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    Laryngeal and hypopharyngeal cancers andoccupational exposure to formaldehyde andvarious dusts: a case-control study in France

    Laurent Laforest, Danile Luce, Paquerette Goldberg, Denis Bgin, Michel Grin,Paul A Demers, Jacques Brugre, Annette Leclerc

    Abstract

    Objectives A case-control study was

    conducted in France to assess possible

    associations between occupational expo-

    sures and squamous cell carcinomas of

    the larynx and hypopharynx.

    Methods The study was restricted to

    men, and included 201 hypopharyngeal

    cancers, 296 laryngeal cancers, and 296

    controls (patients with other tumour

    sites). Detailed information on smoking,

    alcohol consumption, and lifetime occu-

    pational history was collected. Occupa-tional exposure to seven substances

    (formaldehyde, leather dust, wood dust,

    flour dust, coal dust, silica dust, and

    textile dust) was assessed with a job expo-

    sure matrix. Exposure variables used in

    the analysis were probability, duration,

    and cumulative level of exposure. Odds

    ratios (ORs) with their 95% confidence

    intervals (95% CIs) were estimated by

    unconditional logistic regression, and

    were adjusted for major confounding fac-

    tors (age, smoking, alcohol, and when rel-

    evant other occupational exposures).

    Results Hypopharyngeal cancer was

    found to be associated with exposure tocoal dust (OR 2.31, 95% CI 1.21 to 4.40),

    with a significant rise in risk with prob-

    ability (p

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    hypopharyngeal and laryngeal tumours amongwomen, only men were recruited. The studyinitially identified 664 patients meeting thesecriteria. Of these, 136 (20.5%) could not beinterviewed because of health problems(n=40), death before an interview could beconducted (n=11), refusal to participate(n=22), or because they could not be located(n=63). In all, the study finally included 206men with hypopharyngeal cancer, 315 with

    laryngeal cancer, and seven with cancers ofboth the larynx and hypopharynx. Controlswere patients with primary cancers of diVerentsites, selected by frequency matching on ageand recruited between 1987 and 1991 in thesame hospitals as the cases or in similar hospi-tals nearby. The aim was to obtain a controlgroup of the same size as the group of cases oflaryngeal cancer. Of the 355 controls identi-fied, 50 (14%) could not be interviewed,because of medical conditions (n=14), refusal(n=14), or because they could not be located(n=22). To obtain comparable catchmentareas, controls were patients with cancersrequiring the same medical environment as the

    cases.The following sites were selected:rectumor anal canal (n=30), liver or gall bladder(n=15), pancreas (n=11), haematopoietic sys-tem (n=34), bones and cartilage (n=7), skin(melanoma) (n=18), soft tissue (n=11), pros-tate (n=63), testis (n=17), bladder (n=29),other urinary organs (n=27), brain and nerv-ous system (n=18), thyroid (n=18), colon(n=5), and stomach (n=2).

    Occupational physicians specially trained forthis study interviewed both cases and controlsand collected detailed data about demographiccharacteristics, alcohol and tobacco consump-tion, and lifetime occupational history. A morecomplete description of the study design and ofthe characteristics of cases and controls haspreviously been published.25

    Of the 833 subjects included in the study,some were excluded from the analysis: thosewith cancer at more than one site (n=7), thosewho did not answer the questions on alcohol(five cases of laryngeal cancer), and those whodid not drink at all (nine controls, 14 cases oflaryngeal cancer, five cases of hypopharyngealcancer, because it was unclear whether theywere teetotal or former drinkers who hadstopped for health reasons). The final analysisthus included 793 subjects: 296 controls, 201men with hypopharyngeal cancer, and 296with laryngeal cancer. Those with laryngealcancer were divided into anatomical subsites

    according to the classification used by Tuyns etal.4 These sites were the epilarynx (n=97), theglottis (n=102), the supraglottis (n=80), thesubglottis (n=3), and larynx unspecified(n=14).

    OCCUPATIONAL EXPOSURES

    Each job was coded with standard classificationfor occupation (ISCO)27 and industry (ISIC).28

    Occupational exposures were assessed througha job exposure matrix (JEM), developed earlierby three of the authors (PD for wood andleather dust, DB and MG for other substances)

    for a study on sinonasal cancer29 (the JEM isavailable from the authors).

    For each ISCO-ISIC combination and foreach substance, the JEM gives the probabilityof exposure, and the level of exposure incategories. The cut oVpoints used for the cat-egories of level and probability, according tothe substance, are presented in table 1. Whenthe probability of exposure was less than 10%(for wood dust and leather dust) or less than

    1% (for the other substances), the job was con-sidered to be unexposed.

    For a given substance, for each job i of eachsubject, the JEM provides the probability ofexposure Pi and the level of exposure Li. Thejob duration Di was also available. Subjectscould have had several successive jobs iexposed to the same substance throughouttheir working life. Several exposure variableswere calculated to summarise the subjects life-time exposure: maximum probability ofexposure=max (Pi); total duration of exposure(in years)=Di; cumulative level of exposure=Li Pi Di.

    To calculate the cumulative level, quantita-

    tive values (midpoints of the intervals) wereassigned to each category of level and probabil-ity (table 1).

    DATA ANALYSIS

    Each substance was studied independently.Separate analyses were conducted for cancersof the larynx and hypopharynx. Each analysisused the same control group.

    Occupational exposure was first assessed bya dichotomous variable ever versus neverexposed. Quantitative exposure variables wereconverted into categorical variables accordingto their distribution among all subjects. Thenumber of classes ranged from two to four,depending on the frequency of exposure. The

    reference category for each analysis was thenever exposed subjects.

    Table 1 Categories for level and probability of exposuredefined in the JEM for the studied substances and assignedvalues

    Substances

    Level categories Probability categories

    Cut oVpoints*

    Assignedvalue

    Cut oVpoints(%)

    Assignedvalue

    Leather dust Low 1.00 1050 0.30Medium 2.00 5090 0.70High 3.00 >90 1.00

    Wood dust 5 9.00 >90 1.00

    Formaldehyde 1.00 3.00 5090 0.70

    >90 1.00Flour dust 5 10.0 >90 1.00

    Coal dust 2 5.00 >90 1.00

    Silica 0.1 0.200 >90 1.00

    Textile dust 0.5 1.500 >90 1.00

    *Wood dust, flour dust, coal dust, silica, textile dust (mg/m3),and formaldehyde (ppm).

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    The analysis used multivariate unconditionallogistic regression, performed with SAS soft-ware. Adjusted odds ratios (ORs) are reportedwith their 95% confidence intervals (95% CIs).All ORs were adjusted for age (60),alcohol (04 glasses/day; >5 glasses/day) andsmoking (30 pack-years).Preliminary analysis showed that with a finerstratification for age (69), alcohol (13) and smoking (non-smoker, 129 pack-years, 3044, >45) did not substantially alterthe adjusted ORs for occupational exposures.

    Other occupational exposures (includingasbestos and man made mineral fibres) andeducation level (primary school or less, higherthan primary school) were considered to bepossible confounders for any given substanceand were included in the final model if morethan 10 subjects (cases or controls) wereexposed to both the substance under consid-eration and the potential confounder, and if theconfounder changed the OR estimate by morethan 10%. When a dose-response pattern of

    interest was found for a categorised exposurevariable, a test for trend was performed byassigning the score k to the kth level ofexposure (the number 0 was assigned to thereference category) and entering the score intologistic models. We also examined morecomplex logistic models including interactionterms between occupational exposures andage, and alcohol and tobacco consumption.

    For substances other than wood dust andleather dust, further analyses were performedby excluding subjects considered to be exposedwith a probability of exposure less than 10%.

    We also analysed the data according tolaryngeal subsites, and we compared, for each

    substance, the risk of cancer of the epilarynxwith that of cancer of other parts of the larynx(endolarynx) and the hypopharynx.

    To allow for a possible induction period,successive analyses excluded the 5, 10, and 15years of exposure immediately before the refer-ence date (cancer diagnosis).

    In all additional analyses, the ORs wereadjusted for the variables found to be con-founders in the earlier analyses.

    ResultsTable 2 summarises the principal characteris-tics of each of the study groups for educationlevel, age, daily alcohol consumption, andsmoking.

    Table 3 reports the number of exposed sub-jects and the adjusted OR for each substance.Only 19 workers (2.4% of all subjects) wereexposed to leather dust; therefore no furtheranalysis was performed for it. Exposure was

    most frequent for formaldehyde (n=270,34.0%) and silica dust (n=326, 41.1%). Thefrequency of exposure to the other substanceswas 8.1% for textile dust (n=64), 13.4% forcoal dust (n=106), 14.6% for wood dust(n=116), and 7.2% for flour dust (n=57).

    An increased risk of hypopharyngeal cancer,although not significant, was found for expo-sure to formaldehyde. There was a clear dose-response pattern with the probability ofexposure (trend test p

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    Table 3 Risk of cancer of the larynx and hypopharynx, by occupational exposure to each substance

    Larynx Hypopharynx

    Cases/ controls Adjusted OR 95% CI Cases/ controls Adjusted OR 95% CI

    Leather dust:Never exposed 288/288 1.00 198/288 1.00

    Ever exposed 8/8 0.89 0.62 to 1.27 3/8 0.80 0.16 to 4.07Wood dust*:

    Never exposed 249/260 1.00 168/260 1.00

    Ever exposed 47/36 1.00 0.58 to 1.72 33/36 0.89 0.47 to 1.68Probability of exposure (%):

    70 27/18 1.08 0.53 to 2.21 22/18 1.06 0.48 to 2.31Duration of exposure (y):

    10 19/13 1.03 0.46 to 2.30 13/13 1.19 0.48 to 2.95Cumulative level:

    Low (42) 12/9 0.86 0.33 to 2.28 15/9 1.52 0.59 to 3.94Formaldehyde:

    Never exposed 194/211 1.00 118/211 1.00

    Ever exposed 102/85 1.14 0.76 to 1.70 83/85 1.35 0.86 to 2.14Probability of exposure (%):

    50 21/15 1.04 0.44 to 2.47 26/15 3.78 1.50 to 9.49Duration of exposure (y):

    20 30/32 0.96 0.52 to 1.76 28/32 1.51 0.78 to 2.92

    Cumulative level:Low (0.09) 29/30 0.87 0.45 to 1.67 28/30 1.51 0.74 to 3.10Flour dust:

    Never exposed 274/282 1.00 180/282 1.00 Ever exposed 22/14 1.52 0.69 to 3.34 21/14 1.92 0.82 to 4.50

    Probability of exposure (%):90 17/13 1.11 0.47 to 2.60 16/13 1.16 0.46 to 2.91Duration of exposure (y):3 13/8 1.15 0.43 to 1.28 13/8 1.53 0.53 to 4.44Cumulative level:

    Low (20) 12/6 1.59 0.54 to 4.70 8/6 1.51 0.42 to 5.38

    Textile dust:Never exposed 272/275 1.00 182/275 1.00 Ever exposed 24/21 1.22 0.61 to 2.43 19/21 1.63 0.74 to 3.60

    Probability of exposure (%):90 16/11 1.41 0.58 to 3.44 9/11 1.21 0.39 to 3.72Duration of exposure (y):

    7 9/14 0.74 0.28 to 1.95 8/14 1.26 0.43 to 3.65Cumulative level:

    Low (0.3) 13/8 1.37 0.50 to 3.81 9/8 1.24 0.38 to 4.05

    Coal dust:Never exposed 254/270 1.00 163/270 1.00 Ever exposed 42/26 1.67 0.92 to 3.02 38/26 2.31 1.21 to 4.40

    Probability of exposure (%):90 20/13 1.75 0.75 to 4.08 19/13 3.12 1.22 to 8.01Duration of exposure (y):

    20 17/12 1.52 0.64 to 3.58 11/12 2.37 0.86 to 6.52

    Cumulative level:Low (25) 15/9 1.78 0.66 to 4.78 14/9 3.73 1.23 to 11.3

    Silica dust**:Never exposed 173/181 1.00 113/181 1.00 Ever exposed 123/115 0.96 0.65 to 1.40 88/115 0.81 0.50 to 1.31

    Probability of exposure (%):90 38/27 1.23 0.62 to 2.44 28/27 0.98 0.43 to 2.20

    Duration of exposure (y):36 30/29 1.07 0.57 to 1.99 19/29 0.87 0.41 to 1.87

    Cumulative level:Very low (0.100) 32/24 0.95 0.45 to 2.01 23/24 0.73 0.31 to 1.76

    ORs adjusted for age, smoking, and alcohol (see text).*Also adjusted for exposure to formaldehyde (yes/no) and mineral fibres (yes/no) for the larynx, and for exposure to formaldehyde (yes/no) , mineral fibres (yes/no)and asbestos (yes/no) for the hypopharynx.Also adjusted for exposure to coal dust (yes/no) for the larynx, and for exposure to coal dust (yes/no) and asbestos (yes/no) for the hypopharynx.Also adjusted for exposure to formaldehyde (yes/no) for the larynx and hypopharynx.Also adjusted for exposure to formaldehyde (yes/no) and asbestos (yes/no) for the hypopharynx only.Also adjusted for exposure to formaldehyde (yes/no) for the larynx and hypopharynx.**Also adjusted for exposure to coal dust (yes/no) for the larynx, and for exposure to coal dust (yes/no), asbestos (yes/no), and education level (only primary schoolor more) for the hypopharynx.

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    risk increased with cumulative level of expo-sure (p

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    discordant as to laryngeal11 13 4345 and oropha-ryngeal and hypopharyngeal7 35 46 cancers.Similarly, although some authors have foundan increased risk of laryngeal or pharyngealcancers among textile workers,79 47 other stud-ies have failed to confirm these results.13 35 39 48

    Moreover, most textile or wood workers areexposed not only to wood dust or textile dust,but also to numerous other substances, includ-ing solvents, varnishes, dyes, asbestos, and

    formaldehyde.37 49 50 These other substancescan all be potential confounders in studiesbased on job titles.

    Our study has several limitations. Controlswere recruited during a longer period than thecases, but controls diagnosed in 19878 weresimilar to those recruited in 198991 (period ofcases recruitment) for the number of jobs, thelevel of education, the consumption of alcoholand tobacco, and the frequency of occupationalexposures.

    Interviewers were aware of case-controlstatus, which could introduce a bias. However,they were blind to the study hypotheses andcomparisons between interviewers concerning

    the main characteristics of the subjects did notshow important diVerences. This suggests thatan interviewer bias is probably not a majorlimitation in this study.

    The use of a cancer control group limits apossible recall bias. On the other hand, somecancer sites among controls may be associatedwith the occupational exposures under study. Asthe proportion of each cancer site was limited, itis unlikely that such associations seriously biasedthe results. Furthermore, the proportion ofexposed subjects did not diVer between the sites,for all the substances studied.

    The occupational exposures were assessedwith a JEM, which could have entailed

    non-diVerential misclassification and biasedthe ORs towards unity. Such non-diVerentialmisclassification may also be responsible forthe lack of a dose-response pattern in our data.Dosemici et al51 showed that in some situationsnon-diVerential misclassification when expo-sure is assessed by polytomous variables canbias the ORs estimated for intermediate levelsaway from the null and invert the slope of thedose-response trend. Furthermore, the fewsubjects with high levels of exposure may beresponsible for some negative results.

    The few subjects exposed to some sub-stances also necessitated a broad categorisationof the confounders, but as a more stringentcontrol for age, alcohol, and smoking did notaVect the ORs substantially, there is probablyno important residual confounding.

    In this study, we could not consider theimpact of some substances known or suspectedto be carcinogenic to the larynx and pharynxsuch as sulphuric acid and polycyclic aromatichydrocarbons. Future work will expand expo-sure assessment to other substances.

    On the whole, our data suggest an associ-ation between hypopharyngeal cancer andexposure to formaldehyde and coal dust.Further epidemiological investigations are re-quired for confirmation.

    1 International Agency for Research on Cancer. Cancerincidence in five continents. Lyon: IARC, 1997.

    2 Elwood JM, Pearson JC, Skippen DH, et al. Alcohol, smok-ing, social and occupational factors in the aetiology of can-cer of the oral cavity, pharynx and larynx. Int J Cancer1984;15:60312.

    3 Rothman KJ, Cann CI, Flanders D, et al. Epidemiology oflaryngeal cancer. Epidemiol Rev 1980;2:195209.

    4 Tuyns AJ, Esteve J, Raymond L, et al. Cancer of the larynx/hypopharynx, tobacco and alcohol: IARC: internationalcase control study in Varese (Italy), Zaragoza and Navarra(Spain), Geneva (Switzerland) and Calvados (France). IntJ Cancer1988;41:48391.

    5 Gunel P, Chastang JF,Luce D, et al. A study of the interac-tion of alcohol drinking and tobacco smoking among

    French cases of laryngeal cancer. J Epidemiol CommunityHealth 1988;42:3504.

    6 Riboli E, Kaaks R, Esteve J. Nutrition and oral cancer. Can-cer Causes Control 1996;7:14756.

    7 Haguenoer JM, Cordier S, Morel C, et al. Occupational riskfactors for upper respiratory tract and upper digestive tractcancer. Br J Ind Med 1990;47:3803.

    8 Flanders WB, Cann CI, Rothman KJ, et al. Work related riskfactors for laryngealcancer.AmJ Epidemiol1984;119:2332.

    9 Ahrens W, Jockel KH, Patzak W, et al. Alcohol, smoking andoccupational factors in cancer of the larynx: a case controlstudy. Am J Ind Med1991;20:47793.

    10 Burch JD, Howe GR, Miller AB, et al. Tobacco alcoholasbestos and nickel in the aetiology of cancer of larynx: acase control study. J Natl Cancer Inst 1981;67:121924.

    11 Flanders WD, Rothman KJ. Occupational risk for laryngealcancer. Am J Public Health 1982;72:36972.

    12 Gunel P, Engholm G, Lynge E. Laryngeal cancer inDenmark: a nationwide longitudinal study based on regis-ter linkage data. Br J Ind Med 1990;47:4739.

    13 Zagraniski RT, Kesley JL, Walter SD. Occupational risk fac-tors for laryngeal carcinoma: Connecticut 197580. Am JEpidemiol1986;124:6776.

    14 Chan CK, Gee JBL. Asbestos exposure and laryngealcancer: an analysis of the epidemiologic evidence. J OccupMed1988;30:237.

    15 Edelman DA. Laryngeal cancer and occupational exposureto asbestos. Int Arch Occup Environ Health 1989;61:2237.

    16 Liddell FDK. Laryngeal cancer and asbestos. Br J Ind Med1990;47:28991.

    17 Parnes SM. Asbestos and cancer of the larynx: is there arelationship. Laryngoscope 1990;100:25461.

    18 Smith AH, Handley MA, Wood R. Epidemiologicalevidence indicates asbestos causes laryngeal cancer. JOccup Med 1990;32:499507.

    19 Kraus T, Drexler H, Weber A, et al. The association of occu-pational asbestos dust exposure and laryngeal carcinoma.Isr J Med Sci1995;31:5408.

    20 BoVetta P, Jourenkova N, Gustavsson P. Cancer risk fromoccupational and environmental exposure to polycyclic aro-matic hydrocarbons. Cancer Causes Control 1997;8:44472.

    21 Soskolne CL, Zeighami EA, Hanis NM, et al. Laryngealcancer and occupational exposure to sulfuric acid. Am JEpidemiol1984;120:35869.

    22 Soskolne CL, Jhangri GS, Siemiatycki J, et al. Occupationalexposure to sulfuric acid in southern Ontario, Canada, in

    association with laryngeal cancer. Scand J Work EnvironHealth 1992;18:22532.23 Steenland K. Laryngeal cancer incidence among workers

    exposed to acid mists (United States). Cancer Causes Con-trol1997;8:348.

    24 International Agency for Research on Cancer. Wood dust andformaldehyde. Lyon: IARC, 1995;62:1440

    25 Goldberg P, Leclerc A, Luce D, et al . Laryngeal andhypopharyngeal cancer and occupation: results of a casecontrol study. Occup Environ Med 1997;54:47782.

    26 Marchand JL, Luce D, Leclerc A, et al. Laryngeal andhypopharyngeal cancer and occupational exposure toasbestos and man-made vitreous fibers: results of acase-control study. Am J Ind Med2000;37:5819.

    27 International Labour OYce. International standard classifi-cation of occupations. Geneva: International Labour OYce,1968.

    28 United Nations Statistical OYce. International standardindustrial classification of all economic activities. New York:United Nations Statistical OYce, 1968.

    29 Demers PA, Kogevinas M, BoVetta P, et al. Wood dust andsinonasal cancer: pooled reanalysis of twelve case controlstudies. Am J Ind Med1995;28:15166.

    30 Roush GC, Walrath J, Stayner LT, et al. Nasopharyngealcancer, sinonasal cancer and occupation related toformaldehyde: a case control study. J Natl Cancer Inst1987;79:12214.

    31 West S, Hildesheim A, Dosemeci M. Non-viral risk factorsfor nasopharyngeal carcinoma in the Philippines: resultsfrom a case control study. Int J Cancer 1993;55:7227.

    32 Blair A, Stewart PA, OBerg M, et al. Mortality amongindustrial workers exposed to formaldehyde. J Natl CancerInst 1986;76:107184.

    33 Merletti F, BoVetta P, Ferro G, et al. Occupational cancer ofthe oral cavity or oropharynx in Turin Italy. Scand J WorkEnviron Health 1991;17:24854.

    34 Vaughan TL, Strader C, Davis C, et al. Formaldehyde andcancers of the pharynx, sinus and nasal cavity: IOccupational exposures. Int J Cancer 1986;15:67783.

    35 Gustavsson P, Jakobsson R, Johansson H, et al. Occupa-tional exposures and squamous cell carcinoma of the oralcavity, pharynx, larynx and oesophagus: a case-controlstudy in Sweden. Occup Environ Med 1998;55:393400.

    772 Laforest, Luce, Goldberg, et al

    www.occenvmed.com

    http://oem.bmj.com/
  • 8/8/2019 v057p00767

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    36 Stayner LT, Elliot L, Blade L, et al. A retrospective cohortmortality study of workers exposed to formaldehyde in thegarment industry. Am J Ind Med 1988;13:66781.

    37 Berrino F. Occupational factors of upper respiratory tractcancers. In: Hirsch A, Goldberg M, Martin JP, et al, eds.Prevention of respiratory diseases. New York: Marcel Dekker,1993;8196.

    38 Wortley P, Vaughan TL, Davis S, et al. A case control studyof occupational risk factors for laryngeal cancer. Br J IndMed1992;49:83744.

    39 Zheng W, Blot WJ, Shu XO, et al. Diet and other risks fac-tors for laryngeal cancer in Shangai. Am J Epidemiol 1992;136:17891.

    40 Bravo MP, Espinosa J, Calero JR. Occupational risk factorsfor cancer of the larynx in Spain. Neoplasma 1990;37:477

    81.41 Andjelkovitch DA, Janszen DB, Brown MH, et al. Mortality

    of iron foundry workers: IV analysis of a subcohort exposedto formaldehyde. J Occup Environ Med 1995;37:82637.

    42 Puntoni R, Goldsmith DF, Valerio F, et al. A cohort study ofworkers employed in a refractory brick plant. Tumori1988;74:2733.

    43 Wynder EL, Covey LS, Mabuchi K, et al. Environmentalfactors in cancer of the larynx: a second look. Cancer 1976;38:1591601.

    44 Vaughan TL, Davis S. Wood dust exposure and squamouscell cancers of the upper respiratory tract. Am J Epidemiol1991;133:5604.

    45 Brown LM, Mason TJ, Pickle LW, et al. Occupational riskfactors for laryngeal cancer on the Texas Gulf Coast. Can-cer Res 1988;48:19604.

    46 Huebner WW, Schoenberg JB, Kesley JL, et al. Oral andpharyngeal cancer and occupation: a case control study.Epidemiology 1992;3:3009.

    47 Moss E, Lee WR. Occurrence of oral and pharyngealcancers in textile workers. Br J Ind Med 1974;31:22432.

    48 Whitaker CJ, Moss E, Lee WR, et al. Oral and pharyngealcancer in the North-west and West Yorkshire regions ofEngland, and occupation. Br J Ind Med 1979;36:2928.

    49 Nylander LA. Carcinogenic eVects of wood dust:review anddiscussion. Am J Ind Med1993;24:61947.

    50 Kauppinen TP, Partanen TJ, Hernberg SG, et al. Chemicalexposures and respiratory cancer among Finnish wood-workers. Br J Ind Med 1993;50:1438.

    51 Dosemeci M, Waldocher S, Lubin JH. Does non-diVerentialmisclassification of exposure always bias a true eVecttoward the null value ? Am J Epidemiol 1990;132:7468.

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