<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Milewski D</submitter><funding>National Cancer Institute (NCI)</funding><funding>Intramural NIH HHS</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><pagination>364-378</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9843436</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(2)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Rhabdomyosarcoma (RMS) is an aggressive soft-tissue sarcoma, which primarily occurs in children and young adults. We previously reported specific genomic alterations in RMS, which strongly correlated with survival; however, predicting these mutations or high-risk disease at diagnosis remains a significant challenge. In this study, we utilized convolutional neural networks (CNN) to learn histologic features associated with driver mutations and outcome using hematoxylin and eosin (H&amp;E) images of RMS.&lt;h4>Experimental design&lt;/h4>Digital whole slide H&amp;E images were collected from clinically annotated diagnostic tumor samples from 321 patients with RMS enrolled in Children's Oncology Group (COG) trials (1998-2017). Patches were extracted and fed into deep learning CNNs to learn f</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>Predicting Molecular Subtype and Survival of Rhabdomyosarcoma Patients Using Deep Learning of H&amp;E Images: A Report from the Children's Oncology Group.</pubmed_title><pmcid>PMC9843436</pmcid><funding_grant_id>U10CA180886</funding_grant_id><funding_grant_id>U54CA231630</funding_grant_id><funding_grant_id>U10CA098413</funding_grant_id><funding_grant_id>P30CA008748</funding_grant_id><funding_grant_id>U10CA098543</funding_grant_id><funding_grant_id>U10 CA180899</funding_grant_id><funding_grant_id>ZIA BC011002</funding_grant_id><funding_grant_id>U10CA180899</funding_grant_id><pubmed_authors>Barkauskas DA</pubmed_authors><pubmed_authors>Hawkins DS</pubmed_authors><pubmed_authors>Choo-Wosoba H</pubmed_authors><pubmed_authors>Milewski D</pubmed_authors><pubmed_authors>Ladanyi M</pubmed_authors><pubmed_authors>Brown GT</pubmed_authors><pubmed_authors>Shern JF</pubmed_authors><pubmed_authors>Steinberg SM</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Zaki G</pubmed_authors><pubmed_authors>Bode PK</pubmed_authors><pubmed_authors>Hall D</pubmed_authors><pubmed_authors>Chou HC</pubmed_authors><pubmed_authors>Lisle C</pubmed_authors><pubmed_authors>Jung H</pubmed_authors><pubmed_authors>Rudzinski ER</pubmed_authors><pubmed_authors>Somerville B</pubmed_authors><pubmed_authors>Venkatramani R</pubmed_authors><pubmed_authors>Linardic CM</pubmed_authors><pubmed_authors>Skapek SX</pubmed_authors><pubmed_authors>Lo T</pubmed_authors><pubmed_authors>Khan J</pubmed_authors><pubmed_authors>Wei JS</pubmed_authors><pubmed_authors>Kuznetsov IB</pubmed_authors><pubmed_authors>Collins J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Predicting Molecular Subtype and Survival of Rhabdomyosarcoma Patients Using Deep Learning of H&amp;E Images: A Report from the Children's Oncology Group.</name><description>&lt;h4>Purpose&lt;/h4>Rhabdomyosarcoma (RMS) is an aggressive soft-tissue sarcoma, which primarily occurs in children and young adults. We previously reported specific genomic alterations in RMS, which strongly correlated with survival; however, predicting these mutations or high-risk disease at diagnosis remains a significant challenge. In this study, we utilized convolutional neural networks (CNN) to learn histologic features associated with driver mutations and outcome using hematoxylin and eosin (H&amp;E) images of RMS.&lt;h4>Experimental design&lt;/h4>Digital whole slide H&amp;E images were collected from clinically annotated diagnostic tumor samples from 321 patients with RMS enrolled in Children's Oncology Group (COG) trials (1998-2017). Patches were extracted and fed into deep learning CNNs to learn f</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-18T15:44:57.439Z</modification><creation>2025-02-19T04:25:12.796Z</creation></dates><accession>S-EPMC9843436</accession><cross_references><pubmed>36346688</pubmed><doi>10.1158/1078-0432.CCR-22-1663</doi></cross_references></HashMap>