<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ambros IM</submitter><funding>Cancer Research UK</funding><funding>NCI NIH HHS</funding><pagination>3685-3697</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7605396</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>38(31)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>For localized, resectable neuroblastoma without &lt;i>MYCN&lt;/i> amplification, surgery only is recommended even if incomplete. However, it is not known whether the genomic background of these tumors may influence outcome.&lt;h4>Patients and methods&lt;/h4>Diagnostic samples were obtained from 317 tumors, International Neuroblastoma Staging System stages 1/2A/2B, from 3 cohorts: Localized Neuroblastoma European Study Group I/II and Children's Oncology Group. Genomic data were analyzed using multi- and pangenomic techniques and fluorescence in-situ hybridization in 2 age groups (cutoff age, 18 months) and were quality controlled by the International Society of Pediatric Oncology European Neuroblastoma (SIOPEN) Biology Group.&lt;h4>Results&lt;/h4>Patients with stage 1 tumors had an excellent </pubmed_abstract><journal>Journal of clinical oncology : official journal of the American Society of Clinical Oncology</journal><pubmed_title>Age Dependency of the Prognostic Impact of Tumor Genomics in Localized Resectable &lt;i>MYCN&lt;/i>-Nonamplified Neuroblastomas. Report From the SIOPEN Biology Group on the LNESG Trials and a COG Validation Group.</pubmed_title><pmcid>PMC7605396</pmcid><funding_grant_id>23804</funding_grant_id><funding_grant_id>U10 CA180886</funding_grant_id><funding_grant_id>U10 CA180899</funding_grant_id><pubmed_authors>Bown N</pubmed_authors><pubmed_authors>Couturier J</pubmed_authors><pubmed_authors>Van Roy N</pubmed_authors><pubmed_authors>Schleiermacher G</pubmed_authors><pubmed_authors>Beiske K</pubmed_authors><pubmed_authors>Kogner P</pubmed_authors><pubmed_authors>Valent A</pubmed_authors><pubmed_authors>Defferrari R</pubmed_authors><pubmed_authors>Castel V</pubmed_authors><pubmed_authors>Mazzocco K</pubmed_authors><pubmed_authors>De Bernardi B</pubmed_authors><pubmed_authors>Tweddle DA</pubmed_authors><pubmed_authors>Berbegall AP</pubmed_authors><pubmed_authors>Lunec J</pubmed_authors><pubmed_authors>Marques B</pubmed_authors><pubmed_authors>Combaret V</pubmed_authors><pubmed_authors>Villamon E</pubmed_authors><pubmed_authors>Martinsson T</pubmed_authors><pubmed_authors>Mosseri V</pubmed_authors><pubmed_authors>Benard J</pubmed_authors><pubmed_authors>Ladenstein R</pubmed_authors><pubmed_authors>Valteau-Couanet D</pubmed_authors><pubmed_authors>Monclair TF</pubmed_authors><pubmed_authors>Noguera R</pubmed_authors><pubmed_authors>Glogova E</pubmed_authors><pubmed_authors>Holmes K</pubmed_authors><pubmed_authors>Cohn S</pubmed_authors><pubmed_authors>Gross N</pubmed_authors><pubmed_authors>Janousek D</pubmed_authors><pubmed_authors>Pearson ADJ</pubmed_authors><pubmed_authors>Ambros PF</pubmed_authors><pubmed_authors>Michon J</pubmed_authors><pubmed_authors>Hogarty MD</pubmed_authors><pubmed_authors>Park JR</pubmed_authors><pubmed_authors>Jeison M</pubmed_authors><pubmed_authors>Potschger U</pubmed_authors><pubmed_authors>Attiyeh EF</pubmed_authors><pubmed_authors>Beck-Popovic M</pubmed_authors><pubmed_authors>Tonini GP</pubmed_authors><pubmed_authors>Ambros IM</pubmed_authors><pubmed_authors>Caron H</pubmed_authors><pubmed_authors>Pribill I</pubmed_authors><pubmed_authors>Delattre O</pubmed_authors></additional><is_claimable>false</is_claimable><name>Age Dependency of the Prognostic Impact of Tumor Genomics in Localized Resectable &lt;i>MYCN&lt;/i>-Nonamplified Neuroblastomas. Report From the SIOPEN Biology Group on the LNESG Trials and a COG Validation Group.</name><description>&lt;h4>Purpose&lt;/h4>For localized, resectable neuroblastoma without &lt;i>MYCN&lt;/i> amplification, surgery only is recommended even if incomplete. However, it is not known whether the genomic background of these tumors may influence outcome.&lt;h4>Patients and methods&lt;/h4>Diagnostic samples were obtained from 317 tumors, International Neuroblastoma Staging System stages 1/2A/2B, from 3 cohorts: Localized Neuroblastoma European Study Group I/II and Children's Oncology Group. Genomic data were analyzed using multi- and pangenomic techniques and fluorescence in-situ hybridization in 2 age groups (cutoff age, 18 months) and were quality controlled by the International Society of Pediatric Oncology European Neuroblastoma (SIOPEN) Biology Group.&lt;h4>Results&lt;/h4>Patients with stage 1 tumors had an excellent </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Nov</publication><modification>2025-05-29T19:01:14.203Z</modification><creation>2022-02-11T12:21:15.342Z</creation></dates><accession>S-EPMC7605396</accession><cross_references><pubmed>32903140</pubmed><doi>10.1200/JCO.18.02132</doi></cross_references></HashMap>