Interactive Transcript
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Hello and welcome to the PSMA PET Mastery course.
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My name is Dr. Sally Aer and I'm a dual trained radiologist
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and nuclear medicine specialist from Sydney, Australia.
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We are going to start with some basics about PSMA pet,
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talk about why the scans might be indicated
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and how they are conducted
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and then move on to imaging interpretation.
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Okay, let's get started.
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So, prostate cancer is the most common malignancy in men.
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Um, if you discount skin cancers
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and it is the most, the second most common cause
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of cancer related death in men,
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it is diagnosed following detection of a raised PSA
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or prostate specific antigen
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or an abnormal digital rectal examination.
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These examinations are usually prompted when the man
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presents with symptoms
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and these symptoms can include urinary tract symptoms such
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as increased urination overnight
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or noria increased urinary frequency or difficulty emptying
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or completely emptying the bladder.
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Um, although this does have a broad differential including
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benign prostatic hyperplasia, um,
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or they may present with hematuria or blood in the urine.
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And unfortunately in some cases, and we wanna try
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and prevent this, the men can present with symptoms related
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to metastasis such as bone pain in the setting
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of skeletal metastasis to the spine.
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Briefly, we're going to stop here at prostate anatomy
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and we will revisit this later in the course.
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So the prostate, we think about the base being up close
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to the bladder and then the apex being um, more inferiorly.
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So almost like an inverted kind of current or pyramid.
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There are four specific zones,
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but we can combine the central zone
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and transition zone to give the central gland.
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Moving from the base of the gland, we have the central zone,
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which is marked in this kind of dark purple blue
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and that's more posteriorly.
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And at the front is the fibromuscular stroma.
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Now this is important 'cause this doesn't
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contain glandular tissue.
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So invasion of this structure is important when you're
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looking at MRI interpretation, which is well
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outside the scope of this presentation today.
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As we move more inferiorly
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and we've gotten here at axial size two, we are seeing more
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of the transition zone marked in green.
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And then you'll also notice that the urethra starts more
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anteriorly and then moves kind
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of more centrally and posteriorly.
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The more inferiorly you move through the gland relative
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to the remainder of the tissue surrounding it.
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Coming down at three, we've got that transition zone.
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And also at two and three at that posterior
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and lateral aspect of the prostate,
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we have the peripheral zone.
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And this is quite important
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because of the fact that 70%
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of prostate cancers will arise in this peripheral zone
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or the peripheral gland.
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Um, and then coming down towards the apex, you still have
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that peripheral zone as well as more of the transition zone
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and that anterior fibromuscular stroma coming all the way
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down to the apex.
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So 30% of cancers will arise in the central gland,
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which is this blue and green area.
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So we need to be aware that we are looking
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for abnormal increased uptake
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and we are talking about PET in this series,
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abnormal increased uptake in different parts of the gland
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and then considering that in the context
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Of other imaging or the patient's presentation.
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So coming back a section
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and we're just going to think about
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how prostate cancer spreads in the body.
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And I believe that when I'm interpreting my images, one
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of the most important things to do is
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to think about the pathology of the tumor
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and how it spreads through the lymphatics, how it interacts
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with the structures around it.
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And I really use that to hone my search patterns in imaging
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interpretation and lymph nodes are no different.
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So the first place that
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that prostate cancer typically spreads
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to is the pelvic lymph nodes
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and these are the ones contained within the true pelvis.
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And that kind of comes into staging that we'll see later.
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That N one disease is nodes contained within the true pelvis
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below the pelvic brim, but discounting common iliac
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and inguinal lymph nodes, they're considered M1
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or metastasis one or distant nodes.
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Um, but once they have spread to the pelvis, they do tend
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to follow those big vessels.
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So following the iliac vessels
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through the common iliacs into the
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retroperitoneum around the aorta.
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And that's really important when we think about metastasis
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bone far and away, the most common, uh,
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that has been reported, which comes into why traditionally
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prostate cancer was staged with bone scans.
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Um, as we knew that a good proportion
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of metastatic disease did affect the bones
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that said metastasis can go
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to other organs including the lung, the liver,
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pleura, adrenal glands.
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And I have seen some cases that have gone to the brain.
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So thinking about the imaging modalities
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with prostate cancer as well.
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So if we look at diagnostic radiology, we have MRI
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and here's a tumor here at the anterior aspect.
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And then we also have ct, which is really the mainstay
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for imaging of a lot of other tumor modalities.
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And I do a lot of lung cancer as well in addition
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to my general um, PET and PSMA work.
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And I know that for our lung cancer patients diagnostic CT
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so far and away the most um, common investigation
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that we use in radiology, but it's less
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useful in prostate cancer.
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Um, this she case with the blue ring shows
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that the patient does have an enhancing lesion in the
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prostate, but this isn't the norm.
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Often the lesions you cannot see
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and often the lymph nodes that are involved are small
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and with CT we have our size criteria that we use
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for interpretation, but if they are less than a centimeter,
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we may not detect them
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and that's where other modalities really come in handy.
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Um, also with ct it's great for looking at bone lesions, um,
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but if they are not developing a sclerotic
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or a lytic response within the bone, then we may miss them.
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So with as, just to summarize, those limitations of ct um,
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include um, that we have limited assessment
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of the primary tumor in many cases
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and also that there can be a size assessment
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of the node limitation.
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And so we may Ms. Small volume local recurrence,
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which often happens when we have just a small elevation in
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PSA in a previously treated patient.
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In terms of thinking about nuclear medicine,
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we have traditionally relied on technician 99
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and bone scans which use a bisphosphonate
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analog. And so we're looking at
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Osteoblastic activity.
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So the osteoblast takes out the tracer
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for the radiopharmaceutical from the blood
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and deposits it into bone.
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So we have a surrogate measure of bone turnover.
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Um, but this relies on a few things that the fact
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that we need to have bone metastases
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and that those bone metastases are osteoblastic.
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The majority are, but not all are.
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And we don't really get a good sense of the soft tissues,
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particularly the lymph nodes.
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But of course bone scans aren't our only option
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and we now have A-P-S-M-A PET CT
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to help stage these patients
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and that is what this whole mastery course is about today.
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And here's an example. We not only are able
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to image the skeleton in this case,
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which does have quite widespread skeletal metastases,
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but the primary tumor, the soft tissues
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and metastases affecting other organs besides the skeleton.
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So in summary, the limitations of bone scans,
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which have meant that it is less useful compared
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to PSMA PET include that it gives assessment
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of the skeleton only.
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It only also images osteoblast metastases.
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And I do put an asterisk here as we can sometimes see
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NIA in regions of lytic metastases.
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And we do have SPECT cts,
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so the functional plus the low dose CT imaging
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that we confuse together for increasing that interpretation.
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Um, but typically osteoblastic lesions is
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where bone scans shine, which isn't always the case.
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We image, um, patients for bone scans four hours
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after injection of tracer compared to gallium,
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which is we image them an hour after injection.
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So we've got a shorter access, shorter time.
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Um, and then there's also inherent limitations in spatial
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resolution and that we are looking at a scan which is
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sensitive but not necessarily specific.
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And what do I mean by that?
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I mean that a bone scan will pick up any cause
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of increased bone turnover, whether that be infection
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or arthritis or um, even a healing fracture.
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So there's a huge differential
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and sometimes even though it's really useful in detecting
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and very sensitive for osteoblastic metastases,
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there can still be some diagnostic uncertainty with that.
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And just to close off this first section,
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I just thought I would showcase one example of
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how we can use diagnostic radiology with that MRI
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or the multiparametric MRI of the prostate in conjunction
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with our PSMA pets.
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And here is a lesion anteriorly within the gland at the
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base, and corresponding to that focal increased uptake
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of the PSMA ligand tracer,
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which we'll learn about a little bit more in the upcoming
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modules.