<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>56(1)</volume><submitter>Chen W</submitter><funding>Interventional Medicine Research Fund of Jiangsu Medical Association</funding><funding>Jiangsu Province Capability Improvement Project through Science, Technology and Education</funding><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Not all patients benefit from transarterial chemoembolization (TACE) due to the heterogeneity of the tumour burden in intermediate-stage hepatocellular carcinoma (HCC). To compare the outcomes of transarterial chemoembolization (TACE) combined with molecular-targeted agents plus immune checkpoint inhibitors (TACE-MTAs-ICIs) with those of TACE for patients with unresectable hepatocellular carcinoma (uHCC) that were beyond the up-to-seven criteria.&lt;h4>Patients and methods&lt;/h4>Between January 2019 and July 2022, 130 patients diagnosed with uHCC beyond the up-to-seven criteria were retrospectively identified, including 47 patients who received TACE-MTAs-ICIs and 83 patients who received TACE alone. The primary endpoints were overall survival (OS) and progression-free survival (PFS); the secondary endpoints included tumour response and adverse events (AEs).&lt;h4>Results&lt;/h4>There were 43 matched patients. The median OS and PFS times in the TACE-MTAs-ICIs group were significantly longer than those in the TACE group (OS: 27.2 vs. 15.9 months, &lt;i>p&lt;/i> = 0.007; PFS: 15.4 months vs. 4.8 months, &lt;i>p&lt;/i> &lt; 0.001). The objective response rate (ORR) in the TACE-MTAs-ICIs group was higher than that in the TACE group (65.1% vs. 37.2%, &lt;i>p&lt;/i> = 0.010). Reversible AEs (grade 3 or 4) occurred differently in TACE-MTAs-ICIs and TACE groups (83.7% vs. 51.2%, &lt;i>p&lt;/i> = 0.001). Univariate and multivariate analyses revealed that TACE-MTAs-ICIs treatment was an independent favourable prognostic factor for both PFS and OS (&lt;i>p&lt;/i> &lt; 0.001).&lt;h4>Conclusion&lt;/h4>For uHCC patients beyond the up-to-seven criteria, TACE-MTAs-ICIs provided superior ORR and OS. Early combined TACE and systemic treatment should shift for patients who are beyond these criteria.</pubmed_abstract><journal>Annals of medicine</journal><pagination>2419993</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11536643</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Transarterial chemoembolization combined with molecular targeted agents plus immune checkpoint inhibitors for unresectable hepatocellular carcinoma beyond the up-to-seven criteria: a propensity score-matching analysis.</pubmed_title><pmcid>PMC11536643</pmcid><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Zhang JX</pubmed_authors><pubmed_authors>Chen W</pubmed_authors><pubmed_authors>Zhou CG</pubmed_authors><pubmed_authors>Shi HB</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Zu QQ</pubmed_authors><pubmed_authors>Yan HT</pubmed_authors><pubmed_authors>Cheng Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transarterial chemoembolization combined with molecular targeted agents plus immune checkpoint inhibitors for unresectable hepatocellular carcinoma beyond the up-to-seven criteria: a propensity score-matching analysis.</name><description>&lt;h4>Purpose&lt;/h4>Not all patients benefit from transarterial chemoembolization (TACE) due to the heterogeneity of the tumour burden in intermediate-stage hepatocellular carcinoma (HCC). To compare the outcomes of transarterial chemoembolization (TACE) combined with molecular-targeted agents plus immune checkpoint inhibitors (TACE-MTAs-ICIs) with those of TACE for patients with unresectable hepatocellular carcinoma (uHCC) that were beyond the up-to-seven criteria.&lt;h4>Patients and methods&lt;/h4>Between January 2019 and July 2022, 130 patients diagnosed with uHCC beyond the up-to-seven criteria were retrospectively identified, including 47 patients who received TACE-MTAs-ICIs and 83 patients who received TACE alone. The primary endpoints were overall survival (OS) and progression-free survival (PFS); the secondary endpoints included tumour response and adverse events (AEs).&lt;h4>Results&lt;/h4>There were 43 matched patients. The median OS and PFS times in the TACE-MTAs-ICIs group were significantly longer than those in the TACE group (OS: 27.2 vs. 15.9 months, &lt;i>p&lt;/i> = 0.007; PFS: 15.4 months vs. 4.8 months, &lt;i>p&lt;/i> &lt; 0.001). The objective response rate (ORR) in the TACE-MTAs-ICIs group was higher than that in the TACE group (65.1% vs. 37.2%, &lt;i>p&lt;/i> = 0.010). Reversible AEs (grade 3 or 4) occurred differently in TACE-MTAs-ICIs and TACE groups (83.7% vs. 51.2%, &lt;i>p&lt;/i> = 0.001). Univariate and multivariate analyses revealed that TACE-MTAs-ICIs treatment was an independent favourable prognostic factor for both PFS and OS (&lt;i>p&lt;/i> &lt; 0.001).&lt;h4>Conclusion&lt;/h4>For uHCC patients beyond the up-to-seven criteria, TACE-MTAs-ICIs provided superior ORR and OS. Early combined TACE and systemic treatment should shift for patients who are beyond these criteria.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2025-04-04T18:53:44.806Z</modification><creation>2025-04-04T18:53:44.806Z</creation></dates><accession>S-EPMC11536643</accession><cross_references><pubmed>39484705</pubmed><doi>10.1080/07853890.2024.2419993</doi></cross_references></HashMap>