39 research outputs found

    Prostate specific membrane antigen (PSMA) ligands for diagnosis and therapy of prostate cancer

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    <p><b>Introduction:</b> Prostate specific membrane antigen (PSMA) has become an attractive diagnostic and therapeutic target for small molecule ligands. Radionuclide-chelating ligands can be labeled with either <sup>68</sup>Ga for positron-emission-tomography (PET) or <sup>177</sup>Lu for radionuclide therapy.</p> <p><b>Areas covered:</b> In this literature review we evaluate the diagnostic value of <sup>68</sup>Ga PSMA PET/CT and the therapeutic potential of <sup>177</sup>Lu PSMA radioligand therapy (RLT) in patients with prostate cancer. <sup>68</sup>Ga PSMA PET/CT is more accurate than CT for nodal staging and superior to conventional imaging in patients with biochemical recurrence, translating into major changes in clinical management. The preliminary data for <sup>177</sup>Lu PSMA indicates >50% reduction of PSA levels in up to 59% of patients. Severe adverse events occurred <10% of patients after RLT.</p> <p><b>Expert commentary:</b> PSMA ligands for diagnostic and therapeutic purpose will significantly impact the management of patients with prostate cancer.</p

    Reproducibility of the 8 remaining HePs (see Table 3, type A), as the function of reconstruction settings (see in Table 1) and acquisition time.

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    <p>Reproducibility of the 8 remaining HePs (see <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0164113#pone.0164113.t003" target="_blank">Table 3</a>, type A), as the function of reconstruction settings (see in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0164113#pone.0164113.t001" target="_blank">Table 1</a>) and acquisition time.</p
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