Document KRg6eDYdQ57raaXn5aEw9YRb0
Recorded telephone conversation between Dr. J. K. Wagoner & Ms. Selevan of NIOSH and Dr. J. Rafter of & Research - Jan. 4
Sherry
1977
J.R.
SS J. $ J.R. JKW
J.R. JKW J.R. JKW
Let me tell you what I have then we'll kind of be on the same
wave length maybe I have transcript that Ms. Selevan gave at the American Public Health Association on October 20th I have a transcript of that talk I also have a listing of th 94 deceased individuals and a more detailed listing of 17 who died from respiratory causes and finally I have
some tables which I understand were given to the three
companies involved in your probably equivalent to the
report slides
and I think they're
that were shown on the
they are equivalent
Pardon
7
Fra
who
?
So that's where I stand and now I need generally some information so I can understand how they were analyzed and maybe go over it myself so I can report to people that
ask me whether or not I think it's a reasonable analysis
and so forth
Well basically the
underlying assumption of the whole
analyses are
out with ten
ten
persons
that one person person years at
observed for one
observed
risk which is to
equates out
equates say that to ten
person years at risk However there is one additional parameter that added into it because of the fact that
disease causation if not an instantaneous event as manifest
by death
draw out
and that is we analyzed our on a piece of paper a matrix
basic which
data if you
has on one
could
scale axis duration since onset of which for easier
terminology we classify as latency on the you have duration of employment Within
out seven different categories in each one
other axis
if you draw of those axis
total actually
which is
eight being the marginal
cell'1 x 1 you with is
the first category
less than five years
of duration of employment and less than five years since
onset of employment Going over to your right the second
cell is 5 through 19..where have you got duration of
employment on top
on top
Within latency less than five
5 to 9 years it's a nonsense You understand that
years duration of employment cell it's an impossibility o.k.
Yes
Basically let me go back one further you the five variables six variables
step I'll give
that we consider
We
consider
age
whicihs an
always
increasing
function
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we consider calendar time which is an always function we consider interval since onset of which is an always increasing function _.
increasing employment
that's latency is that correct
latency and we consider duration
employment
which is
a static or increasing function depending on whether a
person terminates employment or not Those are your basic
four variables that are considered other than W
in variables such as race and sex Now within each one of
these cells in this big matrix that I had given
we
have a life table in terms of calendar time and you
in five year
intervals
calendar time in
age age five year intervals
The reason that we analyze in terms of these two variables
is that disease is obviously associated with
is also a secular phenomenon terms of
aging disease
and things like this that
diagnostic differences
lung cancer is an increasing function
over time and what we hope to do when we analyze is to control
for these nonsense variables so that later in our final
analyses we can after analyzing for these variables we can
collapse the table and just consider dosage and intervals
since onset holding each of these other variables constant
as we controlled for them in the analyses O.K
Yes
On your axis you have five year intervals less than five
five to nine ten through fourteen fifteen through nineteen
twenty through twenty twenty through twenty
greater equal to thirty and a total which is the
total summation of all the events in that column r laorwgestIn
going down you have the same numeric breakout of less than
five five through nine O.K. What we do is we take each
individual as he comes in we ask the basic
did he get employment
into the life table in
he began employment 1940 the
question in 1940 entered
age he had achieved in
1940 latency 0 because he had just began employment
and the duration of onset of employment of O.
that he has continuous
Assuming
he the
employment passes down through
diagonal of the table both in terms of calendar time
in terms of aging in terms of
in terms of interval since onsetinocfreaesmiplnogymeemnptlouynmteinlt heand
stops employment in which case he no longer increases
in terms of duration of employment but just increases
in terms of onset interval since onset of
O.K. As he ages of course he
employment
He can get out of the life tableproingrets ersmess oifn c tw aolenddiafrferteinmte
events Either he expired in which case he is
from risk of dying at the date that he
removed
expired and is
removed totally from further accumulation of
years at risk of dying at that point in time ro irskhe pe ca rn son
come to the end of the study period when
out of the
everybody drops
study who does not expire O.K. Now if a
continues employment from the date he began employmentperisnon
1940 and the study period ceases in 1975 he will contribute
he five years of risk in cell will contribute five
of risk in cell II O.K because he has spent five yea yr es ars
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at risk of dying as he was accumulating his fifth through his ninth year of employment and he was in his fifth through ninth year since onset of employment at that time And like-
wise five in the third cell 33 five in 55 five in cell 66 and six in cell 77 '73 '74 and '75 O.K. Now let's assume
cell that that
44 five in cell is 1970 '72
we have another
individual that comes through but he dies on the 10th anniversary of his initial employment He will contribute five years at risk in cell II he will contribute five years at risk in
cell 22 and will be removed from the life table at that point
in time as deceased due to the underlying cause as certified on the death certificate O.K. I will take a third individual
who just dies on the fifteen anniversary of his employment initial employment but he only works for ten consecutive
| years
He will
in cell 22 and
of employment
contribute five years
five years in cell II five years in cell 23 two being duration
Its 32
across
the way
the top
that I have it would be
it I
32 in
guess since I
terms of o.k.
have
duration
Essentially he goes on the diagonal and then drops one
cell and then drops out due to the cause of death that he
died from O.KJ You with me
Yes
The only other case that really theoretically can happen
you can work out all sorts of combinations on those would
be a person who was initially employed worked for five years left the industry for five years came back and worked for
another five years Alright That person contributes five
years at risk in cell
in cell 12 one being
at the fifth to ninth
HI he contributes five years at risk
less than five years of duration but
year since onset o.k. and then he
contributes five years at risk in cell 23 during the period that he accumulated his fifth through ninth year of employment but he was in his tenth through his fourteenth years since onset of employment That will be third type of
individual fourth type of individual that can fit into
the life table at
person who begins
risk The
employment
other condition obviously a
in 1920 of our study period
record begins in 1940 because that when the
when our follow up started because we
system or thats
social security
as method of ascertaining whether a person is deceased
or alive and that system really came into effect in 1935
oractually '37 or '38 If that person began in 1920
and was still on the payroll in 1940 then this is the
first date of our study period He will be in cell 5-5
when he enters our period at risk He has accumulated
20 through 24 years of
20th year of the onset
employment he's actually on the of his employment He contributes
no risk during the interval prior to that because he has
no probability of dying otherwise he would not be on the
payroll of 1940 when we had the first chance of picking
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him up O.K
Yes
Basically
from our
you have the in this case
matrix as we send people through
the Vermont Talc workers themselves
Each one of these
of these obviously as they go through each one cells is put into that additional matrix within
the
eight periods through '50
1940 cell of a series of sixteen age groups and approximately
calendar
1945 through 1949
through
54.
O.K. These individual numbers that we
are distributing are individual person years that each
individual contributes that risk of dying during the period
of the study O.K Now to get what one would expect to
have occurred in this population if they had experienced
the same death rate of the control group this case the
U.S. calendar
male
period
population we generate out for the same
that we used in our life table distribution
and the same age groups that we use in our life table
distribution death
per 100,000 population due to
specific causes of death 001 through 0119 ICD code
tuberculosis malignant
-
140 through 199 or 205
comparbilty In order to provide comparability comparability because the coding of
death study
has changed over
deaths in terms of
period of time we interpret our
the revision that was in effect
at the time of death and then we convert that code to a
Sc o o wemdp o haavreability seventh revision code number for ease of handling O.K.
and death statistics as Statistics Division and
We code out the U.S. population
published by the National Vital
put them together using that same
comparability arrangement We take these death rates for
100,000 population specific for five years age groups and five year calendar time periods and bring them back in and multiply them by the person years at risk in the
life table that we just distributed which are now specific
| for calendar time and age
if you -and for ease
group within dosage and
of statistical notation
latency
we will
LYZ abcd say that
lets make it
where abcd
a
is dose
1
b
is
latency ^ is age group 1 and d is calendar time 1 we
take that person year at risk times the death rate of the
general population specific for age group c and calendar
time group b O.K. That generates out the expected numbers
of deaths that would occur in this population within age
group c calendar time period time d experienced
group 1
latency group 1 if they had experienced the death rate
due to that particular cause of the general population
K.
Let me ask you a question
references for the United what was it sex
at this point You use these States and broke them down by
)
sex race cause age calendar time
Oh so there is age in there
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Oh yes Age is in there sex is in there race is in
there
These are race sex specific race
How about job classifications in these
Is there anything like that
Well not at this time here O.K.
clatification at a later time
We'll
get
into that
sub
You mean for the U.S. rate
Yeh I'm just trying to get an idea of what these references give
The rates for the U.S. don't have any
I
see
recupation's information
These are just U.S. general white Yet anything the use of the U.S.
male population rates white male population
general population as a
reference
population tends to
underestimate what one would expect in all things other than age and sex rate
a populatioinf
and calendar time
were the same The rate in being that a working population consists of people who are physically able enough to seek
employment and are medically sound enough to pass routine
company medical examinations in order accepted for employ-
ment They are also well enough to withstand the normal
rigors of a physical type of employment whereas the general population not only includes many of the same people from that industry but all other industries but they also contain the sickly the people who are in hospitals with diagnosed cancer already who have yet to expire and things like that In addition during the war years you tend to find that the
general
medical
population rejects and
in many cases contains many of
things like this which are left
the in the
U.S. population and during those years the population at
risk really was continental U.S. not population overseas
etc. The use of the general population has been referenced
in many articles as producing what we call the
healthy
worker effect and that is in underestimate of the risk
that than
one would
experience if
these nonsense variables
in fact everything were equated
other
Is this information reference available to me in
the library someplace
What the healthy worker effect
No the references that you used for the U.S.
Yes they're published vital statistics
That's what I would ask for
Each year they put out two big volumes on it
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Who puts it out
Public Health
The U.S. Vital Statistics Division
What about the references available someplace
for
Vermont
Are they also
There are two different types of references Either you
can get population and death from the same volume that we
were talking about
causes of death as
for you
many but can from
not the
as large an array of
U.S. The U.S. breaks
out about 251 specific causes of death I think each state
breaks 68 or 56.
Its a less detailed breakout in terms
of specific types of causes of death or the state of
Vermont themselves have their own data available
I would have to contact an agency in Vermont
I would imagine the State Health Department
State Health Department and this this state Health Department
also
has
job
classifications
No no
. job classifications The reason being that
one assumes that the general population as I said before
if anything underestimaant d etoso that it contains because
of the fact that its a large population relative to a very
small restrictive geographic region tends to contain all
segments of the population and is really in sense smoothed
out in terms of risk factors O.K.
Yes I understand
When one gets through with this whole array that we are
talking about where one increments the calendar time and
increments the age and then goes in and calculates another
expected death and goes all the way through for each one
of the cells then we update the cause of death and go into
the second cause of death and do all the same sequentially
through the ek.
When all of this is done we sum over
all calendar periods and all age groups within specific
latency and dosage cell O.K
controlled for age the effects
The reason of age we
being we have now
have standardized
for the effects of age and calendar time and we are really
causation not interested in terms of these as disease
standardized for and held at constant We summarize
over
those and then
within latency
You with me
we sum within dosage over latency and we sum
over dosage to get our marginal total O.K.
a
Yes
Then come
you out
can
the
sum your marginal total and they same O.K which will give you a
had better
grand total
Right of the number of deaths
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Number of deaths both observed number of deaths expected and you can sum your person years because they're additive
also Only for descriptive purposes the actual years of
the marginal total person years or the grand total person
years in any calculation is statiscally in balance because
you in a sense have sacrificed your age calendar time
distribution that consideration O.K. You with me
the general philosphy behind the
Well basically that is
people
were presented by Ms. Selevan on occasion presented the
grand total for various causes of death on other occasion
presented the sub marginal totals according to
intervals since onset of employment as we wish to look at
latency O.K. The reason we wish to look at latency is
if in fact one usually sees or one sees that one has an
excessive risk as measured by the ratio of the observed
over the expected times 100 which is the SMR early in
the game with very short latency one can become very
suspicious of an occupational ideology toward that excessive
risk The reason being that its impossible or very unlikely
that one has instantaneous death due to an exposure for a
chronic disease
Of course there is a problem there and that is in some instances people were exposed a very short time a long time ago and it appears that they have a long latency where you know they have a long time since exposure but they had a very small exposure tends to be misleading in some
cases I would think
Well you've got your option in looking at both spectrums dosage and latency O.K.
The original tables that you've got they just looked at
latency because the effect was much more pronounced there
It was a ten minute presentatioInn the final draft we
also looked at exposure but that opportunity we just
didn't have enough time to give all the data and the pro-
nounced effect was with latency a much lesser effect as
there
Well
was one
with exposure
ee eee ?
Ae tk
can normally say is we that we
pagon
a
hat
hat
wala wala
din
din
really don't know
summ
how much duration of employment it takes to really induce
a disease either it manifests by its diagnosis and
death but if its a chronic disease after a person was exposed
in
terms of diagnosis and death is very minimal
Certainly all of our population studies to date have de-
monstrated that
I'm sorry that
I didn't quite understand that
would you repeat
What I'm saying is that whereas your dose group 1 in your
latency group would be not expected to have an SMR above
100 o.k. the ratio of observed over expected should not
even exceed 1
scale
latency the further you get down removed on the
with the possibility of certain exposure
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if there is an affect you would expect to see an
increasing relative risk
Ratio of observed to
expected If in fact there is an occupational
would increase
ideology if in fact
short term exposure is really associated with this phenomena
O.K.
There is another question that occurs to me and that is
since there you have very few people in your sample
that you are working with does this change what you've just
said for example I can understand that if things would
even out kind in
few people can you
a lot
..can
of people but when mistakes be made by
you have very
making that
assumption because you just have so few people
Well I think one could
hood of overestimating
basis that the test of distribution take into numbers
tend to underestimate but the likeli-
the risk would be unlikely on the
significance uses a Foisson
?
consideration the magnitude of the
Does this test of significance something that you do or is it done by your computer
of
Really we use table Biometrica Volume I Biometrica
Table for Statisticians Persall & Hartley
Its a standard
process that is used internationally in the field
So given an SMR then you would look in this table
Actually the table gives you the bounds on the observed
number of cases
I see
I noticed in one place in these tables you made
comparisons between the expected number for the Vermont
miners and Vermont population excuse me the observed
for the miners and the expected for the Vermont as well
as the observed for the miners and the expected for the
U. S. population
We use two different standard populations to generate our
expected one the U.S. white male population and two the Vermont white male population
Did you use the same table to do the analysis and does the table take into account that you are doing multiple comparisons using the same expected number of people the same observed number of people
No no
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So its like you had several tests to do and you just did
pair comparisons with each of the possible
JKW
Right right
JR
Have you adjusted your P values for that at all
JKW
nept
No no
In this case I would doubt very much if it would
make any difference in light of the extremely large
relative risk And this is going to be heresy that I'm
going to state being a graduate of Harvard University
School of Public Health both in biostatistics and epid^'-
miology but I often view tests of significance to be a
crutch that have been imposed upon the statisticians by
the incompetent medical profession who are too damm
inadept to interpret their own data I would prefer to
biologically interpret the significance of my data as
well as the statistical significance of my data
JR
I should hope anyone would do that
JKW
Too often this is not the case
JR JKW JR JKW JR JKW
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The unfortunate thing is people will
P values and take them as gospel
I
with you
tend to think I
look at
am agreeing
This basically is why we tend to restrict ourselves to just the .05 and anytime you start getting down to the exact and multiple comparisons its ludicrous
Of course times does
the sample
the fact that you reuse the same sample several tend to make the conclusions more dependent upon and less relevant to the total population
It depends on which standard population you are referring to
Well I assume that the underlying population is something along the lines of people who are or will be employed in talc mines that's the inference I guess that's being
No. I mean in which general population
If one does multiple
comparisons and looks at the Vermont population and says let's
look at the U.S. population certainly the first is an in-
dependent step
Yes that's true expect you're using the same observed in
each case that was my point
Could I ask you some specific
questions about the people that had died of respiratory causes
For example on this listing there are about ten of them
where its listed as smoking unknown has this been
updated at all is there new information about that
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I think there is update going on on it yes Obviously
we are attempting to get the complete smoking history as
very possible However I think one has to
I would hope that we are not going to be
using
categorically
smoking as
red herring and let me explain whatI mean on that Single
population of approximately 60 x or current smokers
that
We are not using U.S. white male population rates specifically
for smokers
when one
tends
to say well
you
haven't
considered cigarette smoking and obviously it must be due to
cigarette smoking it is often stated that we would without
consideration being given to the type that a sizable portion
of the general white male population are also current and
x cigarette smokers
In spite of that fact that we do have
smokers vs. smokers and they may cigarette smoking but there is no that at present
differ in quantity of data which would support
The only criticism
. I would have of that is that its
generally true if you have a large sample again the fact that you have a rather small sample cigarette smoking could be more of an influence than if you had a larger sample even though as you mentioned your Pason tables take into
account small numbers
Tel Sy
There are a few other things that I think we ought to consider Since we break the population down into miners and into millers two independent categories and miscellaneous
Miscellaneous are mixed categories both places
people who worked in
O.K.
Yes I know about that
The likelihood of an independent effect of cigarette
smoking in the ideology this diseas that we are
observing seems very small unless one further evokes the
hypothesis that there is job specific smoking patterns within specific corporations in the same geographic area That is why do miners smoke less than millers and if they don't why do we see an excessive risk of malignant respiratory disease in the millers and not the miners
Why also
cancer in
conversely the miners
do we see an excess of but not the millers
respiratory
Well the point is I agree that you can make you can ask these questions except when you've got only like for
example people who died of cancer and if two or three
of them died as a .. which I don't know but if two or
three died as a result of cigarette smoking you know that
really affects the sample
If you had sixty people and
two or three had died as a result
that doesn't effect the
sample
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| We're not pushing on the lung cancer at the present time
Mie
We are not making any conclusions its just that you work would
expect consistent patterns if smoking is truly the cause of the excessives we're observing you would expect the pattern not to be opposite but to be consistent and they are That's the only point I'm making I'm not drawing any conclusions as to the lung cancer at this point
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My point is that its hard to see trends when you have few people
Well the only trend that we're really
is that and respiratory diseasIet is
specifically
striking
identifying
Let me ask you do you have information with regard to length of exposure and period of employment of the people other than the ninety four who died I understand there
was a sample of 405 taken Do you have information on these people who are still alive with regard to things like exposure to tale and working history
oh yes They are distributed in the matrix
This includes everyone living and dead in that 405 people
.
And they are included in the calculation of expected
7
on yes
In order to generate
death you have to have people
in years
and who
observe and expected
are generatinogf course. ,
All of these that adds up
people add up to
to more than 94.
only have
94
there's none of them
I took it to mean that you
Oh no there are 94 deaths
Actually there's a correction there are
people without death certificates and we
two of those 94 to be alive
But its 92
corrected tables
92 we had some had since found now we will have
printints of Is it possible for me to get notes the living people
with regard to length of exposure
That information is confidential
It will be made available
What the living people No No No.
He asked for living people
of person years
You want distribution
;
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Well what I would like is that which gives me a distribution as
exposure
would be helpful something to the regard to the
You don't workers
want
actual
individual
information
about
individual
No I don't need regard to length of employment of history of those
that
I'm interested in distributions with
of exposure of live
live people and if live people
people and also period possible the smoking
1 ( We don't have smoking histories of live people
don't
people
Is it possible for me to get that or can I come and pick it
up or can you send it to me
Can I ask another question
while you are deciding
First of all we do not have cigarette smoking habits patterns
among the surviving O.K. Many of the surviving people no
longer are regularly employed with the companies in question
some of them are dispersed throughout the U.S. and I think
we run into a severe problem of privacy in addition to the
possible harrassment of individuals trying to go
evoke this type of information
Its cumbersome
back
and
O.K. so don't give me their names I don't want What about the length of exposure tables which
length of exposure for living people and period for living people Are those available
them summarize
of employment
Well if you wanted you could have
nothing but work history in it
It
identifiers we would blind out any
could give you that
a master file that has won't have any individual
personal identifiers we
That
ages need
would be fine
I don't care to know their names
Their
would be nice or distribution of their the raw data I can get by with summary
ages data
I don't
A. life table
has
the number of person
we've got all that kind of breakdown the
years per age
person years
group
rather than specific flow for each person in the various exposure category so that you could get that
indirectly from the life table
It would be much less
complicated that way
These are available to me the life tables
Well they certainly will be made available when we have
| our general
meeting here O.K.
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The point is I've been asked by someone who I have to
rely on to pay my salary you know to get this information
as quickly as possible and to try to make some head and
tail out of it
Is it possible that I could come there or
you could send me this kind of information about either
the living or everybody in terms of these life tables or
both
Pause
ling pause
While you are thinking can I ask you a second question
about this
Wait a second we'll try to work this one out
Go ahead shoot your second question
There are 405 people that number of people that were from the people
you talk about is this the total available or is it a sample
It's the total number of people with who worked a minimum
of one year with January 1940 1970 and one day of that time had
at least one day of that time between 1940
and the current year has to be before
of that time had to be at least one day
to be after 1940
So as far as you know it's a complete census as opposed to sample
It's as a matter of fact probably well it's as complete
as we can get considering the problems with the company data and the Health Dept. data what with the Health Dept. data as they had in their data a greater percentage of the
people with the greater exposures and the companies had
more names but the additional names all seemed to be
those people who worked The companies also were who worked there longer
much less than a year
missing quite a few of periods of time and we
like two weeks
the people
think that
this is in some
probably due to the sketchy
of the companies in the past
work histories kept 2 the fact that the
companies have changed quite a few of them have changed
hands several times and the
but we ultimately went with
records were lost in the changes
the Health Dept. records they're
more reliable of their own and there were originally 826
people in the Health Dept. and 405 fit our criteria as <>
described
I can continue asking questions if you want to continue
thinking about the other one We've been trying to get a hold George Lee has been trying to a hold of the death
certificates of the people who died and he would like to
know if you could provide the information with the state in which the death is registered for If I give you those could you find those
regard to three people
out..tell me
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Which people
One is Treffeley West Shall I continue or wait
Treffeley West Who else
The second one is Guyett Daniel his third one was Reil the first name is
first name Edson
and
the
O.K. I can get that information for you it with me right this second I'll have to our original file
I don't look it
have up in
George asked me to ask a second question with regard to
these respiratory deaths he noticed that in your transcript
people died you mention that you had excluded people who had
influenza and pneumonia and he notes that there
from
on the list of malignant respiratory deaths who were
listed as dying from pneumonia or some
Its a coding It's coded by the underlying cause of death
Any causes death for the immediate cause they die instantly of pneumonia but that's not the underlying cause of death and that's not the way they're coded by nosologist a qualified nosologist The tables that I sent you where it had the coding that coding by a professional nosologist and there's either three or four columns depends on how
many causes we found on them prime cause there's contri-
butory case 1 contributory cause 2 contributory cause 3
and the
-
-.
~
is the cause of death
classified under ?
As an example congestive heart failure due to
due to chronic fibrosis of the lung
It would
out necessarily as congestive heart failure
influenza not be coded
It would be coded under the underlying causes
That's the ICD column cause of death
I think that's it
Is that the first
The first cause on the death certificate underlying Yes that's what the column ICD contains
Yes
And then ClC and 3 are ..
Contributory cause 1 contributory cause
O.K. I understand
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So although the immediate cause of death might be pneumonia pneumonia might be a resulting factor from something else and in these death certificates they all were at least according to the physician who attended the patients
O.K. Well I'm out of questions now What can we decide about getting this other data I'll tell you George would really like to come out there he's asked me several times he said that I should press that point I don't want
to become offensive to you
Yes well let me explain my position on this Our general
feeling is that we certainly don't intend to shy away
and certainly would be more than receptive to interact with
other people in the scientific community However we don't
wish to be put in a position and we refuse to be put into
a position of dealing differentially with management and
labano d r my general feeling is
that
since
there are multiple
corporations involved there has been multiple requests
from multiple corporations would prefer that other than
what we're really talking about here that we refrain from
any further distribution of hard raw data pending the joint
meeting of
both
and labor and anyconsultants
wish that they
discuss our
to bring to
interpretation of
very candidly
the data the
go over and analyses any
tendbrought questions that may be resolved
of this nature obviously are to
brought up Meetings a briefing of our
interpretation feeling our interpretation of the data answering any
questions and
opinions that may be certainly
scientifically sounded we have no corner on the market
consistent of course but reserving
data as we so fit consistent
the right to interpret the final with good scientific inter-
pretation and in that sense that I'm a little reluctant
to openly essentially dump our computer volumes that are
least three to four inches thick
of them
a computer dumpout
four
Possibly duplicated
pages and
I means
it's hundreds
and hundreds of
From my personal point of view the problem is that if I
was asked to attend such a meeting and I probably will
it would be very beneficial to me if I had been able to
be
look at the data before going to the meeting otherwise it would seem to me that people would have to take what's given at the meeting go back and digest it and then come and ask for
a second meeting so our point of view is that we would
like to get as much information as possible before the
meeting so that we can come prepared to discuss our feelings at that meeting
Can I ask you a question briefly
Sure
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If you came to a scientific conference do you leave the scientific conference with the feeling that you had to see somebody's basic raw data and entire distribution
before you arrived at a judgement as to the validity of that data and interpretation Forget that you're a consultant for the company Come on
When I go to a conference I hear a paper I usually don't
understand it
so that I have
usually
to take
five minutes
what's given
after they start I'm
in terms of hand outs
lost
and
go home and study it like crazy and look up in the literature
what is necessary to understand it and then if I'm interested
in pursuing it further get in contact with the people that gave the talk and pursue it The point is I really can't say that I would I wouldn't certainly go to a meeting and call somebody a liar or anything like that
Well I'm not asking about liar guilt Scientific protocol
I'm just talking about
Generally if I go to a meeting other than a statistical kind of conference and people present statistical data my experience that I should question that data I'm not saying you obviously know a lot more than I do about this subject so I'm certainly not questioning you but that's my basic feeling I tend to question data when people do statistics
because I've seen so much misuse of it
I don't deny that It's too much garbage in garbage out
My point still is if I have to come to a meeting whereby I'm
going done
to talk I would
intelligently about important work that's being like to have information before that as opposed
to coming in cold and having to say well can we talk in a
week or two weeks when I've had a chance to digest the
information
Well I'll tell you what you tell Mr. Lee that one we will be sending a copy of the paper out at least a week before the meeting o.k. and two at that time with descretion we will provide a couple of pertinent matrixes to give you the answers that you're really after
You couldn't send them before that time
Well basically we're talking about getting the paper out within essentially a week and two days right now so we are not talking about any lies o.k. The thing is that we've attempted to crank up this meeting to occur as fast as we can however in light of the repetitive requests that have come in from Windsor Minerals Johnson & Johnson & Engelhard
I suppose everybody is doing the same thing
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If they wish to have the meeting and wish to have the manuscript then you're going to have to sit back and let
us finish it o.k.
re
n.
What back will
about these three death certificates now can I call or have George call back to get that information or
you send it to us
We'll send them out
We'll send them out we can send them
Do you have an address there that
I can give you my address it's John Rafter Johnson & Johnson Research Center New Brunswick N.J. 08903. So that's Johnson & Johnson Research Center New Brunswick
N.J. 08903
and your phone number Area Code 201-524-5087
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