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Slide, please, Gaetano.

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All right. And now we are back to our main speakers for today.

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Again, as I mentioned at the beginning, our incredible fellow team, they all have

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a number of projects ongoing and have been presenting all around the country and

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the world. So we get to hear some of their recent work that was presented at the CNS.

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And Gaetano, I think you're going to be going first.

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Is that correct?

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Yes, sir.

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All right.

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Let me share my screen.

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All right. Good morning, everyone.

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So today I'll be presenting on our initial results of precision treatment of

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postoperative CSF leaks with ultrasound-guided epidural blood patch.

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And this is a talk that I gave as an oral presentation at CNS in Austin,

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and really was a work of the entire spine team here at Mayo Clinic Florida.

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Florida, as well as Dr. Clendenon and James West.

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I don't have any disclosures relevant to this talk.

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As you know, incidental durotomy is a very well-known complication of spine

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surgery, and if left untreated, it can lead to a persistent CSF leak or

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pseudomeningocele. The reported rate of incidental durotomy ranges from 4 to 16%,

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depending on the index operation.

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If patients develop symptoms of persistent CSF leak,

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first-line treatment is bed rest.

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Other options include oversewing the wound and placement of a lumbar drain,

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and there is the potential need of having to go back to the OR for direct repair.

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While epidural blood patches are routinely used to treat post-anesthesia or post-LP CSF

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leaks, they are not often used after spine surgery for durotomy repair.

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The ultrasound is a great technique that allows radiation-free and

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direct real-time visualization of the pseudomeningocele,

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the dura, and the Tuohy needle.

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But this application in the native spine is often very limited.

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That's magnified in the postoperative spine,

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thanks to the bone work that has been done by removing the bony anatomy and the ligamentous

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there, which allows a window for the ultrasound and for the needle to be

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visualized properly. So in our study, we did a retrospective analysis of patients

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that underwent the US EBP at Mayo Clinic Florida from 2009 to 2020

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for symptomatic pseudomeningocele secondary to spine surgery.

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We collected demographic, procedural, and outcome characteristics.

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The primary outcome of our study was ultrasound EBP success,

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defined as a resolution of the initial symptom that brought the pseudomeningocele to clinic.

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clinical attention, such as postural headaches,

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incisional leak. For our technique, patients are positioned prone.

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The ultrasound is used to localize the pseudomeningocele,

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and the color Doppler can also be adopted to determine if there are any active sites of

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CSF leak of egress. Under ultrasound guidance,

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An 18-gauge Tuohy needle is advanced into the pseudomeningocele and the content is

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aspirated. The needle is then advanced into the epidural space,

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and about 30 mL of autologous blood is injected epidurally in 5 to 10 mL aliquots

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under continuous ultrasound guidance.

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Then, after waiting for 5 to 10 minutes to allow the blood patch to set,

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The ultrasound is then used again to confirm the placement of the patch, and the color

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Doppler can also be used to confirm an absence of CSF egress if that was previously

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identified. Overall, we had 48 patients who underwent a total

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of 61 US EBPs. And you can see that the most frequent index operation was a laminectomy,

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24.5%, and about 36.7% of these cases were revision surgeries.

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And also that the incidental durotomy was unrecognized during the surgery in about 22%

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of cases. You can see here that the median time from surgery to symptom development was

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seven days, and the most frequent symptoms at presentation were

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postural headaches in 64% of cases and incisional leak in 26.5% of cases.

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Here, looking at the results of the EBP under ultrasound guidance,

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You can see that 51% of patients experience resolution of their symptoms after their first

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blood patch, and you can see that the median volume aspirated from the pseudomeningocele

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was 34 mL, and also that another 20% of patients experience resolution of their

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symptoms after subsequent attempts of blood patches.

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Talking about complications, we had about 14% complications in our series,

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And the most frequent one was wound infection in two patients,

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followed by meningitis also in two patients.

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Here is a couple of illustrative cases you can see here.

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Patient that presented with a dural AV fistula.

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And here on the T2 sagittal MRI you can see a fairly large pseudomeningocele.

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After the patient had undergone the laminectomy and obliteration of the AV

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fistula, the patient underwent an ultrasound epidural blood patch.

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The contents of the pseudomeningocele was aspirated and a blood patch placed.

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And then you can see on the postoperative MRI,

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sagittal and axial cut that was done one month after the procedure.

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complete resolution of the pseudomeningocele.

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This is another case of a patient that laminectomy,

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as you can see here on the CT scan on the level above a previous fusion construct,

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and there is an hypodensity there, a collection, fluid collection,

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that was also again identified under the ultrasound where you can see the star there,

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And then the color Doppler was used to identify the active CSF egress there.

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The Tuohy needle, you can see here in white where this big arrow is,

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is inserted. The content of the pseudomeningocele is aspirated,

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as you can see in figure E, and then the blood patch is placed.

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And this is a postoperative scan that documents resolution of the

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pseudomeningocele. Our study carries all the limitations of all single-institution

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retrospective studies,

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therefore further prospective and multicenter studies are needed to confirm the

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generalizability of our data.

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But our study is the first and the largest series describing the adoption of US EBP in

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in patients presenting with persistent pseudomeningocele and CSF leak

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following spine surgery. We found an overall success rate of over 70%,

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with a first-attempt success rate of 50%.

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So this suggests that the utilization of US-guided EBP in expert hands may allow for

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targeted treatment of a large portion of symptomatic postoperative

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pseudomeningoceles. Thank you.

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Gaetano, that's excellent work.

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Congratulations. It's a novel treatment for these non-uncommon problems.

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One thing that I realized I never asked Dr. Miller or

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Dr. Clendenon: what's the consistency of the blood that you're using as the patch,

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And how long is it in between obtaining the autologous blood and actually injecting it?

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I don't know about the time between when the blood is drawn and injected, sir,

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but most of them, I believe, it may have been done at the same time of the

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procedure, sir.

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Yeah, but I mean, they aspirate it and then immediately give it.

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I was just curious about how thick the blood is. Maybe

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Elird, I see Dr. Behrakis who might

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Yeah, I do some of these as well.

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Okay. Yeah, we go right away for the blood.

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So it's right from an IV catheter into the epidural space.

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What's really helpful is the Tisseel fibrin glue.

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So it's human fibrin blood components that we inject,

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and that solidifies much, much quicker and is much more firm.

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With the blood, it's thinner and can get into different

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crevices, while the fibrin glue is a bit more firm.

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So you try to get both properties in there right at the leak.

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Excellent. Yeah. Thanks.

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Thanks, Tiana, I appreciate that.

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Alireza, did you want to give—I see your hand up there.

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Do you want to make a comment?

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Sorry I can't join on camera because I'm

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tied up in the hospital.

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But I would like to second those comments.

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I've done a couple of these cases with Dr. Clendenon. A lot of times what we do is we

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place an arterial line.

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So that way we can reliably draw blood right away as soon as access is identified with the

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ultrasound machine. Fibrin glue has also been something new

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that's been very helpful for these cases.

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One question that I had, and this is something that we always worry about, is the risk of

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infection and meningitis.

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And it's interesting from the data presented,

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that was about two, I believe.

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Any thoughts on looking at the data and anything that we can

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do to make things better or reduce that risk?

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Or is this contributed directly to the block itself?

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Or were there other circumstances on those two patients that got infections?

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Thank you.

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Yes, sir. Excellent question. We had about two patients, about 4% for

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our series. It's a small series, so it's difficult to generalize if that's

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really a 4% for the procedure itself.

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But that was assumed to be related, it was meningitis,

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assumed to be related to the procedure, not like a UTI or any other infections.

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Let's see. We have a question from Dr. Vargas about what

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about the presence of fibrous tissue after the procedure?

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And I think

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So these are usually done

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in scar, that sort of thing.

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Yeah, so these are usually done right after the procedure, it's not too long.

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And that's why it's very difficult to do them anatomically guided.

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That's why the ultrasound really helps to visualize the anatomy.

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And as far as we didn't have any issues as far as going through fibrous tissue for

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the patches.

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Great. Well, thank you so much, Gaetano.

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A couple more points here.

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Dr. Dean mentioned, would emphasize the need to make sure patient is afebrile and has

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normal white blood cell count prior to the blood patch.

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I know that's part of the protocol and a good point.

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Some of these patients are immediate post-op.

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They have an immediate postoperative status, so they might have an elevated white blood

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cell count just from surgery.

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Very, very good point.

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All right. Excellent work, Gaetano.

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And we will go on to the next presentation.

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We have Dr. Garcia who is going to be presenting next.

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Can you see this, Dr. Fox?

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Yes.

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It's advancing by itself.

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All right. Good morning, everyone.

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Today I'm going to be presenting on SPECT CT as a predictor of pain generators in patients

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undergoing intra-articular injections for neck and back pain.

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I think most of you already know of this project.

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It's a project that we did with the spine group under particular mentorship of

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Dr. Abode-Iyamah, and we presented it at Austin at the Congress of Neurological Surgeons.

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As you know, low back pain and also neck pain,

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but there's a lot more literature on low back pain, is one of the main leading causes of

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disability in general, and yet the identification of painful

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generators is still difficult.

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Despite use of multiple morphological-based studies,

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including X-ray, CT, MRI, and also compounded by the fact that sometimes structural

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abnormalities found on scans have no direct correlation with the actual

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pain of the patient, which makes the correct identification of the painful generator

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difficult and therefore the targeted treatment for that painful generator also

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difficult and limited.

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With this in mind, there has been some interest in functional-based tests like SPECT

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to accurately identify those painful generators,

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More recently, a scan has been available which is called the hybrid SPECT CT,

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which at Mayo we have been fortunate to have available for a number of years and with good

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quality, as I'm going to show in one of the example scans.

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So the idea here was to look at facet joint injections,

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targeted injections, and see whether or not the hypothesis that injections targeted at

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positive sites of uptake would do better than injections targeted at foci without uptake.

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To accomplish this, we designed a study with a single institution

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retrospective in which we compared both short and long-term outcomes for patients

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undergoing facet joint injections for neck and back pain.

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Given the large sample size, I was able to do a propensity score match

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to adjust for age, gender, BMI, hypertension,

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and multiple target injections and injection location.

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We did exclude sacroiliac joint injections, given that they are a bit different and they

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should not be grouped all the same with cervical, thoracic, and lumbar injections.

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So these were our main outcomes.

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We looked at immediate positive response, change in VAS two weeks after injection,

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improvement in VAS above 50 and 70% after injection, and need for additional treatment,

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both injection and surgery.

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Importantly, at Mayo, we have people who do call these patients two

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weeks after the procedure who are not implicated in the research.

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So they're able to give us unbiased feedback from the patient regarding patient-

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reported outcomes, which allowed us to really objectify these outcomes.

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So as you can see, we have a large number of patients,

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2,849 patients that were evaluated with SPECT CT within five years.

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Out of these ones, we had 340 with facet injections within 150 days after a SPECT CT.

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Why 150 days? We had to choose a threshold.

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There is no specific literature on the threshold.

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We just had to come up with a threshold that would allow us to look at outcomes that were

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associated with the injection and not associated with something else that could

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have happened in the interlude.

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We had a total of 140 cervical injections,

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21 thoracic injections, and 207 lumbar injections.

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Importantly, 265 were uptake-targeted injections.

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By this we mean that all the injections were targeted at foci of uptake,

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all of them. That was our definition of uptake.

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targeted injections and 75 were non-uptake targeted injections.

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So as you can see here, just an example of a SPECT CT at Mayo,

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with in this particular patient, a right L4-L5 facet joint having uptake that was

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targeted by injection. This is actually one of the cases that was included in this study.

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So here, just some demographics and characteristics of the location and

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characteristics of the injection.

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As you can see, even though there's nothing that is statistically significant,

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it can always compound and have an effect, a confounding effect on the variables.

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Hence why we did the propensity score match to adjust for all these variables.

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And what you can see here is that both on a univariate analysis and a multivariate

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analysis, we did not find statistically
significant differences between non-uptake

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and uptake-targeted injections.

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But when we did look at patients who already
had a failed injection before the SPECT CT

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and in which the surgeon or proceduralist
was able to change the target based on

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the information of the SPECT CT.

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Below, what you can see is that in those patients we do have a benefit.

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And the benefit was particularly greater if there was any change made on the target.

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So that is very suggestive that for a particular set of patients with adequate

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patient selection, you do see a benefit with SPECT CT to guide facet joint injections.

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So basically our conclusions seem to support that, pending adequate patient selection,

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SPECT CT has a benefit in guiding facet injections.

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There are limitations, of course, with our retrospective single

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institution study, but we did use a propensity score to match for confounding

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variables. We have a large sample size, but of course future directions would have to

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be prospective, multi-site, hopefully double-blind clinical trial to

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to accurately discern the impact of SPECT CT in routine clinical practice. And I'll take any

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questions.

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Excellent, Diogo. Really fabulous work.

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And I think this is there's so much potential applicability to using imaging

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biomarkers for better delineating patients' pain.

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Even with the precision of these SPECT

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studies, it shows how challenging it can be to figure out pain generators in the spine.

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And I think this is incredible work with a lot of promise. Based on what you've seen so

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far, who do you think?

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Do you think we should be doing this more or less?

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Or do you think people should have this upfront?

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How do you recommend we use this based on your knowledge of the technique in

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our everyday practice?

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So the patients that I did see have a benefit were patients in which there had already

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been an attempt at an injection.

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Because my understanding is that SPECT CT is sensitive but not necessarily specific.

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So it's difficult to figure out which of those facets that are lighting up are the ones

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that are actually causing pain.

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So when we have the benefit of having a patient that already had a procedure that

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failed, we do know which of those joints did light up.

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but they're not the actual pain generator.

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So we can take those out and pursue the next ones.

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So I do see SPECT CT not as a necessary first line for any patient that has a first

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procedure, but for a recurrent facet injection.

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For a patient who has not benefited from a facet injection,

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I would definitely see benefit there. But of course,

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I think to actually make a recommendation, we'd have to have a double-blind clinical

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trial so we can make a recommendation. Hopefully coming.

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Hopefully so.

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Yeah, and we'll continue to learn more about these imaging biomarkers.

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which I think will be very helpful.

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Dr. Deen makes a great point in the comments as well that we have extremely high

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quality SPECT studies at Mayo, which

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I completely agree. At UF, we didn't do this at all.

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So this was something novel to me.

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seeing here and very impressed with the quality of these studies.

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Excellent work. All right.

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I think we can move on now to our next presentation.

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Dr. Vivas Buitrago, who is going to be speaking about supra-

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marginal resection impact on overall survival for IDH wild-type glioblastoma.

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Perfect. Can you hear me now?

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00:19:31,650 --> 00:19:33,130
Yes. Yes. Thank you, Diogo.

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Let me share the screen here.

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All right. Are you seeing my slide?

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Yes.

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Perfect. Good morning, everyone.

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Thank you for attending to this lecture today.

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So I'm going to present our study that we presented in October this year in CNS.

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The title of this study is Supramarginal Resection Impact on Overall Survival for IDH wild-type

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glioblastoma according to their cell density distribution infiltration profile.

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This is a mathematical model.

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We have no disclosures for this lecture.

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A bit of background regarding the extent of resection in glioblastoma.

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We know that not long ago, the most common surgical recommendation for glioblastoma was

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to perform only a biopsy.

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And this was not only in the United States but worldwide.

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Since the 2000s, we started seeing very important studies from Dr. Lacroix,

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from Dr. McGirt, from Dr. Sanai, from UCSF with Dr. Berger,

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and from Dr. Chaichana and Dr. Quiñones.

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With this data from Hopkins, all of these studies were in favor of performing more

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extensive surgical resection on patients with glioblastoma,

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and the results were pretty much homogeneous,

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identifying that resections above 78% of the contrast enhancement in T1 were associated with

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a significant improvement in overall survival in patients with GBM.

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But furthermore, we see that the gross total resection is a

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is this complete surgical resection of the contrast-enhancing component of the

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tumor that you can see up here.

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But what about the FLAIR component in the T2 sequence? That we have known for

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a while already that there are infiltrated GBM cells within the brain tissue

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that most of the time is not being taken care of,

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resected because of the infiltrated behavior of these

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cells within functional brain tissue that if you resected it,

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you can cause a deficit in the functionality of the patient.

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So we aim with our group at Mayo Clinic to start looking at the extent of the

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supramarginal resection beyond the margins of the contrast-enhancing tumor.

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We have seen that regarding this topic, that has been influenced by the

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results from the good results from external resection beyond

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the margins in low-grade gliomas.

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We see here very important papers from MD Anderson,

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from Hopkins, from Cleveland Clinic, and from UCSF.

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And not all of them have homogeneous results,

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as we found before in the gross total resection for the T1 contrast.

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So we wanted to give it a shot.

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And thanks to all the data that we have at Mayo Clinic with the

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high flow of patients, we were.

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We were able to do this study in which we identified more than 800 patients.

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And we selected only those patients that were IDH wild-type,

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since it's the most aggressive type of GBM that has a less overall survival in total.

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So we only selected those patients that had a gross total resection of the contrast

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enhancement and that they did present before the surgery with some degree of preoperative

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So in total, we included 101 patients.

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We performed all volumetric analysis on all the sequences in the

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contrast enhancement, in the necrosis part, and in the FLAIR for all the patients.

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And we did find in univariate and multivariate analysis that increasing SMR as

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a continuous variable, for the first time we can show that it is statistically

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significant for an increase and improved overall survival in our patient population.

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Furthermore, when we performed a threshold analysis,

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we found that those resections above 20% and less than 60% were the ones that were related

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with a significant increase in overall survival.

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So to summarize our findings, we did this illustration that shows

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In the green part, in the green portion, are the

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percentages from above 20 and less than 60%
that were related with an improved overall

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survival. And we didn't find a significant
benefit in those resections above 60%,

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that is the red portion of the figure here.

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So now we know that increasing SMR is
beneficial for an

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00:25:04,369 --> 00:25:09,329
improved overall survival in our patients with IDH wild-type GBM.

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But we know that there is also a high variability in the radiological presentation

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of our group in general in GBM, but also in IDH wild-type.

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So we partnered with the Mathematical Neuro-oncology Laboratory at Mayo Clinic Arizona,

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with Dr. Kristin Swanson to try to further personalize the

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to try to be more specific with using specific patient characteristics from

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the radiological data.

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And we can see that following our hypothesis at the center of the

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lesion, the one that is in close proximity with

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the contrast enhancement part has a greater tumor burden cell concentration over there.

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And once you are going to the periphery, you see that the density

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of these tumor cells is lower.

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So this is the formula that was used in our patient population.

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In summary, for the interest of time, you can see that in the T1 with contrast, the

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00:26:19,309 --> 00:26:22,309
volume was approximated to a spherical shape.

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And we saw that this portion has a greater cell density compared to the

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cell density in the T2 FLAIR.

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So with these results, we classified our patient population in three

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00:26:39,069 --> 00:26:41,829
groups that were nodular, moderately diffuse,

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and highly diffuse according to their

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00:26:46,150 --> 00:26:49,390
to their tumor cell density and distribution profile.

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So this is a representation from some of the patients that were selected and classified

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and included in these three groups.

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You can see here in the nodular, they have more contrast enhancement than FLAIR.

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And see in the moderate diffuse, you see that there is some more FLAIR in

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the patients surrounding the post-gadolinium T1, and in the highly diffuse

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00:27:16,019 --> 00:27:19,700
you see that the FLAIR is greater than in the other groups.

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00:27:21,859 --> 00:27:26,339
So for this, in the univariate analysis, we saw that this was significant,

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00:27:26,339 --> 00:27:32,180
statistically significant only for moderate and diffuse and highly diffuse.

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00:27:32,220 --> 00:27:34,980
But it was not significant for nodular.

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00:27:35,059 --> 00:27:40,220
This is in univariate, and the same results were obtained for the multivariate analysis.

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00:27:40,500 --> 00:27:44,579
It was statistically significant for moderately and highly diffuse, not for nodular.

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00:27:44,579 --> 00:27:52,980
But when we performed a threshold analysis, we saw that for the nodular, there is actually a

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benefit only in resections from 80 to 100%.

385
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And this is kind of logical because

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00:28:01,039 --> 00:28:04,359
In the nodular, there is not much FLAIR,
as we showed you in the

387
00:28:04,400 --> 00:28:13,200
MRI before. So there is not much
benefit in extending resection beyond the 20%

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00:28:13,200 --> 00:28:16,640
of the contrast enhancement in the
nodular group.

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00:28:17,119 --> 00:28:22,839
In the moderately diffuse,
we found benefits from all the way up to 50%,

390
00:28:22,880 --> 00:28:25,440
as you can see here. And in the highly
diffuse,

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00:28:25,440 --> 00:28:32,039
We only saw benefits beyond 30% all the way up to 90 and 90 plus percent.

392
00:28:33,599 --> 00:28:36,880
So this is very important because now we can,

393
00:28:37,400 --> 00:28:40,119
based on this study, at least in these results,

394
00:28:40,279 --> 00:28:44,599
we see that there is a very important benefit in the

395
00:28:44,640 --> 00:28:47,039
supramarginal resection of these patients.

396
00:28:47,039 --> 00:28:54,279
And of course, based on their radiological characteristics before the surgery,

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00:28:54,660 --> 00:28:59,579
the surgeons can decide how much the patients can need,

398
00:28:59,579 --> 00:29:02,819
a resection, an extent of resection based on this.

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00:29:02,819 --> 00:29:05,619
And for example, in these highly diffuse tumors,

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00:29:05,619 --> 00:29:12,259
we found that this is the maximum SMR correlated with a beneficial overall

401
00:29:12,259 --> 00:29:19,500
survival. You can see that the patients that had a resection above 90% had a

402
00:29:19,500 --> 00:29:22,819
better overall survival than the ones that had less than 90%.

403
00:29:23,140 --> 00:29:27,220
And this patient population had a greater survival of,

404
00:29:27,940 --> 00:29:33,779
if I remember correctly, almost nine months greater than the patients

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00:29:33,779 --> 00:29:39,500
that had a resection with less than 90%. For the moderately diffuse,

406
00:29:39,539 --> 00:29:42,779
The highest SMR percentage was 50,

407
00:29:43,099 --> 00:29:48,059
and this patient presented with a benefit

408
00:29:48,299 --> 00:29:49,980
of an additional seven months.

409
00:29:51,420 --> 00:29:55,099
And in the nodular patients, the highest maximum significant
