Occupational Medicine Advance Access originally published online on August 11, 2006
Occupational Medicine 2006 56(7):485-493; doi:10.1093/occmed/kql083
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A meta-analysis of occupational trichloroethylene exposure and multiple myeloma or leukaemia
ExponentHealth Sciences, 185 Hansen Court, Suite 100, Wood Dale, IL 60191, USA
Correspondence to: Dominik Alexander, ExponentHealth Sciences, 185 Hansen Court, Suite 100, Wood Dale, IL 60191, USA. Tel: 6302743230; e-mail: dalexander{at}exponent.com
| Abstract |
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Background Trichloroethylene (TCE) has been widely used as an industrial solvent and degreasing agent.
Aims We conducted a meta-analysis of epidemiologic studies of occupational TCE exposure and multiple myeloma (MM) or leukaemia.
Methods We identified a total of eight cohort or casecontrol studies that enumerated a TCE-exposed study population and presented relative risk (RR) estimates for MM (n = 7) and/or leukaemia (n = 7). The individual studies included aerospace or aircraft workers (n = 3 studies), workers from a transformer manufacturing plant (n = 1 study) and workers from numerous occupations who, based on biomonitoring or extensive industrial hygiene exposure measurements, were likely exposed to TCE (n = 4). We used random effects models to calculate summary relative risk estimates (SRRE). In addition, we examined heterogeneity across studies and the relative influence of each individual study on the overall meta-analysis.
Results No association was observed for MM (SRRE = 1.05, 95% CI: 0.801.38; P value for heterogeneity = 0.94) or leukaemia (SRRE = 1.11, 95% CI: 0.931.32; P value for heterogeneity = 0.50), based on TCE-exposed subgroup meta-analyses. Study-specific RR estimates for MM ranged between 0.57 and 1.62. RRs for leukaemia ranged between 1.05 and 1.15 in five studies, while one study reported a 2-fold increased RR and another study reported an inverse association of 0.60. All confidence intervals (CIs) for study-specific estimates included 1.0.
Conclusions The results of this meta-analysis do not support an etiologic association between occupational TCE exposure and risk of MM or leukaemia.
Keywords Leukaemia; meta-analysis; multiple myeloma; TCE; trichloroethylene
| Introduction |
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Trichloroethylene (TCE) is a non-flammable, colourless liquid that has been used extensively worldwide for >70 years primarily as a chemical intermediate and industrial solvent to remove grease from metal parts [1,2]. Occupational groups commonly exposed to TCE include aircraft manufacturers, printers, painters, solvent workers, electronic equipment cleaners, mechanics and dry cleaners [35]. Workers involved in metal degreasing, who are exposed to TCE via inhalation, are presumably the most heavily exposed occupational group [6].
TCE is rapidly absorbed from the stomach, intestines and lung and is distributed throughout the body, concentrating in fatty tissues, such as the liver, brain and body fat [7]. The carcinogenicity of TCE based on animal models and epidemiologic studies has been reviewed [1,3,5,8]. Increased risks of liver, lung and kidney tumours have been reported in laboratory mice and rats [7,912]; however, species disparities in TCE metabolism preclude extrapolation to human carcinogenesis. Furthermore, some studies reported no indication of carcinogenic potential in animals [13,14]. Findings from epidemiologic studies have been inconsistent, and TCE has most commonly been associated with increased risks of liver and renal malignancies, as well as with non-Hodgkin's lymphoma [1,3,5,6,8,15,16]. Interpretation is limited, however, by possible occupational or lifestyle confounding factors [6]. In occupational settings, TCE is often one of many possible workplace exposures, further complicating interpretive issues. Moreover, few studies have analytically isolated occupational TCE exposure, often relying on job title or occupational group as a surrogate for exposure, which also hinders interpretation [8].
Several studies have evaluated the association between TCE in community drinking-water and risk of leukaemia, with inconsistent results [1721]. A study of drinking-water contamination in 75 municipalities in New Jersey reported relative risks (RRs) of 1.43 for total leukaemias (95% CI: 1.071.90) and 2.35 for acute lymphocytic leukaemia (95% CI: 1.035.45) among women in the >5.0 ppb TCE-exposure category [18]. No significant associations were reported for men. A California community cancer assessment found no association between long-term exposure to TCE and perchlorate in drinking-water and total leukaemia [standardized incidence ratio (SIR) = 1.02, 99% CI: 0.741.35] [17].
Multiple myeloma (MM) and leukaemia are rare outcomes; thus, combining study findings will allow for quantifiable RR estimates with greater precision than results from single studies. We, therefore, conducted a comprehensive meta-analysis of studies that evaluated occupational TCE exposure and risk of these two haematological malignancies [2229]. In addition, we evaluated other epidemiological studies that evaluated TCE exposure and MM or leukaemia, but were not included in our meta-analysis.
| Methods |
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We conducted a comprehensive literature search using PubMed and identified 284 studies using the keywords [trichloroethylene] or [TCE] and [cancer] or [multiple myeloma] or [leukaemia]. We included a total of eight epidemiological cohort or casecontrol studies that presented RR estimates for International Classification of Diseases (ICD) codes that corresponded to MM or leukaemia or with data that allowed for the calculation of RRs for a TCE-exposed worker population (e.g. TCE used as a solvent among aircraft maintenance workers). Of these studies, six presented results for both MM and leukaemia, while one cohort study presented findings for MM only, and one casecontrol study presented findings for leukaemia only.
We excluded ecological studies of TCE in community drinking-water because study design issues limit their use for making causal inferences. We excluded studies of dry cleaners and laundry workers due to exposure assessment and study design limitations. For example, TCE exposure was not identified specifically in these cohorts, there was little or no TCE exposure for a significant portion of these workers, there was a lack of a distinction between dry cleaners and laundry workers who generally have not been exposed to TCE, and workers were predominantly exposed to chemicals other than TCE, such as perchloroethylene or carbon tetrachloride [4,8,30]. Furthermore, proportionate mortality analyses were conducted in several of these studies, thus, limiting potential causal interpretation. In two of the multiple industry studies that were included, dry cleaners represented a relatively small proportion of the study population, however [28,29]. A total of eight studies met our inclusion/exclusion criteria and, thus, were considered the most informative for making aetiological assessments pertaining to occupational TCE exposure and risk of MM or leukaemia.
Random effects models were used to calculate summary relative risk estimates (SRRE), 95% confidence intervals (CIs), and corresponding P values for heterogeneity. This type of model assumes that the study-specific effect sizes come from a random distribution of effect sizes according to a specific mean and variance. In calculating SRREs, the estimates of the individual studies were weighted by the inverse of the variance, which takes into account the sizes of the study populations. The relative influence of each study on the overall SRRE was examined by generating an SRRE with all studies included in the model, followed by the removal of one study at a time to compare the overall SRRE with SRREs from models that each had one individual study removed. This allowed us to determine the robustness of each analytical model. All analyses were performed using Episheet, a spreadsheet-based analytical package designed for the analysis of epidemiologic data [31].
We generated separate meta-analysis models for MM and leukaemia using data from studies that presented findings for a TCE-exposed subgroup or a population with known occupational TCE exposure. If an individual study presented overall cohort results as well as findings for a TCE-exposed subgroup, we extracted the data pertaining to the specific TCE-exposed population. This was done to provide the most accurate estimate of TCE RR that was available in each study. The lack of data for other exposure metrics (e.g. intensity of exposure) across multiple studies precluded a meta-analysis evaluation of exposureresponse. Two studies presented results based on a lowest and highest TCE exposure category [24,26], while one study presented findings for MM based on duration of TCE exposure [23], and another study presented cumulative TCE exposure findings for MM and leukaemia [22].
The study of Morgan et al. [24] did not provide results specifically for MM, however; MM data for the study period 196093 was provided by one of the study authors (M.K.). The standardized mortality ratio (SMR) was subsequently calculated for the TCE-exposed subgroup. In addition, we calculated SMRs for low and high TCE-exposed workers.
| Results |
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The studies included in this meta-analysis are presented in Table 1. Three US studies included aerospace or aircraft worker cohorts [2224], while four European studies included cohorts of workers from various occupational groups who were exposed to TCE [2629]. In a casecontrol study of US transformer manufacturing plant workers, Greenland et al. [25] presented results for leukaemia, based on TCE job exposure matrices generated by industrial hygienists. In the aerospace and aircraft worker studies, TCE exposure was assessed based on job descriptions, work history information and available industrial hygiene data [2224]. Biomonitoring surveillance for the presence of urinary trichloroacetic acid concentrations (U-TCA), a metabolite of TCE in urine, was performed in three [2628] European worker cohort studies. In the other European worker cohort [29], historical measurement files were used to select TCE-using industries.
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Multiple myeloma
There was no association between occupational TCE exposure and risk of MM (SRRE = 1.05, 95% CI: 0.801.38) (Table 2). The P value for heterogeneity was 0.94, indicating homogeneous findings across studies. All CIs for the individual studies included 1.0, and RR estimates ranged between 0.57 and 1.62. Of the seven studies included in this meta-analysis model, five reported six or fewer exposed MM cases or deaths. Raaschou-Nielsen et al. [29] included 31 MM cases and, based on our influence analysis, accounted for 57% of the relative weight of the SRRE. The exclusion of this study in our sensitivity analysis, however, did not appreciably change the result (SRRE = 1.08, 95% CI: 0.721.64; P value for heterogeneity = 0.88).
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Categories of U-TCA concentrations or levels of TCE-exposure intensity were ascertained in some studies [2729], but we were unable to conduct biological gradient meta-analyses across these studies due to small numbers of exposed cases or deaths. Two studies [24,26] reported elevated RR estimates for high levels of TCE exposure, although findings were not significant and were based on four or fewer exposed cases (Table 3). Boice et al. [23] reported no increasing trend in MM risk based on time since first hire, duration of employment or increasing years of potential routine or intermittent TCE exposure (Table 3). Blair et al. [22] reported a 5-fold non-significant increased risk of incident MM among men in the highest category of cumulative TCE exposure (>25 unit/year: RR = 5.1, 95% CI: 0.6043.7), based on five exposed cases, but did not find similar results based on mortality data (Table 3). The authors also reported an elevated RR for male workers exposed to chemicals other than TCE (RR = 3.7, 95% CI: 0.431.7) (Table 3).
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Leukaemia
Similar to the MM findings, there was no association between occupational TCE exposure and risk of leukaemia (SRRE = 1.11, 95% CI: 0.931.32; P value for heterogeneity = 0.50) (Table 2). Furthermore, five of the individual studies reported associations ranging between 1.05 and 1.15 [2326,29], while one study reported an inverse association (RR = 0.60) [22] and another reported a 2-fold positive association [28]. All CIs for these studies included 1.0. The study of Raaschou-Nielsen et al. [29] contributed 82 leukaemia cases, while the other studies each contributed 16 or fewer leukaemia cases or deaths. The study of Raaschou-Nielson et al. [29] accounted for 64% of the relative weight of the leukaemia meta-analysis, but its removal from the analysis did not markedly alter the overall result (SRRE = 1.05, 95% CI: 0.771.41; P value for heterogeneity = 0.40), nor did the removal of Hansen et al. [28], the study with the greatest magnitude of increased risk (SRRE = 1.08, 95% CI: 0.901.28). There was a lack of heterogeneity of findings across the remaining studies with the removal of Hansen et al. [28] (P value for heterogeneity = 0.690). Greenland et al. [25], the only casecontrol study included in our meta-analysis (leukaemia only), reported an odds ratio (OR) for TCE exposure among transformer manufacturing workers (OR = 1.10, 95% CI: 0.462.66). Removal of this study did not change the meta-analysis results (SRRE = 1.10, 95% CI: 0.901.35). Furthermore, the removal of any one of the individual studies in the MM or leukaemia meta-analyses did not alter the SRRE by >7%.
Anttila et al. [26] reported a non-significant positive association for the high category of U-TCA exposure (100+ µmol/l: SIR = 2.65, 95% CI: 0.726.78), based on four cases (Table 3). Among aerospace or aircraft workers, Morgan et al. [24] reported weak, non-significant associations for the high and low categories of TCE exposure, while Blair et al. [22] found no increasing risk of leukaemia among men or women, based on increasing categories of cumulative exposure to TCE (Table 3).
| Discussion |
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The relative homogeneity of findings across studies of TCE-exposed workers for MM and leukaemia allowed for the application of meta-analysis modelling to more precisely estimate the association between occupational TCE exposures and risk of these rare malignancies. Other than the study of Raaschou-Nielsen et al. [29], the individual studies analysed were relatively small, with 16 or fewer TCE-exposed MM or leukaemia cases; thus, the aetiological interpretation of each individual study is limited by low statistical power to detect an association if one truly exists. By combining results from studies in a meta-analysis, we were able to produce relatively precise SRRE. Based on our meta-analyses, there is no epidemiological evidence to support a causal relationship between occupational TCE exposure and risk of MM or leukaemia (Table 2). The overall findings were robust, as they did not vary markedly with the addition and/or deletion of the study of Raaschou-Nielsen et al. [29], which contributed >49% of exposed cases in both meta-analyses. Findings from individual studies that analysed various categories of TCE exposure, such as cumulative duration of exposure or mean U-TCA concentration classifications, are not supportive of an aetiological association between TCE exposure and MM or leukaemia. These individual analyses, however, were limited by few or no exposed cases/deaths in the exposure subcategories (Table 3).
In a 2000 review of >80 published papers and letters, Wartenberg et al. [8] examined the cancer epidemiology of persons exposed to TCE. The authors combined results from individual cohort studies and reported no overall significant associations for MM [incidence: SIR = 1.50, 95% CI: 0.703.30; mortality: SMR = 1.00, 95% CI: 0.601.90 (note: after erratum corrected [32])] or leukaemia (incidence: SIR = 1.00, 95% CI: 0.502.10; mortality: SMR = 1.00, 95% CI: 0.701.30), based on the analysis of Tier I studies, which were considered the most informative for TCE characterization [8]. In our meta-analysis, we included data from two recent cohorts [28,29] and new data for MM from the study of Morgan et al. [24] that were not incorporated into the analysis of Wartenberg et al. [8]. In addition, Wartenberg et al. [8] found no statistically significant associations for MM or leukaemia, based on combined analysis of studies of dry cleaner and laundry workers, in which persons were exposed to various solvents including TCE. Recent cohort studies of dry cleaning and laundry workers have been inconsistent, with associations above and below 1.0 [30,33,34].
Other studies that evaluated worker populations that were potentially exposed to TCE, reported findings that are consistent with our results of no association between occupational TCE exposure and MM or leukaemia. These studies neither identified a TCE-exposed subpopulation nor provided results specific to TCE, therefore, were not included in our meta-analysis. In a cohort of >14 000 aircraft manufacturing company workers, Garabrant et al. [35] reported non-significant inverse associations for leukaemia and aleukaemia (SMR = 0.82, 95% CI: 0.471.34), and for neoplasms of other lymphatic and haematopoietic tissue (SMR = 0.65, 95% CI: 0.211.52). There were no individual exposure measurements, but the authors reported that 37% of jobs entailed exposure to TCE. Ritz [36] reported no associations for leukaemia and aleukaemia, or for cancer of lymphatic tissue, a category that included MM, in a cohort of uranium-processing workers exposed to TCE, cutting fluids and kerosene. Chang et al. [37] reported non-significant inverse associations for cancer of the lymphatic and haematopoietic tissue among male (SIR = 0.73, 95% CI: 0.271.60) and female (SIR = 0.65, 95% CI: 0.371.05) workers in an electronics factory who were potentially exposed to TCE prior to 1968. Zhao et al. [38] reported no significant associations for combined categories of non-Hodgkin's lymphoma and leukaemia mortality (high exposure: RR = 1.30, 95% CI: 0.523.23) or incidence (high exposure: RR = 0.20, 95% CI: 0.031.46) among California aerospace workers exposed to TCE. Leukaemia was not analysed as a separate outcome; therefore, we did not include this study in our meta-analysis.
Interpretation of findings should be done with consideration of potential limitations in the studies included in our meta-analyses. The workforce cohorts from each study were presumably exposed to numerous and heterogeneous occupational exposures, which may have confounded individual study findings. Blair et al. [22], for example, reported elevated risks, albeit non-significant, for several chemicals including methylene chloride, freon, acetone and jet fuel. The study cohort in Raaschou-Nielsen et al. [29] was composed of a wide variety of TCE-using industries, including iron and metal, electronics, painting and printing. Despite these possible limitations, individual findings across studies were generally consistent, and none of the study-specific associations was statistically significant.
The evaluation of findings from individual epidemiological studies using meta-analysis techniques provided the opportunity to examine the relationship between occupational TCE exposure and the risk of developing two relatively rare haematological malignancies, MM and leukaemia. We were able to calculate a more precise summary RR estimate given the relative homogeneity of findings across individual studies. The results from our meta-analyses are not supportive of a causal role of occupational TCE exposure and risk of developing MM or leukaemia.
| Conflicts of interest |
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The authors have consulted for a number of private and governmental clients on health issues related to occupational and environmental TCE exposure. This research was partially supported by the TCE Issues Group, a group of companies involved in TCE remediation.
| References |
|---|
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- Weiss NS. Cancer in relation to occupational exposure to trichloroethylene. Occup Environ Med 1996;53:15.[ISI][Medline]
- Feldman RG. Trichloroethylene. In: Occupational and Environmental Neurotoxicology. Philadelphia, PA: Lippincott-Raven, 1999; 189213.
- Wong O. Carcinogenicity of trichloroethylene: an epidemiologic assessment. Clin Occup Environ Med 2004;4:557589, vii.[CrossRef][Medline]
- Raaschou-Nielsen O, Hansen J, Thomsen BL et al. Exposure of Danish workers to trichloroethylene, 19471989. Appl Occup Environ Hyg 2002;17:693703.[CrossRef][Medline]
- Lynge E, Anttila A, Hemminki K. Organic solvents and cancer. Cancer Causes Control 1997;8:406419.[CrossRef][ISI][Medline]
- International Agency for Research on Cancer. Trichloroethylene. In: IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. World Health Organization, 1995.
- US Department of Health and Human Services, Public Health Service. National Toxicology Program. Report on Carcinogens, Eleventh Edition, 2005.
- Wartenberg D, Reyner D, Scott CS. Trichloroethylene and cancer: epidemiologic evidence. Environ Health Perspect 2000;108(Suppl. 2):161176.
- Maltoni C, Lefemine G, Cotti G, Perino G. Long-term carcinogenicity bioassays on trichloroethylene administered by inhalation to Sprague-Dawley rats and Swiss and B6C3F1 mice. Ann N Y Acad Sci 1988;534:316342.[Abstract]
- NTP. Carcinogenesis studies of trichloroethylene (without epichlorohydrin) (CAS No. 79-01-6) in F344/N rats and B6C3F1 mice (gavage studies). Natl Toxicol Program Tech Rep Ser 1990;243:1174.[Medline]
- NTP. Toxicology and carcinogenesis studies of trichloroethylene (CAS No. 79-01-6) in four strains of rats (ACI, August, Marshall, Osborne-Mendel) (gavage studies). Natl Toxicol Program Tech Rep Ser 1988;273:1299.[Medline]
- Rhomberg LR. Dose-response analyses of the carcinogenic effects of trichloroethylene in experimental animals. Environ Health Perspect 2000;108(Suppl. 2):343358.
- Henschler D, Romen W, Elsasser HM, Reichert D, Eder E, Radwan Z. Carcinogenicity study of trichloroethylene by longterm inhalation in three animal species. Arch Toxicol 1980;43:237248.[CrossRef][ISI][Medline]
- Henschler D, Elsasser H, Romen W, Eder E. Carcinogenicity study of trichloroethylene, with and without epoxide stabilizers, in mice. J Cancer Res Clin Oncol 1984;107:149156.[CrossRef][ISI][Medline]
- McLaughlin JK, Blot WJ. A critical review of epidemiology studies of trichloroethylene and perchloroethylene and risk of renal-cell cancer. Int Arch Occup Environ Health 1997;70:222231.[CrossRef][ISI][Medline]
- Harth V, Bruning T, Bolt HM. Renal carcinogenicity of trichloroethylene: update, mode of action, and fundamentals for occupational standard setting. Rev Environ Health 2005;20:103118.[Medline]
- Morgan JW, Cassady RE. Community cancer assessment in response to long-time exposure to perchlorate and trichloroethylene in drinking water. J Occup Environ Med 2002;44:616621.[ISI][Medline]
- Cohn P, Klotz J, Bove F, Berkowitz M, Fagliano J. Drinking water contamination and the incidence of Leukemia and non-Hodgkin's lymphoma. Environ Health Perspect 1994;102:556561.[ISI][Medline]
- Costas K, Knorr RS, Condon SK. A case-control study of childhood leukemia in Woburn, Massachusetts: the relationship between leukemia incidence and exposure to public drinking water. Sci Total Environ 2002;300:2335.[CrossRef][Medline]
- Fagliano J, Berry M, Bove F, Burke T. Drinking water contamination and the incidence of leukemia: an ecologic study. Am J Public Health 1990;80:12091212.
[Abstract/Free Full Text] - Vartiainen T, Pukkala E, Rienoja T, Strandman T, Kaksonen K. Population exposure to tri- and tetrachloroethylene and cancer risk: two cases of drinking water pollution. Chemosphere 1993;27:11711181.[CrossRef]
- Blair A, Hartge P, Stewart PA, McAdams M, Lubin J. Mortality and cancer incidence of aircraft maintenance workers exposed to trichloroethylene and other organic solvents and chemicals: extended follow up. Occup Environ Med 1998;55:161171.[Abstract]
- Boice JD Jr, Marano DE, Fryzek JP, Sadler CJ, McLaughlin JK. Mortality among aircraft manufacturing workers. Occup Environ Med 1999;56:581597.[Abstract]
- Morgan RW, Kelsh MA, Zhao K, Heringer S. Mortality of aerospace workers exposed to trichloroethylene. Epidemiology 1998;9:424431.[CrossRef][ISI][Medline]
- Greenland S, Salvan A, Wegman DH, Hallock MF, Smith TJ. A case-control study of cancer mortality at a transformer-assembly facility. Int Arch Occup Environ Health 1994;66:4954.[CrossRef][ISI][Medline]
- Anttila A, Pukkala E, Sallmen M, Hernberg S, Hemminki K. Cancer incidence among Finnish workers exposed to halogenated hydrocarbons. J Occup Environ Med 1995;37:797806.[ISI][Medline]
- Axelson O, Selden A, Andersson K, Hogstedt C. Updated and expanded Swedish cohort study on trichloroethylene and cancer risk. J Occup Med 1994;36:556562.[ISI][Medline]
- Hansen J, Raaschou-Nielsen O, Christensen JM et al. Cancer incidence among Danish workers exposed to trichloroethylene. J Occup Environ Med 2001;43:133139.[ISI][Medline]
- Raaschou-Nielsen O, Hansen J, McLaughlin JK et al. Cancer risk among workers at Danish companies using trichloroethylene: a cohort study. Am J Epidemiol 2003;158:11821192.
[Abstract/Free Full Text] - Travier N, Gridley G, De Roos AJ, Plato N, Moradi T, Boffetta P. Cancer incidence of dry cleaning, laundry and ironing workers in Sweden. Scand J Work Environ Health 2002;28:341348.[ISI][Medline]
- Andersson T, Ahlbom A. Episheet Software: Spreadsheets for the Analysis of Epidemiologic Data, K. Rothman, 2004. Available at: http://members.aol.com/krothman/episheet.xls.
- Boice JD Jr, McLaughlin JK. Errors in TCE analysis. Environ Health Perspect 2001;109:A108A109.[ISI][Medline]
- Blair A, Petralia SA, Stewart PA. Extended mortality follow-up of a cohort of dry cleaners. Ann Epidemiol 2003;13:5056.[CrossRef][ISI][Medline]
- Ji J, Hemminki K. Occurrences of leukemia subtypes by socioeconomic and occupational groups in Sweden. J Occup Environ Med 2005;47:11311140.[CrossRef][ISI][Medline]
- Garabrant DH, Held J, Langholz B, Bernstein L. Mortality of aircraft manufacturing workers in southern California. Am J Ind Med 1988;13:683693.[ISI][Medline]
- Ritz B. Cancer mortality among workers exposed to chemicals during uranium processing. J Occup Environ Med 1999;41:556566.[ISI][Medline]
- Chang YM, Tai CF, Yang SC et al. Cancer incidence among workers potentially exposed to chlorinated solvents in an electronics factory. J Occup Health 2005;47:171180.[CrossRef][ISI][Medline]
- Zhao Y, Krishnadasan A, Kennedy N, Morgenstern H, Ritz B. Estimated effects of solvents and mineral oils on cancer incidence and mortality in a cohort of aerospace workers. Am J Ind Med 2005;48:249258.[CrossRef][ISI][Medline]
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