<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang KL</submitter><funding>Shin Kong Wu Ho-Su Memorial Hospital</funding><pagination>18</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7819176</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>To investigate maximum tolerated dose (MTD) of axitinib, a selective vascular endothelial growth factor receptor 1-3 inhibitor, in combination with radiotherapy (RT) for advanced hepatocellular carcinoma (HCC).&lt;h4>Methods&lt;/h4>This phase I study followed the rule of traditional 3 + 3 design. Major eligibility included: (1) patients with advanced HCC unsuitable for surgery, radiofrequency ablation or transarterial chemoembolization, or who failed after prior local-regional treatment; (2) failure on sorafenib or no grant for sorafenib from health insurance system. Eligible patients with advanced HCC received axitinib for total 8 weeks during and after RT. Three cohorts with axitinib dose escalation were planned: 1 mg twice daily (level I), 2 mg twice daily (level II) and 3 </pubmed_abstract><journal>Radiation oncology (London, England)</journal><pubmed_title>Axitinib in combination with radiotherapy for advanced hepatocellular carcinoma: a phase I clinical trial.</pubmed_title><pmcid>PMC7819176</pmcid><funding_grant_id>SKH-8302-106-DR-27</funding_grant_id><pubmed_authors>Huang YY</pubmed_authors><pubmed_authors>Huang SC</pubmed_authors><pubmed_authors>Ko HL</pubmed_authors><pubmed_authors>Chi KH</pubmed_authors><pubmed_authors>Lin YM</pubmed_authors><pubmed_authors>Chi MS</pubmed_authors><pubmed_authors>Yang KL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Axitinib in combination with radiotherapy for advanced hepatocellular carcinoma: a phase I clinical trial.</name><description>&lt;h4>Background&lt;/h4>To investigate maximum tolerated dose (MTD) of axitinib, a selective vascular endothelial growth factor receptor 1-3 inhibitor, in combination with radiotherapy (RT) for advanced hepatocellular carcinoma (HCC).&lt;h4>Methods&lt;/h4>This phase I study followed the rule of traditional 3 + 3 design. Major eligibility included: (1) patients with advanced HCC unsuitable for surgery, radiofrequency ablation or transarterial chemoembolization, or who failed after prior local-regional treatment; (2) failure on sorafenib or no grant for sorafenib from health insurance system. Eligible patients with advanced HCC received axitinib for total 8 weeks during and after RT. Three cohorts with axitinib dose escalation were planned: 1 mg twice daily (level I), 2 mg twice daily (level II) and 3 </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jan</publication><modification>2025-04-27T00:43:21.48Z</modification><creation>2021-02-21T01:54:59Z</creation></dates><accession>S-EPMC7819176</accession><cross_references><pubmed>33472666</pubmed><doi>10.1186/s13014-020-01742-w</doi></cross_references></HashMap>