<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(6)</volume><submitter>Young K</submitter><pubmed_abstract>Ramucirumab, a fully humanized monoclonal antibody directed against vascular endothelial growth factor receptor 2, is the first targeted agent to have demonstrated an improvement in survival, as a single agent or in combination, in a molecularly unselected population in gastro-oesophageal cancer. Now that second-line treatment is routinely considered for patients with advanced gastro-oesophageal cancer, ramucirumab, with its favourable toxicity profile compared with cytotoxic treatment, provides a valuable additional treatment option.</pubmed_abstract><journal>Therapeutic advances in gastroenterology</journal><pagination>373-83</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4622287</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Ramucirumab for advanced gastric cancer or gastro-oesophageal junction adenocarcinoma.</pubmed_title><pmcid>PMC4622287</pmcid><pubmed_authors>Young K</pubmed_authors><pubmed_authors>Smyth E</pubmed_authors><pubmed_authors>Chau I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ramucirumab for advanced gastric cancer or gastro-oesophageal junction adenocarcinoma.</name><description>Ramucirumab, a fully humanized monoclonal antibody directed against vascular endothelial growth factor receptor 2, is the first targeted agent to have demonstrated an improvement in survival, as a single agent or in combination, in a molecularly unselected population in gastro-oesophageal cancer. Now that second-line treatment is routinely considered for patients with advanced gastro-oesophageal cancer, ramucirumab, with its favourable toxicity profile compared with cytotoxic treatment, provides a valuable additional treatment option.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Nov</publication><modification>2024-11-21T09:26:52.72Z</modification><creation>2019-03-27T02:00:51Z</creation></dates><accession>S-EPMC4622287</accession><cross_references><pubmed>26557893</pubmed><doi>10.1177/1756283x15592586</doi><doi>10.1177/1756283X15592586</doi></cross_references></HashMap>