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Greetings and welcome to EHA 
Unplugged, the official podcast 

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channel of the European 
Hematology Association EHA. 

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Hi everyone, My name is Wilson 
Lim, a medical writer for EHA. 

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I'm sitting here today with 
Professor Gregor Horman to talk 

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about AI, artificial 
intelligence in hematology. 

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Professor Orman, would you 
introduce yourself please? 

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Yeah. 
Hi. 

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My name is Gregor Herman. 
I'm a clinical pathologist or 

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specialist in laboratory 
medicine working at the MLL of 

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the Munich Leukemia Laboratory 
in Germany. 

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The M&L is one of the largest 
laboratories focusing on 

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patients with leukemia and 
lymphoma and diagnosis of bone 

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marrow and blood samples. 
So when we talk about artificial

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intelligence, AI, the first 
thing that comes to mind is all 

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the large language models such 
as ChatGPT and and Gemini. 

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Many, many people are unaware of
the other models that can be 

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applied that are applied in 
healthcare. 

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Can you share with us some 
examples of that? 

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It's a huge spectrum of AI to be
applied in healthcare, for 

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example, where we are mainly 
focusing on is of course using 

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AI for our diagnostic processes.
And there we are mainly applying

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a particular kind of AI machine 
learning or more specifically 

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deep learning, where we try to 
get the information out of our 

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data and use them in a 
scientific way. 

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With those AI machine 
approaches, for example, we are 

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doing soda morphology or we are 
doing chromosome on Banach 

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analysis. 
Both of those techniques focus 

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on imaging. 
So our technicians, our soda 

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geneticists, our haematologists 
have to assess those images and 

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tell what kind of cells are 
these, what type of chromosomes 

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are these? 
And we can use here deep neural 

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networks, a kind of machine 
learning approach to align those

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pictures to the classes of cells
or the classes of chromosomes. 

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So we extract the features out 
of the picture and then have the

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network aligning the cell to a 
particular class. 

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For example telling this is a 
blast and this is very helpful. 

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As to the cells are pre 
annotated, of course you need 

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all the data digital. 
First of all, we have to 

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photograph all the cells from 
the peripheral blood smear or 

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from the bone marrow smear or 
have the metaphases digital 

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available and then we can apply 
those AI models to help us in 

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the classification of the 
particular cells. 

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This is nothing that the EI is 
doing alone. 

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This is definitely a Co working 
between the EI and our trained 

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personal. 
So each and every cell is then 

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reviewed by a trained medical 
personnel and then we have a 

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final report to be assigned. 
Still, this addition of AI was 

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very helpful in our processes, 
in particular inside genetics. 

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This has really streamlined our 
reporting. 

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We are much faster now. 
We can deliver the report faster

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to the patient and therefore 
help the patient care directly. 

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So does AI help? 
Yes. 

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So we can use health data to 
predict and help us with certain

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tasks. 
So what I've just elaborated on 

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was a rather easy task. 
Just tell me what is this cell? 

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What is this chromosome? 
So we have a picture as an input

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and the classification as an 
output, rather straightforward. 

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Of course, we can also ask more 
complex questions. 

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For example, is this picture 
associated with a certain 

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genotype or is this picture 
associated with a certain 

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outcome of the patient? 
So then we are talking about the

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CS classification 
prognostication. 

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EI can also be used for this. 
Again, we typically are then 

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using machine learning 
approaches. 

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We can use this with supervised 
or unsupervised machine 

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learning. 
And a particular unsupervised 

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machine learning also helps us 
to identify new classes of the 

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CS where we would not have 
thought about. 

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We have so much data now 
available in the area of 

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genomics, where we struggle as 
humans to interpret all those 

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data, to find patterns in this 
large field of data. 

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And here AI is helpful to point 
to certain classes that are 

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biologically similar depending 
on the genotype, on the other 

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features. 
And then we as the humans of the

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medical doctors have to figure 
out if those classes are then 

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meaningful in terms of 
treatment, in terms of 

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prognostication, and how to deal
with this. 

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From all accounts, this also 
leads to a huge improvement in 

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efficiency. 
How long would you say it takes 

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to process for example image and
karyotyping? 

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Would you say 10 seconds more or
less? 

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Even faster. 
Now we are in the range of one 

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second. 
So it's really just get it 

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started and it's done. 
So that's not a bottleneck. 

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The system is really fast. 
And to get this into context, a 

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well trained technician who is 
doing this karyotyping leads 

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about one minute for one 
metaphase and you have to do 

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multiple of those to assess one 
case. 

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So you typically need half an 
hour to assess a case. 

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And now this is pre prepared. 
It still takes some time, but 

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for reviewing and this is much 
faster than doing everything 

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from the scratch. 
Do you think we can still 

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improve this? 
There's always room for 

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improvement, so in the past we 
have been focusing on normal 

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chromosomes. 
The mast majority of those are 

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normal, and we also can assign a
numeric operation, meaning just 

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one chromosome in addition of 1 
chromosome missing. 

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This nicely works, however, when
we're talking about structural 

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operations, for example, a 
translocation that leads to a 

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fusion of the chromosomes. 
BCR Able would be such an 

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example with the philadelphic 
chromosome. 

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This needs to be specifically 
trained to also recognise those 

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structurally abnormal 
chromosomes, and that's what 

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we're currently doing. 
We're training the system with 

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the most frequent and most 
relevant structural operations 

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to also have them automatically 
key assigned. 

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You mentioned morphology. 
Are there any morphology AI 

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models as advanced as the Kyo 
Typing 1? 

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Well, the current typing was the
first one out there and it is 

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really something that we have in
place in our routine diagnostic 

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application for a couple of 
years now. 

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Therefore, we have a lot of 
experience with this and also 

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other labs are already using 
this approach and we know it's 

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really helpful also in in their 
hands in the field of 

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sodomorphology. 
We are a little bit beyond this.

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We need to imply this in our own
lab right now. 

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This is perfectly fine. 
And we're currently in this 

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transition phase to see how 
robust the workflow is to be 

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also applicable for example, in 
other labs. 

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So if any of our listeners wants
want to get to know more about 

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the Kyo typing process, it's AI.
For example the benefits or what

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it take to set it up? 
How and where can they find more

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about it? 
You can contact us, we can get 

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in touch. 
There is always room for 

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collaboration. 
We have a designated AI team in 

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our laboratory and currently 
there are five people working 

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full time on AI applications in 
this diagnostic field. 

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In medicine. 
We are enlarging in this team 

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right now up to 10 people that 
will work at AI and for example,

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with the Carrot typing model. 
This has been a cooperation with

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Meta systems, is also available 
via them directly. 

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So shifting gear a bit here, can
you tell us a bit about how we 

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can use AI to determine patient 
prognosis? 

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Yes. 
So when we're talking about 

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prognosis and hematology, we now
rely on rather well simple 

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models because we need to handle
those. 

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For example, if you think about 
acute mild leukemia, then we 

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have the ELN certification in 
three different risk groups of 

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this of utmost importance for 
treatment of patients with AML. 

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The patients are assigned to 
this risk groups based typically

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on one marker 1 genetic 
operation found inside genetics 

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or molecular genetics and this 
makes the risk group for this 

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patient. 
This is straightforward 

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physician can deal with this 
type of information perfectly 

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fine. 
However, we are losing kind of 

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complexity because in many 
instances we have combinations 

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of multiple mutations and 
together with other operations 

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and to assess this type of 
complexity here AI can help. 

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There are a number of studies 
out there that just asked are 

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there biological subclasses 
within AML that can be assigned 

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to a different biology or to 
different outcome? 

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And this more evidence based 
specification taking into 

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account the complexity of the 
disease will be an interesting 

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way to move the field forward. 
So the principle behind this is 

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it applicable more widely, for 
example to MDSMPNS etcetera. 

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Yes, it's the principle is 
applicable for all those types 

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of diseases. 
For MD's, we now have the IPSSM 

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that has come out in parallel. 
There have been multiple 

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publications on other 
approaches, including also EI 

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for certification of those 
patients and machine learning is

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an issue there. 
Moving forward, to what extent 

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do you think you'll be able to 
implement this in your 

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laboratory, for example? 
Yeah, they can be implemented 

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and they have already been 
implemented to some extent. 

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The important thing is you have 
to carefully validate your 

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model. 
You need to know the 

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performance, how well is it 
working, what are problems, what

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are cases where it doesn't work.
And this is really careful 

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validation process that is of 
utmost importance before you can

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apply this into a clinical 
practice. 

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When we are talking about what 
we are currently doing, this are

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rather narrow questions that we 
are asking, for example, how to 

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assign the class of the cell. 
And this is what we will call a 

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uni model AI, just one input and
one output format. 

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In the future, there are now 
proposals and models out there 

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that can deal with multiple 
formats multimodal AI. 

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This will be a very interesting 
topic to see how the field is 

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moving with this. 
We are not there as a current 

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state to implement this in 
routine practice, but this will 

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be of utmost importance to move 
forward. 

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So what is synthetic data? 
It's a pretty hot topic at the 

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moment. 
Would you be able to explain 

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more about it? 
Yeah, that's a interesting and 

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rather new field within 
generation of data with AI. 

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So large language models are 
kind of generative AI, and this 

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is also something a little bit 
in this direction. 

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So we're not just analysing 
data, but we're producing data 

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with this. 
What does this mean? 

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You have a large data set. 
Big data is still an issue 

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there. 
You have a large data set of 

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real patients for example, and 
you then train a model to 

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produce patients data sets that 
are like the real ones but not 

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perfect copy of the real ones. 
So we've slide modifications and

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those new data sets are then 
called synthetic data sets. 

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What are pros of this of this 
approach? 

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You have better patient privacy 
as the real patient data are 

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then not needed for sharing any 
more. 

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You can share those slightly 
modified data, but we can also 

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augment the data set, increase 
the number at least to some 

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extent and to make some studies 
more powerful with this. 

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That's an emerging field. 
We will have to see for what 

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applications is really useful in
clinical practice and where the 

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limitation of this technique 
are. 

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So for all our listeners who was
also interested in synthetic 

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data, we will have a specific 
podcast on that with Professor 

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Matteo de la Porta. 
If you're interested, please 

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keep an eye out for today 
episode by subscribing to the 

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EHA Unplugged Podcast channel. 
So taking all the things that 

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you've spoken about, along with 
the language models, being able 

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to suggest reports and other 
communications, this is moving 

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towards an AI doctor. 
What is your take on this? 

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Well, we should not overestimate
what AI is currently able to do.

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So those models are helpful in 
many instances. 

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They can well help us get rid of
the boring stuff to do and then 

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focus on the complex things. 
Right now, AI will not be able 

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to solve all the very 
complicated cases and really get

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up with much new information on 
a single case. 

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This is really something where 
the human is still in the front.

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However, it is a matter of 
working with the eye, not 

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against the eye, so it should 
really help us in our process 

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and not replace what we are 
doing in this combination of 

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human intelligence together with
the eye is definitely the way to

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go for it. 
So what you're saying is that we

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shouldn't be afraid of AI, but 
rather we should embrace this 

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change and move forward with it?
Absolutely agree. 

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So don't be afraid, try to learn
about AI and here EHA can be 

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very helpful with those training
activities, trying to learn 

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about their pros, the cons, the 
limitations, how you can use AI,

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how you can use AI in a way that
was really helpful for you in 

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your daily practice. 
And yeah, just you this 

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opportunity, it's a great area 
where we're leaving right now 

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and we should not only focus on 
negative sides, but really get 

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into the doing with this. 
There was a wonderful quote at 

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the end of your talk here at the
EHA 2024 Congress. 

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Would you be able to share it 
again with our listeners here? 

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Yeah, the quote is from Eric 
Topple, one of the most famous 

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physicians dealing with AI. 
And he said AI will not replace 

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physicians, but physicians using
AI will replace physicians not 

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using AI. 
It's a very interesting quote, 

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yes. 
Thank you very much, Professor 

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Holman for this wonderful talk 
and also thank you for everyone 

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listening. 
If you're interested in more 

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podcasts, do stay tuned and 
check out our EHA Unplugged 

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channel. 
Until then, have a nice one.

