Upload
kathleen-m-gardner
View
212
Download
0
Embed Size (px)
Citation preview
AMERICAN JOURNAL OF INDUSTRIAL MEDICINE 42:296–308 (2002)
Occupations and Breast Cancer Risk AmongChinese Women in Urban Shanghai
Kathleen M. Gardner, MT (ASCP), MSPH,1 Xiao Ou Shu, MD, PhD,1� Fan Jin, MD,2
Qi Dai, MD, PhD,1 Zhixian Ruan, BS,2 Shirley J. Thompson, PhD,3 James R. Hussey, PhD,3
Yu Tang Gao, MD,2 and Wei Zheng, MD, PhD1
Background Although, an elevated risk of breast cancer has been suggested for a numberof occupations, many earlier studies were limited by selection biases, the incompleteassessment of job histories, and the inability to control for confounding.Methods We examined the relationship between occupational history and breast cancerrisk using data from a population-based case-control study of 1,458 cases and 1,556 age-matched controls (90% response rate) conducted in Shanghai, China. Unconditionallogistic regression models were used to derive odds ratios (ORs) and 95% confidenceintervals (95% CIs) of breast cancer risk associated with occupations and duration ofemployment adjusting for non-occupational risk factors.Results The following occupations were found to be associated with an increased riskof breast cancer: laboratory technicians (OR 9.94, 95% CI 1.20–82.37), telephone andtelegraph operators (OR 4.63, 95% CI 1.85–11.59), leather and fur processors (OR 3.25,95% CI 1.11–9.53), and glass-manufacturing workers (OR 2.08, 95% CI 1.14–3.82).A dose–response pattern for years of employment was observed for leather and fur pro-cessors (P¼ 0.02) and glass-manufacturing workers (P¼ 0.01). Stratified analyses alsorevealed dose–response relationships between the risk of breast cancer and years ofemployment as inspector and product analysts among pre-menopausal women (P¼ 0.02),and as farmers among post-menopausal women (P¼ 0.04).Conclusions This study found that several occupations are associated with an increasedrisk of breast cancer among women. Studies examining various occupational exposures inthese high-risk occupations are warranted to identify carcinogens that may play a role inthe increasedbreastcancerrisk. Am. J. Ind. Med. 42:296–308, 2002.�2002Wiley-Liss, Inc.
KEY WORDS: breast cancer; occupations; employment; cancer; occupationalexposures
INTRODUCTION
Breast cancer incidence varies from nation to nation
[Parkin and Muir, 1992; Nab et al., 1994]. Although, China
has one of the lowest incidence rates of this malignancy in the
world, Shanghai, the largest industrial city on the east coast of
China, experienced a 40% increase in breast cancer incidence
from 1972 to 1989 [Jin et al., 1993a], with an 80–100% in-
crease among women between the ages of 35 and 44 [Jin et al.,
1993b]. Screening practices have remained the same in China
and, therefore, cannot be considered major contributors to
this increase in breast cancer [Jin et al., 1993b]. The increase
� 2002Wiley-Liss, Inc.
1Department of Medicine, and Vanderbilt-Ingram Cancer Center, Vanderbilt University,Nashville,Tennessee 37232-8300
2Department of Epidemiology, Shanghai Cancer Institute, Shanghai 200032, People’sRepublic of China
3Norman J. Arnold School of Public Health, University of South Carolina, South Carolina29203
Contract grant sponsor: USPHS; Contract grant number: R01CA64277.*Correspondence to: Xiao Ou Shu,Vanderbilt University Medical Center, Health Services
Research, 6th floor, Medical Center East, Nashville,TN 37232-8300.E-mail: [email protected]
Accepted10 June 2002DOI10.1002/ajim.10112. Published online inWiley InterScience
(www.interscience.wiley.com)
coincides with a decrease in age at menarche, an increase
in age at menopause [Jin et al., 1993a], and a delayed onset of
pregnancy [Jin et al., 1993b] among successive birth cohorts.
However, menstrual and reproductive factors can only ex-
plain 40–50% of the breast cancer within this population
[Gao et al., 2000]. During this same period, China has also
experienced rapid advancements in industrialization. It is
possible that occupational exposures resulting from this surge
of industrialization [He, 1998] may have contributed, in part,
to the increase in breast cancer incidence in China.
Over the last decade, a number of epidemiologic studies
have explored the association between occupations and breast
cancer. Possible increased risk of breast cancer has been
suggested for health care workers [Doebbert et al., 1988;
Sankila et al., 1990; Belli et al., 1992; Bulbulyan et al.,
1992; Rubin et al., 1993; Zheng et al., 1993; Morton, 1995;
Schenck, 1997; Petralia et al., 1998a, 1999a; Pollan and
Gustavsson, 1999], teachers [Threlfall et al., 1985; Rubin
et al., 1993; Schenck, 1997; Petralia et al., 1998a; Pollan and
Gustavsson, 1999; Simpson et al., 1999], clerical workers
[Threlfall et al., 1985; Ewertz, 1988; Bulbulyan et al., 1992;
Rubin et al., 1993; Zheng et al., 1993; Calle et al., 1998;
Pollan and Gustavsson, 1999; Simpson et al., 1999],
agricultural workers (farmers) [Petralia et al., 1998b; Pollan
and Gustavsson, 1999; Settimi et al., 1999], and rubber and
plastic manufacturers [Chiazze and Ference, 1981; Cantor
et al., 1995; Petralia et al., 1998a]. However, evidence on
the relationship between occupations and breast cancer risk
remains inadequate, and conflicting results from previous
studies may be due to methodological limitations. Many
studies were based on mortality data and, thus, may suffer
from survival biases [Chiazze and Ference, 1981; Katz, 1983;
Threlfall et al., 1985; Doebbert et al., 1988; Wong, 1990;
Bulbulyan et al., 1992; Rubin et al., 1993; Kogevinas et al.,
1994; Wong et al., 1994; Sala-Serra et al., 1996; Calle et al.,
1998; Burnett et al., 1999; Petralia et al., 1999a]. Other
studies obtained limited job histories [Katz, 1983; Threlfall
et al., 1985; Doebbert et al., 1988] and/or lacked information
on other breast cancer risk factors [Cantor et al., 1995] and,
thus, may have suffered from misclassification errors in ex-
posure assessment and/or confounding effects. Some case-
control studies were also limited by low response rates
[Doody et al., 1995; Petralia et al., 1998b, 1999b]. Low
employment rates for women in some study populations
could further jeopardize results of past studies.
The recently completed Shanghai Breast Cancer Study
was designed to overcome many limitations of earlier studies.
This study was conducted in a population where virtually all
women work and hold relatively stable jobs over time. In this
report, we examined the relationship between occupations
and breast cancer risk focusing first on the suggestive high-
risk occupations (healthcare workers, teachers, clerical
workers, farmers, and rubber and plastic manufacturers) that
have been linked to breast cancer in earlier studies. We then
evaluated the association of breast cancer risk with other
occupations.
MATERIALS AND METHODS
The Shanghai Breast Cancer Study, a population-based
case-control study, was conducted between August 1996 and
March 1998 among Chinese women between the ages of 25
and 64 who were permanent residents of Shanghai with no
former history of cancer, and who were willing to undergo an
in-person interview. Relevant institutional review boards
approved the use of human subjects in this study and a written
consent was obtained from all study participants. Newly
diagnosed, pathologically confirmed breast cancer cases, as
defined by ICD-9 code 174, were identified through both a
rapid case ascertainment system and the population-based
Shanghai Cancer Registry. Potentially eligible controls were
randomly selected from female residents of the general popu-
lation using the Shanghai Resident Registry, a registry for all
permanent residents of Shanghai, and frequency matched to
cases by age (5 years). The number of controls in each age-
specific stratum was pre-determined using the age distribu-
tion of the 1990–1993 incident breast cancer cases reported
to the Shanghai Cancer Registry. Controls were considered
eligible for the study only if they were still residing at the
address recorded in the residential registry at the time of
interview.
Information was collected from participants during an
in-person interview using a structured questionnaire. The
questionnaire obtained data on demographics, physical acti-
vity, diet, smoking, drinking, history of benign breast disease,
family history of breast cancer, weight history, detailed
menstrual, and reproductive history, and an in-depth
occupational history. Occupational history included up to
four occupations, held for a minimum of 3 years, with cor-
responding starting and stopping dates and occupational
physical assessment. Additional occupational information
included ever working on a farm and a detailed history of
pesticide exposure.
Job titles were coded by a three level hierarchy coding
system [National Bureau of Statistics, 1982]. The 3-digit level
corresponds to 301 specific occupational titles, the 2-digit
level corresponds to 63 occupational categories and the 1-digit
level corresponds to seven general occupational categories
[National Bureau of Statistics, 1982]. Based on published
literature, we selected five occupations (healthcare workers,
teachers, clerical workers, agricultural workers, and rubber
and plastic workers) as high-risk groups and performed an
in-depth evaluation of these occupations in relation to breast
cancer. A systematic evaluation of all other occupational
groups was also conducted by using the corresponding 1- or
2-digit codes.
To measure the association of occupations and breast
cancer risk, unconditional logistic regression analyses were
Occupations and Breast Cancer Risk 297
used to calculate adjusted odds ratios (ORs) and 95%
confidence intervals (95% CIs) for all women combined and
stratified by menopausal status. All variables that have been
found to be associated with a high risk of breast cancer in
this study were considered as potential confounders, and
adjusted for in the logistic regression models. These include
age, education level, age at menarche, age at menopause/pre-
menopause, age at first live birth/nulliparity, family history
of breast cancer, history of fibroadenoma, body mass index
(kg/m2) (BMI), waist-to-hip ratio (WHR), height and leisure
physical activity. Age was coded as a continuous variable.
All others were treated as categorical variables. Ever having
held a specific occupation and the duration of that occupation
provided two measures by which occupations were inves-
tigated in this study. Duration of the occupation was dicho-
tomized as � 10 years vs. > 10 years of employment in a
particular occupation. To determine whether there was a
dose–response relationship for duration of employment in a
suggestive high-risk occupation, a test for trend was per-
formed by assigning the score 0 for never having held that
occupation, 1 for having held the occupation for � 10 years,
and 2 for having held that occupation for > 10 years, and
then, entering this score into the logistic model as a con-
tinuous variable. Since menopausal status was missing for
6 cases and 4 controls, these subjects were excluded from
multivariate logistic regression analysis. All analyses were
performed using PC-SAS, version 8.0, (SAS Institutes, Inc.,
Cary, NC), and all tests were two-sided.
RESULTS
The participation rate of subjects was acceptable. Of the
1,602 eligible cases, 109 (6.8%) chose not to participate, 17
(1.1%) could not be located, and 17 (1.1%) died before
interview, resulting in a 91.1% response rate. One additional
case had to be eliminated from this occupational study due to
incomplete occupational information. Of the 1,724 eligible
controls, 166 (9.6%) chose not to participate, and 2 (0.1%)
died before interview, resulting in a 90.3% response rate.
Table I compares cases and controls on the distribution
of demographic, menstrual, and reproductive factors among
all women, pre- and post-menopausal women. In general,
cases were slightly older, more educated, younger at menar-
che, older at first live birth, taller, heavier, had a higher WHR,
and were more likely to have a family history of breast cancer
and a history of fibroadenoma than controls. Among pre-
menopausal women, compared with controls, cases were
older, older at first live birth, older at menopause, had a higher
WHR, and were more likely to have a family history of breast
cancer and a history of fibroadenoma. Among post-
menopausal women, cases were taller, heavier, more edu-
cated, younger at menarche, older at first live birth, and were
less likely to engage in leisure physical activity, and more
likely to have a history of fibroadenoma than controls.
Table II presents the ORs of breast cancer risk associated
with ever being employed in the five primary occupations of
interest and by the duration of employment. The five primary
occupational groups of interest were generally not related to
the risk of breast cancer. However, upon examining 3-digit
occupations among health care workers, we found that labo-
ratory technicians (consisting of 7 cases and 1 control) had a
tenfold increased risk of breast cancer (ORADJ, 9.94, 95% CI
1.20–82.37) (data not shown in table). No significant in-
creased risks were found for other health care occupations
examined, including doctors, nurses, pharmacists, and public
health workers (data not shown). A suggestive increased risk
of 19% was present for women ever being employed as cleri-
cal workers (ORADJ, 1.19, 95% CI 0.95–1.47). Women who
worked as clerical workers for � 10 years had a 48% incre-
ased risk of breast cancer (ORADJ, 1.48, 95% CI 1.08–2.03).
This elevated risk was mainly confined to post-menopausal
women (ORADJ, 2.07, 95% CI 1.21–3.81). Women who
remained in the job as clerical workers for > 10 years were
not at increased risk, whether examining all women or women
by menopausal status. Women working as farmers for over
10 years were twice as likely to develop breast cancer
(ORADJ, 2.08, 95% CI 1.15–3.74). This increased risk was
seen among both pre-menopausal (ORADJ, 1.72, 95% CI
0.87–3.41) and post-menopausal women (ORADJ, 2.75, 95%
CI 0.78–9.76), although, the point estimates did not reach
statistical significance. Stratified analyses also revealed a
dose–response relationship between the risk of breast cancer
and years of employment as farmers among post-menopausal
women (P¼ 0.04).
Table III shows breast cancer risks for women working
in all 1- and 2-digit occupations. Statistically elevated risks
of breast cancer were found in the following occupations:
postal and communication workers (ORADJ, 2.98, 95% CI
1.50–5.92), leather and fur processors (ORADJ, 3.25, 95% CI
1.11–9.53), and glass-manufacturing workers (ORADJ, 2.08,
95% CI 1.14–3.82). A reduced risk of breast cancer was
found among lawyers (ORADJ, 0.10, 95% CI 0.01–0.87) and
commercial workers (ORADJ, 0.80, 95% CI 0.63–1.00).
After stratifying by menopausal status, an increased
risk of breast cancer among postal and communication
workers was observed for both pre- (ORADJ, 2.47, 95% CI
1.05–5.82) and post-menopausal women (ORADJ, 4.03, 95%
CI 1.26–12.90). The occupation responsible for the in-
creased risk among postal and communication workers was
telephone and telegraph operators (ORADJ, 4.63, 95% CI,
1.85–11.59) (data not shown in table). A statistically signi-
ficant increased risk of breast cancer was not observed among
leather and fur processors, after stratification by meno-
pausal status, due to small numbers. Glass-manufacturing
workers were 2.7 times more likely to develop pre-meno-
pausal breast cancer (ORADJ, 2.70, 95% CI 1.20–6.05), and
had a 39% increased, but non-significant risk of devel-
oping post-menopausal breast cancer (ORADJ, 1.39, 95% CI
298 Gardner et al.
TABLE I. Comparison of Cases and Controls on Breast Cancer Risk Factors forAllWomen,Pre- and Post-MenopausalWomen in Shanghai*
All women Pre-menopausal women Post-menopausal women
Case (1458)(%)
Control (1556)(%) P value
Case (951)(%)
Control (990)(%) P value
Case (501)(%)
Control (562)(%) P value
Age (years)25^34 2.8 5.3 4.3 8.2 0.2 0.235^44 35.9 36.4 53.5 55.6 2.4 2.745^54 38.8 33.4 41.6 36.0 33.3 28.855^64 22.6 24.9 <0.01 0.5 0.3 <0.01 64.1 68.3 0.47
EducationNo formal education 3.6 5.5 0.5 0.4 9.6 14.4Elementary 8.5 8.4 3.2 2.5 18.4 18.5Middleþ high 74.3 75.4 84.7 88.0 54.5 53.6Prof.þ college 13.6 10.7 0.01 11.6 9.1 0.23 17.6 13.5 0.05
Age atmenarche� 12 9.4 8.4 8.4 8.8 11.3 7.813^16 80.1 77.2 82.8 79.8 74.7 72.8� 17 10.5 14.4 <0.01 8.8 11.4 0.13 14.0 19.4 0.02
Age at first birth/nulliparity< 30 73.8 80.3 70.7 76.3 79.8 87.530^34 17.0 13.2 19.6 16.5 12.2 7.5� 35 4.1 2.6 4.5 3.1 3.4 1.6Nulliparity 5.1 3.9 <0.01 5.2 4.1 0.04 4.6 3.4 <0.01
Age atmenopause/pre-menopause<45 5.8 7.9 16.8 21.745^47 6.6 6.2 19.2 17.148^50 12.0 13.7 34.7 37.9> 50 10.1 8.4 29.3 23.3Pre-menopause 65.5 63.8 0.05 0.04
Family history of breast cancerYes 3.7 2.4 3.5 1.9 4.2 3.4No 96.3 97.6 0.04 96.5 98.1 0.03 95.8 96.6 0.49
History of fibroadenomaYes 9.6 5.0 10.0 5.5 9.0 4.3No 90.4 95.0 < 0.01 90.0 94.5 < 0.01 91.0 95.7 < 0.01
BMI (kg/m2)< 20.70 20.3 24.4 24.3 28.4 12.8 17.420.71^22.79 23.9 25.4 26.7 28.3 19.0 20.122.80^25.10 26.8 25.3 26.7 23.9 26.8 27.9> 25.10 29.0 24.9 < 0.01 22.3 19.4 0.08 41.6 34.5 0.05
WHR� 0.764 19.5 25.0 22.9 30.2 13.2 15.80.765^0.800 25.3 26.8 28.2 28.2 20.0 24.00.801^0.835 25.0 23.0 23.8 21.9 27.3 24.7> 0.835 30.2 25.3 < 0.01 25.1 19.6 < 0.01 39.5 35.4 0.16
Height (cm)� 155.0 23.4 26.8 19.4 19.8 30.3 39.1155.1^159.0 30.2 27.5 28.5 27.0 33.7 28.5159.1^162.0 21.0 23.0 22.5 24.9 18.2 19.8> 162.0 25.4 22.7 0.03 29.6 28.3 0.59 17.8 12.6 < 0.01
(Continued )
Occupations and Breast Cancer Risk 299
0.52–3.71). Risk of pre-menopausal breast cancer was also
elevated among inspectors and product analysts (ORADJ,
1.49, 95% CI 1.06–2.08), and other service workers (ORADJ,
9.40, 95% CI 1.09–81.03). Risk of post-menopausal breast
cancer was elevated, but not statistically significant among
wood preparation workers (ORADJ, 3.63, 95% CI 0.93–
14.18).
Additional analyses were conducted for occupations that
showed a high-risk of breast cancer based on our preliminary
analyses to evaluate the occupational association by the dura-
tion of employment (Table IV). A positive dose–response
pattern associated with duration of employment was observed
for postal and communication workers (P for trend< 0.01),
leather and fur processors (P for trend¼ 0.02), and glass-
manufacturing workers (P for trend¼ 0.01). Indeed, a signi-
ficant relationship was observed between breast cancer risk
and employment for> 10 years as postal and communication
workers (ORADJ, 3.42, 95% CI 1.33–8.81), leather and fur
processors (ORADJ, 10.51, 95% CI 1.27–86.80), and glass-
manufacturing workers (ORADJ, 2.71, 95% CI 1.09–6.77).
A dose–response relationship was also observed for pre-
menopausal breast cancer among glass-manufacturing
workers (P for trend¼ 0.02) (3.37, 95% CI 0.89–12.73
for > 10 years of employment), and inspector and product
analysts (P for trend¼ 0.02) (ORADJ, 1.61, 95% CI 1.04–
2.49 for > 10 years of employment). Risk of post-meno-
pausal breast cancer also increased with the duration of
employment among postal and communication workers
(P for trend¼ 0.03) (ORADJ, 4.53, 95% CI 0.92–22.42 for
> 10 years of employment).
DISCUSSION
Healthcare workers [Doebbert et al., 1988; Belli et al.,
1992], teachers [Threlfall et al., 1985], clerical workers
[Threlfall et al., 1985; Ewertz, 1988; Bulbulyan et al., 1992;
Rubin et al., 1993; Zheng et al., 1993; Calle et al., 1998;
Pollan and Gustavsson, 1999; Simpson et al., 1999], agri-
cultural workers [Pollan and Gustavsson, 1999; Band et al.,
2000], and rubber and plastic manufacturers [Chiazze and
Ference, 1981] have previously been found to have a higher
risk of breast cancer. While we did not find health care
workers to be at increased risk of breast cancer as a whole,
analysis on individual health care occupations revealed a
significant tenfold increased risk of breast cancer among
laboratory technicians, consistent with several earlier studies
[Belli et al., 1992; Dosemeci et al., 1992; Andersen et al.,
1999]. Suggested potential exposures that may contribute to
this increased risk among health care workers are infectious
agents, sterilizing agents, ionizing radiation, cytostatic
drugs, and other toxic chemicals in addition to a high level
of stress [Katz, 1983; Sankila et al., 1990].
In this study, we also found that women employed as
farmers for over 10 years were two times more likely to
develop breast cancer than women never employed as far-
mers. Although, it has been suggested that women working
with pesticides may be at increased risk of breast cancer
due to the proposed estrogenic effects of these chemicals
[Labreche and Goldberg, 1997], earlier studies have gene-
rally not found a significantly increased risk of breast cancer
among farmers [Petralia et al., 1998b; Settimi et al., 1999].
Some of these studies were apparently limited by lack of sta-
tistical power to detect an association by menopausal status
[Petralia et al., 1998b; Settimi et al., 1999] and duration of
employment [Settimi et al., 1999]. In a recent population-
based case-control study, crop farmers, a subgroup of far-
mers, were found to have a tenfold increased risk of breast
cancer after adjusting for other risk factors [Band et al., 2000].
Interestingly, the vast majority of women who have ever
worked on farms in our study were crop farmers. Studies
stemming from large cohorts of women farmers will be
needed to confirm this association.
Women ever employed in leather and fur processing had
over a threefold increased risk of breast cancer as compared
to women never employed in this occupation. Moreover,
women employed for more than 10 years had over a tenfold
increased risk for breast cancer, although, the estimate was
based on only 7 cases and 1 control. Previous studies have
TABLE I. (Continued )
All women Pre-menopausal women Post-menopausal women
Case (1458)(%)
Control (1556)(%) P value
Case (951)(%)
Control (990)(%) P value
Case (501)(%)
Control (562)(%) P value
Leisure physical activityYes 18.7 25.2 14.0 15.5 27.5 42.6No 81.3 74.8 < 0.01 86.0 84.5 0.36 72.5 57.4 < 0.01
*Subjectswithmissingvalueswereexcludedfromanalysis.
300 Gardner et al.
TABLE
II.AdjustedORsofBreastCancerAssociatedWithaprioriH
igh-RiskOccupationsbyEverEm
ployedandbyD
urationofEmployment(�10and>
10Years)intheOccupationofInterestforAllW
omen,Pre-
andPost-MenopausalW
omeninShanghai*
, **
Allwom
enPre-menopausal
Post-menopausal
Cases
(1452)
Controls
(1552)
ORa
Trendtest
( Pvalue)
Cases
(951)
Controls
(990)
ORb
Trendtest
( Pvalue)
Cases
(501)
Controls
(562)
ORa
Trendtest
( Pvalue)
Medical&publichealthw
orkerc
7778
0.94(0.67^
1.13)
3543
0.74
(0.48^
1.24)
4235
1.19(0.72^
1.97)
�10yearsofemployment
1017
0.57
(0.26^
1.28)
511
0.44(0.15^1.30)
56
0.82
(0.24^
2.80)
>10yearsofemployment
6761
1.04(0.72^
1.51)
0.93
3032
0.89
(0.53^
1.50)
0.44
3729
1.27(0.74
^2.20)
0.43
Teacherc
127
111
1.06(0.79^
1.42)
5046
0.89
(0.58^
1.38)
7765
1.20(0.79^
1.81)
�10yearsofemployment
3133
0.92(0.55^
1.54)
1821
0.83
(0.43^
1.60)
1312
1.15(0.49^
2.70)
>10yearsofemployment
9678
1.12(0.79^
1.58)
0.60
3225
0.94(0.53^
1.67)
0.70
6453
1.21(0.78^
1.89)
0.39
Clerical&relatedworkerd
219
192
1.19(0.95^
1.47)
141
131
1.06(0.81^
1.39)
7761
1.32(0.90^
1.94)
�10yearsofemployment
103
761.48(1.08^2.03)
6957
1.28(0.87^
1.86)
3419
2.07
(1.21^3.81)
>10yearsofemployment
116
116
1.00(0.76^
1.32)
0.40
7274
0.91(0.64^
1.29)
0.97
4342
1.01(0.63^
1.62)
0.46
Farmerc
262
250
1.09(0.89^
1.34)
224
217
0.99(0.79^
1.24)
3832
1.65(0.97
^2.81)
�10yearsofemployment
228
229
1.02(0.82^
1.26)
198
202
0.94(0.74
^1.19)
3027
1.54(0.86^
2.76)
>10yearsofemployment
3420
2.08
(1.15^3.74)
0.13
2615
1.72(0.87^
3.41)
0.68
84
2.75
(0.78^
9.76)
0.04
Rubber&plasticproductm
akerc
3125
1.39(0.80^
2.40)
2316
1.51(0.78^
2.94)
89
1.12(0.41
^3.11)
�10yearsofemployment
1210
1.37(0.58^
3.23)
76
1.22(0.40^
3.73)
54
1.60(0.40^
6.45)
>10yearsofemployment
1915
1.40(0.69^
2.84)
0.26
1610
1.70(0.75^
3.85)
0.19
35
0.74
(0.16^3.41)
0.98
*Referencegroupconsistedofwom
enneverhavingtheoccupationofinterestcorrespondingtothegroupofwom
enbeingexamined.
**Excludedfromanalysis
durationofemploymentonw
omenwithincompleteinformationonlengthofemployment.
a Adjustedforage,education,ageatmenarche,everhavingalive
birth,ageatfirstlivebirth,menopausalstatus,ageatmenopause,familyhistoryofbreastcancer,historyoffibroadenom
a,WHR,BMI,height,andleisurephysicalactivity.
b Adjustedforallabovepotentialconfoundersexceptageatmenopause.
c Two-digitoccupations.
d One-digitoccupations.
301
TABLE
III.
AdjustedORsofBreastCancerAssociatedWithOne-Digitand
Two-DigitCodedOccupationsHeldfor3
orMoreYearsforAllW
omen,Pre-and
Post-MenopausalW
omeninShanghai*
Allwom
enPre-menopausal
Post-menopausal
Case(1458)
Control(1556)
ORADJa(95%
CI)
Case(951)
Control(990)
ORADJb(95%
CI)
Case(501)
Control(562)
ORADJa(95%
CI)
Professionalc
443
442
0.90(0.75^
1.10)
254
263
0.82
(0.65^
1.03)
187
176
1.14(0.82^
1.59)
Scientific
researcher
97
1.10(0.39^
3.09)
64
1.26(0.34^
4.70)
33
0.94(0.17^5.13)
Industrialtechnician
3840
0.79
(0.48^
1.30)
1616
0.82
(0.39^
1.74)
2224
0.80
(0.40^
1.61)
Administratorsinscience
1720
0.87
(0.44^
1.70)
1614
1.11(0.53^
2.34)
15
0.22
(0.03^
1.94)
Aircraft&shipengineer
52
2.05
(0.38^
11.19)
00
NA5
22.35
(0.41
^13.34)
Medical&publichealthworker
7778
0.94(0.67^
1.31)
3543
0.77
(0.48^
1.24)
4235
1.19(0.72^
1.97)
Econom
ists&
financialplanner
178
182
0.95(0.75^
1.19)
132
137
0.90(0.68^
1.17)
4545
1.11(0.70^
1.76)
Lawyer
18
0.10(0.01
^0.87)
04
NA1
40.21
(0.02^
2.16)
Teacher
127
111
1.06(0.79^
1.42)
5046
0.89
(0.58^
1.38)
7765
1.20(0.79^
1.81)
Professionalartist
146
2.34
(0.80^
6.79)
73
1.84(0.46^
7.33)
62
3.42
(0.61^
19.22)
Culturalworker
1833
0.56
(0.31^
1.01)
1421
0.63
(0.31^
1.28)
412
0.36
(0.11^1.17)
Leaderc
9190
1.03(0.75^
1.40)
5649
1.05(0.70^
1.59)
3441
1.01(0.61^
1.67)
Leaderparty/massorganization
4028
1.47(0.88^
2.46)
2616
1.47(0.77^
2.83)
1312
1.56(0.67^
3.61)
Leadertown/streetcommittee
1318
0.75
(0.36^
1.57)
35
0.59
(0.14^2.52)
1013
0.92(0.39^
2.17)
Leaderbusinessorganization
4951
0.94(0.62^
1.43)
3230
0.97(0.57^
1.63)
1721
0.88
(0.44^
1.78)
Clerical&relatedworkerc
219
192
1.19(0.95^
1.47)
141
131
1.06(0.81^
1.39)
7761
1.32(0.90^
1.94)
Administrativeclerk
161
152
1.08(0.85^
1.38)
105
100
1.04(0.77^
1.40)
5552
1.03(0.67^
1.59)
Politicalandsecuritypersonnel
4039
0.96(0.60^
1.52)
2828
0.87
(0.50^
1.51)
1211
1.09(0.46^
2.62)
Postal/com
municationw
orker
3112
2.98
(1.50^5.9
2)18
82.47
(1.05^5.82)
134
4.03
(1.26^12.90)
Otherclerical&relatedworker
34
0.72
(0.16^3.34)
13
0.38
(0.04^
3.71)
21
1.78(0.15^21.44)
Commercialworkerc
162
203
0.80
(0.63^
1.00)
121
153
0.79
(0.61^
1.04)
3949
0.80
(0.50^
1.27)
Salesmanandshopassistant
143
164
0.91(0.71^
1.16)
104
126
0.87
(0.65^
1.15)
3737
1.05(0.64^
1.75)
Service
workerc
225
262
0.95(0.78^
1.17)
155
167
1.01(0.79^
1.30)
6994
0.87
(0.60^
1.27)
Publicservice
worker
170
189
1.00(0.79^
1.26)
111
118
1.03(0.77^
1.37)
5870
1.00(0.67^
1.50)
Cook
5576
0.82
(0.57^
1.18)
4253
0.84
(0.55^
1.28)
1323
0.78
(0.37^
1.63)
Agriculturalworkerc
273
264
1.09(0.89^
1.33)
233
226
1.00(0.80^
1.25)
4037
1.44(0.87^
2.41)
Farmer
262
250
1.09(0.89^
1.34)
224
217
0.99(0.79^
1.24)
3832
1.65(0.97
^2.81)
Forester
76
1.29(0.43^
3.90)
64
1.18(0.49^
6.37)
12
0.35
(0.03^
4.44)
Production&
relatedworkerc
871
946
1.06(0.90^
1.25)
596
601
1.12(0.92^
1.37)
272
343
0.90(0.67^
1.21)
Metalrefiningw
orker
2831
1.00(0.59^
1.72)
1615
1.16(0.56^
2.42)
1216
0.71
(0.31^
1.61)
Chem
icalprocessors&related
2324
0.96(0.53^
1.73)
1218
0.69
(0.32^
1.47)
116
1.60(0.57^
4.49)
Rubber&plasticproductm
aker
3125
1.39(0.80^
2.40)
2316
1.51(0.78^
2.94)
89
1.12(0.41
^3.11)
Textileworker
150
199
0.82
(0.65^
1.03)
102
129
0.84
(0.63^
1.12)
4770
0.83
(0.55^
1.26)
Leatherandfurprocessor
125
3.25
(1.11^9.53)
84
2.98
(0.87^
10.17)
31
6.37
(0.63^
64.16)
Tailor
7284
0.90(0.65^
1.26)
5152
1.00(0.66^
1.51)
2132
0.78
(0.42^
1.42)
(Con
tinue
d)
302
TABLE
III.
(Continued)
Allwom
enPre-menopausal
Post-menopausal
Case(1458)
Control(1556)
ORADJa(95%
CI)
Case(951)
Control(990)
ORADJb(95%
CI)
Case(501)
Control(562)
ORADJa(95%
CI)
Foodandbeverageprocessor
2017
1.32(0.68^
2.57)
1211
1.17(0.50^
2.73)
86
1.39(0.45^
4.26)
TobaccoP
roductmaker
31
4.59
(0.46^
4.71)
20
NA1
11.39(0.08^
23.53)
WoodPreparationW
orker
1312
1.21(0.54^
2.68)
59
0.61
(0.20^
1.86)
83
3.63
(0.93^
14.18)
Paperandpaperproductmaker
1012
0.89
(0.37^
2.12)
88
0.92(0.34^
2.50)
24
0.89
(0.15^5.39)
Printersandrelatedworker
2227
0.93(0.52^
1.66)
1217
0.77
(0.36^
1.66)
1010
1.32(0.52^
3.36)
Stonecuttersandcarver
11
1.39(0.09^
22.73)
01
NA1
0NA
Blacksmithsand
toolmaker
144
155
1.03(0.80^
1.32)
9290
1.03(0.75^
1.41)
164
1.02(0.68^
1.55)
Machineryfitterand
assembler
5768
0.96(0.66^
1.39)
3543
0.86
(0.54^
1.38)
2225
1.09(0.59^
2.03)
Electricalfitter/relatedworker
7494
0.92(0.67^
1.27)
5156
0.98(0.66^
1.47)
2338
0.72
(0.41
^1.26)
Plum
ber&
welder
4042
1.14(0.72^
1.79)
2925
1.27(0.73^
2.23)
1117
0.80
(0.36^
1.79)
Glass-manufacturingw
orker
3018
2.08
(1.14^3.82)
209
2.70
(1.20^6.0
5)10
91.39(0.52^
3.71)
Painter
1813
1.46(0.69^
3.07)
118
1.16(0.46^
2.95)
74
1.56(0.44^
5.55)
Otherproduction/relatedworker
3639
0.97(0.60^
1.55)
2425
0.89
(0.50^
1.60)
1214
0.98(0.43^
2.23)
Constructionw
orker
1020
0.65
(0.30^
1.43)
412
0.41(0.13^1.30)
68
1.12(0.37^
3.40)
Engine&Equipm
entOperator
78
1.13(0.40^
3.19)
54
1.53(0.40^
5.91)
24
0.58
(0.10^3.35)
Materialequipmentoperator
3936
1.25(0.78^
2.02)
3024
1.43(0.81^
2.52)
912
0.87(0.35^
2.18)
Transportationequipment
2827
1.10(0.63^
1.92)
2114
1.44(0.71^
2.89)
713
0.59
(0.22^
1.60)
Inspector&
productanalyst
134
122
1.24(0.94^
1.60)
9668
1.49(1.06^2.08)
3853
0.82
(0.51^
1.30)
Othertransportationw
orker
108
131
0.89
(0.67^
1.17)
7784
0.91(0.65^
1.27)
3147
0.82
(0.50^
1.34)
*Referencegroupconsistedofwom
enneverhavingtheoccupationofinterestcorrespondingtothegroupofwom
enbeingexamined.
a Adjustedforage,education,ageatmenarche,everhavingalive
birth,ageatfirstlivebirth,menopausalstatus,ageatmenopause,familyhistoryofbreastcancer,historyoffibroadenom
a,WHR,BMI,height,andleisurephysicalactivity.
b Adjustedforallabovepotentialconfoundersexceptageatmenopause.
c One-digitoccupations.
303
TABLE
IV.AdjustedORsofBreastCancerAssociatedWithSuggestiveH
igh-RiskOccupationsbyEverEm
ployedandbyD
urationofEmployment(�10and>10Years)WithintheO
ccupationofInterestforAll
Wom
en,Pre-and
Post-MenopausalW
omeninShanghai* Al
lwom
enPre-menopausal
Post-menopausal
Case
(1452)
Control
(1552)
ORa
Trendtest
( Pvalue)
Case
(951)
Control
(990)
ORb
Trendtest
( Pvalue)
Case
(501)
Control
(562)
ORa
Trendtest
( Pvalue)
Postal/Com
municationw
orkerc
3112
2.98
(1.50^5.9
2)18
82.47
(1.05^5.82)
134
4.03
(1.26^12.90)
�10yearsofemployment
136
2.54
(0.94^
6.86)
84
2.34
(0.68^
8.04)
52
3.05
(0.64^
19.17)
>10yearsofemployment
186
3.42
(1.33^8.81)
<0.01
104
2.60
(0.80^
8.48)
0.05
82
4.53
(0.92^
22.42)
0.03
Leather&
furprocessorc
125
3.25
(1.11^9.53)
84
2.98
(0.87^
10.17)
31
NA�10yearsofemployment
54
1.46(0.36^
5.96)
43
1.93(0.42^
8.95)
01
NA>10yearsofemployment
71
10.51(1.27^86.8)
0.02
41
6.18(0.67^
56.89)
0.06
30
NANA
Woodpreparationw
orkerc
1312
1.21(0.54^
2.69)
59
0.61
(0.20^
1.86)
83
3.63
(0.93^
14.18)
�10yearsofemployment
56
0.78
(0.23^
2.59)
25
0.39
(0.7^2.03)
31
3.14(0.30^
33.12)
>10yearsofemployment
86
1.71(0.58^
5.02)
0.46
34
0.95(0.20^
4.39)
0.56
52
3.89
(0.74
^20.57)
0.07
Glass-manufacturingw
orkerc
3018
2.08
(1.14^3.82)
209
2.70
(1.20^6.0
5)10
91.39(0.52^
3.71)
�10yearsofemployment
1411
1.67(0.74
^3.77)
116
2.34
(0.84^
6.50)
35
0.73
(0.16^3.42)
>10yearsofemployment
167
2.71
(1.09^6.77)
0.01
93
3.37
(0.89^
12.73)
0.02
74
2.21
(0.59^
8.26)
0.34
Inspector&
productanalystc
134
122
1.24(0.94^
1.60)
9668
1.49(1.06^2.08)
3853
0.82
(0.51^
1.30)
�10yearsofemployment
5750
1.32(0.88^
1.98)
3731
1.33(0.81^
2.19)
2018
1.17(0.59^
2.32)
>10yearsofemployment
7772
1.16(0.82^
1.63)
0.21
5937
1.61(1.04^2.49)
0.02
1835
0.61
(0.33^
1.14)
0.21
*Referencegroupconsistedofwom
enneverhavingtheoccupationofinterestcorrespondingtothegroupofwom
enbeingexamined.
a Adjustedforage,education,ageatmenarche,everhavingalive
birth,ageatfirstlivebirth,menopausalstatus,ageatmenopause,familyhistoryofbreastcancer,historyoffibroadenom
a,WHR,BMI,height,andleisurephysicalactivity.
b Adjustedforallabovepotentialconfoundersexceptageatmenopause.
c 2-digitoccupations.
304
generally found a non-significant elevated risk of breast
cancer among leather and tanning workers [Bulbulyan et al.,
1992; Goldberg and Labreche, 1996; Weiderpass et al., 1999],
although a retrospective cohort study in Shanghai failed to
find any association [Petralia et al., 1998a]. Possible sources
of exposure that might increase the risk of breast cancer
among these workers would include benzene and chlorinated
solvents [Goldberg and Labreche, 1996; Labreche and
Goldberg, 1997], and high levels of exposure to leather dust
[Weiderpass et al., 1999].
A twofold increased risk for breast cancer was found for
glass-manufacturing workers consisting of glass workers,
potters, enamelware, and porcelain workers. The few studies
that have examined the relationship between glass-manu-
facturing workers and breast cancer only found a 40–50%
non-significant increased risk for breast cancer [Petralia et al.,
1998a; Pollan and Gustavsson, 1999]. Yet, a recent study
found a significant fourfold increased risk of breast cancer
among pre-menopausal women working in material proces-
sing (mine, rubber, metal, glass, or clay) [Band et al., 2000].
Sources of exposure to various chemicals and industrial
dusts have been suggested in this line of work for pancreatic
cancer [Ji et al., 1999] and lung cancer [Jahn et al., 1999].
More recently, studies have demonstrated that dust in cera-
mic manufacturing industry contains pesticides (dioxins)
[Ferrario and Byrne, 2002]. The firing process itself may
further emit dioxins into the workplace [Ferrario and Byrne,
2002], thereby possibly exposing glass-manufacturing work-
ers to these proposed mammary carcinogens by dermal
exposure and inhalation.
Breast cancer risk was also elevated among pre-
menopausal inspectors and analysts and post-menopausal
wood preparation workers. These elevated risks would not
have been detected if the data had not been stratified by
menopausal status. However, numbers become rather small
when stratifying by menopausal status resulting in instability
and a loss of power. Yet, since employment for > 10 years in
these two occupations further increased the risk of breast
cancer, these findings are further substantiated. Sources of
carcinogenic exposure in these potentially high-risk occupa-
tions might include a multitude of chemicals, including
solvents and remnants of pesticides, in addition to high levels
of exposure to wood dusts in the wood preparation workers.
In this study, we also found that women in postal and
communication occupations were three times more likely to
develop breast cancer as compared to women never work-
ing in these occupations and risk increased with duration of
employment. Postal and communication workers consist
of only three occupations: (1) post office administrators,
(2) telephone and telegraph operators, and (3) other postal
and communication workers. Examining each of these speci-
fic occupations revealed that the increased risk seen in postal
and communication workers was due to a fourfold significant
increased risk among telephone and telegraph operators.
Aside from the Shanghai retrospective cohort study that
found only a non-significant increased risk of breast cancer
among postal and communication workers [Petralia et al.,
1998a], no other studies have addressed the risk of this group
in relation to breast cancer. Among telephone and telegraph
operators, many studies have found a significantly incre-
ased risk of breast cancer [Morton, 1995; Brinton and
Devesa, 1996; Goldberg and Labreche, 1996; Tynes et al.,
1996; Pollan and Gustavsson, 1999; Simpson et al., 1999].
Other studies only found a non-significant increased risk
[Bulbulyan et al., 1992; Calle et al., 1998; Petralia et al.,
1998a] or no increased risk of breast cancer [Band et al.,
2000]. The hypothesized source of exposure for telephone
and telegraph operators is their exposure to electromagnetic
fields (EMFs) [Goldberg and Labreche, 1996]. The pineal
gland, responsible for secreting melatonin, undergoes a re-
duction in the secretion of this hormone due to exposure from
EMFs, thereby, allowing an increase in the production of
estrogen increasing cellular proliferation of the breast [Cohen
et al., 1978; Stevens, 1987; Gammon and John, 1993; Caplan
et al., 2000]. As recently noted in a review on breast cancer
and EMFs, experimental data and epidemiological studies
focusing on this relationship further substantiates a possible
biologically plausible association between EMFs and breast
cancer risk [Caplan et al., 2000]. Moreover, a meta-analysis
of 24 epidemiologic studies examining the relationship
between EMFs and breast cancer among women resulted in a
pooled estimated relative risk (RR 1.12, 95% CI 1.09–1.15)
with study risk estimates ranging from 0.6 to 1.64 [Erren,
2001]. Not finding an increased risk among electrical workers
in this study, however, suggests that the underlying cause of
breast cancer among telephone and telegraph operators may
be a result of an exposure other than EMFs.
An increased risk of breast cancer was also found among
clerical workers, most notably, among the subgroup of cleri-
cal workers consisting of postal and communication workers
(as mentioned above). However, the patterns of association
for job duration differed for clerical workers and the subgroup
of postal and communication workers. The increased risk for
clerical workers existed for those employed � 10 years, and
the increased risk among postal and communication workers
existed for those employed > 10 years. Analysis of clerical
workers excluding postal and communication workers did
not alter the results for clerical workers. When analysis was
restricted to women who had worked exclusively as clerical
workers, only pre-menopausal women had worked � 10
years. These women had an elevated risk of breast cancer
(ORADJ, 6.55, 95% CI 0.72–59.89 based on 5 cases and 1
control). The perplexing increased risk among women
working as clerical workers for � 10 years could be due to
an unidentified risk factor or may very well be a chance
finding. A possible explanation for the observed increased
risk of post-menopausal breast cancer among short-term
clerical workers could be that women previously employed
Occupations and Breast Cancer Risk 305
in high-risk occupations might have been transferred to
clerical positions due to declining health.
Several occupations found to be associated with an
increased risk of breast cancer in this study may stem from
occupational exposures that may be classified as endocrine
disrupters, exogenous chemicals that alter endocrine func-
tion [McGlynn, 2001]. Xenoestrogens, one class of endocrine
disrupters, consist of exogenous chemicals with estrogenic
properties, such as aromatic and halogenated solvents and
organochlorines that are lipophilic and can build up in the
fatty tissue of the breast [Labreche and Goldberg, 1997].
These weak estrogens may increase the risk of breast cancer
by increasing cellular proliferation [Davis et al., 1993]. Some
xenoestrogens have proven to be mammary carcinogens in
animals [Labreche and Goldberg, 1997]. Solvents, such as
polycyclic aromatic hydrocarbons (PAH) (e.g., benzene,
toluene, xylene) are potential carcinogens that may behave
as xenoestrogens. Exposures to these solvents may occur in
many of the occupations found to be associated with an in-
creased risk of breast cancer in our study, including laboratory
workers, leather and fur processors, glass-manufacturing
workers, and inspector and product analysts. Women work-
ing in agriculture may also be exposed to xenoestrogens by
way of certain organochlorine pesticides [Morton, 1995],
such as DDT [Soto et al., 1995], although, the current litera-
ture examining the relationship between pesticides and breast
cancer has been inconsistent [Aronson et al., 2000]. Large
cohort studies of women examining the appropriate biomar-
kers of carcinogens and/or xenoestrogens are needed to
advance the current knowledge.
Caution needs to be taken when making conclusions
from this study due to the multiple comparisons conducted.
To minimize Type I error, we gave more emphasis to positive
associations with a priori hypothesis and/or a dose–
response. On the other hand, small numbers for various
occupations may jeopardize finding a significant association
even if one is present. This may be especially true when
examining the association between occupations and breast
cancer by menopausal status. Another potential drawback to
this study could be uncontrolled confounding that may exist
from environmental exposures outside the workplace.
Exposures in-utero, infancy, childhood, and adolescence
may very well be important missing links to the mystery of
this multifactorial disease. An additional limitation is that
occupations and occupational groups rather than the
occupational exposures were evaluated in this study.
Masking of associations can occur since occupational titles
and occupational groups are crude surrogates for occupa-
tional exposures. Although cases of this study are only
slightly older than controls (mean ages, 49.7 for cases and
47.3 for controls), age differences may vary widely within
certain occupations leading to unequal exposure opportunity.
However, we found no significant age differences between
cases and controls within occupations where significant
associations were observed. Finally, the genetic make-up of
certain subgroups of the study population may make them
more prone to exposures to carcinogens and/or endocrine
disruptors in the workplace that may influence their risk of
breast cancer. Not taking into consideration genetic suscept-
ibility factors may hinder finding some associations between
occupations and breast cancer.
Our study has many strength. Not only is this a
population-based case-control study that uses incident cases,
the detailed collection of reproductive, menstrual, and life-
style factors allows for full adjustment for traditional breast
cancer risk factors. High response rates for both cases and
controls minimized selection bias. Plus, the lower back-
ground risk of breast cancer among Chinese women may
provide a window of opportunity to examine the association
between occupations and breast cancer with less impact from
other breast cancer risk factors. Moreover, the occupational
stability that exists in the Chinese population [Zheng et al.,
1993] enhances the ability to find occupations that may pre-
dispose women to breast cancer. In this study population,
93% of study participants reported having no more than
three occupations. Our in-depth assessment of occupational
histories reduced the exposure misclassification that may
have occurred in other studies that had information on only
one occupation. Plus the average duration of employment for
our study participants was 24 years. Errors in recall may be
minimized in this study population, since the Chinese are
more apt to remain in the same occupation [Zheng et al.,
1993]. Another real advantage of this study is that it takes
into account a thorough occupational history, whereas
many previous studies did not. In our study, 1 year or less
elapsed between jobs for 91% of women, demonstrating
that we have captured a relatively complete occupational
history for the vast majority of women. Moreover, examining
the occupations for women by menopausal status in addition
to examining the occupations for all women provided
leverage for finding occupations that may increase the risk
of breast cancer in pre- or post-menopausal women only.
In summary, this study provides preliminary insights
into the associations between occupations and the risk of
breast cancer among Chinese women from urban Shanghai.
Future studies are needed to examine the association between
breast cancer risk and specific occupational exposures in
these suspected high-risk occupations to identify the res-
ponsible mammary carcinogen(s) in order to develop further
preventive measures for breast cancer.
ACKNOWLEDGMENTS
We thank Dr. Wanquing Wen for his expert assistance in
SAS programming and Dr. Martha Shrubsole for her valuable
comments on the manuscript.
306 Gardner et al.
REFERENCES
Andersen A, Barlow L, Engeland A, Kjaerheim K, Lynge E, Pukkala E.1999. Work-related cancer in the Nordic countries. Scand J WorkEnviron Health 25 (Suppl 2):1–116.
Aronson KJ, Miller AB, Woolcott CG, Sterns EE, McCready DR,Lickley LA, Fish EB, Hiraki GY, Holloway C, Ross T, Hanna WM,SenGupta SK, Weber JP. 2000. Breast adipose tissue concentrations ofpolychlorinated biphenyls and other organochlorines and breast cancerrisk. Cancer Epidemiol Biomarkers Prev 9:55–63.
Band PR, Le ND, Fang R, Deschamps M, Gallagher RP, Yang P. 2000.Identification of occupational cancer risks in British Columbia. Apopulation-based case-control study of 995 incident breast cancer casesby menopausal status, controlling for confounding factors. J OccupEnviron Med 42:284–310.
Belli S, Comba P, De Santis M, Grignoli M, Sasco AJ. 1992. Mortalitystudy of workers employed by the Italian National Institute of Health,1960–1989. Scand J Work Environ Health 18:64–67.
Brinton LA, Devesa SS. 1996. Etiology and pathogenesis ofbreast cancer. In: Harris JR, Lippman ME, Morrow M, Hellman S,editors. Diseases of the breast. Philadelphia, PA: Lippincott-Raven.p 159–168.
Bulbulyan M, Zahm SH, Zaridze DG. 1992. Occupational cancermortality among urban women in the former USSR. Cancer CausesControl 3:299–307.
Burnett C, Robinson C, Walker J. 1999. Cancer mortality in health andscience technicians. Am J Ind Med 36:155–158.
Calle EE, Murphy TK, Rodriguez C, Thun MJ, Heath CW, Jr. 1998.Occupation and breast cancer mortality in a prospective cohort of USwomen. Am J Epidemiol 148:191–197.
Cantor KP, Stewart PA, Brinton LA, Dosemeci M. 1995. Occupationalexposures and female breast cancer mortality in the United States.J Occup Environ Med 37:336–348.
Caplan LS, Schoenfeld ER, O’Leary ES, Leske MC. 2000. Breast cancerand electromagnetic fields—A review. Ann Epidemiol 10:31–44.
Chiazze L, Jr., Ference LD. 1981. Mortality among PVC-fabricatingemployees. Environ Health Perspect 41:137–143.
Cohen M, Lippman M, Chabner B. 1978. Role of pineal gland inetiology and treatment of breast cancer. Lancet 2:814–816.
Davis DL, Bradlow HL, Wolff M, Woodruff T, Hoel DG, Anton-CulverH. 1993. Medical hypothesis: Xenoestrogens as preventable causes ofbreast cancer. Environ Health Perspect 101:372–377.
Doebbert G, Riedmiller KR, Kizer KW. 1988. Occupational mortality ofCalifornia women, 1979–1981. West J Med 149:734–740.
Doody MM, Mandel JS, Boice JD, Jr. 1995. Employment practices andbreast cancer among radiologic technologists. J Occup Environ Med37:321–327.
Dosemeci M, Alavanja M, Vetter R, Eaton B, Blair A. 1992. Mortalityamong laboratory workers employed at the U.S. Department ofAgriculture. Epidemiology 3:258–262.
Erren TC. 2001. A meta-analysis of epidemiologic studies of electricand magnetic fields and breast cancer in women and men. Bioelec-tromagnetics Suppl 5:S105–S119.
Ewertz M. 1988. Risk of breast cancer in relation to social factors inDenmark. Acta Oncol 27:787–792.
Ferrario J, Byrne C. 2002. Dibenzo-p-dioxins in the environment fromceramics and pottery produced from ball clay mined in the UnitedStates. Chemosphere 46:1297–1301.
Gammon MD, John EM. 1993. Recent etiologic hypotheses concern-ing breast cancer. Epidemiologic Rev 15:163–168.
Gao YT, Shu XO, Dai Q, Potter JD, Brinton LA, Wen W, Sellers TA,Kushi LH, Ruan Z, Bostick RM, Jin F, Zheng W. 2000. Associationof menstrual and reproductive factors with breast cancer risk:Results from the Shanghai Breast Cancer Study. Int J Cancer 87:295–300.
Goldberg MS, Labreche F. 1996. Occupational risk factors for femalebreast cancer: A review. Occup Environ Med 53:145–156.
He F. 1998. Occupational medicine in China. Int Arch Occup EnvironHealth 71:79–84.
Jahn I, Ahrens W, Bruske-Hohlfeld I, Kreuzer M, Mohner M, PohlabelnH, Wichmann HE, Jockel KH. 1999. Occupational risk factors for lungcancer in women: Results of a case-control study in Germany. Am J IndMed 36:90–100.
Ji BT, Silverman DT, Dosemeci M, Dai Q, Gao YT, Blair A. 1999.Occupation and pancreatic cancer risk in Shanghai, China. Am J IndMed 35:76–81.
Jin F, Devesa SS, Zheng W, Blot WJ, Fraumeni JF, Jr., Gao YT. 1993a.Cancer incidence trends in urban Shanghai, 1972–1989. Int J Cancer53:764–770.
Jin F, Shu XO, Devesa SS, Zheng W, Blot WJ, Gao YT. 1993b. Incidencetrends for cancers of the breast, ovary, and corpus uteri in urbanShanghai, 1972–89. Cancer Causes Control 4:355–360.
Katz RM. 1983. Causes of death among registered nurses. J Occup Med25:760–762.
Kogevinas M, Ferro G, Andersen A, Bellander T, Biocca M, Coggon D,Gennaro V, Hutchings S, Kolstad H, Lundberg I. 1994. Cancer mortalityin a historical cohort study of workers exposed to styrene. Scand J WorkEnviron Health 20:251–261.
Labreche FP, Goldberg MS. 1997. Exposure to organic solvents andbreast cancer in women: A hypothesis. Am J Ind Med 32:1–14.
McGlynn KA. 2001. Environmental and host factors in testicular germcell tumors. Cancer Invest 19:842–853.
Morton WE. 1995. Major differences in breast cancer risks amongoccupations. J Occup Environ Med 37:328–335.
Nab HW, Mulder PG, Crommelin MA, Heijden LH, Coebergh JW.1994. Is the peak in breast cancer incidence in sight? A study conductedin the southeastern Netherlands. Eur J Cancer 30A:50–52.
National Bureau of Statistics. 1982. Standard classification of industriesand occupations used for the third national census. Beijing: BeijingOffice of the National Census of the State Council. p 1–75.
Parkin DM, Muir CS. 1992. Cancer incidence in five continents.Comparability and quality of data. IARC Sci Publ 120:45–173.
Petralia SA, Chow WH, McLaughlin J, Jin F, Gao YT, Dosemeci M.1998a. Occupational risk factors for breast cancer among women inShanghai. Am J Ind Med 34:477–483.
Petralia SA, Vena JE, Freudenheim JL, Marshall JR, Michalek A,Brasure J, Swanson M, Graham S. 1998b. Breast cancer risk and lifetimeoccupational history: Employment in professional and managerialoccupations. Occup Environ Med 55:43–48.
Petralia SA, Dosemeci M, Adams EE, Zahm SH. 1999a. Cancermortality among women employed in health care occupations in 24 U.S.states, 1984–1993. Am J Ind Med 36:159–165.
Petralia SA, Vena JE, Freudenheim JL, Michalek A, Goldberg MS, BlairA, Brasure J, Graham S. 1999b. Risk of pre-menopausal breast cancerand patterns of established breast cancer risk factors among teachers andnurses. Am J Ind Med 35:137–141.
Occupations and Breast Cancer Risk 307
Pollan M, Gustavsson P. 1999. High-risk occupations for breast cancerin the Swedish female working population. Am J Public Health 89:875–881.
Rubin CH, Burnett CA, Halperin WE, Seligman PJ. 1993. Occupationas a risk identifier for breast cancer. Am J Public Health 83:1311–1315.
Sala-Serra M, Sunyer J, Kogevinas M, McFarlane D, Anto JM. 1996.Cohort study on cancer mortality among workers in the pulp and paperindustry in Catalonia, Spain. Am J Ind Med 30:87–92.
Sankila R, Karjalainen S, Laara E, Pukkala E, Teppo L. 1990. Cancerrisk among health care personnel in Finland, 1971–1980. Scand J WorkEnviron Health 16:252–257.
Schenck AP. 1997. Occupation and breast cancer: A population-based,case-control study of women in North Carolina (Dissertation). ChapelHill: University of North Carolina.
Settimi L, Comba P, Carrieri P, Boffetta P, Magnani C, Terracini B,Andrion A, Bosia S, Ciapini C, De Santis M, Desideri E, Fedi A, LuccoliL, Maiozzi P, Masina A, Perazzo PL, Axelson O. 1999. Cancer riskamong female agricultural workers: A multi-center case-control study.Am J Ind Med 36:135–141.
Simpson J, Roman E, Law G, Pannett B. 1999. Women’s occupation andcancer: Preliminary analysis of cancer registrations in England andWales, 1971–1990. Am J Ind Med 36:172–185.
Soto AM, Sonnenschein C, Chung KL, Fernandez MF, Olea N, SerranoFO. 1995. The E-SCREEN assay as a tool to identify estrogens: An
update on estrogenic environmental pollutants. Environ HealthPerspect 103 (Suppl 7):113–122.
Stevens RG. 1987. Electric power use and breast cancer: A hypothesis.Am J Epidemiol 125:556–561.
Threlfall WJ, Gallagher RP, Spinelli JJ, Band PR. 1985. Reproductivevariables as possible confounders in occupational studies of breast andovarian cancer in females. J Occup Med 27:448–450.
Tynes T, Hannevik M, Andersen A, Vistnes AI, Haldorsen T. 1996.Incidence of breast cancer in Norwegian female radio and telegraphoperators. Cancer Causes Control 7:197–204.
Weiderpass E, Pukkala E, Kauppinen T, Mutanen P, Paakkulainen H,Vasama-Neuvonen K, Boffetta P, Partanen T. 1999. Breast cancer andoccupational exposures in women in Finland. Am J Ind Med 36:48–53.
Wong O. 1990. A cohort mortality study and a case-control study ofworkers potentially exposed to styrene in the reinforced plastics andcomposites industry. Br J Ind Med 47:753–762.
Wong O, Trent LS, Whorton MD. 1994. An updated cohort mortalitystudy of workers exposed to styrene in the reinforced plastics andcomposites industry. Occup Environ Med 51:386–396.
Zheng W, Shu XO, McLaughlin JK, Chow WH, Gao YT, Blot WJ.1993. Occupational physical activity and the incidence of cancer ofthe breast, corpus uteri, and ovary in Shanghai. Cancer 71:3620–3624.
308 Gardner et al.