<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Villaruz LC</submitter><funding>NCI NIH HHS</funding><pagination>26</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4836185</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(6)</volume><pubmed_abstract>Recognition of the vascular endothelial growth factor (VEGF) pathway as a key mediator of angiogenesis has led to the clinical study of several VEGF and VEGF receptor (VEGFR) targeted therapies in non-small-cell lung cancer (NSCLC). These targeted therapies include neutralizing antibodies to VEGF (bevacizumab and aflibercept) and VEGFR-2 (ramucirumab) and tyrosine kinase inhibitors (TKIs) with selectivity for the VEGFRs. Bevacizumab and ramucirumab are associated with survival advantages in the treatment of advanced NSCLC: bevacizumab in the first-line setting in combination with carboplatin/paclitaxel and ramucirumab in combination with docetaxel in the second-line setting. The VEGFR-2 TKIs have been associated with responses and improved progression-free survival in selected NSCLC settings; however, this level of activity has thus far been insufficient to confer significant survival advantages. This review will focus on the current state of VEGF targeted therapies in NSCLC.</pubmed_abstract><journal>Current oncology reports</journal><pubmed_title>The role of anti-angiogenesis in non-small-cell lung cancer: an update.</pubmed_title><pmcid>PMC4836185</pmcid><funding_grant_id>P30 CA047904</funding_grant_id><pubmed_authors>Villaruz LC</pubmed_authors><pubmed_authors>Socinski MA</pubmed_authors></additional><is_claimable>false</is_claimable><name>The role of anti-angiogenesis in non-small-cell lung cancer: an update.</name><description>Recognition of the vascular endothelial growth factor (VEGF) pathway as a key mediator of angiogenesis has led to the clinical study of several VEGF and VEGF receptor (VEGFR) targeted therapies in non-small-cell lung cancer (NSCLC). These targeted therapies include neutralizing antibodies to VEGF (bevacizumab and aflibercept) and VEGFR-2 (ramucirumab) and tyrosine kinase inhibitors (TKIs) with selectivity for the VEGFRs. Bevacizumab and ramucirumab are associated with survival advantages in the treatment of advanced NSCLC: bevacizumab in the first-line setting in combination with carboplatin/paclitaxel and ramucirumab in combination with docetaxel in the second-line setting. The VEGFR-2 TKIs have been associated with responses and improved progression-free survival in selected NSCLC settings; however, this level of activity has thus far been insufficient to confer significant survival advantages. This review will focus on the current state of VEGF targeted therapies in NSCLC.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Jun</publication><modification>2024-11-08T17:39:55.656Z</modification><creation>2019-03-27T02:11:54Z</creation></dates><accession>S-EPMC4836185</accession><cross_references><pubmed>25947099</pubmed><doi>10.1007/s11912-015-0448-y</doi></cross_references></HashMap>