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The Impact of Statins on the Survival of Patients with Advanced Hepatocellular Carcinoma Treated with Sorafenib or Lenvatinib
DC Field | Value | Language |
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dc.contributor.author | Han, JE | - |
dc.contributor.author | Kim, J | - |
dc.contributor.author | Cheong, JY | - |
dc.contributor.author | Kim, SS | - |
dc.contributor.author | Lim, SG | - |
dc.contributor.author | Yang, MJ | - |
dc.contributor.author | Noh, CK | - |
dc.contributor.author | Lee, GH | - |
dc.contributor.author | Eun, JW | - |
dc.contributor.author | Park, B | - |
dc.contributor.author | Cho, HJ | - |
dc.date.accessioned | 2024-03-14T04:52:32Z | - |
dc.date.available | 2024-03-14T04:52:32Z | - |
dc.date.issued | 2024 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/32330 | - |
dc.description.abstract | We aimed to evaluate the survival benefits of coadministering statins and multityrosine kinase inhibitors (TKIs) in patients with advanced hepatocellular carcinoma (HCC). Data from the Health Insurance Review and Assessment Service in Korea (2010–2020) were utilized. Statin use (≥28 cumulative defined daily doses) was analyzed, with 1534 statin users matched to 6136 non-users (1:4 ratio) using propensity scores. Primary and secondary outcomes were overall survival (OS) and progression-free survival (PFS). Statin use significantly improved OS (hazard ratio [HR] 0.77, 95% confidence interval [CI] 0.72–0.82, p < 0.001) and PFS (HR 0.78, 95% CI 0.74–0.84, p < 0.001). Continuous or post-TKI statin users had better OS, while discontinuation after TKI use led to poorer OS. Both lipophilic and hydrophilic statins improved OS and PFS, particularly with ≥730 cumulative defined daily doses. In conclusion, combining statins and TKIs in patients with advanced HCC yielded significant survival benefits, influenced by statin dosage and duration. Continuous statin administration post-TKI treatment is crucial for improving outcomes in patients with HCC. | - |
dc.language.iso | en | - |
dc.title | The Impact of Statins on the Survival of Patients with Advanced Hepatocellular Carcinoma Treated with Sorafenib or Lenvatinib | - |
dc.type | Article | - |
dc.identifier.pmid | 38254739 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10813381 | - |
dc.subject.keyword | hepatocellular carcinoma | - |
dc.subject.keyword | hydrophilic statin | - |
dc.subject.keyword | lipophilic statin | - |
dc.subject.keyword | multityrosine kinase inhibitor | - |
dc.subject.keyword | sorafenib resistance | - |
dc.subject.keyword | statin | - |
dc.contributor.affiliatedAuthor | Han, JE | - |
dc.contributor.affiliatedAuthor | Cheong, JY | - |
dc.contributor.affiliatedAuthor | Kim, SS | - |
dc.contributor.affiliatedAuthor | Lim, SG | - |
dc.contributor.affiliatedAuthor | Yang, MJ | - |
dc.contributor.affiliatedAuthor | Noh, CK | - |
dc.contributor.affiliatedAuthor | Lee, GH | - |
dc.contributor.affiliatedAuthor | Eun, JW | - |
dc.contributor.affiliatedAuthor | Park, B | - |
dc.contributor.affiliatedAuthor | Cho, HJ | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.3390/cancers16020249 | - |
dc.citation.title | Cancers | - |
dc.citation.volume | 16 | - |
dc.citation.number | 2 | - |
dc.citation.date | 2024 | - |
dc.citation.startPage | 249 | - |
dc.citation.endPage | 249 | - |
dc.identifier.bibliographicCitation | Cancers, 16(2). : 249-249, 2024 | - |
dc.identifier.eissn | 2072-6694 | - |
dc.relation.journalid | J020726694 | - |
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