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    <title>Knut Håkon Hole | Theragnostic Imaging</title>
    <link>https://www.theragnostics.no/en/author/knut-hakon-hole/</link>
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    <description>Knut Håkon Hole</description>
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      <title>Knut Håkon Hole</title>
      <link>https://www.theragnostics.no/en/author/knut-hakon-hole/</link>
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      <title>Localization of primary prostate cancer: FACBC PET/CT compared with multiparametric MRI using histopathology as reference standard</title>
      <link>https://www.theragnostics.no/en/publications/hole-2021-localization/</link>
      <pubDate>Fri, 15 Oct 2021 00:00:00 +0000</pubDate>
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      <description>&lt;hr&gt;
&lt;p&gt;FACBC (anti-1-amino-3-&lt;sup&gt;18&lt;/sup&gt;F-fluorocyclobutane-1-carboxylic acid) is a FDA-approved PET-tracer in patients with suspected recurrent prostate cancer. In the diagnostic work-up of primary prostate cancer, accurate localization of the index tumor is needed for image-guidance of biopsies. We therefore assessed the performance of FACBC PET/CT to detect and localize the index tumor and compared it to multiparametric MRI (mpMRI) using whole-mount histopathology as reference standard. Twenty-three patients with biopsy-proven prostate cancer had FACBC PET/CT and mpMRI within two weeks prior to prostatectomy. FACBC PET/CT was acquired as 14 minutes list-mode and re-binned into seven 2-minutes intervals. Static FACBC was the acquired data from 4-6 minutes, whereas the dynamic FACBC included all seven intervals. Two radiologists and two nuclear medicine physicians independently interpreted the images and consensus was reached in case of discrepancy. Static PET detected 15 of 23 (65%) of the index tumors, dynamic PET detected 14 of 22 (64%), and MRI detected 20 of 23 (87%). To assess the extent of the tumor, the interpreters delineated the tumor in a 12-regions sector-based template. True positive, true negative, false positive and false negative sectors were recorded based on the template drawings and whole-mount histopathology. Both static and dynamic FACBC PET had sensitivity of 40% and specificity of 99%, whereas MRI had sensitivity of 81% and specificity of 100%. Our data indicate that FACBC PET/CT may be useful but that mpMRI is better for localizing the index tumor in patients with prostate cancer.&lt;/p&gt;
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      <title>Robotic salvage pelvic lymph node dissection for locoregional recurrence after radical prostatectomy: a single institution experience</title>
      <link>https://www.theragnostics.no/en/publications/hopland-2021-robotic/</link>
      <pubDate>Sun, 01 Aug 2021 00:00:00 +0000</pubDate>
      <guid>https://www.theragnostics.no/en/publications/hopland-2021-robotic/</guid>
      <description>&lt;hr&gt;
&lt;p&gt;To assess treatment response (PSA &amp;lt; 0.2 ng/ml), need for additional therapy and complication rate after robot assisted salvage pelvic lymph node dissection (sPLND). Analysis of outcomes data from radical prostatectomy (RP) patients consecutively operated with robot assisted sPLND due to biochemical recurrence and positron-emission tomography (PET)/computed tomography (CT)-detected nodal recurrence of pelvic lymph nodes. Sixty-nine patients underwent robotic sPLND after a median time of 47 months post- RP. Sixty-four patients (93%) had malignant lymph nodes upon histological assessment of sPLND specimen. Twenty patients (29%) achieved PSA &amp;lt; 0.2 ng/ml 6 weeks postoperatively. After median (IQR) follow-up of 15 months (10-27), fourteen patients (20%) still had PSA &amp;lt; 0.2 ng/ml without additional therapy and forty-one patients (59%) had started additional therapy. No significant predictor for treatment response was found. Postoperative complications occurred in 14 patients (20%). Eleven of these complications were classified as Clavien-Dindo grade 1. Oncological benefit of sPLND as the only salvage procedure seems to be limited, though almost one third of patients achieved treatment response. Clinical trials are needed to determine if sPLND as part of a multimodal treatment may improve outcome.&lt;/p&gt;
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      <title>18F-Fluciclovine PET for Assessment of Prostate Cancer with Histopathology as Reference Standard: A Systematic Review</title>
      <link>https://www.theragnostics.no/en/publications/seierstad-2021-sup-18-supf-fluciclovine/</link>
      <pubDate>Thu, 01 Apr 2021 00:00:00 +0000</pubDate>
      <guid>https://www.theragnostics.no/en/publications/seierstad-2021-sup-18-supf-fluciclovine/</guid>
      <description>&lt;hr&gt;
&lt;p&gt;The PET tracer &lt;sup&gt;18&lt;/sup&gt;F-fluciclovine (Axumin) was recently approved in the United States and Europe for men with suspected prostate cancer recurrence following prior treatment. This article summarizes studies where systematic sector-based histopathology was used as reference standard to assess the diagnostic accuracy of the tracer &lt;sup&gt;18&lt;/sup&gt;F-fluciclovine PET in patients with prostate cancer.&lt;/p&gt;
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    <item>
      <title>Prostate-Specific Membrane Antigen PET for Assessment of Primary and Recurrent Prostate Cancer with Histopathology as Reference Standard: A Systematic Review and Meta-Analysis</title>
      <link>https://www.theragnostics.no/en/publications/hernes-2021-prostate-specific/</link>
      <pubDate>Thu, 01 Apr 2021 00:00:00 +0000</pubDate>
      <guid>https://www.theragnostics.no/en/publications/hernes-2021-prostate-specific/</guid>
      <description>&lt;hr&gt;
&lt;p&gt;Prostate-specific membrane antigen PET is a promising diagnostic tool in prostate cancer. The gold standard for the detection of prostate tumor and lymph node metastases is histopathology. The aim of the present review was to investigate accuracy measures of &lt;sup&gt;68&lt;/sup&gt;Ga/&lt;sup&gt;18&lt;/sup&gt;F-labeled prostate-specific membrane antigen PET tracers in primary and recurrent prostate cancer with systematic sector-based histopathology as the reference standard. A systematic literature search was performed and 34 studies were included. Overall, prostate-specific membrane antigen PET showed high specificity, but variable sensitivity to localize known prostate cancer and detect pelvic lymph node metastases.&lt;/p&gt;
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