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Similar recurrence after curative treatment of HBV-related HCC, regardless of HBV replication activity
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 김범경 | - |
| dc.contributor.author | 김승업 | - |
| dc.contributor.author | 노윤호 | - |
| dc.contributor.author | 김미나 | - |
| dc.date.accessioned | 2024-10-04T02:29:57Z | - |
| dc.date.available | 2024-10-04T02:29:57Z | - |
| dc.date.issued | 2024-08 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/200515 | - |
| dc.description.abstract | Background and aims Antiviral therapy (AVT) is required in patients with newly diagnosed hepatitis B virus (HBV)related hepatocellular carcinoma (HCC), if HBV DNA is detectable. We compared the risk of recurrence according to HBV replication activity at the curative treatment of HBV-related HCC. Methods Patients with HBV-related HCC who underwent surgical resection or radiofrequency ablation between 2013 and 2018 were enrolled in this retrospective cohort study. Patients were categorized into two groups according to HBV replication activity at the curative treatment of HBV-related HCC (group 1: patients who met the AVT indication for HBV-related HCC due to detectable HBV DNA but did not meet the AVT indication if without HCC; group 2: patients who met the AVT indication, regardless of HCC). Results In the entire cohort (n = 911), HCC recurred in 303 (33.3%) patients during a median followup of 4.7 years. After multivariate adjustment, group 2 showed a statistically similar risk of HCC recurrence (adjusted hazard ratio [aHR] = 1.18, P = 0.332) compared to that of group 1. In addition, group 2 showed statistically similar risks of early (< 2 years; aHR = 1.31) and late (≥ 2 years; aHR = 0.83) recurrence than that of group 1 (all P>0.05). Propensity score matching and inverse probability of treatment weighting analysis also yielded similar risks of HCC recurrence between the two groups (all P>0.05, log-rank tests). Conclusions The risk of HCC recurrence in patients who received curative treatment for newly diagnosed HBV-related HCC was similar regardless of HBV replication activity, if AVT was properly initiated. © 2024 Kim et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | - |
| dc.description.statementOfResponsibility | open | - |
| dc.format | application/pdf | - |
| dc.language | English | - |
| dc.publisher | Public Library of Science | - |
| dc.relation.isPartOf | PLOS ONE | - |
| dc.rights | CC BY-NC-ND 2.0 KR | - |
| dc.subject.MESH | Aged | - |
| dc.subject.MESH | Antiviral Agents / therapeutic use | - |
| dc.subject.MESH | Carcinoma, Hepatocellular* / pathology | - |
| dc.subject.MESH | Carcinoma, Hepatocellular* / virology | - |
| dc.subject.MESH | DNA, Viral / genetics | - |
| dc.subject.MESH | Female | - |
| dc.subject.MESH | Hepatitis B / complications | - |
| dc.subject.MESH | Hepatitis B / virology | - |
| dc.subject.MESH | Hepatitis B virus* / physiology | - |
| dc.subject.MESH | Humans | - |
| dc.subject.MESH | Liver Neoplasms* / pathology | - |
| dc.subject.MESH | Liver Neoplasms* / virology | - |
| dc.subject.MESH | Male | - |
| dc.subject.MESH | Middle Aged | - |
| dc.subject.MESH | Neoplasm Recurrence, Local* / virology | - |
| dc.subject.MESH | Retrospective Studies | - |
| dc.subject.MESH | Virus Replication* | - |
| dc.title | Similar recurrence after curative treatment of HBV-related HCC, regardless of HBV replication activity | - |
| dc.type | Article | - |
| dc.contributor.college | College of Medicine (의과대학) | - |
| dc.contributor.department | BioMedical Science Institute (의생명과학부) | - |
| dc.contributor.googleauthor | Mi Na Kim | - |
| dc.contributor.googleauthor | Beom Kyung Kim | - |
| dc.contributor.googleauthor | Heejin Cho | - |
| dc.contributor.googleauthor | Myung Ji Goh | - |
| dc.contributor.googleauthor | Yun Ho Roh | - |
| dc.contributor.googleauthor | Su Jong Yu | - |
| dc.contributor.googleauthor | Dong Hyun Sinn | - |
| dc.contributor.googleauthor | Soo Young Park | - |
| dc.contributor.googleauthor | Seung Up Kim | - |
| dc.identifier.doi | 10.1371/journal.pone.0307712 | - |
| dc.contributor.localId | A00441 | - |
| dc.contributor.localId | A00487 | - |
| dc.contributor.localId | A00654 | - |
| dc.relation.journalcode | J02540 | - |
| dc.identifier.eissn | 1932-6203 | - |
| dc.identifier.pmid | 39186715 | - |
| dc.contributor.alternativeName | Kim, Mina | - |
| dc.contributor.affiliatedAuthor | 김범경 | - |
| dc.contributor.affiliatedAuthor | 김승업 | - |
| dc.citation.volume | 19 | - |
| dc.citation.number | 8 | - |
| dc.citation.startPage | e0307712 | - |
| dc.identifier.bibliographicCitation | PLOS ONE, Vol.19(8) : e0307712, 2024-08 | - |
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