Interactive Transcript
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So in the second part of our first section, we're going
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to be looking at the emergence of PSMA ligand PET scans
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and how they have really changed the game in the assessment
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of patients with prostate cancer.
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And so PSMA stands for prostate specific membrane antigen,
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and that's a transmembrane type two glycoprotein.
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And this is physiologically expressed on the surface
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of many cells all around the body.
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And as we can see here with our normal, well,
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this is a patient with disease,
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but we can see normal uptake in multiple AL organs,
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including saliva, glands, liver, spleen, bowel,
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and excretion by the renal tract.
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So it's not only seen in prostate cells,
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it's not only seen in prostate cancer cells,
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but where it becomes useful is
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that it is upregulated in cells that have prostate cancer.
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So those cells become more avid to the tracer
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because of increased expression of PSMA antigen.
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So the PSMA ligand RADIOPHARMACEUTICALS were developed
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through the two thousands.
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And I will pause here just to say
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that PSMA ligand is really the name of
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what the radiopharmaceutical that we're injecting is.
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Um, it's a ligand that binds to the antigen,
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which is present on the cell surface
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for patients with prostate cancer.
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And that's how we image it.
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But you will notice that I will use the term
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interchangeably, um,
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and just assumed if I'm talking about PSMA
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radiopharmaceutical, I'm talking about the PSMA ligand
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and talking about the binding
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and the uptake in the tissues in the body.
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So with its development, it was fantastic
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because all of a sudden we had a quite reasonably specific,
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um, trace of the assessment
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and treatment of prostate cancer.
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And traditionally, FDG pet, which is our workhorse PET,
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wasn't so good at imaging patients with prostate cancer
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because of the way that the cells interacted with glucose.
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Um, not all of them being particularly glucose avid
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or hypermetabolic two radiopharmaceuticals have emerged, um,
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although are quite a number on the market,
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and that depends on variable practice.
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But, um, in my experience, the ones
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that I use in my practice are Gallium 68, PSMA 11,
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which we'll shorten to gallium 68 PSMA
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or just PSMA in the upcoming modules.
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And this is one of the most widely used tracers worldwide,
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um, but also one that will come across as well
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as F 18 DCF pile, also called F 18 PSR.
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And that uses the positron emitter of fluorine 18,
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whereas Gallium 68 PSA, as the name suggests,
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uses gallium 68 as the positron emitter
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in terms of PS a's emergence into practice.
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And there's been a lot of studies
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that have demonstrated the utility
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of these imaging investigations
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for diff patients at different stages along
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their prostate cancer journey.
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So in one study, which was performed at, um,
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in Sydney at actually at my hospital, it was found
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that a 51% change in management was occurring in patients
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referred for this PET scan, which is fantastic.
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Um, and that change in management may relate
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to surgical resection.
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Radiotherapy be that external beam brachytherapy
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or suitability for LUTETIUM 1 77 PSMA,
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which is a theranostic agent where we
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Swap out the Gallium 68
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and put in the beta emitter LUTETIUM 1 77.
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But we will come back to that in some upcoming modules
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or systemic therapy,
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and that includes androgen deprivation
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therapy agents as well.
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What the study did notice, however,
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that the management change was more common in patients
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with biochemical failure with a low PSA,
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so low volume disease, and it's just starting to emerge.
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So really low PSAs,
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and that encountered a 62% change in management as opposed
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to 51% in the overall cohort.
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It noticed that there was less change for primary staging,
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particularly with no change in prostatectomy rates.
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However, when a management change was evoked,
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it often was about, you know, treatment
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of local regional disease, particularly whether
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or not to give radio therapeutic pelvic nodes which were
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involved, um, even though previously going undetected.
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So there's also a role, um, for A-P-S-M-A pet, which is a,
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it's a total body imaging modality.
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So there is a role for detection
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of clinically significant incidental findings.
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And in this, this is a rotating MIP
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or a MIP projection maximum intensity,
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which we'll see in upcoming modules used quite a lot.
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Um, but here with the purple arrow is the site
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of primary disease in the prostate focal uptake.
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But in this case, there was also another abnormality seen in
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the thorax, which was found
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to be an incidentally detected primary lung cancer.
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Note that the lung cancer,
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even though it isn't a prostate cancer metastasis
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or anything to do with the prostate cancer,
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still has a little bit of PSMA uptake.
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And this is a pitfall that we will also revisit in upcoming
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modules.