WEBVTT

00:00:00.000 --> 00:00:19.440
Music.

00:00:19.945 --> 00:00:23.485
Hello and welcome everybody. This is Joe from StartupRate.io,

00:00:23.625 --> 00:00:29.365
your startup podcast and YouTube blog from Germany, bringing you yet another interview today.

00:00:29.625 --> 00:00:32.525
Today, I do have Giuseppe here with me. Hey, how are you doing?

00:00:33.325 --> 00:00:37.965
Hi, Jan. Nice to meet you. Thank you for having me here. It's totally my pleasure.

00:00:38.045 --> 00:00:39.185
A little disclaimer here.

00:00:39.405 --> 00:00:42.985
Today, we do the first interview on my new computer.

00:00:42.985 --> 00:00:48.445
I was building StartupRate.io on a laptop that was first produced in 2015,

00:00:48.745 --> 00:00:55.725
and now I upgraded it seriously to a computer together with a friend who actually

00:00:55.725 --> 00:00:57.565
called the computer only the beast.

00:00:57.805 --> 00:01:01.425
So let's see how this is performing and if everything works.

00:01:01.825 --> 00:01:08.305
I actually have not all the cables yet, so that means I'm working only on one monitor, but I'm sure.

00:01:08.465 --> 00:01:12.325
I keep my fingers crossed so that everything goes well.

00:01:14.085 --> 00:01:19.865
Yeah, in Germany, thumbs press, but we do both that and everything will be totally fine.

00:01:20.065 --> 00:01:24.685
Today's episode is sponsored by StartupRaven.com, the fastest and most efficient

00:01:24.685 --> 00:01:29.825
way to find new investors, startups to connect and cooperation partners.

00:01:30.485 --> 00:01:34.485
Giuseppe, you are an Italian living in Munich.

00:01:34.665 --> 00:01:40.385
Funny note here, I've heard a lot of people from Munich referring to it as the

00:01:40.385 --> 00:01:42.065
most northern city of Italy.

00:01:42.985 --> 00:01:46.265
Yeah, exactly. So Munich is seen as the most northern city of Italy.

00:01:46.385 --> 00:01:51.505
It's because of the climate, because of the... No, it's really nice to be here.

00:01:51.605 --> 00:01:53.465
It's very close to Italy, as you know.

00:01:53.825 --> 00:01:58.345
And the atmosphere, the way of living is quite similar.

00:01:59.045 --> 00:02:02.345
And except the food. So the food we had to import.

00:02:05.085 --> 00:02:08.025
So you're not a fan of Weisswurst for breakfast?

00:02:08.645 --> 00:02:13.605
Not really. Maybe once a year I have Weisswurst. But then I go back to my Italian

00:02:13.605 --> 00:02:17.125
dishes, gnocchi and tagliatelle.

00:02:17.365 --> 00:02:20.485
And, you know, we have good food. We have a big variety there.

00:02:21.145 --> 00:02:24.945
I have to admit that they both have a certain place in my life,

00:02:24.985 --> 00:02:28.605
but actually don't tell anybody. But I prefer Weisswurst for dinner.

00:02:29.385 --> 00:02:34.505
Okay, don't tell anybody. This would be a crime in Bavaria. So don't do that.

00:02:36.505 --> 00:02:42.085
Exactly. Giuseppe, you are today here because we will talk about a serious topic,

00:02:42.285 --> 00:02:45.885
diagnosing tumors, speeding up this diagnostics.

00:02:46.165 --> 00:02:50.565
You are from a company called Viva Scope.

00:02:50.785 --> 00:02:54.325
Can you tell us a little bit about this company and the history?

00:02:54.405 --> 00:03:00.265
Because when we talked before, you told me about a very, very interesting setup here.

00:03:00.385 --> 00:03:07.485
So you're not necessarily a startup anymore. You do your R&D in Rochester, upstate New York.

00:03:07.565 --> 00:03:12.825
You're headquartered in Munich, and you have production facilities in Europe and the US.

00:03:12.965 --> 00:03:16.265
So can you walk us a little bit through all that stuff?

00:03:16.990 --> 00:03:19.690
Yeah so the whole story i mean i'm i'm now

00:03:19.690 --> 00:03:23.030
19 years with the company quite a long of time and

00:03:23.030 --> 00:03:28.070
but it started even before and it started with the in vivo application so today

00:03:28.070 --> 00:03:33.910
we will not hear a lot about in vivo diagnostic and xvivo diagnostic in vivo

00:03:33.910 --> 00:03:39.730
diagnostic was the first area of application and it's quite interesting how

00:03:39.730 --> 00:03:42.790
it started they developed the product which was

00:03:42.870 --> 00:03:45.750
supposed to check the effect of hair removal,

00:03:45.970 --> 00:03:48.570
which is a pure aesthetic application.

00:03:49.930 --> 00:03:55.430
And they wanted to see how good the quality is when you remove hair, how good the cut is.

00:03:55.710 --> 00:04:01.310
And then they realized, wow, we can see much more in the skin. We can see cells.

00:04:01.490 --> 00:04:05.650
We can see different layers in the skin. What can we do with this information?

00:04:06.050 --> 00:04:11.730
And then they started to investigate. And by now, we can use this in vivo technology,

00:04:12.150 --> 00:04:19.650
which had its origin in aesthetic, to diagnose very accurate skin diseases in

00:04:19.650 --> 00:04:21.850
vivo before cutting out anything.

00:04:22.450 --> 00:04:27.890
Okay, this is how it started. The other technology we are offering is ex vivo.

00:04:28.110 --> 00:04:30.050
This is I have to remove tissue.

00:04:30.650 --> 00:04:35.550
And here I want to have a very fast diagnosis. This is a bit the history.

00:04:35.550 --> 00:04:40.710
We may get into the background because we're talking today about diagnosing

00:04:40.710 --> 00:04:44.050
cancer, especially skin cancer. And...

00:04:45.581 --> 00:04:50.861
Everybody was thinking, fast diagnosis, you get a good diagnosis anyways.

00:04:51.181 --> 00:04:57.501
But actually, guys, listen, when you get tissue removed, you want to have the

00:04:57.501 --> 00:05:01.461
results as fast as possible to know if it's in cancer or not.

00:05:01.601 --> 00:05:04.741
Right now, how long can it take to get the diagnosis?

00:05:05.261 --> 00:05:10.261
It takes, unfortunately, quite long, 10 days up to three weeks.

00:05:10.961 --> 00:05:16.321
And this is far too long. I'm not a doctor. I have a commercial background,

00:05:16.581 --> 00:05:23.361
but I was quite shocked when I started in this area to see how long it takes to get a result.

00:05:23.601 --> 00:05:29.301
So today I can order whatever I want digitally on the Internet.

00:05:29.421 --> 00:05:33.681
I can get it the next day. But if I want to know if I have a tumor or not,

00:05:33.781 --> 00:05:35.241
I need to wait so long time.

00:05:35.941 --> 00:05:39.161
And then I started to try to understand why is this?

00:05:39.341 --> 00:05:43.661
What's the reason for that? On the other side, when we talk about skin cancer,

00:05:43.781 --> 00:05:49.801
so we're going to talk today about in vivo application means skin and all diseases

00:05:49.801 --> 00:05:53.601
around skin and the ex vivo application with the other device.

00:05:54.341 --> 00:06:01.681
It's all type of tumors from prostate cancer to breast cancer, lung cancer and so on.

00:06:02.161 --> 00:06:08.801
In the area of skin, there is an over excision rate. Let's say there is a lot

00:06:08.801 --> 00:06:12.061
of biopsies done which are not necessary.

00:06:12.421 --> 00:06:17.881
So over 60% of this removal are done because there is a suspect.

00:06:18.221 --> 00:06:22.701
But, you know, skin, I can look with my eyes. I can use a lens.

00:06:23.081 --> 00:06:26.381
But I always stay at the surface. I see the top of the iceberg.

00:06:26.641 --> 00:06:30.881
I don't know what's below, what's happening. How big is the iceberg? Going to crash or not?

00:06:31.281 --> 00:06:36.081
So it's the same for skin cancer. And so we have the difficulties to understand,

00:06:36.281 --> 00:06:40.261
or the dermatologists have the difficulty to understand what's happening below.

00:06:40.681 --> 00:06:47.041
Before risking to get a melanoma, they just remove it. But then after two weeks, you get the result.

00:06:48.129 --> 00:06:54.089
Was nothing, was a benign lesion. So in the in vivo area, we want to avoid that

00:06:54.089 --> 00:06:59.289
too much biopsies are taken and benign lesions are sent to the laboratory.

00:06:59.889 --> 00:07:07.869
This is the aim for the in vivo. Ex vivo, we want to know immediately what is there.

00:07:08.309 --> 00:07:13.909
In the best case, this is our target, which we're managing, when the patient

00:07:13.909 --> 00:07:15.429
is there in the hospital.

00:07:16.849 --> 00:07:21.609
That's very important. You're talking about unnecessary biopsies.

00:07:21.669 --> 00:07:27.529
We may tell our audience the doctor is not really able to tell from just looking

00:07:27.529 --> 00:07:31.249
at it if it's cancers or not.

00:07:31.449 --> 00:07:37.029
So that means there needs to be some tissue removed, sent into a certain laboratory,

00:07:37.349 --> 00:07:42.389
and then really thoroughly cut under a microscope.

00:07:42.529 --> 00:07:47.309
And they have specialists to look at it. And I do believe that's the process

00:07:47.309 --> 00:07:49.649
when you guys come in, right?

00:07:49.849 --> 00:08:00.109
Yeah, exactly. So every tumor in the world needs to be judged by this doctor called pathologist.

00:08:00.349 --> 00:08:05.569
The pathologist is the only one which can tell if a tumor is there,

00:08:05.669 --> 00:08:08.189
independent of its skin or the other types of tumors.

00:08:08.969 --> 00:08:14.889
The process, the base of his judgment is an image.

00:08:15.489 --> 00:08:19.669
And the image is now achieved by a process called histology.

00:08:20.869 --> 00:08:27.169
Unfortunately, this process called histology to get the image is today in 2024,

00:08:27.649 --> 00:08:31.349
an analogue procedure, so tissue is removed.

00:08:32.439 --> 00:08:39.379
There are three types of these procedures. So the most common one was the paraffin section.

00:08:39.639 --> 00:08:41.619
I don't know how deep I should enter into these details.

00:08:41.999 --> 00:08:46.079
Paraffin section is one of these. It takes minimum 24 hours.

00:08:46.319 --> 00:08:50.279
Here they take the tissue, they embed in paraffin, they cut it in slices,

00:08:50.359 --> 00:08:51.879
and then they put it into chemicals.

00:08:51.919 --> 00:08:56.479
And then 24 hours later, they have an image, which is on a glass slide,

00:08:56.599 --> 00:08:58.939
and the pathologist is looking at it.

00:08:59.899 --> 00:09:04.219
Since ever there was the wish to have a faster way of doing diagnosis,

00:09:04.439 --> 00:09:07.259
of doing histology, of getting these images.

00:09:07.679 --> 00:09:14.219
And in 1894 the so-called frozen section was invented.

00:09:14.579 --> 00:09:21.059
Here we have the advantage that it takes less time, but the tissue is frozen,

00:09:21.279 --> 00:09:26.219
cut into slices, analog, and then put into chemicals.

00:09:26.539 --> 00:09:29.679
This freezing up the tissue creates some problems.

00:09:30.719 --> 00:09:35.839
It creates artifacts and every time I cut something and I put it into paraffin

00:09:35.839 --> 00:09:40.099
or frozen, I lose the tissue, I lose the probe because it's dead.

00:09:40.339 --> 00:09:42.179
I cannot use it for further investigations.

00:09:43.739 --> 00:09:49.419
And this is the problem of the current system. It's still made in an analog way.

00:09:49.879 --> 00:09:56.519
What we do is, we do it digitally. In vivo we image the skin in a digital way

00:09:56.519 --> 00:10:01.139
and we see what's going on, if there's a need of excising or not.

00:10:01.479 --> 00:10:06.919
Ex vivo we have a tissue which we just put on the machine, we scan it and we

00:10:06.919 --> 00:10:13.839
get an image like the pathologist knows today, this kind of H&E like image it's called.

00:10:15.614 --> 00:10:24.694
Big advantage time i preserve the tissue i can act much faster than than with the analog system.

00:10:25.614 --> 00:10:29.434
And we're talking here about minutes so it's

00:10:29.434 --> 00:10:32.354
not a small change that you improve by

00:10:32.354 --> 00:10:35.834
a bit it's from weeks to minutes

00:10:35.834 --> 00:10:41.134
and that's that's a big big improvement the

00:10:41.134 --> 00:10:44.574
other problem we have today is that worldwide we

00:10:44.574 --> 00:10:47.674
have 20 million cases of

00:10:47.674 --> 00:10:50.474
cancer which need to

00:10:50.474 --> 00:10:53.434
be diagnosed by whom you learn the lesson

00:10:53.434 --> 00:10:56.834
all the tests by the pathologists

00:10:56.834 --> 00:11:00.014
so did the number of cases

00:11:00.014 --> 00:11:03.254
is increasing in a drastic way we're expecting in

00:11:03.254 --> 00:11:06.154
2040 30 million it's not saying me is

00:11:06.154 --> 00:11:12.794
the WHO saying this and on this this number of pathologists which are able to

00:11:12.794 --> 00:11:19.714
make a diagnose I would expect also a big increase but here's the problem worldwide

00:11:19.714 --> 00:11:24.134
we have 84,000 pathologists,

00:11:24.874 --> 00:11:27.734
covering 90% of the

00:11:27.734 --> 00:11:30.454
cancer cases yeah this is a

00:11:30.454 --> 00:11:36.554
far too low number and the tendency is decreased in number of pathologists and

00:11:36.554 --> 00:11:43.254
not increased in number of pathologists it's a huge problem yeah so when we

00:11:43.254 --> 00:11:45.014
have more and more cancer cases

00:11:45.014 --> 00:11:49.694
less and less pathologists who's gonna diagnose all these cases means.

00:11:51.056 --> 00:11:54.636
If i'm lucky i get my result after i don't know how many months if

00:11:54.636 --> 00:11:58.476
i'm not lucky i will die before i get my diagnosis and

00:11:58.476 --> 00:12:01.336
here we need to change things we need

00:12:01.336 --> 00:12:04.596
to make the process much efficient much

00:12:04.596 --> 00:12:08.516
more efficient i cannot bake pathologists but

00:12:08.516 --> 00:12:11.676
i can make this analog process in a

00:12:11.676 --> 00:12:16.336
digital way cutting down the time and reducing

00:12:16.336 --> 00:12:23.096
or let's say reducing the time needed to get to the diagnose to get to the image

00:12:23.096 --> 00:12:30.416
yeah we may add here that of course for everybody who had ever a biopsy done

00:12:30.416 --> 00:12:36.136
and it was not yet determined if it's cancer or not this is quite a stressful full time.

00:12:36.276 --> 00:12:41.736
But we should also emphasize that this could give you a week's head start in

00:12:41.736 --> 00:12:46.956
the best case to start your treatment, which may at the end have a decisive

00:12:46.956 --> 00:12:48.436
impact on your treatment.

00:12:48.676 --> 00:12:51.596
So that's where you guys are really coming in.

00:12:52.276 --> 00:12:58.556
It's amazing. Just to tell you a story, I was last week in Rome at our reference

00:12:58.556 --> 00:13:00.416
center, Unicampus Biomedical,

00:13:00.736 --> 00:13:06.236
with a fantastic pathologist, Ana Crescenzi, she's a wonderful, progressive doctor,

00:13:06.476 --> 00:13:12.416
and I assisted to a procedure, so we had a patient, suspect of pancreas,

00:13:12.436 --> 00:13:14.916
you know, pancreas is very, very aggressive,

00:13:15.156 --> 00:13:22.316
we have a mortality of 95% in this area, he came in, then Professor Di Matteo

00:13:22.316 --> 00:13:29.396
used the endoscope, so he took anaesthesia, of course, endoscopic examination,

00:13:29.756 --> 00:13:31.196
we took a biopsy.

00:13:32.276 --> 00:13:35.056
Which are liquid biopsies in this case, not firm.

00:13:35.576 --> 00:13:40.696
And then immediately they brought it to the machine. They scanned the probe.

00:13:40.876 --> 00:13:42.796
And within three minutes, we

00:13:42.796 --> 00:13:47.816
saw that, number one, what they took out of the body is of good quality.

00:13:48.016 --> 00:13:50.696
That's also a challenge when I cannot see this immediately.

00:13:51.216 --> 00:13:56.436
And number two, we saw that it's an aggressive tumor.

00:13:58.856 --> 00:14:04.756
So very bad for the patient. Normally now, this probe would have gone to the

00:14:04.756 --> 00:14:09.356
laboratory, after two weeks he would get his result, and then there's another

00:14:09.356 --> 00:14:13.316
process called molecular analysis in order to know what kind of treatment you need.

00:14:13.796 --> 00:14:17.216
It would have taken four weeks until he can start the treatment.

00:14:17.636 --> 00:14:23.416
On this day, I was quite flashed because I saw there's an aggressive tumor.

00:14:23.916 --> 00:14:26.096
She then took the probe.

00:14:27.416 --> 00:14:33.576
And scraped a bit of the cells into another container and put it in another device.

00:14:34.036 --> 00:14:37.396
And the molecular analysis was done within three hours.

00:14:37.636 --> 00:14:47.596
So within one day, this patient got his analysis, aggressive type of pancreas

00:14:47.596 --> 00:14:51.496
tumor, and he got also the,

00:14:52.216 --> 00:14:57.816
therapy he needs the information that is needed to start the therapy this is

00:14:57.816 --> 00:15:03.596
a revolution this is a change of paradigm it's like when they invented the plane not a car,

00:15:04.376 --> 00:15:12.476
it's changing completely the workflow cutting down the time from weeks in this

00:15:12.476 --> 00:15:18.396
case four weeks to one day and for me this is emotional yeah this is very because

00:15:18.396 --> 00:15:20.756
everybody which has a case in the family,

00:15:21.496 --> 00:15:27.956
uh can understand what the problem is there are many people out there don't even know about this.

00:15:28.776 --> 00:15:33.976
Time needed to get the diagnosis they trust the system the system is relying

00:15:33.976 --> 00:15:38.556
on an analog system but i don't want to wait 10 days do you want to wait 10

00:15:38.556 --> 00:15:40.576
days if you have a suspect of pancreas,

00:15:41.336 --> 00:15:47.936
or lung biopsy no no i don't i wouldn't want to wait that long this is this

00:15:47.936 --> 00:15:54.076
is incredible that we We don't know and we realize once we are affected or once

00:15:54.076 --> 00:15:58.616
our beloved are affected or friends are affected, we realize, wow.

00:15:59.816 --> 00:16:03.456
And there is an urgency because the situation is not getting better, it's getting worse.

00:16:03.716 --> 00:16:10.996
So it's not saying us, the prediction of cancer is increasing in a drastic way.

00:16:11.096 --> 00:16:15.936
And the guys which can say, tell you there's a cancer are decreasing.

00:16:15.936 --> 00:16:22.596
There are 40% over 55% down the way of retirement.

00:16:23.036 --> 00:16:28.076
The workload is increasingly high of the remaining people.

00:16:28.296 --> 00:16:35.656
And especially in Germany, I just read yesterday, it's one pathologist per 48,000

00:16:35.656 --> 00:16:40.536
inhabitants, means the worst value in Europe, in Germany.

00:16:41.476 --> 00:16:49.016
I would expect not Germany. So there's even worse situation in this country.

00:16:49.949 --> 00:16:55.369
But in general, we have some differences in the distribution.

00:16:55.629 --> 00:16:58.569
But in general, worldwide, we have a big problem.

00:16:59.309 --> 00:17:03.929
I see. And when you've been talking about this biopsy, by the way,

00:17:03.969 --> 00:17:10.169
liquid biopsy is just that you don't extract tissue, but liquid. So simple as it gets.

00:17:12.009 --> 00:17:18.029
So today, there's the tendency, which is good, to be less and less invasive.

00:17:18.029 --> 00:17:23.129
So in the former times, they took big chunks out of your body.

00:17:23.249 --> 00:17:29.109
They had a big probe, big tissue in order to make the process.

00:17:29.389 --> 00:17:34.509
Today, when I have suspect of lung cancer or pancreas or thyroid,

00:17:34.729 --> 00:17:41.309
they try to go with a nice needle and take some sample, very little sample.

00:17:41.309 --> 00:17:47.629
So imagine this system, this analog system, which was built based on big chunks,

00:17:47.809 --> 00:17:53.229
has to now handle these small little samples. And this is quite impossible.

00:17:53.469 --> 00:18:00.549
There's no other way to do a fast diagnosis with this analog technology.

00:18:02.569 --> 00:18:07.629
It takes time. It needs to go to the laboratory. The patient goes home. So there's a process.

00:18:07.789 --> 00:18:12.289
After two weeks, they find out the biopsy was not good.

00:18:12.349 --> 00:18:15.789
Please come back, which is the worst, worst case. We have to do it again.

00:18:16.069 --> 00:18:23.629
Or after 10 days, we did the process and you have unfortunately two more we need to treat you.

00:18:23.969 --> 00:18:32.449
So for us, as we use it like a scanner, it's very easy to have liquid biopsies

00:18:32.449 --> 00:18:34.709
or small fragments of biopsies.

00:18:34.709 --> 00:18:39.189
So we see that in the market, or let's say in this area,

00:18:39.948 --> 00:18:45.828
There's an increasing number of small and liquid biopsies, which is good for us.

00:18:46.028 --> 00:18:52.728
But the more we have this minimal invasive biopsies, the more that the current system is challenged.

00:18:52.988 --> 00:18:58.108
So we have the advantage of you put it on the scanner, you scan it and then

00:18:58.108 --> 00:19:01.208
whatever it is, whatever size it is, we can see it immediately.

00:19:01.448 --> 00:19:02.768
So this is another big advantage.

00:19:03.848 --> 00:19:09.068
And there's a funny story. Sorry, how did we get there? How did Anna Glashensky get there?

00:19:09.768 --> 00:19:14.448
We went for Neurology Congress in Rome before COVID.

00:19:14.988 --> 00:19:20.088
And then we did the Congress. We all flew home. And then COVID started.

00:19:20.348 --> 00:19:22.608
And we had no access to this machine anymore.

00:19:23.088 --> 00:19:28.428
And Anna was in this hospital. And she also at the same time got a little sponge,

00:19:28.568 --> 00:19:32.608
a little matrix in order to bind this little and liquid biopsies.

00:19:32.808 --> 00:19:38.428
So thanks to COVID, she had the time. and to test this solution and to find

00:19:38.428 --> 00:19:42.348
out that there is a new way of having a fast evaluation in a digital way.

00:19:42.428 --> 00:19:46.568
So this is also some positive aspect of COVID.

00:19:47.428 --> 00:19:53.008
So these two years where she had the machine, she managed to develop all this

00:19:53.008 --> 00:19:54.328
application, which is fantastic.

00:19:55.585 --> 00:20:01.845
When you've been talking about getting faster digitally, the first thing that

00:20:01.845 --> 00:20:08.205
came to mind, hey, you got less and less pathologists and everybody is talking about AI right now.

00:20:08.205 --> 00:20:15.565
Now, I do totally understand that there are much higher levels of certainty, of trust, of testing,

00:20:15.845 --> 00:20:20.905
of processes that need to be done before you could even think about introducing

00:20:20.905 --> 00:20:26.145
even an AI-assisted diagnosis for pathologists here.

00:20:27.365 --> 00:20:31.105
My question would be, are you guys already working on stuff like that?

00:20:31.325 --> 00:20:36.545
Yeah, we need to. I mean, it's obvious. We will not change the number of pathologists so quickly.

00:20:37.385 --> 00:20:42.345
If it's not a political change, a push, but even so, if somebody would decide

00:20:42.345 --> 00:20:47.565
today to invest in the promotion or let's say in the education of new pathologists,

00:20:47.805 --> 00:20:50.305
then it would take years.

00:20:50.885 --> 00:20:57.305
We will need AI because even we make the process fast and digital,

00:20:57.645 --> 00:21:03.605
we need to support the pathologists in the daily work.

00:21:03.605 --> 00:21:08.445
Thanks to the fact that we do it digitally, we have now the possibility with

00:21:08.445 --> 00:21:11.165
the digital image to feed AI system.

00:21:11.505 --> 00:21:21.405
We did this with our partner university and Professor Hartmann from the LMU in Munich for BCCs.

00:21:21.465 --> 00:21:27.645
It's the most current skin cancer, the so-called white skin cancer.

00:21:27.765 --> 00:21:33.105
The black skin cancer is called melanoma. And she won with our device,

00:21:33.245 --> 00:21:37.305
with the software, the first prize, the German Medical Award.

00:21:37.405 --> 00:21:38.845
So it was a nice moment for us.

00:21:39.685 --> 00:21:46.065
But this is only the beginning. We have now also developed together with another

00:21:46.065 --> 00:21:49.965
company an AI judging the sample.

00:21:50.105 --> 00:21:53.345
So I want to know if I take with my endoscope out of the body,

00:21:53.465 --> 00:21:55.925
the biopsy is good of quality or not.

00:21:56.285 --> 00:21:59.665
And here AI can help us immediately to check the adequacy.

00:22:00.225 --> 00:22:08.285
The next step would be to check adequacy and to make a kind of preliminary diagnosis

00:22:08.285 --> 00:22:14.445
to support the pathologist or to indicate where the area are.

00:22:14.585 --> 00:22:17.805
You could see very nicely where are the cells which are important.

00:22:18.025 --> 00:22:19.945
Are they there? Are they enough?

00:22:20.845 --> 00:22:26.125
So, when we talk about biopsy, it's important to have a good,

00:22:26.125 --> 00:22:34.045
adequate probe, means enough cells that I can use to do all the consecutive examination.

00:22:34.625 --> 00:22:40.145
The first one is histology to understand I have tumor, I have no tumor.

00:22:40.956 --> 00:22:46.496
Is it aggressive or not? The second one which they adopt is the immunohistochemistry

00:22:46.496 --> 00:22:49.316
to better understand the typology of the tumor.

00:22:49.496 --> 00:22:54.956
And the third one is the molecular analysis to know which therapy is fitting

00:22:54.956 --> 00:22:58.916
to you or to me, Giuseppe, or to my sister.

00:22:59.096 --> 00:23:03.396
So we are all different. So we need individual so-called medicine.

00:23:03.676 --> 00:23:06.116
We need to have individual treatment.

00:23:06.456 --> 00:23:09.376
Not everybody can have the same treatment.

00:23:09.576 --> 00:23:12.556
It's impossible. it's not efficient it can be

00:23:12.556 --> 00:23:15.736
good the most efficient treatments the doctors

00:23:15.736 --> 00:23:19.756
are talking about you have a certain molecular composition

00:23:19.756 --> 00:23:24.716
of tumor and then they have treatments they call it a key it fits in luck and

00:23:24.716 --> 00:23:28.896
then they can really efficiently treat it that's what you're talking about individual

00:23:28.896 --> 00:23:36.036
medicine right yeah yeah so we need for every individual I'm receptive to type A,

00:23:36.216 --> 00:23:40.196
you're receptive to type B because of the DNA,

00:23:40.396 --> 00:23:46.016
and then you need the drug made for type A or made for type B.

00:23:46.296 --> 00:23:51.996
So what Anna told me was very interesting is today, when you do the normal way,

00:23:52.116 --> 00:23:57.536
you have a suspect of lung cancer, for example, you go make the investigation,

00:23:57.816 --> 00:24:00.736
the imaging, then they take the biopsy, goes to the laboratory,

00:24:00.876 --> 00:24:05.256
and they see it's an aggressive tumor, they have to do a molecular analysis,

00:24:05.396 --> 00:24:08.476
and it takes four weeks, four to five weeks.

00:24:08.956 --> 00:24:13.796
So what do they do with the patient in between? They cannot wait five weeks

00:24:13.796 --> 00:24:15.596
doing nothing. They start,

00:24:16.380 --> 00:24:19.780
a general treatment which has a cost for the system.

00:24:20.760 --> 00:24:27.500
Imagine one month of treatment for lung cancer is 60 000 euros in cost.

00:24:27.800 --> 00:24:33.700
So they just start a general treatment to do something in the hope it's good

00:24:33.700 --> 00:24:40.060
until the specific result comes where they can use the right drug.

00:24:40.440 --> 00:24:44.540
The problem is that you cannot stop after four weeks the general treatment.

00:24:44.660 --> 00:24:48.200
You need to finish the cycle, she explained to me. You have to finish until

00:24:48.200 --> 00:24:54.840
this is then ready, and you can then start, in some cases, after six weeks the

00:24:54.840 --> 00:24:57.140
specific treatment, which is crazy.

00:24:58.900 --> 00:25:05.020
We lose time. We spend resources on a drug which doesn't make sense,

00:25:05.700 --> 00:25:10.820
and then we put in danger the life of the patient.

00:25:10.820 --> 00:25:14.680
She said some patients cannot wait all this time and they just die.

00:25:15.300 --> 00:25:17.140
It sounds terrible.

00:25:18.020 --> 00:25:23.880
I say this, but if you think about your relatives, to say he died because it

00:25:23.880 --> 00:25:25.540
took too long to get the diagnosis.

00:25:26.100 --> 00:25:30.180
How crazy is that? This is really something very serious.

00:25:31.520 --> 00:25:36.020
Independent that you're working in this field, but it's just crazy to say he

00:25:36.020 --> 00:25:40.700
died without knowing what he had. or he died because it took too long to get the diagnosis.

00:25:40.860 --> 00:25:46.600
So there's an urgent need because of many reasons to improve the system,

00:25:46.740 --> 00:25:54.940
to digitalize the system, to have digital images which can be seen remotely and not on site.

00:25:55.580 --> 00:25:58.820
There are some countries where the pathologist is driving by car.

00:25:58.980 --> 00:26:02.980
By car he's driving to a clinic to assist during a surgery process.

00:26:03.620 --> 00:26:14.140
How crazy, I don't have to say it's nonsense, so it's a waste of resources which we don't have.

00:26:16.251 --> 00:26:23.411
You guys are really making an effort to shorten the diagnosis and establish

00:26:23.411 --> 00:26:27.611
even a better diagnosis with helping with remote.

00:26:27.871 --> 00:26:31.911
So my understanding is in the future, there will be options for remote.

00:26:32.031 --> 00:26:34.091
In the future, there will be options for AI.

00:26:34.811 --> 00:26:40.171
Are you also looking for, before we get into a little bit into the future,

00:26:40.311 --> 00:26:43.451
where are you guys currently available?

00:26:43.451 --> 00:26:46.991
Because as we already said, you have the headquarter in Munich,

00:26:47.131 --> 00:26:51.651
you have R&D in upstate New York at the Great Lakes. Have you been there?

00:26:51.791 --> 00:26:53.991
Oh, yeah. Did you wear warm socks?

00:26:54.811 --> 00:26:58.971
In the wintertime, wintertime is quite tough in Rochester.

00:26:59.211 --> 00:27:02.351
I think due to the climate changes, also a bit changed there.

00:27:02.351 --> 00:27:13.151
But I remember flying to Rochester from Newark by this little propeller plane and a stormy night.

00:27:13.551 --> 00:27:18.491
And I see only the runway from the, you know, the cockpit was open, the door was open.

00:27:18.571 --> 00:27:22.251
You could see the snow and the plane, and he was like doing like this.

00:27:22.351 --> 00:27:25.251
And at the last minute doing like this, you know, was crazy.

00:27:25.391 --> 00:27:31.311
But summertime, Finger Lakes, wineries, really fantastic. One time I had the

00:27:31.311 --> 00:27:39.691
luck to fly via Toronto, I took the car and I passed Niagara Falls and then I drove on to Rochester.

00:27:40.291 --> 00:27:44.471
So beautiful, beautiful area, especially the Finger Lakes is fantastic.

00:27:44.691 --> 00:27:46.091
I love it. I love it very much.

00:27:47.431 --> 00:27:54.031
This is a nice, nice area. I would assume you guys are vivoscopes currently

00:27:54.031 --> 00:27:59.211
available in Europe, meaning the European Union and the United States.

00:27:59.211 --> 00:28:02.491
Anywhere else we just started in india uh

00:28:02.491 --> 00:28:05.591
it was um an idea which came

00:28:05.591 --> 00:28:08.711
into my mind why not india it's 1.4 billion people

00:28:08.711 --> 00:28:14.431
and we hired indian colleagues which we appreciate very much and we did our

00:28:14.431 --> 00:28:20.511
first demo tour and uh after the first demo tour that this i think the indians

00:28:20.511 --> 00:28:25.291
are really amazing yeah they got so excited so progressive doctors and they

00:28:25.291 --> 00:28:26.591
have a big problem they have even

00:28:26.731 --> 00:28:33.331
higher workload than we have and it immediately ordered four devices now after one month.

00:28:33.471 --> 00:28:36.531
So this is for me, it's wow, they're fast, they're clever.

00:28:38.111 --> 00:28:44.611
We need to learn a bit of the speed and dynamic of Indian people.

00:28:45.451 --> 00:28:49.831
In Europe, we have 50 centers by now.

00:28:51.166 --> 00:28:56.926
The latest one is really made me happy is a pediatric center in Ancona means

00:28:56.926 --> 00:29:03.986
for babies and children because I didn't also not know that sometimes when you

00:29:03.986 --> 00:29:06.346
have this Hirschsprung disease is called,

00:29:06.466 --> 00:29:12.446
you need to do a kind of surgery and the babies are put under anesthesia for quite a long time.

00:29:12.546 --> 00:29:17.226
So we could reduce the time for anesthesia by two hours, which is immense.

00:29:17.226 --> 00:29:22.206
So, this makes a big difference for the babies.

00:29:22.366 --> 00:29:25.166
So, I think this is a fantastic application.

00:29:25.686 --> 00:29:32.586
And I just got the news that the first oral lecture was accepted to the World

00:29:32.586 --> 00:29:34.546
Congress for Patriotic Oncology.

00:29:35.866 --> 00:29:41.826
I think we all wanted our babies, our children, are feeling well and that they get the best treatment.

00:29:43.246 --> 00:29:50.326
Yeah, we have 50 centers throughout Europe. We have roughly five now in U.S.

00:29:50.346 --> 00:29:54.186
U.S. is quite tough with the regulation.

00:29:54.526 --> 00:29:59.406
You need to prove by big studies that you are allowed to do this.

00:29:59.466 --> 00:30:01.826
So we have Mandy Anderson, Memorial St.

00:30:01.906 --> 00:30:08.106
Catherine, New York, with fantastic scientists and doctors.

00:30:09.446 --> 00:30:14.466
Professor Krishnamurti Savitri, she's a pathologist, very, very progressive.

00:30:15.166 --> 00:30:22.686
Manu Jain pathologist. So it's nice to see how these pathologists are pushing the technology.

00:30:23.026 --> 00:30:28.786
So it's nice because pathologists are used to this analog process,

00:30:28.946 --> 00:30:31.806
but they saw and understood that this is a help for them.

00:30:31.886 --> 00:30:34.286
It's a relief. They can sit at big monitors.

00:30:34.586 --> 00:30:40.486
They can judge the sample from the office or from home. And it's not a threat.

00:30:40.646 --> 00:30:43.646
We're just changing the way of doing

00:30:43.646 --> 00:30:47.326
histology we do it digital and funny

00:30:47.326 --> 00:30:50.606
enough when I started my first job at the Japanese company

00:30:50.606 --> 00:30:53.366
at the time we were the first introducing the digital

00:30:53.366 --> 00:30:59.146
camera so before we used the camera with the film so we made pictures we took

00:30:59.146 --> 00:31:03.966
the film out we said it to laboratory waited to get the results and now it's

00:31:03.966 --> 00:31:12.286
basically the same also in this field in a much more important field the pathology histopathology,

00:31:12.446 --> 00:31:15.166
yeah, the diagnosis area.

00:31:15.486 --> 00:31:20.866
And so it's nice, it's nice to have this, this kind of repeating of the history

00:31:20.866 --> 00:31:22.206
in a higher level, let's say.

00:31:22.446 --> 00:31:27.866
I see. Um, are you guys looking currently for somebody to join your journey?

00:31:27.946 --> 00:31:32.126
So are you looking for talented people? We're looking at getting more and more

00:31:32.126 --> 00:31:34.546
important, we need, of course, it's kind of a.

00:31:36.132 --> 00:31:38.872
Challenging you need to know a lot uh as i

00:31:38.872 --> 00:31:42.012
mentioned i i studied uh mba uh but

00:31:42.012 --> 00:31:45.472
uh i had to learn a lot about skin tumors what

00:31:45.472 --> 00:31:48.892
is a melanoma what is the basis cell carcinoma tinea keratosis inflammatory

00:31:48.892 --> 00:31:54.572
diseases what is the prostate cancer why they take 18 biopsies out of your prostate

00:31:54.572 --> 00:32:00.792
to know if you have prostate cancer breast breast core biopsy fine needle needle

00:32:00.792 --> 00:32:02.572
biopsy, fine needle aspiration,

00:32:03.112 --> 00:32:05.432
lung, how do they do this?

00:32:05.572 --> 00:32:10.532
So it's a lot. It's really a lot to learn, but it's a fantastic way to combine

00:32:10.532 --> 00:32:17.852
your job with something really makes sense, which helps in a tremendous way.

00:32:18.252 --> 00:32:23.632
It helps to improve and to get fast results. And it helps you.

00:32:25.012 --> 00:32:32.492
It helps me when I'm affected. And the probability to get the cancer is unfortunately increasing.

00:32:32.812 --> 00:32:37.292
So we have to think about if it happens, where do I go?

00:32:37.452 --> 00:32:43.972
Do I go to a center offering old type or do I go to a center offering digital,

00:32:44.092 --> 00:32:46.412
new, progressive approach?

00:32:47.712 --> 00:32:51.832
And on the one side, we're looking for talented people.

00:32:52.112 --> 00:32:56.832
Of course, we are a middle-sized company. We are not Siemens,

00:32:56.932 --> 00:33:00.752
we are not General Electric, so it takes more time, it takes more resources,

00:33:00.912 --> 00:33:05.392
and let's say we need then to just do it all by ourselves.

00:33:05.732 --> 00:33:11.872
Thanks God we won many grants last year, which allow us or supports us,

00:33:12.032 --> 00:33:18.532
but you know, medicine is a very slow moving object.

00:33:18.532 --> 00:33:23.012
Checked to change things takes long time.

00:33:24.612 --> 00:33:33.572
Yeah, I do understand that some of it is just to reduce the risk of of potential misdiagnosis.

00:33:33.772 --> 00:33:36.832
Are you guys are also open to talk to new investors?

00:33:38.032 --> 00:33:44.972
Of course, always. I mean, I was, I am a firm believer of collaborations,

00:33:45.292 --> 00:33:49.012
in terms of combining different technologies together,

00:33:49.252 --> 00:33:53.172
in terms of bringing people with knowledge inside,

00:33:53.412 --> 00:33:58.152
in terms of bringing resources to speed up the process because as I mentioned,

00:33:58.332 --> 00:34:03.792
it's an urgent, urgent problem and the more power we have to change things,

00:34:04.012 --> 00:34:09.492
the more, let's say, the more we have the chance to also save people.

00:34:09.492 --> 00:34:14.452
Yeah, we're talking about people's life, that's definitely an issue.

00:34:15.859 --> 00:34:21.619
And we now have a lot of big companies knocking at the door. I'm quite happy.

00:34:22.979 --> 00:34:29.659
And I'm looking forward to these new collaborations. But our doors are open for more.

00:34:32.379 --> 00:34:36.259
Giuseppe, it was really great having you as a guest. You could totally tell

00:34:36.259 --> 00:34:39.659
you are an Italian the way you've been talking.

00:34:39.759 --> 00:34:45.099
I like it when I do have a guest who has really an interesting and important

00:34:45.099 --> 00:34:46.839
topic and can talk a lot about it.

00:34:47.299 --> 00:34:51.039
We're now running almost at thirty five minutes recording time here.

00:34:51.159 --> 00:34:53.739
So I'd like to say thank you. Milagros.

00:34:54.339 --> 00:34:55.899
That's a little bit of a veto.

00:34:56.599 --> 00:35:01.399
I hope I hope it was a bit interesting. I tend to not stop.

00:35:01.599 --> 00:35:04.679
I was want to stop. So thank you so much.

00:35:04.759 --> 00:35:08.939
It was great to talk about this problem and possible solutions.

00:35:08.939 --> 00:35:17.539
And I wish you a fantastic day and week ciao ciao ciao,

00:35:22.399 --> 00:35:32.059
that's all folks find more news, streams events and interviews at www.startuprad.io

00:35:32.059 --> 00:35:34.639
remember sharing is caring.

00:35:35.600 --> 00:35:49.717
Music.

