<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(4)</volume><submitter>Schmitz-Winnenthal FH</submitter><funding>VAXIMM AG</funding><pubmed_abstract>VXM01 is a first-in-kind orally applied tumor vaccine based on live attenuated &lt;i>Salmonella&lt;/i> typhi carrying an expression plasmid encoding VEGFR2, an antigen expressed on tumor vasculature and a stable and accessible target for anti-angiogenic intervention. A recent randomized, placebo-controlled, phase I dose-escalation trial in advanced pancreatic cancer patients demonstrated safety, immunogenicity and transient, T-cell response-related anti-angiogenic activity of four priming vaccinations applied within one week. We here evaluated whether monthly boost vaccinations are safe and can sustain increased frequencies of vaccine-specific T cells. Patients with advanced pancreatic cancer were randomly assigned at a ratio of 2:1 to priming with VXM01 followed by up to six monthly boost vacci</pubmed_abstract><journal>Oncoimmunology</journal><pagination>e1303584</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5889207</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A phase 1 trial extension to assess immunologic efficacy and safety of prime-boost vaccination with VXM01, an oral T cell vaccine against VEGFR2, in patients with advanced pancreatic cancer.</pubmed_title><pmcid>PMC5889207</pmcid><pubmed_authors>Springer M</pubmed_authors><pubmed_authors>Wieckowski S</pubmed_authors><pubmed_authors>Knebel P</pubmed_authors><pubmed_authors>Koc R</pubmed_authors><pubmed_authors>Haefeli WE</pubmed_authors><pubmed_authors>Springfeld C</pubmed_authors><pubmed_authors>Buchler MW</pubmed_authors><pubmed_authors>Lubenau H</pubmed_authors><pubmed_authors>Podola L</pubmed_authors><pubmed_authors>Mikus G</pubmed_authors><pubmed_authors>Grenacher L</pubmed_authors><pubmed_authors>Schmitz-Winnenthal FH</pubmed_authors><pubmed_authors>Bucur M</pubmed_authors><pubmed_authors>Hohmann N</pubmed_authors><pubmed_authors>Beckhove P</pubmed_authors><pubmed_authors>Schmidt T</pubmed_authors><pubmed_authors>Breiner KM</pubmed_authors><pubmed_authors>Keller AV</pubmed_authors><pubmed_authors>Friedrich T</pubmed_authors></additional><is_claimable>false</is_claimable><name>A phase 1 trial extension to assess immunologic efficacy and safety of prime-boost vaccination with VXM01, an oral T cell vaccine against VEGFR2, in patients with advanced pancreatic cancer.</name><description>VXM01 is a first-in-kind orally applied tumor vaccine based on live attenuated &lt;i>Salmonella&lt;/i> typhi carrying an expression plasmid encoding VEGFR2, an antigen expressed on tumor vasculature and a stable and accessible target for anti-angiogenic intervention. A recent randomized, placebo-controlled, phase I dose-escalation trial in advanced pancreatic cancer patients demonstrated safety, immunogenicity and transient, T-cell response-related anti-angiogenic activity of four priming vaccinations applied within one week. We here evaluated whether monthly boost vaccinations are safe and can sustain increased frequencies of vaccine-specific T cells. Patients with advanced pancreatic cancer were randomly assigned at a ratio of 2:1 to priming with VXM01 followed by up to six monthly boost vacci</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2026-04-07T23:22:49.723Z</modification><creation>2019-03-26T22:37:18Z</creation></dates><accession>S-EPMC5889207</accession><cross_references><pubmed>29632710</pubmed><doi>10.1080/2162402X.2017.1303584</doi><doi>10.1080/2162402x.2017.1303584</doi></cross_references></HashMap>