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    <Identifier>26urobay26</Identifier>
    <IdentifierDoi>10.3205/26urobay26</IdentifierDoi>
    <IdentifierUrn>urn:nbn:de:0183-26urobay266</IdentifierUrn>
    <ArticleType>Meeting Abstract</ArticleType>
    <TitleGroup>
      <Title language="en">Prospective evaluation of &#91;68Ga&#93;-FAPI-PET&#47;MRI for loco-regional staging of muscle-invasive bladder cancer</Title>
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        <PersonNames>
          <Lastname>Laukhtina</Lastname>
          <LastnameHeading>Laukhtina</LastnameHeading>
          <Firstname>Ekaterina</Firstname>
          <Initials>E</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Medical University of Vienna, Department of Urology, Vienna, Austria</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="yes">author</Creatorrole>
      </Creator>
      <Creator>
        <PersonNames>
          <Lastname>Shariat</Lastname>
          <LastnameHeading>Shariat</LastnameHeading>
          <Firstname>Shahrokh F.</Firstname>
          <Initials>SF</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Medical University of Vienna, Department of Urology, Vienna, Austria</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
      </Creator>
      <Creator>
        <PersonNames>
          <Lastname>Hassler-Di Fratta</Lastname>
          <LastnameHeading>Hassler-Di Fratta</LastnameHeading>
          <Firstname>Melanie</Firstname>
          <Initials>M</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Medical University of Vienna, Department of Urology, Vienna, Austria</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
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      <Creator>
        <PersonNames>
          <Lastname>Hacker</Lastname>
          <LastnameHeading>Hacker</LastnameHeading>
          <Firstname>Marcus</Firstname>
          <Initials>M</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Medical University of Vienna, Department of Biomedical Imaging and Image-guided Therapy, Devision of Nuclear Medicine, Vienna, Austria</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
      </Creator>
      <Creator>
        <PersonNames>
          <Lastname>Muin</Lastname>
          <LastnameHeading>Muin</LastnameHeading>
          <Firstname>Dina</Firstname>
          <Initials>D</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Medical University of Vienna, Department of Biomedical Imaging and Image-guided Therapy, Devision of Nuclear Medicine, Vienna, Austria</Affiliation>
        </Address>
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          <Corporatename>German Medical Science GMS Publishing House</Corporatename>
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        <Address>D&#252;sseldorf</Address>
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    <SubjectGroup>
      <SubjectheadingDDB>610</SubjectheadingDDB>
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    <DatePublishedList>
      <DatePublished>20260506</DatePublished>
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    <Language>engl</Language>
    <License license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
      <AltText language="en">This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License.</AltText>
      <AltText language="de">Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung).</AltText>
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      <Meeting>
        <MeetingId>M0645</MeetingId>
        <MeetingSequence>26</MeetingSequence>
        <MeetingCorporation>Bayerische Urologenvereinigung</MeetingCorporation>
        <MeetingCorporation>&#214;sterreichische Gesellschaft f&#252;r Urologie und Andrologie</MeetingCorporation>
        <MeetingName>52. Tagung der Bayerischen Urologenvereinigung und der &#214;sterreichischen Gesellschaft f&#252;r Urologie und Andrologie</MeetingName>
        <MeetingTitle></MeetingTitle>
        <MeetingSession>Prostata-, Urothel- &#38; Nierenzellkarzinom klinisch, operativ, systemisch, experimentell</MeetingSession>
        <MeetingCity>W&#252;rzburg</MeetingCity>
        <MeetingDate>
          <DateFrom>20260506</DateFrom>
          <DateTo>20260508</DateTo>
        </MeetingDate>
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    <ArticleNo>26urobay26</ArticleNo>
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      <MainHeadline>Text</MainHeadline><Pgraph><Mark1>Introduction:</Mark1> Fibroblast activation protein (FAP) is frequently overexpressed by cancer-associated fibroblasts in various tumor types, including bladder cancer. This study aimed to evaluate the performance of &#91;68Ga&#93;-FAPI-PET imaging for loco-regional staging in patients with MIBC. </Pgraph><Pgraph><Mark1>Methods:</Mark1> In this prospective investigator-initiated study, consecutive MIBC patients planned for RC were enrolled. All patients underwent both &#91;68Ga&#93;-FAPI-PET&#47;MRI and standard &#91;18F&#93;-FDG-PET&#47;CT prior to NAC and again prior to RC. The primary outcome of interest was the diagnostic accuracy of &#91;68Ga&#93;-FAPI-PET&#47;MRI and&#47;or &#91;18F&#93;-FDG-PET&#47;CT for local and nodal staging in MIBC patients. The specificity, sensitivity, PPV, and NPV of imaging modalities for local and nodal staging were assessed, with pathology results at RC serving as the reference test. </Pgraph><Pgraph><Mark1>Results:</Mark1> We included twenty-two MIBC patients treated with RC; among them, fourteen (64&#37;) received NAC. Fifteen patients (68&#37;) had residual bladder tumor at RC. In ten patients, &#91;68Ga&#93;-FAPI demonstrated significant expression in the primary tumor located in the bladder wall, resulting in a sensitivity of 60&#37;, specificity of 85&#37;, PPV of 89&#37;, and NPV of 50&#37;. Similarly, &#91;18F&#93;-FDG-PET&#47;CT demonstrated a sensitivity of 60&#37;, specificity of 100&#37;, PPV of 100&#37;, and NPV of 54&#37; for primary tumor detection. The median number of removed lymph nodes was 32 (range 2 to 78). Seven patients (32&#37;) had lymph node metastases on the RC pathology report. For lymph node detection, &#91;68Ga&#93;-FAPI-PET&#47;MRI and &#91;18F&#93;-FDG-PET&#47;CT resulted in identical sensitivity (33&#37;), specificity (93&#37;), PPV(69&#37;), and NPV (75&#37;). </Pgraph><Pgraph><Mark1>Conclusion:</Mark1> In this study, &#91;68Ga&#93;-FAPI-PET&#47;MRI demonstrated similar diagnostic accuracy to &#91;18F&#93;-FDG-PET&#47;CT for locoregional tumor staging in MIBC patients; both modalities had a moderate sensitivity but high specificity for detecting primary tumors and lymph node metastases. These findings indicate that &#91;68Ga&#93;-FAPI-PET could be a viable alternative imaging tool for MIBC staging, though both imaging modalities&#47;tracers underperform for ruling out a cancer. Further studies are needed to validate &#91;68Ga&#93;-FAPI-PET&#8217;s reliability and clinical utility.</Pgraph></TextBlock>
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