<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Miller KE</submitter><funding>NCI</funding><funding>NCRR NIH HHS</funding><funding>Nationwide Insurance Innovation Fund</funding><funding>NCI NIH HHS</funding><funding>NIH</funding><pagination>498-506</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8846434</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(3)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Previously, clinical trials of experimental virotherapy for recurrent glioblastoma multiforme (GBM) demonstrated that inoculation with a conditionally replication-competent Δγ&lt;sub>1&lt;/sub>34.5 oncolytic herpes simplex virus (oHSV), G207, was safe. Following the initial safety study, a phase Ib trial enrolled 6 adult patients diagnosed with GBM recurrence from which tumor tissue was banked for future studies.&lt;h4>Patients and methods&lt;/h4>Here, we analyzed tumor RNA sequencing (RNA-seq) data obtained from pre- and posttreatment (collected 2 or 5 days after G207 injection) biopsies from the phase Ib study patients.&lt;h4>Results&lt;/h4>Using a Spearman rank-order correlation analysis, we identified approximately 500 genes whose expression pattern correlated with survival duration. Man</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>Immune Activity and Response Differences of Oncolytic Viral Therapy in Recurrent Glioblastoma: Gene Expression Analyses of a Phase IB Study.</pubmed_title><pmcid>PMC8846434</pmcid><funding_grant_id>P01 CA071933</funding_grant_id><funding_grant_id>R01 CA217179</funding_grant_id><funding_grant_id>U54 CA232561</funding_grant_id><funding_grant_id>R01-CA217179</funding_grant_id><funding_grant_id>U54-CA232561</funding_grant_id><funding_grant_id>R01 CA222903</funding_grant_id><funding_grant_id>R01-CA222903</funding_grant_id><funding_grant_id>M01 RR000032</funding_grant_id><pubmed_authors>Cassady KA</pubmed_authors><pubmed_authors>Miller AR</pubmed_authors><pubmed_authors>Prasad N</pubmed_authors><pubmed_authors>Leavenworth JW</pubmed_authors><pubmed_authors>Clements J</pubmed_authors><pubmed_authors>Miller KE</pubmed_authors><pubmed_authors>Aban IB</pubmed_authors><pubmed_authors>Gillespie GY</pubmed_authors><pubmed_authors>Roth JC</pubmed_authors><pubmed_authors>Mardis ER</pubmed_authors><pubmed_authors>Markert JM</pubmed_authors><pubmed_authors>Schieffer KM</pubmed_authors><pubmed_authors>Whitley RJ</pubmed_authors><pubmed_authors>Leraas K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immune Activity and Response Differences of Oncolytic Viral Therapy in Recurrent Glioblastoma: Gene Expression Analyses of a Phase IB Study.</name><description>&lt;h4>Purpose&lt;/h4>Previously, clinical trials of experimental virotherapy for recurrent glioblastoma multiforme (GBM) demonstrated that inoculation with a conditionally replication-competent Δγ&lt;sub>1&lt;/sub>34.5 oncolytic herpes simplex virus (oHSV), G207, was safe. Following the initial safety study, a phase Ib trial enrolled 6 adult patients diagnosed with GBM recurrence from which tumor tissue was banked for future studies.&lt;h4>Patients and methods&lt;/h4>Here, we analyzed tumor RNA sequencing (RNA-seq) data obtained from pre- and posttreatment (collected 2 or 5 days after G207 injection) biopsies from the phase Ib study patients.&lt;h4>Results&lt;/h4>Using a Spearman rank-order correlation analysis, we identified approximately 500 genes whose expression pattern correlated with survival duration. Man</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2026-05-31T02:35:36.01Z</modification><creation>2025-04-07T04:06:24.381Z</creation></dates><accession>S-EPMC8846434</accession><cross_references><pubmed>35105718</pubmed><doi>10.1158/1078-0432.CCR-21-2636</doi></cross_references></HashMap>