounders including age (as the time metric); sex; body mass index (BMI); cigarette, cigar, and pipe smoking status; number of cigarettes/cigars/pipes smoked on average; years of each type of tobacco use; home exposure to secondhand smoke; educational attainment; classification of the last occupation; and consumption of alcohol, fruits, vegetables, fish, and shellfish. We also adjusted all models for area-level indicators of socioeconomic status (SES) based on data from Statistics Netherlands: Percent of individuals below the 40th percentile and percent of individuals above the 80th percentile of the Dutch income distribution were calculated at both the neighborhood and “COROP area scale.” The COROP areas were defined in 1970 by the Dutch Coordination Commission for Regional Research Program to be a geographic region consisting of a city and the surrounding economic and social region. Missing indicator variables were created as needed for all variables. In sensitivity analyses, each a priori confounder (or group of confounders) was added to our basic models to determine if it (they) changed the association of any exposure on the risk of overall lung cancer by 10% (Greenland 1989). These confounders were then included in an alternate multivariable model to determine the sensitivity of our findings to our a priori selections. In sensitivity analyses to adjust our variance estimates for potential nonindependence among participants living in similar areas, we included random effects for each of the COROP areas in our multivariable models.

We performed stratified analyses by cigarette smoking status (current, former, never), overall tobacco use (current, former, never), and sex and created multiplicative interaction terms to assess effect modification. We also used multiplicative interaction terms to test effect modification by study follow-up period (original vs. extended). To test for heterogeneity in effect estimates across lung cancer subtypes, we used partial likelihood ratio tests from polytomous regressions using the publically available SUBTYPE macro (Kuchiba et al. 2014). A p-value of 0.05 was used to denote statistical significance.

Measurement error adjustment. We used the regression calibration method to adjust for bias due to exposure measurement error (Rosner et al. 1990; Spiegelman et al. 1997), using the publicly available BLINPLUS macro (Logan and Spiegelman 2012). First, we obtained the basic and multivariable adjusted HRs and 95% CIs as described above. Next, in the validation study, we regressed the measures of personal exposure on ambient exposure while controlling for age and sex. Then, measurement error–corrected point and interval estimates of the HRs were calculated by combining the uncorrected HRs from the Cox model with the validation study exposure regressions using a multivariate version of the following equation: βˆ1 = βˆ1*/γˆ1 where βˆ1 is the measurement error–corrected effect estimate, βˆ1* is the uncorrected effect estimate, and γˆ1 is the slope of the regression of personal exposure on exposure surrogate estimated in the validation study. The variance for the measurement error–corrected estimates incorporates the variance from estimating β1* in the main study, as well as from estimating γ1 in the validation study using the multivariate delta method.

As shown in previous simulation studies (Kuha 1994; Rosner et al. 1989, 1990; Spiegelman et al. 1997, 2001), regression calibration can be reliably performed when a number of assumptions have been satisfied. The assumptions include the following: a) The relationship between the personal and ambient exposure must be linear and homoscedastic, b) the associations between outcome and exposure must be linear on the scale of the link function used, c) the degree of measurement error is not severe, d) the measurement error is nondifferential, and e) the ambient exposure measure would not be associated with the outcome of interest if personal exposures were available. We examined the validity of the linearity assumptions using restricted cubic regression splines. Homoscedasticity in the validation study model was assessed by calculating the correlation between the predicted values and the absolute residuals from the linear regression models, and the statistical significance of deviations was assessed with the White test (White 1980). The magnitude of measurement error was examined by calculating βˆ12σˆ2, where σˆ2 is the residual variance from the regression of the personal exposures on the ambient exposures. Simulation studies have found that measurement error corrections are accurate when β12σ2 < 0.5 (Kuha 1994). Nondifferential measurement error is reasonably assumed in this setting, where the exposure is measured prospectively and objectively, and participants subsequently followed for the occurrence of lung cancer. The fifth assumption is assumed to hold, because there is no reason to assume that ambient exposures would be associated with lung cancer independently of associations with personal exposures. In addition to the above assumptions, we must make the empirically unverifiable transportability assumption that the slope of the regression of the personal exposure on the ambient exposures found in the validation study would be similar to the one that would be found in the main study population. All data analyses were performed in SAS 9.3 (SAS Institute Inc.).

Results

Cases were more likely to smoke cigarettes, cigars, and pipes than subcohort members, and were more exposed to secondhand smoke from a spouse (Table 1). They were also more likely to be male, to be less educated, and to work in blue-collar occupations. There was little difference in the measures of exposure and area-level SES between the cases and subcohort members, and the distributions of BMI and age were similar.

Table 1.

Baseline (1986) characteristics of the lung cancer cases and the subcohort from the Netherlands Cohort Study on Diet and Cancer (n = 7,881).

Characteristic Cases (n = 3,355) Subcohort (n = 4,666)
Median (IQR)
Age (years) 62 (7) 61 (7)
Fruit and fruit preserves consumed (g/day) 106 (146) 145 (150)
Vegetables consumed (g/day) 165 (102) 175 (102)
Fish and shellfish consumed (g/day) 8 (20) 7 (20)
Percent neighborhood < 40th percentile of income 41 (11) 40 (10)
Percent neighborhood > 80th percentile of income 17 (12) 18 (13)
Percent COROP area < 40th percentile of income 41 (9) 41 (9)
Percent COROP area > 80th percentile of income 19 (5) 19 (5)
Average black smoke 1987–1996 (μg/m3) 16.7 (4.0) 16.6 (4.0)
Average NO2 1987–1996 (μg/m3) 38.0 (11.0) 37.8 (11.1)
Average PM2.5 1987–1996 (μg/m3) 28.3 (2.4) 28.3 (2.5)
Percent
Male 85.3 48.9
Marital status
Married 84.3 78.1
Single, divorced, widowed 15.6 21.5
Missing 0.1 0.4
Cigarette-smoking status
Never 6.8 36.3
Former 29.5 35.1
Current 63.8 28.6
Cigar-smoking status
Never 77.3 87.4
Former 6.6 5.4
Current 15.4 6.5
Pipe-smoking status
Never 87.3 92.5
Former 3.4 3.6
Current 8.2 3.1
Cigarette-smoking spouse
Never 41.3 30.8
Former 17.1 27.8
Current 34.2 31.6
NA or missing 7.4 9.9
Alcohol consumption (g/day)
< 0.4 (abstainer) 14.5 22.2
0.4–4 18.3 27.0
5–14 22.8 21.7
15–29 22.6 15.0
≥ 30 18.2 8.8
Missing 3.6 5.3
Educational attainment
Primary/lower vocational school 24.4 20.3
High school 55.0 51.5
Higher vocational or university 19.9 27.3
Missing 0.8 0.9
BMI (kg/m2)
< 20 3.7 3.5
20 to < 25 50.6 48.2
25 to < 30 38.2 38.3
≥ 30 4.0 6.4
Missing 3.6 3.6
Last occupation
Blue collar 36.7 26.7
Low white collar 12.6 15.8
White collar 20.7 19.8
Other 14.7 15.5
Last occupation ≥ 40 years ago 1.6 5.0
Never paid employment 1.4 6.5
Missing 12.4 10.7
Abbreviations: IQR, interquartile range; NA, not applicable.
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In age- and sex-adjusted models, HRs for all three pollutants and the measures of traffic exposure were above the null for associations with all lung cancer cases and with the specific histological subtypes (Table 2). There was no statistically significant evidence of heterogeneity across subtypes (all p-for-heterogeneity > 0.19). In models adjusted for our full set of a priori confounders, the HRs generally remained positive. All forms of tobacco use, educational attainment, marital status, occupation, diet, alcohol consumption, and neighborhood- and COROP-level SES were included in the parsimonious multivariable models, and results were similar to those from the a priori multivariable models (see Supplemental Material, Table S1). Although the random term for COROP area was statistically significant for many models (data not shown), the HRs from models accounting for potential clustering were similar to our main models (see Supplemental Material, Table S1). There was no evidence of effect modification by cigarette-smoking status, other tobacco use, sex, or follow-up period (p-values for interaction > 0.05; data not shown).

Table 2.

Associations of increases in average black smoke, NO2, or PM2.5 exposures 1987–1996 or baseline address traffic measures with incident lung cancer 1986–2003 overall and by subtype.

Exposure All lung cancer HR (95% CI) Squamous-cell carcinoma HR (95% CI) Small-cell carcinoma HR (95% CI) Large-cell carcinoma HR (95% CI) Adenocarcinoma HR (95% CI)
No. of cases 3,355 1,298 573 498 737
Black smoke (10 μg/m3)
Basic modela 1.23 (1.08, 1.40) 1.16 (0.96, 1.40) 1.24 (0.96, 1.60) 1.22 (0.94, 1.59) 1.42 (1.14, 1.78)
Multivariable modelb 1.16 (1.02, 1.32) 1.14 (0.94, 1.38) 1.24 (0.95, 1.61) 1.22 (0.91, 1.62) 1.14 (0.90, 1.44)
NO2 (30 μg/m3)
Basic modela 1.24 (1.05, 1.47) 1.09 (0.86, 1.38) 1.21 (0.87, 1.69) 1.26 (0.89, 1.78) 1.65 (1.24, 2.21)
Multivariable modelb 1.29 (1.08, 1.54) 1.24 (0.96, 1.61) 1.37 (0.95, 1.97) 1.33 (0.90, 1.97) 1.29 (0.93, 1.78)
PM2.5 (10 μg/m3)
Basic modela 1.12 (0.89, 1.40) 1.02 (0.73, 1.41) 1.11 (0.71, 1.72) 1.17 (0.73, 1.87) 1.44 (0.98, 2.11)
Multivariable modelb 1.17 (0.93, 1.47) 1.15 (0.82, 1.61) 1.12 (0.71, 1.77) 1.37 (0.83, 2.26) 1.12 (0.74, 1.70)
Living near a major road
Basic modela 1.18 (0.96, 1.45) 1.15 (0.87, 1.54) 1.39 (0.96, 2.00) 1.28 (0.86, 1.91) 1.15 (0.81, 1.63)
Multivariable modelc 1.12 (0.92, 1.37) 1.08 (0.80, 1.44) 1.40 (0.96, 2.02) 1.25 (0.83, 1.88) 1.05 (0.75, 1.47)
Traffic intensity on the nearest road (10,000 mvh/24 hr)
Basic modela 1.06 (0.96, 1.17) 1.07 (0.95, 1.21) 1.08 (0.89, 1.32) 1.03 (0.86, 1.23) 1.05 (0.92, 1.20)
Multivariable modelc 1.02 (0.93, 1.12) 1.03 (0.91, 1.15) 1.06 (0.87, 1.29) 1.01 (0.84, 1.21) 0.99 (0.86, 1.14)
Traffic intensity in a 100-m buffer (335,000 mvh/24 hr)
Basic modela 1.15 (1.01, 1.31) 1.21 (1.01, 1.44) 1.13 (0.87, 1.46) 1.03 (0.79, 1.35) 1.20 (0.97, 1.49)
Multivariable modelc 1.10 (0.97, 1.24) 1.17 (0.98, 1.39) 1.15 (0.89, 1.47) 0.98 (0.75, 1.29) 1.10 (0.89, 1.36)
aAdjusted for age and sex. bAdditionally adjusted for cigarette-, cigar-, and pipe-smoking status; years and amount of cigarette, cigar, and pipe smoking; secondhand smoke exposure; educational status; occupational status; marital status; BMI; alcohol consumption; intake of fruits, vegetables, and fish; and neighborhood- and COROP-level SES. cAdjusted for all covariates in the default multivariable model plus regional and urban background black smoke.
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There was no evidence of deviation from linearity or evidence of deviation from homoscedasticity for any of the examined exposures in the validation data [Table 3, calculated with data from Van Roosbroeck et al. (2008a)]. Based on β12σ2, the magnitude of measurement error was well within the bounds of the Kuha criterion [β12σ2 < 0.5 (Kuha 1994)] for validity of regression calibration for BS (β12σ2s of 0.008, 0.007, 0.011, 0.010, and 0.007 for all cases, squamous-cell carcinoma, small-cell carcinoma, large-cell carcinoma, and adenocarcinomas, respectively), and for PM2.5 (β12σ2s of 0.316, 0.279, 0,224, 0.634, and 0.224 for all cases, squamous-cell carcinoma, small-cell carcinoma, large-cell carcinoma, and adenocarcinomas, respectively). However, the Kuha criterion was not satisfied for NO2 (β12σ2s of 2.052, 1.753, 2.523, 2.281, and 2.033 for all cases, squamous-cell carcinoma, small-cell carcinoma, large-cell carcinoma, and adenocarcinomas, respectively). Therefore, any error corrections for NO2 would not be appropriate.

Table 3.

Exposure information from the validation study (Van Roosbroeck et al. 2008a) available for measurement error correction.

Data PM2.5 absorbancea (10–5/m) NO2 (μg/m3) PM2.5 (μg/m3)
n 172 209 174
Measured personal exposure (mean ± SD) 1.71 ± 0.70 26.9 ± 11.3 16.8 ± 11.2
Measured ambient exposure (mean ± SD) 1.61 ± 0.63 32.0 ± 8.4 18.2 ± 10.0
Ratio of personal and ambient SDs 1.11 1.35 1.12
Correlation of personal and ambient exposures 0.78 0.04 0.45
Validation model R2 0.62 0.22 0.21
p-Value for test of heteroscedasticity 0.74 0.14 0.77
σ2 0.044 0.326 1.004
Deattenuation factorb 0.87 0.05 0.50
aPM2.5 absorbance was measured in the validation study and is used to adjust models for black smoke. bThe deattenuation factor is calculated by multiplying the ratio of the personal and ambient exposure standard deviations by the correlation between the personal and ambient measures.
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After adjustment for measurement error, the HRs for BS and PM2.5 were further from the null than the HRs before adjustment, with increases of 0–3.3% for BS and 9.7–37.2% for PM2.5 (Table 4). The magnitude of the percent increase in the width of the confidence intervals was generally an order of magnitude larger, with increases of 10.2–23.3% for BS and 108.0–216.8% for PM2.5.

Table 4.

Measurement error–adjusted associations per interquartile range increase in black smoke or PM2.5 exposures on the risk of incident lung cancer 1986–2003 overall and by subtype.

Exposure All cases HR (95% CI)a Squamous-cell carcinoma HR (95% CI)a Small-cell carcinoma HR (95% CI)a Large-cell carcinoma HR (95% CI)a Adenocarcinoma HR (95% CI)a
Black smoke (10 μg/m3) 1.19 (1.02, 1.39) 1.17 (0.93, 1.47) 1.28 (0.94, 1.75) 1.26 (0.90, 1.76) 1.17 (0.89, 1.54)
Percent increase in HRb 2.6 2.6 3.2 3.3 0.0
Percent increase in 95% CIsc 23.3 22.7 22.7 21.1 10.2
PM2.5 (10 μg/m3) 1.37 (0.86, 2.17) 1.32 (0.67, 2.61) 1.25 (0.50, 3.15) 1.88 (0.68, 5.21) 1.25 (0.54, 2.89)
Percent increase in HRb 17.1 14.8 11.6 37.2 9.7
Percent increase in 95% CIsc 142.6 145.6 150.0 216.8 108.0
aMultivariable model was adjusted for age and sex; cigarette-, cigar-, and pipe-smoking status; years and amount of cigarette, cigar, and pipe smoking; secondhand smoke exposure; educational status; occupational status; marital status; BMI; alcohol consumption; intake of fruits, vegetables, and fish; and neighborhood- and COROP-level SES. b[(HRmultivariable – HRmeasurement error)/HRmultivariable] × 100. c{[(UCLmultivariable – LCLmultivariable) – (UCLmeasurement error – LCLmeasurement error)]/(UCLmultivariable – LCLmultivariable)} × 100.
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Discussion

In this extended follow-up of the NLCS, HRs were above the null for risks of overall and histologic subtype–specific lung cancer for exposures to BS, NO2, PM2.5, and with measures of traffic at the baseline address, even after adjustment for a number of lifestyle and dietary factors, and personal and area-level SES. Associations were positive for all histologic subtypes; however, there was no statistically significant heterogeneity observed. Adjustment for measurement error to account for the differences between personal and ambient exposures led to modest increases in the HRs for BS (0–3.3%) and moderate increases in the HRs for PM2.5, (9.7–37.2%), along with substantial widening of the confidence intervals (10.2–216.8%).

Adjustment for various aspects of measurement error has become more common in studies of air pollution in recent years. Several methods have been proposed to address the impact of potential errors induced due to the spatial modeling of exposure (Molitor et al. 2007; Sheppard et al. 2012; Szpiro and Paciorek 2013; Szpiro et al. 2011). Others have adjusted estimates of the effects of air pollution on some health end points for the differences between personal and ambient point exposures (Avery et al. 2010a, 2010b; Holliday et al. 2014). These authors used random-effects meta-analysis of literature-based reported correlations between personal and ambient exposures to impute personal exposures for the main study.

Although there was little evidence of effect modification by follow-up period, our results had HRs of greater magnitude and more were statistically significant compared with our previous findings in this cohort (Beelen et al. 2008). For example, in the present analysis, the HR for BS was 1.16 (95% CI: 1.02, 1.32, per 10 μg/m3), compared with an equivalent HR of 1.03 (95% CI: 0.78, 1.34) in our previous analysis. Additionally, we observed HRs > 1 with exposures to PM2.5 and NO2, which were not observed in the previous analysis. However, although we had previously observed differences in these associations by smoking status, we did not observe statistically significant differences by smoking status in the present analysis.

Most studies of PM2.5 on lung cancer risk have reported positive associations, even with a wide variety of approaches to exposure assessment, and a mix of incident and mortality studies (Cao et al. 2011; Carey et al. 2013; Cesaroni et al. 2013; Hart et al. 2011; Hystad et al. 2013; Jerrett et al. 2013; Katanoda et al. 2011; Krewski et al. 2009; Lepeule et al. 2012; Lipsett et al. 2011; McDonnell et al. 2000; Puett et al. 2014; Raaschou-Nielsen et al. 2013). Our measurement error–corrected and –uncorrected HRs for PM2.5 on overall lung cancer incidence are near the higher end of the distribution of results from previous studies (see Supplemental Material, Table S2). In a recent meta-analysis that included the estimate from our previous NLCS lung cancer analysis, the risk ratio for a 10-μg/m3 increase was estimated to be 1.09 (95% CI; 1.04, 1.14) (Hamra et al. 2014).

A large number of studies from around the world have also reported that NO2 exposures are positively associated with lung cancer risk (Abbey et al. 1999; Carey et al. 2013; Cesaroni et al. 2013; Filleul et al. 2005; Hart et al. 2011; Heinrich et al. 2013; Hystad et al. 2013; Jerrett et al. 2013; Katanoda et al. 2011; Krewski et al. 2009; Lipsett et al. 2011; Nyberg et al. 2000; Raaschou-Nielsen et al. 2013; Villeneuve et al. 2014; Yorifuji et al. 2013). Our HR of 1.29 (95% CI: 1.08, 1.54 for each 30-μg/m3 increase in NO2) is near the center of the distribution of findings from previous studies (see Supplemental Material, Table S3). As with PM2.5, positive associations have been reported based on a wide variety of study types from around the world, with a number of different approaches to exposure assessment.

To our knowledge, only two other population-based studies have explored the associations of BS or related measures with risk of lung cancer. In the French Pollution Atmospherique et Affections Respiratoires Chronique (PAARC) study, exposure to BS in seven French cities was associated with an increased risk of lung cancer (adjusted HR = 1.03; 95% CI: 0.92, 1.15 for each 10-μg/m3 increase) (Filleul et al. 2005). The multi-country European Study of Cohorts for Air Pollution Effects (ESCAPE) used PM2.5 absorbance as a marker of BS, and also observed positive associations (HR = 1.12; 95% CI: 0.88, 1.42, per 10–5/m increase) (Raaschou-Nielsen et al. 2013).

Results of studies examining the impact of roadway proximity on the risk of lung cancer risk have been more mixed. In addition to our previous analysis, a number of other studies have examined distance to roadway or traffic intensity as an exposure (Cesaroni et al. 2013; Hystad et al. 2013; Puett et al. 2014; Raaschou-Nielsen et al. 2011, 2013; Vineis et al. 2006). Similar to our findings, these studies have generally observed modest increases in lung cancer risk. Given the heterogeneity in methods and definitions, however, the different metrics are difficult to compare, and few studies have observed statistically significant results.

Although we observed HRs of different magnitudes for the different lung cancer subtypes we examined, there was no statistically significant heterogeneity among the subtypes. Differences of effect among subtypes are of great interest, but to date only a limited number of studies have examined histological subtype–specific effects. This interest in differences by subtype is motivated by differences in risk observed with exposures to cigarette smoking. For example, small-cell carcinoma, squamous-cell carcinoma, and adenocarcinomas have been the subtypes most closely associated with cigarette smoking (Boyle et al. 2010; Tse et al. 2009). Stronger associations with various pollutants have been observed for adenocarcinomas and squamous-cell carcinomas. Specifically, in ESCAPE, elevated HRs were observed in models of PM2.5 exposure restricted to these two subtypes when compared with models of all cases (Raaschou-Nielsen et al. 2013). In a case–control study in Canada, subtype-specific results for PM2.5 and NO2 were mixed, with a suggestion of a larger risk for adenocarcinomas compared with other subtypes (Hystad et al. 2013). Positive associations with exposures to PM were also observed for adenocarcinomas compared with all lung cancer cases in a study of U.S. nurses (Puett et al. 2014).

This study has several limitations. We used exposures based on the baseline home address as a proxy for actual exposures over time. However, a number of studies have also demonstrated that land-use regressions, such as the one used here, are quite robust to historical changes (Cesaroni et al. 2012; Eeftens et al. 2011; Gulliver et al. 2013). Our inability to incorporate changes in residence during the study period would have induced further exposure misclassification. Another limitation is that we were not able to adjust our analyses of NO2 (due to violations in the required assumptions) and the traffic proximity and volume measures (due to a lack of data in the validation study) for measurement error. The high β12σ2 for NO2 is likely attributable to the presence of indoor sources or low air exchange rates, which have been consistently observed in other studies (Kousa et al. 2001; Lai et al. 2004; Rotko et al. 2001; Sahsuvaroglu et al. 2009; Zipprich et al. 2002). Given the differences in measurement error for PM2.5 and BS, it is not possible to determine the potential magnitude error that would be observed for NO2. We are also not able to quantify the impact of indoor sources of NO2 on lung cancer risk. Therefore, our NO2 associations should be treated with caution and interpreted only as the ambient effects of these exposures. Last, as with all studies, residual confounding is a concern. Our study was not able to update potential confounders, such as smoking or diet, after baseline, and we were missing information on potential confounders such as secondhand smoke and occupation for around 10% of the study participants.

Our validation study and measurement error approach also have some limitations. Information was available from only 45 individuals, with a few more than 200 individual sampling sessions. This limits our ability to examine personal characteristics that may impact the personal and ambient exposure relationships. We were not able to directly measure BS in the validation study, and instead measured PM2.5 absorbance, which is measured from another type of filter. However, these two measurements are highly correlated (R2 = 0.94) (Roorda-Knape et al. 1998), so this is unlikely to be a major source of error. There were also a number of differences between the population measured in the validation study and the individuals in the subcohort. For example, the validation study was composed of nonsmokers in a single metropolitian area of the Netherlands, and it was conducted after the NLCS follow-up. If there are substantially different relationships of personal to ambient exposure measures between the members of the validation study and NLCS, then the assumption of transportability would be violated, and it would not be appropriate to measurement error correct. The personal concentrations are affected by both indoor and outdoor sources. For studies on outdoor air pollution, it has been argued that personal exposure to outdoor- and indoor-generated particles should be considered separately (Wilson and Brauer 2006; Wilson et al. 2000). The correlation between outdoor exposure and the personal exposure to ambient origin pollution is the most relevant correlation, but difficult to assess. One method is to exclude the main indoor source from the study, as was done in the present validation study by excluding smokers.

This study also has major strengths. The long follow-up period and high rate of case ascertainment have provided us with a large number of cases with information on histological subtype. This allows us to examine the impact of a number of pollutants on subtype-specific risks, which to date has been possible in only a handful of studies. Our use of regression calibration to adjust for bias due to measurement error in predicted ambient pollutant concentrations in relation to personal exposure measurements, though imperfect, provides a sense of the level of underestimation in studies that are unable to perform this correction for measurement error bias.

In conclusion, in this large study based in the Netherlands, we observed an elevated risk of overall and histologic subtype–specific incident lung cancer with long-term exposure to BS, NO2, PM2.5, and with measures of traffic at the baseline address. The HRs increased after correction for measurement error, although the impact of the adjustment for measurement error varied between the two pollutants where adjustment was possible. Correction for measurement error also resulted in substantial losses in precision. These findings add support to a growing body of literature on the effects of air pollution on lung cancer, as well as to the recent classification of air pollution as a human carcinogen by IARC (Loomis et al. 2013).

Supplemental Material

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Footnotes

This work was supported by the National Institute of Environmental Health Sciences/National Institutes of Health (grant R01 ES009411).

The authors declare they have no actual or potential competing financial interests.

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