<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Gauvain K</submitter><funding>National Center for Advancing Translational Sciences</funding><funding>American Cancer Society</funding><funding>NCATS NIH HHS</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><pagination>28-36</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5909807</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Noninvasively predicting early response to therapy in recurrent pediatric brain tumors provides a challenge. 3,4-dihydroxy-6-[&lt;sup>18&lt;/sup>F]fluoro-L-phenylalanine (&lt;sup>18&lt;/sup>F-FDOPA) PET/MRI has not been previously studied as a tool to evaluate early response to antiangiogenic therapy in children. The purpose of this study was to evaluate the safety and feasibility of using &lt;sup>18&lt;/sup>F-FDOPA PET/MRI to assess response to bevacizumab in children with relapsed brain tumors.&lt;h4>Materials and methods&lt;/h4>Six patients with recurrent gliomas (5 low-grade, 1 high-grade) planned to undergo treatment with bevacizumab were enrolled. &lt;sup>18&lt;/sup>F-FDOPA PET/MRI scans were obtained prior to and 4 weeks following the start of treatment, and these were compared with the clinic</pubmed_abstract><journal>Neuro-oncology practice</journal><pubmed_title>&lt;sup>18&lt;/sup>F-FDOPA PET/MRI for monitoring early response to bevacizumab in children with recurrent brain tumors.</pubmed_title><pmcid>PMC5909807</pmcid><funding_grant_id>P30 CA091842</funding_grant_id><funding_grant_id>UL1 TR002345</funding_grant_id><funding_grant_id>K08 CA154790</funding_grant_id><funding_grant_id>P30 CA013148</funding_grant_id><funding_grant_id>IRG-58-010-56</funding_grant_id><funding_grant_id>K08CA154790</funding_grant_id><pubmed_authors>Ponisio MR</pubmed_authors><pubmed_authors>Leeds H</pubmed_authors><pubmed_authors>Goyal M</pubmed_authors><pubmed_authors>Rubin J</pubmed_authors><pubmed_authors>Barone A</pubmed_authors><pubmed_authors>McConathy J</pubmed_authors><pubmed_authors>Parent E</pubmed_authors><pubmed_authors>Grimaldi M</pubmed_authors><pubmed_authors>Gauvain K</pubmed_authors></additional><is_claimable>false</is_claimable><name>&lt;sup>18&lt;/sup>F-FDOPA PET/MRI for monitoring early response to bevacizumab in children with recurrent brain tumors.</name><description>&lt;h4>Background&lt;/h4>Noninvasively predicting early response to therapy in recurrent pediatric brain tumors provides a challenge. 3,4-dihydroxy-6-[&lt;sup>18&lt;/sup>F]fluoro-L-phenylalanine (&lt;sup>18&lt;/sup>F-FDOPA) PET/MRI has not been previously studied as a tool to evaluate early response to antiangiogenic therapy in children. The purpose of this study was to evaluate the safety and feasibility of using &lt;sup>18&lt;/sup>F-FDOPA PET/MRI to assess response to bevacizumab in children with relapsed brain tumors.&lt;h4>Materials and methods&lt;/h4>Six patients with recurrent gliomas (5 low-grade, 1 high-grade) planned to undergo treatment with bevacizumab were enrolled. &lt;sup>18&lt;/sup>F-FDOPA PET/MRI scans were obtained prior to and 4 weeks following the start of treatment, and these were compared with the clinic</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Mar</publication><modification>2025-04-04T14:02:21.618Z</modification><creation>2019-07-30T07:00:30Z</creation></dates><accession>S-EPMC5909807</accession><cross_references><pubmed>29692922</pubmed><doi>10.1093/nop/npx008</doi></cross_references></HashMap>