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  <ref-type name="Journal Article">17</ref-type>
  <contributors>
    <authors>
      <author>Obrecht-Sturm, Denise</author>
      <author>Schömig, Lena</author>
      <author>Mynarek, Martin</author>
      <author>Bison, Brigitte</author>
      <author>Schwarz, Rudolf</author>
      <author>Pietsch, Torsten</author>
      <author>Pfister, Stefan M</author>
      <author>Sill, Martin</author>
      <author>Sturm, Dominik</author>
      <author>Sahm, Felix</author>
      <author>Kortmann, Rolf-Dieter</author>
      <author>Gerber, Nicolas U</author>
      <author>von Bueren, André O</author>
      <author>Fleischhack, Gudrun</author>
      <author>Schüller, Ulrich</author>
      <author>Nussbaumer, Gunther</author>
      <author>Benesch, Martin</author>
      <author>Rutkowski, Stefan</author>
    </authors>
    <subsidiary-authors>
      <author>Brainbank (Bonn)</author>
    </subsidiary-authors>
  </contributors>
  <titles>
    <title>Treatment response as surrogate to predict risk for disease progression in pediatric medulloblastoma with persistent magnetic resonance imaging lesions after first-line treatment.</title>
    <secondary-title>Neuro-Oncology</secondary-title>
  </titles>
  <periodical>
    <full-title>Neuro-Oncology</full-title>
  </periodical>
  <publisher>Oxford Univ. Press</publisher>
  <pub-location>Oxford</pub-location>
  <isbn>1522-8517</isbn>
  <electronic-resource-num>10.1093/neuonc/noae071</electronic-resource-num>
  <language>English</language>
  <pages>1712 - 1722</pages>
  <number>9</number>
  <volume>26</volume>
  <abstract>This study aims at clarifying the impact of persistent residual lesions following first-line treatment for pediatric medulloblastoma.Data on 84 pediatric patients with medulloblastoma and persistent residual lesions on centrally reviewed magnetic resonance imaging (MRI) at the end of first-line therapy were analyzed.Twenty patients (23.8%) had residual lesions in the tumor bed (R+/M0), 51 (60.7%) had distant lesions (R0/M+) and 13 (15.5%) had both (R+/M+). Overall response to first-line therapy was minor or partial (≥ 25% reduction, minor response [MR]/PR) for 64 (76.2%) and stable disease (SD) for 20 patients (23.8%). Five-year post-primary-treatment progression-free (pptPFS) and overall survival (pptOS) were superior after MR/PR (pptPFS: 62.5 ± 7.0%[MR/PR] vs. 35.9 ± 12.8%[SD], P = .03; pptOS: 79.7 ± 5.9[MR/PR] vs. 55.5 ± 13.9[SD], P = .04). Furthermore, R+/M + was associated with a higher risk for progression (5-year pptPFS: 22.9 ± 17.9%[R+, M+] vs. 72.4 ± 12.0%[R+, M0]; P = .03). Watch-and-wait was pursued in 58 patients, while n = 26 received additional treatments (chemotherapy only, n = 19; surgery only, n = 2; combined, n = 3; valproic acid, n = 2), and their outcomes were not superior to watch-and-wait (5-year pptPFS: 58.5 ± 7.7% vs. 51.6 ± 10.7% P = .71; 5-year pptOS: 76.3 ± 6.9% vs. 69.8 ± 9.7%, P = .74). For the whole cohort, 5-year pptPFS by molecular subgroup (58 cases) were WNT: 100%, SHH: 50.0 ± 35.4%, group-4, 52.5 ± 10.5, group-3 54.2 ± 13.8%; (P = .08).Overall response and extent of lesions can function as surrogate parameters to predict outcomes in pediatric MB patients with persistent lesions after first-line therapy. Especially in the case of solitary persistent medulloblastoma MRI lesions, additional therapy was not beneficial. Therefore, treatment response, extent/kind of residual lesions and further diagnostic information need consideration for indication of additional treatments for persisting lesions.</abstract>
  <notes/>
  <label>PUB:(DE-HGF)16, ; 0, ; </label>
  <keywords>
    <keyword>Humans</keyword>
    <keyword>Medulloblastoma: diagnostic imaging</keyword>
    <keyword>Medulloblastoma: pathology</keyword>
    <keyword>Male</keyword>
    <keyword>Child</keyword>
    <keyword>Female</keyword>
    <keyword>Magnetic Resonance Imaging: methods</keyword>
    <keyword>Cerebellar Neoplasms: diagnostic imaging</keyword>
    <keyword>Cerebellar Neoplasms: pathology</keyword>
    <keyword>Disease Progression</keyword>
    <keyword>Child, Preschool</keyword>
    <keyword>Adolescent</keyword>
    <keyword>Follow-Up Studies</keyword>
    <keyword>Prognosis</keyword>
    <keyword>Retrospective Studies</keyword>
    <keyword>Survival Rate</keyword>
    <keyword>Infant</keyword>
    <keyword>Neoplasm, Residual: diagnostic imaging</keyword>
    <keyword>Neoplasm, Residual: pathology</keyword>
    <keyword>MRI</keyword>
    <keyword>children</keyword>
    <keyword>medulloblastoma</keyword>
    <keyword>persistent residual disease</keyword>
  </keywords>
  <accession-num/>
  <work-type>Journal Article</work-type>
  <dates>
    <pub-dates>
      <year>2024</year>
    </pub-dates>
  </dates>
  <accession-num>DZNE-2024-01108</accession-num>
  <year>2024</year>
  <custom2>pmc:PMC11376455</custom2>
  <custom6>pmid:38578306</custom6>
  <urls>
    <related-urls>
      <url>https://pub.dzne.de/record/271966</url>
      <url>https://doi.org/10.1093/neuonc/noae071</url>
    </related-urls>
  </urls>
</record>

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