Document 3NaK4QzGMwVze19MrXZqKMgqa
FILE NAME: Smoking (SMOK) DATE: 1956 Nov
DOC#: S M O K O ll
DO CUM ENT DESCRIPTION: Journal Article - Environmental Causes of Cancer of the Lung Other Than Tobacco Smoke
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i nt er im Session --Seattle, W a s h i n g t o n November 25-26, 1956
VOLUME XXX
NUMBER 2
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OFFICIAI. PUBLICATION
A GUST 1.358
PUBLICATION OFFICE, CHICAGO, ILLINOIS EXECUTIVE OFFICE, 112 EAST CHESTNUT STIC ET, CHICAGO l , ILLINOIS
E n tered o s S econd C lass Idg.Cor a t th e P o stciiice a t C h icag o , Illinois C op y rig h t, li)56, by to ...merican College of C hest P hysicians
: ;; i :
Environmental Causes of Cancer of the Lung Other Than Tobacco Smoke
W. C. H U E P E R , M.D.
Bethesda, Maryland
The recognized or strongly suspected environmental causes of cancer of the respiratory system form an important segment of the environmental carcinogenic spectrum.
1. With one exception all so far known exogenous respiratory carcinogens wore discovered during the last 25 years (Table I), that is, during the period in which a remarkable and progressive rise in the number and frequency of cancers of the lung was observed in most industrialized countries (Fig. 1).
2. The various respiratory carcinogens are more or less well defined chemical or physical agents and/or are associated with distinct occupa tional activities engaged in by circumscribed workers groups (Table If).
3. The clinical, epidemiologic, pathologic and experimental observations related to these agents all of which act through the respiratory route
TABLE I
OCCUPATIONAL RESPIRATORY CARCINOGENS AND CANCERS RECORDED DURING PA S T 75 Y E A R S; T H E I R CAUSES, S IT E S AND N U M BERS
Agent
Arsenic Asbestos Chromates Nickel
Coal Tar Petroleum
Oils Isopropyl Oil
Radioactive Chemicals
o k e of Cancer
bung
Lung
Lung'
Lung Notes and
Nasal Sinus
Lung
Lung and Larynx
Lung Larynx Nasal Sinus
Lung
Nasal Sinus
TOTAL
Discovered
1930 193d 1932 1932
1936 1936
1946
1879 1931
Num'iiT of i'cv-onled Cases
Cthor
U.K.A. Cou alivies
Total
7
:l 6
23
20
92
112
75
(5
140
0
84
84
0
51
51
0
53
53
7
33
40
1
0
4
0
6
0
0
625
3
0
123 1,019
1 4 6
625
3
1,142
National Cancer Institute; National Institutes of Health; Public Health Service; IT. S. D epartm ent of Health, Education and Welfare.
Presented at a Symposium, 21st Annual Meeting, American College of Chest Phy sicians, Atlantic City, New .Jersey, Ju n e 2, 1955.
;
142
W. C. H E P E E
August, ion*;
i
ri'oresen o r cancel
sw-Tie occ pu'.m-ana
carcinoji
pdotren
D c-spi
on reco: observe' cvidcnc-
.C
TiVde
I' x wl'S
TABLE II--SPECIFIC
Alien !. Arumm
C hrominm
Nickel _ Iron Radioactive
Substances Isopropyl Oil Coal T a r Fuine;.
Pen oiw m
OH .s
WORKER GROUPS WITH SPECIFIC RESPIRATORY CANCER HAZARDS
______________ W o r k e r G r o u p s
Manufacturers, handlers, and users of arsenical insecticides; arsenic smelter workers; taxidermists; sheep dip worker- ; copper smelter workers
Chromate m a nufa cture rs including p la : maintenance workers; chrome pigment handlers
Nickel-coppor matte refinery workers
Iron ore (hematite) miners ?
Radioactive ore (pitchblende) miners; miners of nonradioactive ores working in radioactive mines
Isopropyl alcohol manufacturers
Coke oven operators; gas house retort workers
Paralbn presses; male wo. sers and drill..' ;
: me ; metal lathe
Arsenic Asbesti Frylli
.;;- v n in
Nickel
-.re ri
Radio;
Sub
Isoprt oil
Polve Hydr
soo
Petn Deri-
oil Caso Diesi Ex h; C asc
Eoo
voi. x x x
ENVIRONMENTAL CAUSES OF CANCER
143
represent the only reliable factual evidence available on the causation of cancers in different parts of f l u respiratory tract (Table III). Although some occupational, medicinal and experimental observations suggest that pnimonary carcinogenesis may ensue after a non-respiratory contact with carcinogens, there exists no valid evidence incriminating hereditary or endogenous factors as primary causal agents of Iranian lung1cancer.
Despite the fact that the total number of occupational pulmonary cancers on record is relatively small, the comparatively high cancer attack rates observed among the different worker groups studied provide weighty evidence in favor of actual causal associations between an exposure to the specific agents and the subsequent development of respiratory cancers (Table IV). The reported number oil cases of occupational respiratory cancers doubtlessly represent only a fraction of the total number which
TABLE III ENVIRONMENTAL LUNG CANCER SCORE BOARD
Arsenic Asbestos
Beryllium Chromni m
Nickel
i ron Radioactive
Substances
Isoproi: vl oil
Poiyoyulic Kyuroc arbons
coal t a r , binii, pitch
Petroleum Derivatives
oil mist Gasoline Diesel engine Exhaust
Gasoline Epoxides
Site of Cancer
c
- UiJ
tv
C
1 H
a U 3
X
b
.S 'H.
Is PZ o Skin
X
X X
Population Affected
Type of Evidence
B
e
! _i 5
a li
l
3 ^U
oS oS u5
1
o
X ?X
X ?X
?
X
X ?X
(J
?
11 1
li X M
X X
?
X
X
X
X
X
X
X
Skin
X
X Bor e
X
X
X
Hem at. tissue
Conn, tissue
XX X
X
X
XX
XX
X
Skin Skin
X ?X ,,
X
X
X ? ?
X ?
Experimental Evidence
e
Other organs
Bone Bone Conn, tissue Bone C o n n , tissue
Bon <3 Conn, tissue Hemal,
tissue, etc.
Skin Conn, tissue,
etc.
Sk, n Conn, tissue
Skin
Skin
144
W. C. H U E P E R
August, 1956
TABLE IV RESPIRATORY CANCER ATTACK RATES BY
ENVIRONMENTAL CARCINOGENS
Affents
Aromatic hydrocarbons: Coal ta r iuraes Petroleum oils
Carbon and silicon poly mors:
Isopropyl oil Asbestos
Metals : Arsenic Chromates Nickel
Ionizing- radiation : Radioactive area
Sites of
Cancers
Lung' Lung;
Paranasal sinuses
Larynx Lung
incidence in
Poymiation at Risk
500:100,000 2000:100,000
10:100
............
Lung
Lung
Marcs
)
1'n r a u a s a l sinuses
yf.
Lung
J
............
329:100,000 574:100,000
Lung'
............
Attack Rates
Percent Morbidity
Mortality
of All
Rate
Rate
C a n c e r ---------------------------------------------
Deaths
P e r 100,000
45% 55%
134.5 ........ (normal
6.5) .........................
........
13.2-20% asbes-
t(o0s.i8s-2a.4u%topsied
normal)
......................... (42x
normal)
(2 On ........ normal)
145.7 males (10.9 normal)
146-338
........ ........
(50-80% of all deaths)
occurred. Some of the lung cancers were certainly mistaken for tubercu losis, pulmonary abscesses, silicosis, asbestosis, siderosis or other forms of chronic pulmonary disease. Another portion of these tumors was recog nized as of occupational origin but not made a matter of public record, while a third fraction developed in workers many years after they had left the hazardous occupation and when the causal relations to their previously sustained exposum,-! had been obscured by the passage of time (Table V. Page 156).
The almost exclusive occurrence of occupational king cancers in male
TABLE VI LATENT PERIODS OF ENVIRONMENTAL RESPIRATORY CANCERS
Agent
Asbestos Chrom sites Nickel Tar fumes Isopropyl oil Ionizing radio Lon
Average Latent Period
Lunff
18 15 22 16
....
25 - 35
Ranjre of Latent Period
15 - 48
,5-47 6-30 9-23
....
7 - 50
Nares & Naiad Sinuses
Average Latent .Period
Rantu of
Latent
Period
....
....
....
ii
3-26
....
10
6-16
25
19 - 32
jlKik
ri*
> M*j
f
'f A S A A 8!lfIL:k'frM:
, , C
i
'* sw __
,r' ?;-v
i i fitos
' *r *>-'-1
,
' * ' * `~
` siiV.
voi. x x x
ENVIRONMENTAL CAUSES OF CANCER
145
workers is in good agreement with the fact th at males are predominantly employed in occupations having lung cancer hazards. One oi; the known exceptions in this respect are the lung cancers found in female ashes n workers. The male-female ratio of lung cancers among workers who bestosis cancer of the lung is for this reason at the low level of 2.3:1, indicating that with an equalization of the degree of exposure there
FIGURE 2 (Reproduced by permission of the British Empire Cancer Campaign.)
|
rKgpi-T-w "
1.
W. C. H U E P E
Aujrusl, 19r,i;
HISTOLOGIC TYPE
TARLI!I VII OF O CC UPATIONAL RE SPI IIA T 0 R Y CANCERS
Agent
T:u' Fumes Nickel Chromium Asbestos Radioactive
Gases & Dust Nickel
Radioactive iases & Dust
Isopropyl ttn
Organ
Lung Lung Luna1 iamg
au na Nwes and
Nasal Sinus Xaves and
Nasal Sinus iSares and
Nasal Sinus
Squamous Col Carcinoma With or Without.
C o r n i . i'.co' i o n
'flou ml Cull o r A n a p l a s t i c or Cat Cell P olym orphic
Cardncwia Carcinoma
Adeno carcinoma
o
2
4
3
2
11
3
2
6
14
!)
7
1
3
6
1
OO I s J
4
VP. XXX
o; cryp etio'ogx
Occui like othi The rei ;rg und a niultic asbestos PCmon with sid '0 canee tional .
ir. m utui
s;
]
s.arre tu have- an
JCVV C.t
n-p'-' a s 't
develops a tendency toward an equalization of liability to lung cancer.
w, -, ia<
Several types of industrial lung cancers, such as those caused by radio
iT-Ooiain
;
active substances, chrome pigments, and coal ta r fumes, show a definite
Since lb
shift into younger age groups than those observed in cancers of the lung
bn ' sno
o r a s i , whit* m i s s , m v m m t s , 19m
( eowafo a. lew]
4 M jxuteA fiath Sates par 100,000, ISiifcs 8*1 Pepatati
Whiff
oo OQ o (
U?
<[ Uoi
s [1 sc
FIGURE 3
Voi. XXX
ENVIRONMENTA i.. CAUSES OF CANCER
147
of cryptogenetic origin, but characteristic of cancers of occupational etiology.
Occupational respiratory cancers moreover have long latent periods litre other cancers of known industrial or environmental origin (Table V I). The relatively massive exposure to carcinogens not infrequently prevail ing under occupational conditions may perhaps account for the fact that a multicentric genesis of several types of occupational lung cancer, i.e. a/oestosis cancer and radioactive cancer, is not infrequently observed.
Pulmonary fibrosis associated with silicosis in radioactive ore minces or mih siderosis in hematite miners seems to decrease the individual liability m cancerous developments in the lungs thus affected. While many occupa. onal lung cancers are of .squamous cell type, many others display an ir,mature cr round cell type or exhibit glandular structures. In fact, several different histologic types of cancers may occasionally occur in the same tumor mass (Table V II). Thus, no special histologic type seems to have any fixed relation to any specific causal factor. Occupational respira tory cancers critically studied exhibit a general symptomatic pattern common to and characteristic of environmental cancers.
4. Many of the agents incriminated in occupational respiratory carcino genesis, such as arsenicals, radioactive substances, coal tar and petroleum oils, had previously been known as important causes of occupational and medicinal cancers of the skin developing usually upon cutaneous exposure. Since the mucosa of the respiratory tract may be considered as an inverted, but specialized entodermal extension of the ectodermal outer lining of the
RESPIRATORY SYSTEM CANCER DEATH RATES BY AGE AND SEX White Population,Urban States and Rural States,'United S tate s, 1349
Sic.tr s with less than 4 0 % urban papulation colled rural, and states with mere then 0% urbe;-
popihation called urban. Rural state* V t > i \ SO, Mi$5nAr^N.G^5.G,W.Vu.1Ky. Urban stater: R.l, Mass,NX, N.J.,Calif,D.C.
SO U R C E1 V i t a l S ta tis tic s of the Um 'cd S ta le s , 194;
STATISTICAL RESEARCH S Z G T m
19 5 0 P o p u io tio n Censu3 o f th e U nited S tates
AMERICAN CANCER
9*53
FIGURE 4
148
W. C. H U E P E R
August,
TABLE Vili
THE TIME TABLE OF DISCOVERIES OF OCCUPATIONAL CANCERS
N am e of Aironi
Dnto
Discoveror
Organs yviTootod
Nature of Exposure
Chemicals: Organic Soot
1775 Pott
Skin (Scrotum) Occupational
Coal T ar (Lignite)
1.87(j Volkmann
Skin
Occupational
Con: T ar (Bituminous) 1892 Dutlin
Skin
Occupational
Coal T ar (Anthracite) 1910 Zweig
Skin
Occupational
Coal Tar (Fumes)
IffilG ICaushata
Lung
Occupational
Creosote Oil
1920 O'Donovan
Skin
Occupational
Anthracene Oil
1908 Oliver
SlU;l
Occupational
Paraffin Oil
Bell
Skin
(Shale Oil)
1870
Occupational
Petroleum Still Coke
1890 Derville and
Skin
G uermongrez
Occupational
Petroleum Paraffin Oil 1910 Sehamhorg
Skin
Occupational
Ptrole u)a i a.:1uie: tia g Oil
Heller litio
Skin
Occupational
Shale Lubricating Oil 1910 Wiisbn
Sim
Occupational
Benzol
1928 Deimv and Borgmano
Blood Form ing Tissues
Occupational
Aromatic Amines (live Intermediates)
Rohn. 1895
Bladder, Ureter Kidney
Occupational
Isopropyl Oil Mustard (las Chemicals : Inorganic Arsenic
Asbestos Chromates Nickel Physical Agents : Ultraviolet Radiation Roentgen-Radiation
Radioactive Substances
1940 1953
Haie and ITueper
Yamaha, Hirose & Miyanrishi
Nasal Sinuses, Larynx Lung
Lung
Occupational Occupational
1822 1887 1900
1935
1935
1 932
Paris Hutchinson Saupe
Lynch & Smith
Pfeil
Grer.feil
Skin Skin Lung
Lung
Lung
Nasal Cavity & Sinuses, Lung
Occupational Medicinal Occupational
Occupational
Occupational
Occupational
1894 Unna
1902 1906 .1911
1922 1879 1923 1928
Frieden Wyes Von Jagic,
Scinvartz & von Siebenrock Beck
Haerting & Hesse MeNcal, Ward
& Willis Loewy
1931 M ar 'and
Sk ;n
Skin Skin. Blood Form ing
Tissues
Bone Lung
Skin
Blood Forming; Tissues
Bone
Occupational Environmental Occupational Medicinal Occupational
Medicinal Occupational
Occupational
Occupational
Occupational
Vf'. XXX
LI
b or] y, .or y
cmopg oyoy a "on or sin
y 'oup
: wie hove s fo r di
refii ho we .ons fact b iny v, prodi)
Ita
The ating
V,:!. XXX
ENVIRONMENTAL CAUSES OF CANCER.
149
LUNG
\B LE IX
CANCER DEATH R t f ' PER 1,000 D EATH S OF ALL FOR SEVEN (7) INDUSTRIAL GROUPS IN OHIO, 1947 AMONG 5,-309 MALE CANCER DEATH S (MANCUSO)
CAUSES
Industry
Iron and steel Transportation Agriculture Rubber and plastics Stone, clay, glass Non-ferrous metal Mining and quarrying
TOTAL
Respiratory Cancer
2.18 2.91 0.82 2.34 0.63 3.22 1.53 1.76
body, the development of cancers from these structures following a respira
tory contact with the mentioned exogenous carcinogens appears to be a phenomenon in line with previous experience (Table V III).
5. Although the existing factual data on occupational respiratory car
cinogens are at present limited to relatively restricted worker groups and
apply to a comparatively small number of cancers of the respiratory organs,
a considerable amount of circumstantial evidence suggests that identical or similar respiratory cancer hazards may prevail for much larger worker
groups having occupational contacts with the known carcinogens. Epidemi
ologic studies on lung cancer death rates made in this country and Europe
rave shown the existence of marked variations in the liability to lung cancer
for different large occupational groups (Tunic I X ) . Some of them revealed
- definitely excessive frequency of pulmonary cancer (Table X, XI, and XII) as well as of cutaneous cancer. The possible significance of these observa tions in perms of occupational lung cancer hazards is evident from the fact that there are over 5,000,000 employed in American industries sustain
ing various degrees of exposure to combustion, distillation a n d cracking
products of coal, petroleum and other carbonaceous matter (soot, carbon
(Continued on, ,
' .79)
TABLE X
LUNG CANCER FREQUENCY AMONG OPERATING AND NO N-O PERATiXG RAILROAD W ORKERS
Railroad
A B
Period
1940 - 1950 1939 - 1949
Total No. Lung Cancers
29
104
Lun g ' C hikumv Oporaljnp; HR
Workers
No. Per Cent
24 83
59 57
Lunc; Cancers N o n - O p e r a tin}?
RR Workers
No. Per Cent
5 17
15 14
X-uofc C a n c e r s Undetermined
RR Workers No. Per Cent
30 29
There were four timer as many non-operating RR workers in one company as oper ating ones, who represented train personnel, round house and track workers.
150
W. C. H U E P E R
August, J.95C
TABLE XI OCCUPATIONAL GROUPS W ITH AN EXCESSIVE LUNG CANCER INCIDENCE
Occupational Group
M( tal workers, welders, nders and polishers,
. i e makers, tool a F die foundry vu i'uvrK,
in- al moulders, lathe workers, etc. (;igar run mrfacturers an c! iolneeonir is
Engineers, mechanics, machinists, plumbers, etc.
Painters, and decorators
Tar workers, road workers, asphalters, paviours, stokers, patent fuel workers, furnace men, foundry laborers, rollers, etc.
Potential Kespiratory Carcinogens
Investigator
Metal dust, lubricating oil mist
Borst; Kennaway and Kennaway; Turner and Grace; Mueller; Dublin and Vane, Wynder and Graham; McLaughlin; Brealow et al.
Tobacco dust, insecticides, soot
S ey farth ; Borst; Kenna-
way; Engcr; Veraiuya, L rinkmarm
Metal dust, soot, lubricating oil
BECC* 1944 & 1952:
Gillespie; Turner and Grace; Mueller; Wynder and Graham
Meta! pigments, coal ta r dyes, carbon black, asphalt paints, solvents, vehicles
(lacquers, resins synthetic phr sics)
BECC 1944; Mueller; Dublin and Vane; Fulton; Wynder and Graham
Tar and pilch fumes and dust, soot
Kennaway and Kennaway; F u lto n ; BECC 1952 Regis-
trar-General (1938) ; McLaughlin
*Report of the British Empire Cancer Campaign.
TABLE XII
LUNG CANCER MORTALITY IN SEVERAL COUNTIES OP .MONTANA 1947-1948 (LULL AND WALLACE)
County and
Total
Population 11)40
Major Industry
Deer Lodge Copper 13,627 Smelting
Silver Bow Copper 58,207 Mining
Cascade 41,499
Copper Mining
Smelting
Gallatin 18,269
Agriculture
Number Lung Cancers
Male Female
21 0
....
....
27 2
....
....
20
5
....
1
0
....
Tot.il
21 29 25
t
Total Cancer deaths
98
Per Cent Lung Cancer
Male
Female
80.8
0.0
259
22.6 1.5
....
299
12.7 3.5
Annual Lung Cancer Death . K ate p er 100,000
Male
Female
145.7
0
* --
....
48.6
3.9
....
....
46.3 12.3
8!
3.0
0.0
5.2
0
....
....
The estimated crude death r..:e for lung cancer among white males in the entire United Ctalcs in 1947 is 10.9 per 100,000 population.
The workers employed in copper ore mining' and smelting inhale dust and fumes of arsenic contained in the are and released as a by- and waste-product during the smelting nrocess.
, .,
Vo!. XXX
LUNG Ci
CAN!
Type
G"oa ..oun
Othe
Terri
S-VNDA
(
(IMA
' Gado **Mctr<
,;:i'* U r b a * `S:::* R u r a
vol. x x x
ENVIRONMENTAL CAUSES OF CANCER
loi
TABLE XIII
LUNG CANCER M O RTA LITY E N N I S IN A U ST R IA P E R 1,000 D E A T H S (J. H E E B IC H AND R. NEUBO LD )
Community Vienna C ' s 60,000 - 1,000,000 ( m s N ,000 - 60,000 Rest of Austria
Total .32.7 18.2 18.4 10.3
Males 59.0 31.6 32.3 17.3
FcmicIoB 7.8 5.0 3.9 3.7
TABLE XIV
CANCER OF THE LUNG AND LARYNX, ENGLAND AND WALES 1946 - 1949 (K E N N A W A Y AND K E N N A W A Y )
u 5 j g-s u l fcll d *c- o!
1
T y n e of C o m m u n ity Greater London County Borough Other Urban Districts Rural Districts
Lunf? Cancer P a t i o - N u m b e r of `P e r s o n s
Producing One Death
Male
Female
100
100
129
137
160
156
233
185;:'-
Mole 100 125 148 170
rer
Persons Death 0
Female
100 55 60 42
TABLE XV
STANDARDIZED MORTALITY RATIOS* FOR LUNG CANCER MORTALITY OF SELECTED SITES IN URBAN AND RURAL COUNTIES OF OHIO, W H IT E MALES, 25-64 YEARS
(MANCUSO, Th. F., MacF A E L A N E , E. M. AND P O R T E R F I E L D , J. D.)
Cancer Si--- uS Years Included
Riirhl Metropolitan Seven Other Counties** Urbanized Counties*** "Rural Counties****
Lung, 1947-1951
122.9
81.8
68.6
s
- Ratio-- Observed Deaths
Ci
------------------------- x 100
*
Expected Deaths
"" Metropolitan County: Counties with cities of 100,000 or more in 1950 (91 per cent urban).
Urban County: Counties with cities with populations between 50,000 and 100,000 in 1950 (66.2 per cent urban).
Rural County: Counties with communities with populations below 50,000 in 1950 (41.4 per cent u rb a n ), comprising 73 counties.
Ci
W. c. H U E P E R
August , 90
LUNG
GANGER
TABLE XVI
D E A T H R A T E S I N 25 S T A T E S O F T H E IN 1940 AND 194S
CRUDE DEATH RA T E S PER 100,000
UNITED
STATES
INDUSTRIALIZED STATES
Stillo
IMli
.1948
Connecticut
8.5
li.i
RI ino is
8.1
8.?
Marybtno
6.5
8.4
Massari inset ;
10.1
10.2
bile :b o'OO
5.7
7.1
Mew Hampshire
7.4
10.1
New Jersey
9.7
9.7
New York
10.3
11.9
Ohio
6,0
7.3
Pennsylvania
6.7
8.4
Rhode Island
8.7
7.4
STATES WITH REGIONAL INDUS?!; UVTJZATION
St aU>
fi.m;
1948
Florida
6.8
7.4
Louisiana
6.5
8.5
Missouri
7.3
9.4
Montana
10.0
8.8
Nebraska
5.7
8.0
AGRICU LTU RAL STATE :i
Stato
L0 4 6
1948
Alabama
4.0
5.1
Arkansas
3.6
5.4
New Mexico
2.6
.3.0
North Carolina
3.1
4.0
North Dakota
5.6
4.1
Oregon
4.1
4.4
South Carolina
3.6
3.7
Washington
5.1
4.2
IVyo rin g
4.9
3.9
The death rates for the year 1946 were taken from "r|,he American Cancer Society. Inc., 1949, Cancer Death Ratos for oach State in the L o b ro States by Site" (3) ; those For the year 1941; wore pet breed by the National Office of Vital Statistics.
Vo'. XXX
LUNG
AC
a;-.
MO
Fri mury C
11 - w toss Aliarla
Xew i ^I;;I . ..
> 4
..-over .ban F r
Chicane
F itts ",u Detroit Larynx AiU at;
irmin Den vex San E-
Chicag
'bo -or sit
vBiom<
.T-MKbv : 1
.A/: :
: . "
-M '
.
C " V#b
W W uu
. I
0'P'i 3N
V.,'. \ K X
E N V IR O N M E N T A L CA U SES OP1 CANCER
153
TABLE NVII LUNG CANCER MORTALITY AND POPULATION
ENGLAND
DENSITY
(STOCKS)
Groups of adjacent towns with over 200,000 occupied dwellings: London and Suburban A re a ..................................................... 156 Birmingham and Suburban A re a .......................................... 134 Manchester and Suburban A re a ............................................ 159 Liverpool and Suburban A re a ................................................. 162 Leeds and Suburban A re a ......................................................... 132
Sheffield with 124,000 occupied dwellings............................................. ......... 135 Newcastle and Gateshead with 87,000 occupied dwellings.................. -..... 114 A ggregate of 6 towns with 50,000 to85,000 occupied dwellings............ 113 A " g r t e of 3 towns w ith 40,000 to50,000 occupied dwelling's............ 107 A.ggnwate of 12 towns with 30,000 to40,000 occupied dwellings............ 104 Aggregate of 13 towns w ith 20,000 to30,000 occupied dwellings............ 100 Aggregate of 29 towns with less than 20,000 occupied dwellings............ 89
TABLE XVIII
IN C ID E N C E OF R E S P IR A T O R Y CANCER, 1937 AND 947 MORBIDITY RATES FOR NINE METROPOLITAN CENTERS, BY SEX
P E R 100,000 POPULATION*
Primary Site arid City
Bronchus and bang
A iUinta
Orleans
J.i-.11idS
Birmingham
Denver
San j
>co
' bjr _
i*mini' s'h
Detroit
Males
Pernales
Total
1937 1947
Per cent Increase
PM7
j
?
Per cent Increase jpMV
Per cent j947 Incvonsc
5.0 13.4 : os 1.0 5.3 400 2.3
207
:i 3.1 39.1 198 2.8 4.2
50 7.0 20.8 174
5.9 29.0 392 0.5 0.4 1180 8.1 j b',2 ahn
4.5 IS.9 320 2.1 3.9
86 3.3 11.0
!
0.1 21.9 1.41 4.2 8.1
93 U.b 14.8
j 5.6 34.3 120 3.9 8.1 10c 5.1 29.S i j.2
13.3 29.3 .122 4.8 7.0 . 63 8.8 13.0 105
9.7 26.j 169 4.9 5.5
12 7.8 15.6 114
12.6 32.0 154. 2.3 5.7 148 7.6 19.0
I 1 o ! j t-- 3!j'
L r V .y n x
1
.du; i
1.4 4.0 .SO 0.3 0.3
0.9
1 02
X O !ns
11.3 14.9
32 0.4 1.0 150 A .i) .Ci
36
Dallas
3.2 5.3
66 1.5 0.4
73 2.3 2.7
17
Birmingham
1.4 4.0 186 0.0 1.3
0.7 2.6 271
Denver
2.0 4.1 105 0.0 0.0 ..... 0.9 2.0 122
San Francisco
4.5 8.8
96 0.2 0.8 300 2.4 4.6
92
Chicago
6.7 7.0
4 0.4 0.6
50 3.5 3.7
6
Pittsburgh
4.4 8.0
82 0.4 0.8 100 2.4 4.4
83
Detroit
3.5 6.4
83 0.4 0.3 -- 25 2.0 3.4
70
'"Biometries Section, National Cancer Institute. 1
v 1
'NS5
*c;
w. c.. H U E P KR
August , 10"
X X
A ROM.
AS)
) o.yo
bbtCOS. .'Aid Cli co ntact inhnbn, as ar.se
0. Si been fc 0 '0:n ; sustain .srens. V corcma tOS is i elbuent special '. '.sor c in soot industr
' ' . V ' V)() };
.v . , ; ;.a c
A 't h
uncos i
mut
voi. x x x
ENVIRONMENTAL CAUSES OF CANCER
155
TABLE XIX
AROMATIC HYDROCARBON ESTIMATED IN ONE-MINUTE SAMPLES OF DIESEL EXHAUST WITH VARYING LOAD AND ENGINE REVOLUTION SPEED WITH FUEL INJECTION INEFFICIENCY (P. KOTIN)
RPM LeaI 1000 0
3 /A i/2 8/4 4/4 1200 0 1/4
1/2 3/4 4/4 1400 0 1/4 3/2 3/4 4/1
Quantities Expressed in U gm ./M inute
Conciiiion
Compression Release
Pyrene CPD. X pByerennze
137
22 146
Compression Release
267
76 465
Compression Release
536 175 772
Compression Release
3.300
640 1320
Compression Release
2500
639
876
Compression Release
208
0
9
Compression Release
257
0
47
Compression Release
448 278 437 ,
Compression Release
888 488 432
Compression Release
1912
614 1706
Compression Release
188
0
80
Compression Release
177
56
78
Compression Release
220
76 1372
Compression Release
734 837 892
Compression Release
822 346 1687
BenzFerylene
22 42 124 610 3.265 79 10 171 930 976
0 0 368 1071 944
aAntnhtrho-no . 0 43
223 472 469
4.3 24 197 320 944 20 " 16 69 577 656
b:acks, t a r f umes and dust, pitch and asphalt dust and fun ms, lubricating
and
ng oil mists and fogs, engine exhausts) ; over 2,000,000 with
com acl i;j metal fumes, vapors ancl dusts; and many thousands of others
imuding for occupational reasons other occupational carcinogens, such
as si'senicais; asbestos and radioact ive materials.
I. Since some of the recogni.A'd occupational respiratory agents have
a.'.aii found among the local ami 'or general air pollutants particularly of
c l a n and industrialized areas, people living and working in such regions
ain beyond any doubt an attenuated form of exposure to ibese careino-
g ; While inhalation contact with chromium compounds (chromite ore,
chsomates, chrome pigments), beryllium compounds, arsenicais and asbes-
to- is usually of local character and depends upon the release of specific
effluents by certain industrial plants or the use of certain chemicals for
special purposes (pesticides, antirusting agents), respiratory exposure to
other carcinogens air pollutants, such as polycyclic hydrocarbons contained
in soot, exhaust fumes of gasoline and diesel engines and fumes from
industrial furnaces, oxidized unsaturated aliphatic hydOcarbons from
evaporated or non-corubusted gasoline acted upon by atmospheric oxidants,
and radioactive matter, is of more or less generalized nature.
Although the atmospheric concentrations of carcinogens encountered
under these conditions are considerably below those prevailing with occu-
6
W . C. HIJ'EPER
Ausrust, 95B
ENVIRONMENTAL CANCER OF LUNG IN FORMER C H R O M ATE WORKERS
W.. XXX
AR0MA1
GA SOL
Trends in selected e n v ir o n m e n t a l fac to r s
United States, 1900-1953 (1924-1926=100)
F IG U R E 5A
p at;on a] C-'G t11st t genicali
In f;i
of limy densely Some, y populat 'vere bt
A si: rates n of Aus' Fiy. 2, States the siz therefc factors except: of air envi.ro rates,
urban-
the im dustry duetio
1. 1
dofne
produ
of cer
O C
Vo;, x x x
ENVIRONMENTAL CAUSES OF CANCER
157
TABLE XX
AROMATIC HYDROCARBONS ESTIMATED IN ONE-MINUTE SAMPLES OF GASOLINE EXHAUST WITH VARYING ENGINE REVOLUTION SPEEDS (P. KOTIN)
IPM 500 1000 1500 2000 2500 8000 1500
Q u an tities IpNprc: sod i n U g m . a t 0 L e a d
Pyrene
CPU. X
Benzpyrene Benzperlone A nthanthrenc
225
289
120
235
; ;Y
439
325
61
177
102
507
266
33
60
36
oV4
142
40
73
27
346
127
25
70
31
121
25
13
85
J. 4
48
5
10
39
15
Rational exposures, numerous epidemiologic observations on the geographi cal distribution of lung cancer suggest that they are nevertheless carcinogenically effective.
In fact, the first observations on an appreciable rise in the frequency of lung cancer were reported from the highly industrialized cities of densely populated Saxony during the first two decades of this century, dome years later it was found that high lung cancer rates existed for the population of the industrialized territory of the Ruhr valley, while they were below average for the agricultural region of the Main valley.
A similarly irregular distribution pattern of lung cancer frequency rates was recently established for urban-inclustrialized and rural regions o' Austria, England and the United States (Table XIII, XIV, XV, XVI; big. 2, Fig. 3). There is moreover evidence from England and the United States showing that in general the lung cancer death rates incren.- c with the size of the community and the population density (YUnc X V II) and therefore display a certain amount of parallelism between these two factors and the presumptive degree of air pollution. However, definite exceptions to this rule have also been noted indicating that the quality of air pollutants may play a role and/or that additional, still unknown environmental factors may he active in controlling lung cancer attack rates, on a local level (Table W i l l ) . It is finally noteworthy that this urban-rural distribution pattern of lung cancer death rates conforms with the increased exposure of urban popidations to known environmental inriustry-reloi ed carcinogens and their progressively increased use and pro duction particularly in urban areas (Tables XIX, XX; Figs. 4, 5, 5A).
CONCLUSIONS
1. The evidence presented definitely establishes the fact that some well defined exogenous physical and chemical agents are causally involved in the production of occupational cancers of the respiratory system of members of certain restricted worker groups.
2. Since epidemiologic studies of various large worker groups and of the
158
W. C. H U E P E R
August, 1956
membership of special occupations have shown marked differences in their Jung cancer death rates and in view of the fact that excessive lung cancer death rates h a v e b een found in o ccu p a tio n a l g ro u p s w ith occupational exposure to known industrial respiratory carcinogens, it is likely that in dustry-related factors account for a much larger number of lung cancers than that on record.
3. The demonstration of recognized environmental respiratory carcino gens in the atmosphere especially of urban areas and of consistently and markedly higher lung cancer death rates for urban populations over rural populations strongly suggests that industry-related air pollutants may play a causal role in the causation of lung cancer and its recent consider able increase in frequency in practically all industrialized countries.
4. While occupational and indu-ary-related carcinogenic air pollutants seem to play an important role ir. the causation of lung cancer and its recent increase in frequency, it is obvious that 1'ey are not the only factors responsible for pulmonary carcinogenesis.
5. Research on the etiology of lung cancer therefore should be conducted on a broad basis, including not only inhalants but also agents entering the body through noil-respiratory routes.
EES Phi Eft
1. La evidencia quo se presenta definidamente asienta el hecho de que algunos agentes exogenos, fsicos y qumicos determinados, influyen causalmente en la produccin ele cnceres ocupaeionaffs del aparato respiratorio en ciertos grupos limitados de trabajadores.
2. Puesto que los estudios epidemiolgicos de varios grandes grupos de trabajadores han mostrado notables diferencias en la frecuencia de las muertes por canee]' del pulmn, en vista de que se han encontrado excesi vas proporciones de muertes por cncer del pulmn en grupos de trabaja dores que debido a sus ocupaciones sufren exposicin a substancias carcinognicas respiratorias industriales, es posible que los factores en rela cin con la industria tengan mucho mayor nmero de cnceres en su haber de lo que se concede.
3. La demostracin de la existencia de carcingenos respiratorios en la atmsfera especialmente de reas urbanas con mucho mayor proporcin de muertes por cncer que en las reas rurales, fuertemente sugiere que hay polucin de aire por las industrias que pue de desempear un papel causal en el cncer del pulmn y su aumento reciente en pirticamente todos los pases industrializados.
4. Si bien los agentes carcinognicos que polueionan el aire en los am bientes industriales profesionales parecen desempear un papel importante en la gnesis fiel cncer y en su reciente aumento de frecuencia, es obvio que no son los responsables nicos de la carcinogenesis pulmonar.
5. La investigacin sobre la etiologa del cncer del pulmn por tanto debe conducirse sobre una base amplia que incluya no slo los agentes inhalados sino tambin aqullos que ingresan en el organismo por otras vas adems de las respiratorias.
Vo!. xc
1. F ragi
Krfi Respi grup]
2. Beru:
D ife
enkrt keits: vulie
mum
Pbikt sino
emop soldi
W erI
ge ge-
im Z
uvst kreb; alien . 4. Luft Zush r.ahn stanc
5.
HU '
einsc ande
V,,I. X X X
ENVIRONMENTAL CAUSES OF CANCER
159
SCH L SSF OLGERU NGEN
1. Die vorgebrachten Belege stellen abschliessend die Tatsache ausser Drage, dass einige klar abgegrenzte exogene physikalische und chemische Krfte urschlich beteiligt sind bei der Entstehung des Berufskrebses des Respirationstraktes von Angehrigen bestimmter beschrnkter Berufs gruppen.
2. Nachdem epidemiologische Untersuchungen von verschiedengrossen Serufsgruppen und von Angehrigen spezieller Berufe ausgesprochene Differenzen ergeben haben hinsichtlich ihrer SterblichkeitsziiTor an Lung enkrebs, und im Hinblick auf die Tatsache, dass bermssige Sterblich keitsziffern an Lungenkrebs bei Berufsgruppen gefunden wurden mit be ruflicher Exposition auf bekannte industrielle carcinogene Stoffe der At mungsorgane, ist es wahrscheinlich, dass auf die Industrie zu beziehende Faktoren fr eine viel grssere Zahl von Lungenkrebsen verantwortlich sind als oie berliefert ist.
. Der Nachweis von anerkannten, durch die Umgebung bedingten carcinogenoi Stoffen des Bespirationstraktes in der Atmosphre besonders in stdtischen Bereichen und von gleichmssig und ausgesprochen hheren uterbkichkeitsziffern an Lungenkrebs unter der stdtischen Bevlkerung gegenber der lndlichen Bevlkerung legt die Vermutung nahe, dass die im Zusammenhang mit der Industrie stehenden Luftverunreinigungen eine irschiiciie Rolle spielen knnten fr das Zustandekommen des Lungen krebses und seine krzliche betrchtliche Hufigkeitszunahme in praktisch allen industrialisierten Lndern.
4. Whrend berufsbedingte und auf die Industrie bezgliche carcinogene Luftverunreinigungen eine bedeutende Rolle ,zu spielen scheinen fr das Zustandekommen des Lungenkrebses und seine jngste Haufigkeitszunnhme, liegt es auf der Hand, dass dies nicht die einzigen, fr das Zu standekommen von LungenkrcV verantwortlichen Faktoren sind.
5. Forschungen ber die Aetiologie des Lungenkrebses mssen daher auf breiter Basis ausgefhrt worden und nicht nur inhalieruaro Stoffe einschliessen, sondern auch solche Bestandteile, die in den Krner auf anderem Wege als ber die Atmung eindringen.