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Hello, I'm Shalom Buchbinder,
from the Montefiore Medical Center in the Bronx, and I'd like to
acknowledge my international colleagues from the Jerusalem College of
Technology, and Hadassah Hebrew University Medical Center, that participated
in this research. Our research is aimed at improving the ability to evaluate
micro-calcifications which are found on mammography. If a cluster of calcifications
is found on mammography, and are ... the physician does not have a good
feel as to whether it is malignant or benign, potentially a computerized
system can be used to diagnose the possibility or the probability of the
cluster being malignant. We initially looked at approximately 50 different
features of clusters of micro-calcifications, and we determined that there
were eight features that were very, very important in differentiating
benign from malignant clusters of micro-calcifications.
Initially what we did,
was, we um, we had the computer analyze 260 cases of micro-calcification.
And it determined values; above a certain threshold, something was assumed
to be malignant, below a certain threshold, something was assumed to be
benign, and there was a very tight indeterminate range. And, if a cluster
of calcification met criteria, it was given a point for malignancy, and,
if it met benign criteria, it was given no points for malignancy, or a
zero.
We sum the numbers of
each one of these features, and we analyzed the summation, and we were
able to identify a positive predictive value of about 67 percent, and
a true positive fraction over a false positive fraction, a so called ROC
curve, at an area of about 0.81. Then we analyzed the clusters of calcification,
the different parameters, and we said- not all parameters should be equally
weighted.
Not all clusters of calcifications
have features that are of equal importance. We know, for example, that
a calcification, or a cluster of calcification, that is made up of very,
very fine calcifications that are a circle, are very rarely, if ever,
malignant. And we know, as a calcification gets to be more and more irregular,
it is more likely that it would be malignant. So we said that not all
features were equally important, and we actually, again, re-analyzed the
260 cases, and we looked at each one of these features to determine how
important was it ultimately in differentiating benign from malignant clusters
of calcification?
Then, what we did was,
we looked at each one of these features, saying how strongly was it malignant?
Okay, and that was given a value. We multiplied by its relative weight
in importance of differentiating benign from malignant calcifications,
and each one of these points then received a value. And we reanalyzed
that data, and we were able to improve the positive predicative value,
which is; how often when we recommend something to be biopsied is it indeed
going to be malignant? We improved the positive predictive value from
a very good 67 percent to a 79 percent. And we improved the accuracy rate
from 69 percent to an 83 percent. And again, we kept the sensitivity at
98 percent. So what this system is able to do, in my belief, is that we
will be able to decrease the amount of unnecessary biopsies as a first
result of this type of analysis. Currently, when a recommendation is made
in the community, it has about a ten to 30 percent positive predictive
value. So, ten out of a hundred clusters will indeed be malignant, or
30 out of a hundred clusters will be malignant. What we're able to do
is raise that number to- of those that we want to be biopsy- we can get
up to about 79 percent will be malignant. So we will be able to obviate
many, many patients from receiving unnecessary biopsies. Therefore, obviously,
you'll alleviate the anxiety, the uncertainty, when you're told that you
may have an abnormality. Certainly, financial considerations will play
into this, in that the cost for the unnecessary biopsies will be reduced,
and we're very, very hopeful that this type of system, in conjunction
with the full field digital mammography, will significantly improve mammography's
ability to correctly identify abnormalities, and also to correctly identify
structures that need not be biopsied.
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