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                    <text>Itom ID Number

01764

Author

Fingerhut, Marilyn A.

Corporate Author
ROpOrt/ArtiOlO TltlO Review of Exposure and Pathology Data for Seven
Cases Reported as Soft Tissue Sarcoma Among
Persons Occupational^ Exposed to DioxinContaminated Herbicides

Journal/Book Title
1984

Year
Month/Day
Color

'

Number of Images

17

Descpipton Notes

Monday, June 11, 2001

Page 1765 of 1793

�187

REVIEW OF EXPOSURE AND PATHOLOGY DATA FOR SEVEN CASES
REPORTED AS SOFT TISSUE SARCOMA AMONG PERSONS OCCUPATIONALLY
EXPOSED TO DIOXIN-CONTAMINATED HERBICIDES

Marilyn, A. Fingerhut, Ph.D*
William E. Halperin, M.D., M.P.H.*
Patricia A. Honchar, Ph.D*
Alexander B. Smith, M.D., M.S.*
David H. Groth, M.D.*
William 0. Russell, M.D.**

*National Institute for Occupational Safety and Health
Cincinnati, Ohio 45226
**North Ridge General Hospital and Cancer Foundation,
Fort Lauderdale, Florida 33334

This paper is a work of the U.S. Government; therefore
copyright does not apply.

From

Public Health Risks of the Dioxins,
proceedings of a symposium held on
. October 19-20, 1983 at The Rockefeller
University, New York City. Edited by
William W. Lowrance. Published by William
Kaufmann, Los Altos, California, 1984.

�188 Fingerhutetal.

Data from two Swedish studies (1,2) and a review of four U.S.
studies (3) of dioxin-exposed workers have suggested that
occupational exposure to dioxin-contaminated products is associated
with an increased risk of soft tissue sarcoma (STS). Soft tissue
sarcomas are malignant neoplasms arising throughout the body from
mesenchymal supporting tissue other than bone (4). The principal
types of histopathologic subtypes and their frequencies 'are listed in
Table 1.
:

Table 1. Histopathologic varieties of sarcoma of soft tissue.*
r
&gt;
tPercentage of
Histopathological Variety
Total Cases
r

Rhabdomyosarcoma

19.2 "'

Fibrosarcoma

19.0

Liposarcoma

18.2

Malignant fibrohistiocytoma

10.5

Sarcoma of Soft Tissue,
type unspecified

10.0

Synovial sarcoma

6.9

Leiomyosarcoma

6.5

Malignant schwannoma

4.9

Angiosarcoma

2.7

Other types

1.9

* Table presented in Suit, H.D., Sarcoma of soft tissue, CA-A Cancer
Journal for Clinicians 1978; 28:284-295.

The percentages were derived from a study of 1,215 sarcomas by the
Task Force for Sarcoma of Soft Tissue of the American joint Committee
on Cancer (5).
Dioxins are generated as unintended contaminants during the
chemical manufacture of chlorinated phenoxy acetic acids and
chlorinated phenols. The most toxic of the 75 dioxin isomers,
2,3,7,8-tetrachlorodibenzodioxin (2,3,7,8-TCDD), is generated during

�Review of Reported Soft, Tissue Sarcoma Cases 189

the production of trichlorophenol (TCP) and its derivative, the
herbicide 2/4,5-trichlorophenoxyacetic acid (2,4,5-T). Industrial
workers who produce chlorinated phenoxy acetic acids and
chlorophenols, and herbicide applicators who spray these products,
potentially have been exposed to the products and their dioxin
contaminants. In 1977, several cases of soft tissue sarcoma were
reported among Swedish lumberjacks who had had prior exposure to
phenoxy herbicides. This clinical observation led researchers in
Sweden to conduct two separate case control studies (1,2). Both
studies found that persons with occupational exposure to phenoxy
acids or chlorophenols had a fivefold increased risk of developing a
soft tissue sarcoma.
At" about the same time, four studies (6-9) were conducted in~j&gt;
U.S. manufacturing plants of workers exposed to the herbicide 2,4,5-T
and its chemical precursor, trichlorophenol. The dioxin isomer
contaminating these products is the most toxic form, 2,3,7,8-TCDD.
None of the four studies found any statistically significant excess
in total mortality or in death from cancer which was attributed to
dioxin exposure. However, each cohort was small and of insufficient
statistical power to allow adequate evaluation of rare causes of
death. Honchar (3) reviewed the deaths in the four cohorts, and
found that three (2.9%) of the total 105 deaths in the merged cohorts
were reported to be from soft tissue sarcoma. Based on national
statistics, only 0.07% of deaths was expected to be due to this
cause. Table 2 lists these three deaths as Cases 1 to 3.
Subsequently, Dr. Ralph Cook of Dow Chemical Company reported a
fourth, living person in one of these cohorts as having a soft tissue
sarcoma (10). This individual, Case 4, is now deceased. Dr. Marion
Moses of Mt. Sinai reported an additional case of soft tissue sarcoma
in an individual (Case 5) employed at one of the same four chemical
manufacturing sites (11). Subsequently, two additional persons,
Cases 6 and 7, were reported to have soft tissue sarcomas (12). They
worked at a chemical manufacturing site which produced 2,4,5-T, but
which had not been previously studied, and their exposures had not
been confirmed at the time of the reports.

�190 Fingerhutetal.

Table 2. Exposure data from original publications for the seven
U.S. workers.

Case
Number

Type of
Exposure

Type of
Report

Reference

TCP

Mortality Study

Zack, J. and Suskind, R.S,
Journal of Occupational
Medicine 1980; 22;11-14.

2,4,5-T

Mortality Study

Zack, J. and Gaffey, W.R.
Environmental Science
Research 1983; 26;575-591.

TCP

Mortality Study

Cook, R.R. et al.
Journal of Occupational
Medicine T980; 22:530-32.

TCP

Case Report

Cook, R.R. Lancet 1981,;
i:618-619. ^

TCP, 2,4,5-T

Case Report

Moses, M. and Selikoff,
I.J. Lancet 1981; i:
1370.

6

Chlorophenols

Case Report

Johnson, F.E. et al.
Lancet 1981; i:40.

7

Chlorophenols

Case Report

Johnson, F.E. et al.
Lancet 1981; i:40.

We have obtained detailed employment records, medical and
pathological reports, tissue specimens and death certificates for
these seven individuals and present here detailed descriptions of our
occupational and pathologic reviews. We hope, through this report,
to focus attention on the problems associated with the study of soft
tissue sarcomas in dioxin-exposed populations. In addition to our
work at the National Institute for Occupational Safety and Health
(NIOSH), studies of the health effects of dioxin are underway at the
Centers for Disease Control (CDC), the Veterans Administration (VA),
the National Institutes of Health (NIH), and various state agencies
in this country. Other organizations, both here and abroad, are also
conducting studies of soft tissue sarcoma, and the International
Agency for Research on Cancer (IARC) of the World Health Organization
is considering an International Dioxin Registry.

�Review of Reported Soft Tissue Sarcoma Cases

191

EXPOSURE DATA FOR THE SEVEN CASES
Table 3 presents the exposure history of each individual. We
used a rigorous criterion of exposure. An individual was considered
exposed to products contaminated with 2,3,7,8-TCDD

if he had a

company record of assignment to a department producing
trichlorophenol or 2,4,5-T.

Table 3.

Work history information for the seven U.S. workers.
'Duration of
Exposure
(Years)

Case
Number

Facility

Years of
Employment

1

A

1946-1978

TCP Operator

1.9 •"

2

A

1946-1972

2,4,5-T Operator

2.0

3

B

1950-1975

Maintenance

3.5

4

B

1951-1982

TCP Operator
Plant Mechanic
(TCP Department)

19.0

job
Title

5

A

1943-1975

Maintenance Service

6

C

1978-1980

Production Worker

7

C

1951-1980

Production Worker

11 days

The work histories confirmed the original reports that Cases 1, 2,
and 4 were production workers assigned to the trichlorophenol or
2,4,5-T departments. Case 3 was a maintenance worker identified by
the company as assigned to a building where trichlorophenol was
produced.

Case 5 was a maintenance and service worker for 32 years

in a chemical manufacturing site which produced trichlorophenol,
2,4,5-T, and many other chemicals, but he had no record of specific
assignment to a trichlorophenol or 2,4,5-T department. Case 6 worked
two and one-half years in a plant which made 2,4,5-T. He was a
production worker but had no record of assignment to the 2,4,5-T
area. Case 7 is the father of Case 6 and was a production worker at
the same facility for 29 years. His work history showed no record of
assignment to the 2,4,5-T area, although he did work for 11 days

�192 Fingerbut etal.

following hire in 1951 in a pentachlorophenol area. Pentachlorophenol is contaminated with hexa-, hepta- and octachlorinated isomers
of dioxin, but does not contain 2,3,7,8-TCDD. These last three
individuals illustrate some of the difficulties encountered in
attempting to verify exposure in chemical workers. In general,
production workers qlo have records of regular assignment to specific
departments within &lt;|:omplex chemical manufacturing plants, although
their records do not show temporary changes in assignments. However,
maintenance workers such as Case 5 often work throughout an entire
facility and never have recorded assignments in specific departments
From our examination of their work histories we concluded that these
three workers did not meet our stringent criterion of exposure,
they had no recordsjof assignment to a 2,4,5-T or trichlorophenol
process. However, absence of such documentation does not eliminate
i
'
the possibility than they were exposed to dioxin contaminated
products during their routine activities.

PATHOLOGY DATA FOR THE SEVEN CASES

Table 4 summarizes clinical observations obtained from company
medical records, hospital records, and pathology reports for the
seven individuals. All cases were reported to have soft tissue
sarcomas.

Table 4.

Medical information for the seven U.S.

Case
Number

Tumor

1

Malignant fibrous
histiocytoma

Onset of
Tumor

workers.

Age at
Onset

Chloracne

1978

58

yes
yes

Adenocarcinoma,
bladder
Liposarcoma,
rectum

1958

34

1972

49

3

Fibrosarcoma

1973

52

dermatitis

4

Malignant fibrous
histiocytoma

1979

58

yes

Neurogenic sarcoma

1980

57

no

2

�Review of Reported Soft Tissue Sarcoma Cases 193

Table 4.

Continued.

Case
Number

Tumor

6

Fibrosarcomatous
mesothelioma

1980

33

no

Liposarcoma

1980

53

no

7

Onset of
Tumor

Age at
Onset

Chloracne

Cases 1, 2, and 4 had records of diagnosed chloracne. Case 3 had
dermatitis of the face and neck while assigned to the trichlorophenol
building during a period when 49 trichlorophenol workers developed
chloracne (8). But no chloracne was found in the records of Cases 5,
6, and .7.
V

Table 5 presents data on the latency of the tumors (time from
first exposure to diagnosis of the tumor) for each individual.

Table 5.

Latency of tumors for seven U.S. workers.

Case
Number

First Assignment
to 2,4,5-T or TCP
Department

STS Tumor
Onset

Latency*
(Years)

Age
at
Onset

1

1949

1978

29

58

2

1950

1971

21

49

3

1964

1973

9

52

4

1951

1979

28

58

5

never

1980

N.A.**

57

6

never

1980

N.A.

33

7

never

1980

N.A.

53

* Time from first exposure to onset of tumor.
** Not applicable.

Adequate latency for development of cancer was experienced by the
four individuals with records of assignment to trichlorophenol or
2,4,5-T departments (Cases 1 to 4). Since no records of specific
departmental assignment to TCP or 2,4,5-T departments exist for the

�194 Fingertmt et al.

remaining three individuals, latency cannot be assigned for exposure
to 2,3,7,8-TCDD,

DEATH CERTIFICATE DATA VS. PATHOLOGIC DIAGNOSES
AND ICD CODING CATEGORIES

Table 6 compares the diagnoses made by the attending pathologists
with the information on the death certificates.

Table 6. Comparison of death certificate data with original
pathologic diagnoses for the seven U.S. workers.
1

Case
Number

Death
Certificate

1

Malignant fibrous
histiocytoma

Malignant fibrous
histiocytoma

2

Liposarcoma

Liposarcoma

3

Pibrosarcoma

Fibrosarcoma

4

Malignant fibrous
histiocytoma

Malignant fibrous
histiocytoma

5

Carcinomatosis

Myxoid neurogenic
sarcoma

Metastatic
mesothelioma

Fibrosarcoma consistent
with fibrosarcomatous
mesothelioma

N.A.*

Myxoid liposarcoma

7
* Not applicable.

Original
Pathology

"

Individual is alive,

Of the six deceased cases, all of whom had hospital diagnoses of soft
tissue sarcoma, only four had soft tissue sarcoma noted on their
death certificates (Cases 1 to 4). A similar finding was noted in a
study of the accuracy of death certificates conducted by Percy et al.
in 1981 (13). They reviewed almost 50,000 hospital diagnoses and
death certificates and found that of 252 soft tissue sarcomas
diagnosed in hospital records, only 142 death certificates for those
individuals (55%) reported the soft tissue sarcomas. Hence using

�Review of Reported Soft Tissue Sarcoma Cases

195

death certificates as the primary source of cases may lead to
underascertainment of cases.
We found in our review that all four death certificates with
notations of soft tissue sarcoma (Cases 1 to 4) belonged to persons
who had diagnoses of soft tissue sarcoma made by the attending
pathologists. In contrast, Percy (13) found in her large study that
only 56% of death certificates with notation of soft tissue sarcoma
were supported by hospital records with the diagnoses of soft tissue
sarcoma. Hence using death certificates as the primary source of
cases and not confirming hospital or pathologic information may
lead to overascertainment. Researchers conducting epidemiologic
studies should be fully aware of possible underascertainment or
overascertainment.
Table 7 illustrates another issue in the use of death
certificate data: consistency in classification by nosologists, the
experts who code cause of death from death certificates according to
the rules of the International Classification of Disease System
(14).

Table 7. Comparison of death certificate information and nosologic
coding of the information.
Case
Number
1

ICD Category*
Original
Honchar
Publication**
Review***

Death
Certificate
Malignant fibrous
histiocytoma

173.9

171

*

World Health Organization, Manual of the International
Statistical Classification Diseases, injuries and Causes of
Death, Geneva. Ninth Revision, 1975.

**

Zack, J.A. and Suskind, R.S.
1980; 22:11-14.

Journal of Occupational Medicine

*** Honchar, P.A. and Halperin, W.E.

Lancet 1981; i:26S-269.

Case 1 was reported in the original publication as having a malignant
fibrous histiocytoma, which was coded in ICD Category 173.9, "Other
malignant neoplasm of skin, site unspecified". Honchar indicated in

�196 Rngerhutfital.

her review (3) that the choice of her nosologist was ICD 171,
"Malignant neoplasm of connective and other soft tissue".
Misclassification in ICD categories could introduce significant
error. The data in Table 7 suggest that coding by more than one
trained nosologist may be desirable.
Another important issue of classification not addressed by this
review has serious implications for studies of soft tissue sarcoma.
The international Classification of Disease System is a site-oriented
classification scheme. Therefore, sarcomas that develop in the
parenchymatoas organs such as the uterus or stomach are coded into
the ICD categories for the organ site. Only soft tissue sarcomas of
the supporting tissue of the body not specified as arising in organs
are coded in the ICD Category 171. It is possible, therefore, to
select soft tissue sarcoma cases for case control studies in two
ways. For the early Swedish studies (1,2) cases were selected by
their histopathologic characteristics; approximately 60% of these
cases are coded in categories other than ICD 171 (15). A current
case control study in New Zealand (16) includes only soft tissue
sarcoma cases coded as ICD 171. Such differences in study design
must be recognized when evaluating results. The problem presented by
the ICD dual classification scheme is slightly different for cohort
mortality studies. It is possible to compare sarcomas coded as ICD
171 with those arising in the national population; however, we are
not aware of population rates for soft tissue sarcoma coded into
other ICD categories.

ORIGINAL REPORT DATA VS. NEW REVIEW DATA

Table 8 compares the original pathologic diagnoses for the seven
individuals with the diagnoses selected in two independent pathologic
reviews of tissue specimens.

�Review of Reported Soft Tissue Sarcoma Cases 197

Table 8. Comparison of the original pathology reports with reports
of two reviewers.*
Original
Pathology

Case
Number

Review
#1

Review
#2

Malignant fibrous
histiocytoma

Malignant fibrous
histiocytoma

Malignant fibrous
histiocytoma

Invasive pleomorphic
liposarcoma

Poorly differentiated
carcinoma

Carcinoma, poorly
differentiated

Fibrosarcoma

Clear cell carcinoma
spindle cell
with spindling, renal renal carcinoma

4

Malignant fibrous
histiocytoma

Malignant fibrous
histiocytoma

Malignant
'
schwannoma

5

Myxoid neurogenic
sarcoma

Leiomyosarcoma

Malignant fibroh ist iocy tomcux

Malignant
schwannoma

Malignant
schwannoma

6

Fibrosarcoma
Liposarcoma

Myxoid liposarcoma

Myxoid
. liposarcoma

* The tissue specimens were reviewed by one of the authors (W.O.R.)
and also by Franz M. Enzinger, M.D. and Sharon M. Weiss, M.D. of the
Armed Forces Institute of Pathology, Washington, DC.

Although all seven individuals received diagnoses of soft tissue
sarcoma by the original pathologists, only five of the cases were
diagnosed as soft tissue sarcoma in each of the two reviews.

In both

reviews Cases 2 and 3 were identified as carcinomas rather than
sarcomas.

These results indicate that review of tissue specimens by

pathologists with expertise in diagnosing soft tissue sarcomas is
necessary

for epidemiologic studies.

A difficult problem arises for

cohort mortality studies because there is no comparison group for
cases ascertained by expert pathologists.

Rates of disease commonly

used for comparison are those taken from compilations of population
rates based on information from death certificates.
The adequacy of diagnosis of histological subtypes of soft tissue
sarcoma is another issue raised by the data in Table 8. Although the
original pathologists and the reviewers all agreed that five
individuals had soft tissue sarcomas, they agreed on the histological
subtype for only two individuals, Cases 1 and 7.

Even the expert

�198 Ftagerhutetal.

reviewers disagreed on subtype diagnoses for Cases 4 and 5. Because
of the difficulties involved in diagnosing the histological subtypes,
particularly when only a limited amount of tissue is available for
review, we recommend that epidemiologic studies continue to focus on
the outcome soft tissue sarcoma, and assess the distribution of
subtypes only cautiously and with a recognition of the limitations
involved.
The next two tables summarize the exposure histories and the
pathologic findings and compare them to the information published in
the original reports. Table 9 presents data for the four production
workers identified in company studies (6-10) as, 2,4,5-T/ or
&gt;•
trichlorophenol-exposed workers.
r
•X

Table 9. Comparison of original reports with results from this
review for production workers identified by companies as TCP* or
2,4,5-T workers.
Case
Number

Reported Exposure
This
Original
Review
Reoort

Cause of death
Original
This
Report
Review

1

TCP

TCP

STS

STS

2

2,4,5-T

2,4,5-T

STS

Carcinoma

3

TCP

TCP

STS

Carcinoma

4

TCP

TCP

STS

STS

* Terms: TCP, trichlorophenol; 2,4,5-T, 2,4,5-trichlorophenoxyacetic
acid; STS, soft tissue sarcoma.

The reported exposures were confirmed by documentation that the four
individuals had been assigned to 2,4,5-T or TCP processes. All had
been reported as having soft tissue sarcomas, but we report that the
two expert pathologists confirm that only two individuals (Cases 1
and 4) had soft tissue sarcomas. Both of these individuals worked in
trichlorophenol processes, had diagnosed chloracne, and were present
during incidents of unusual operating conditions with probable
exposure to 2,3,7,8-TCDD. The histological subtype of malignant
fibrous histiocytona was selected by all three pathologists for Case
1. Case 4 also received a diagnosis of malignant fibrous

�Bevlew of Reported Soft Tissue Sarcoma Cases

199

histiocytoma from the original pathologist and one reviewer. The
second reviewer identified the subtype as a neurogenic schwannoma.
Table 10 presents the same comparison for the three individuals
originally described in case reports by physicians (11,12).

Table 10. Comparison of original reports with results from this
review for production workers originally described as case reports
by physicians.
Case
Number

Reported Exposure
Original
This
Report
Review

Pathologic Diagnosis
Original
This
/
Report
Review

5

Possibly
2,4,5-T,*
TCP

None

STS

STS

6

Possibly
chlorophenols

None

STS

STS

7

Possibly
chlorophenols

PCP

STS

STS

* Terms: 2,4,5-T, 2,4,5-trichlorophenoxyacetic acid; TCP,
trichlorophenol; PCP, pentachlorophenol; STS, soft tissue sarcoma.

Review of the tissue specimens for all three workers were confirmed
that they had soft tissue sarcomas. Examination of the work history
records of the individuals did not document assignment to 2,4,5-T or
trichlorophenol departments. However, Case 7 worked briefly upon
hire in a pentachlorophenol department.

CONCLUSION
Swedish research (1,2) has drawn attention to the issue of soft
tissue sarcoma and dioxin exposure. While each of the original four
U.S. studies (6-9) reported non-positive findings, a reanalysis (3)
and further reports (10,11) strengthened the suspicion that an
association might exist. Honchar (3) and Cook (10) called for
detailed examination of the data. We present the detailed assessment
of exposure history and pathologic diagnosis and report that of the
four soft tissue sarcoma cases identified by death certificates among

�200 Fingerhut et al.

the TCP and 2,4,5-T workers, two are confirmed following pathologic
review of tissues as soft tissue sarcoma.

It Is not possible to use

our data to draw a definitive conclusion regarding the suspected
association because we are not aware of any population rates for soft
tissue sarcoma based upon pathologic review of tissue specimens.
Cases 5, 6 and 7 were originally described in.the literature as
individual case reports. All three are confirmed as cases of soft
tissue sarcoma.

Our review of their work histories did not find any

record of assignment to 2,4,5-T or trichlorophenol departments,
although Case 7 worked briefly in a pentachlorogfhenol department/ a
product contaminated with isomers of dioxin considered to be less
toxic than 2,3,7,8-TCDD. Although these workers do not meet our ,
stringent criterion of exposure by virtue of assignment 'to a 2,4,5-T
or TCP department, we cannot exclude the possibility that they had
undocumented contact with 2,4,5-T or TCP.
This review examines the complexities in evaluating the dioxin
exposure of individuals and the pathologic diagnoses of soft tissue
sarcoma. It emphasizes the need for carefully-designed large
epidemiologic studies to adequately assess whether there is an
association of soft tissue sarcoma with exposure to dioxincontaminated products.

We have shown that the use of the death

certificate, even with the original pathologic diagnosis may lead to
overascertainment or underascertainment of cases of soft tissue
sarcoma.

Finally, we reassert that further research, particularly

the completion of National Institute for Occupational Safety and
Health studies based upon approximately 6,000 U.S. workers, is
necessary to confirm or refute the association first suggested in the
Swedish studies.

ABSTRACT
We have reviewed medical and exposure records and pathology
specimens of seven U.S. chemical workers reported in the.literature
to be cases of soft tissue sarcoma (STS) and to have had dioxin
exposure. The cases were of interest because two Swedish studies
demonstrated a strong association between STS and dioxin exposure.

�Review of Reported Soft Tissue Sarcoma Cases 201

Four U.S. workers from four small mortality cohorts had been reported
to have died of soft tissue sarcoma. We found that these individuals
had employment records of assignment to production of TCP and 2,4,5-T
which are contaminated with the most toxic dioxin isomer,
2,3,7,8-tetrachlorodibenzo-p-dioxin (2,3 ,1,8-TCDD), but pathologic
review of their tissue indicates that only two are cases of soft
tissue sarcoma. Three additional individuals had been described by
physicians as case reports. They are confirmed as cases of soft
tissue sarcoma, but we did not find any record of assignment to these
production departments. One person worked briefly in the production
of pentachlorophenol, which is contaminated with other isomers of.
i
'
dioxin. We suggest that identification of cases of STS through
either .death certificates alone or through pathology records can lead
to errors of ascertainment. We reassert that further research,
particularly the completion of studies by the National Institute for
Occupational Safety and Health based upon approximately 6,000 U.S.
workers, is necessary to confirm or refute the association first
suggested in the Swedish studies.

�202 Fingerhut et al.

REFERENCES
1. Hardell, L. and Sandstrom, A.

Case-Control Study:

Soft-Tissue

Sarcomas and Exposure to Phenoxyacetic Acids or Chlorophenols.
British Journal of Cancer 1979; 39:711-717.
2. Eriksson, FT., Berg, N., Hardell, L., Moller, T. and
Alexson, o.

Soft-Tissue Sarcomas and Exposure to Chemical

Substances:

A Case-Referent Study.

British Journal of

Industrial Medicine 1981; 38:27-33.
3. Honchar, P.A., and Halperin, W.E. 2,4 ,5-Trichloropl^enol and £oft
Tissue Sarcoma. Lancet 1981; i:268-269.
4. Suit, H.D. Sarcoma of Soft Tissue.
Clinicians 1978; 28:284-295.
5. Russell, W.o. et al.

CA-A Cancer Journal for-

A Clinical and Pathological Staging System

for Soft Tissue Sarcomas.

Cancer 1977; 40:1562-1570.

6. Zack, J.A. and Suskind, R.S. The Mortality Experience of Workers
Exposed to Tetrachlorodibenzodioxin in a Trichlorophenol
Process,

journal of Occupational Medicine 1980; 22:11-14.

7. ott, M.G., Holder, B.B. and Olson, R.D.

A Mortality Analysis of

Employees Engaged in the Manufacture of
2,4,5-Trichlorophenoxyacetic Acid. Journal of Occupational
Medicine 1980; 22:47-50.
8. Cook, R.R., Townsend, J.C. and Ott, M.G. Mortality Experience
of Employees Exposed to 2,3,7,8-Tetrachlorodibenzo-p-dioxin
(TCDD).

Journal of Occupational Medicine 1980; 22:530-532.

9. Zack., J.A. and Gaffey, W.R. A Mortality Study of Workers
Employed at The Monsanto Company plant in Nitro, West Virginia.
Environmental Science Research 1983; 26:575-591.

�Review of Reported Soft Tissue Sarcoma Cases

10. Cook, R.R.

Dioxin, Chloracne and Soft Tissue Sarcoma.

203

Lancet

1981; 1:618-619.
11. Moses, M. and Selikoff, I.J.

Soft Tissue Sarcomas, Phenoxy

Herbicides and Chlorinated Phenols.

Lancet 1981; i:1370.

12. Johnson, P.E., Kugler, N.A. and Brown, s.M.
and Chlorinated Phenols.

Soft Tissue Sarcomas

Lancet 1981; i:40.

13. Percy, C., Stanek, E. and Gloeckler, L.

Accuracy of Cancer Death

Certificates and Its Effect on Cancer Mortality Statistics.
American Journal of Public Health 1981; 71:242-250'.
14. World Health Organization, Manual of the International Statistical
_ .
„

__

_ B ^ « _ ^ «
_ ~ w ^ _ B v

w ^
_ ^

___

—.^^—^^^ff^—i-

Classification of Diseases, Injuries and Causes of Death (1975)
Ninth Revision.

Geneva, 1977.

15. Summarized from Exhibit 1299, prepared by L. Hardell for the
U.S. Environmental Protection Agency, October 24, 1979.
16. Smith, A.H. et al.

Do Agricultural Chemicals Cause Soft Tissue

Sarcoma?

initial Findings of a Case Control Study in New

Zealand.

Community Health Studies 1982; 6:114-119.

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            <description>A related resource from which the described resource is derived</description>
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                <text>BioScience</text>
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            <description>A point or period of time associated with an event in the lifecycle of the resource</description>
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                <text>1978-10-01</text>
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                <text>Biology Briefs: 2,4,5-T Called Safe</text>
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            <name>Subject</name>
            <description>The topic of the resource</description>
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                <text>herbicide regulation</text>
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                <text>Great Britain</text>
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