<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yuan G</submitter><funding>the Postdoctoral Research Foundation of China</funding><funding>Natural Science Foundation of Guangdong Province</funding><funding>the National Natural Science Foundation of China</funding><pagination>68</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10924872</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>To explore the efficacy and safety of Transarterial chemoembolization (TACE) in combination with immune checkpoint inhibitors (ICIs) and tyrosine kinase inhibitors (TKIs) in patients with unresectable hepatocellular carcinoma (uHCC).&lt;h4>Methods&lt;/h4>456 patients with HCC receiving either TACE in combination with ICIs and TKIs (combination group, n = 139) or TACE monotherapy (monotherapy group, n = 317) were included from Apr 2016 to Dec 2021 in this retrospective study. We employed propensity score matching (PSM), performed 1:2 optimal pair matching, to balance potential bias.&lt;h4>Results&lt;/h4>The mean follow-up time is 24.7 months (95% CI 22.6-26.8) for matched patients as of March 2022. After matching, the combination group achieved longer OS and PFS (median OS:21.9 vs. 16.3 months, P = 0.022; median PFS: 8.3 vs. 5.1 months, P &lt; 0.0001) than TACE monotherapy group. The combination group had better objective response rate (ORR) and disease control rate (DCR) (ORR: 52.5% vs. 32.8%, P &lt; 0.001; DCR: 82.7% vs. 59.6%, P &lt; 0.001). Subgroup analysis showed that patients who received "TKIs + ICIs" after the first TACE procedure (after TACE group) achieved longer OS than those before the first TACE procedure (before TACE group) (26.8 vs. 19.2 months, P = 0.011). Adverse events were consistent with previous studies of TACE-related trials.&lt;h4>Conclusions&lt;/h4>TACE plus TKIs and ICIs appeared to deliver longer PFS and OS in HCC patients than TACE monotherapy. "TKIs + ICIs" co-treatment within 3 months after the first TACE procedure might be a better medication strategy.</pubmed_abstract><journal>Discover. Oncology</journal><pubmed_title>Transarterial chemoembolization with/without immune checkpoint inhibitors plus tyrosine kinase inhibitors for unresectable hepatocellular carcinoma: a single center, propensity score matching real-world study.</pubmed_title><pmcid>PMC10924872</pmcid><funding_grant_id>82102879</funding_grant_id><funding_grant_id>2021A1515012518</funding_grant_id><funding_grant_id>2021M691468</funding_grant_id><funding_grant_id>2022A1515010526</funding_grant_id><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Ruan J</pubmed_authors><pubmed_authors>Zang M</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Huang W</pubmed_authors><pubmed_authors>Hu X</pubmed_authors><pubmed_authors>Li Q</pubmed_authors><pubmed_authors>Li R</pubmed_authors><pubmed_authors>Pang H</pubmed_authors><pubmed_authors>Yuan G</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transarterial chemoembolization with/without immune checkpoint inhibitors plus tyrosine kinase inhibitors for unresectable hepatocellular carcinoma: a single center, propensity score matching real-world study.</name><description>&lt;h4>Objectives&lt;/h4>To explore the efficacy and safety of Transarterial chemoembolization (TACE) in combination with immune checkpoint inhibitors (ICIs) and tyrosine kinase inhibitors (TKIs) in patients with unresectable hepatocellular carcinoma (uHCC).&lt;h4>Methods&lt;/h4>456 patients with HCC receiving either TACE in combination with ICIs and TKIs (combination group, n = 139) or TACE monotherapy (monotherapy group, n = 317) were included from Apr 2016 to Dec 2021 in this retrospective study. We employed propensity score matching (PSM), performed 1:2 optimal pair matching, to balance potential bias.&lt;h4>Results&lt;/h4>The mean follow-up time is 24.7 months (95% CI 22.6-26.8) for matched patients as of March 2022. After matching, the combination group achieved longer OS and PFS (median OS:21.9 vs. 16.3 months, P = 0.022; median PFS: 8.3 vs. 5.1 months, P &lt; 0.0001) than TACE monotherapy group. The combination group had better objective response rate (ORR) and disease control rate (DCR) (ORR: 52.5% vs. 32.8%, P &lt; 0.001; DCR: 82.7% vs. 59.6%, P &lt; 0.001). Subgroup analysis showed that patients who received "TKIs + ICIs" after the first TACE procedure (after TACE group) achieved longer OS than those before the first TACE procedure (before TACE group) (26.8 vs. 19.2 months, P = 0.011). Adverse events were consistent with previous studies of TACE-related trials.&lt;h4>Conclusions&lt;/h4>TACE plus TKIs and ICIs appeared to deliver longer PFS and OS in HCC patients than TACE monotherapy. "TKIs + ICIs" co-treatment within 3 months after the first TACE procedure might be a better medication strategy.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-04T12:58:37.612Z</modification><creation>2025-04-04T12:58:37.612Z</creation></dates><accession>S-EPMC10924872</accession><cross_references><pubmed>38460053</pubmed><doi>10.1007/s12672-024-00917-1</doi></cross_references></HashMap>