<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Zhang Q</submitter><pubmed_abstract>&lt;b>Background:&lt;/b> Simmitecan is a potent inhibitor of topoisomerase I with anti-tumor activity. This phase Ib trial was conducted to investigate the safety and anti-tumor effect of simmitecan alone or in combination with other drugs. &lt;b>Methods:&lt;/b> Eligible patients with advanced solid tumor had no further standard treatment options. Patients were allocated to receive simmitecan alone, simmitecan in combination with 5-fluorouracil (5-FU)/leucovorin (LV), or simmitecan in combination with thalidomide, 14 days a cycle, until disease progression or unacceptable toxicity occurred. &lt;b>Results:&lt;/b> A total of 41 patients were enrolled, with a median age of 55 (range 29-69) years. Among them, 13 patients received simmitecan monotherapy, 10 received simmitecan + 5-FU/LV, and 18 received simmitec</pubmed_abstract><journal>Frontiers in pharmacology</journal><pagination>833583</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9355729</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A Phase Ib Study of the Simmitecan Single Agent and in Combination With 5-Fluorouracil/Leucovorin or Thalidomide in Patients With Advanced Solid Tumor.</pubmed_title><pmcid>PMC9355729</pmcid><pubmed_authors>Shen L</pubmed_authors><pubmed_authors>Deng T</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Guo W</pubmed_authors><pubmed_authors>Yu Q</pubmed_authors><pubmed_authors>Ba Y</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors><pubmed_authors>Yang F</pubmed_authors><pubmed_authors>Yuan J</pubmed_authors><pubmed_authors>Cai H</pubmed_authors><pubmed_authors>Peng Z</pubmed_authors><pubmed_authors>Lu M</pubmed_authors><pubmed_authors>Cao Y</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Liu D</pubmed_authors><pubmed_authors>Gong J</pubmed_authors><pubmed_authors>Qi C</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Phase Ib Study of the Simmitecan Single Agent and in Combination With 5-Fluorouracil/Leucovorin or Thalidomide in Patients With Advanced Solid Tumor.</name><description>&lt;b>Background:&lt;/b> Simmitecan is a potent inhibitor of topoisomerase I with anti-tumor activity. This phase Ib trial was conducted to investigate the safety and anti-tumor effect of simmitecan alone or in combination with other drugs. &lt;b>Methods:&lt;/b> Eligible patients with advanced solid tumor had no further standard treatment options. Patients were allocated to receive simmitecan alone, simmitecan in combination with 5-fluorouracil (5-FU)/leucovorin (LV), or simmitecan in combination with thalidomide, 14 days a cycle, until disease progression or unacceptable toxicity occurred. &lt;b>Results:&lt;/b> A total of 41 patients were enrolled, with a median age of 55 (range 29-69) years. Among them, 13 patients received simmitecan monotherapy, 10 received simmitecan + 5-FU/LV, and 18 received simmitec</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-09T14:11:09.2Z</modification><creation>2024-11-19T22:29:19.41Z</creation></dates><accession>S-EPMC9355729</accession><cross_references><pubmed>35935841</pubmed><doi>10.3389/fphar.2022.833583</doi></cross_references></HashMap>