<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu CH</submitter><funding>NCI NIH HHS</funding><pagination>926-933.e1</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12483467</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>33(8)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>To investigate the safety of replacing doxorubicin with tirapazamine in conventional transarterial chemoembolization (TACE) in an Asian population with hepatocellular carcinoma (HCC), and to determine the optimal tirapazamine dose for phase II studies.&lt;h4>Materials and methods&lt;/h4>This was a phase I, 3 + 3 dose-escalation study for patients with unresectable early- and intermediate-stage HCC who received 5, 10, or 20 mg/m&lt;sup>2&lt;/sup> of intra-arterial (IA) tirapazamine followed by ethiodized oil/gelatin sponge-based embolization. Key eligibilities included HCCs no more than 10 cm in diameter, prior embolization allowed, Eastern Cooperative Oncology Group performance status of 0 or 1, Child-Pugh score of 5-7, and platelet count of ≥60,000 μL. Dose-limiting toxicity (DLT) was</pubmed_abstract><journal>Journal of vascular and interventional radiology : JVIR</journal><pubmed_title>Phase I Dose-Escalation Study of Tirapazamine Chemoembolization for Unresectable Early- and Intermediate-Stage Hepatocellular Carcinoma.</pubmed_title><pmcid>PMC12483467</pmcid><funding_grant_id>P30 CA062203</funding_grant_id><pubmed_authors>Liu CH</pubmed_authors><pubmed_authors>Abi-Jaoudeh N</pubmed_authors><pubmed_authors>Peng CM</pubmed_authors><pubmed_authors>Chen PJ</pubmed_authors><pubmed_authors>Tyan YS</pubmed_authors><pubmed_authors>Hwang JI</pubmed_authors><pubmed_authors>Liang PC</pubmed_authors><pubmed_authors>Giiang LH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phase I Dose-Escalation Study of Tirapazamine Chemoembolization for Unresectable Early- and Intermediate-Stage Hepatocellular Carcinoma.</name><description>&lt;h4>Purpose&lt;/h4>To investigate the safety of replacing doxorubicin with tirapazamine in conventional transarterial chemoembolization (TACE) in an Asian population with hepatocellular carcinoma (HCC), and to determine the optimal tirapazamine dose for phase II studies.&lt;h4>Materials and methods&lt;/h4>This was a phase I, 3 + 3 dose-escalation study for patients with unresectable early- and intermediate-stage HCC who received 5, 10, or 20 mg/m&lt;sup>2&lt;/sup> of intra-arterial (IA) tirapazamine followed by ethiodized oil/gelatin sponge-based embolization. Key eligibilities included HCCs no more than 10 cm in diameter, prior embolization allowed, Eastern Cooperative Oncology Group performance status of 0 or 1, Child-Pugh score of 5-7, and platelet count of ≥60,000 μL. Dose-limiting toxicity (DLT) was</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2026-06-04T00:20:22.337Z</modification><creation>2026-05-03T03:12:00.757Z</creation></dates><accession>S-EPMC12483467</accession><cross_references><pubmed>35504436</pubmed><doi>10.1016/j.jvir.2022.04.031</doi></cross_references></HashMap>