Cited 79 times in
Addition of tumor multiplicity improves the prognostic performance of the hepatoma arterial-embolization prognostic score
DC Field | Value | Language |
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dc.contributor.author | 김도영 | - |
dc.contributor.author | 김범경 | - |
dc.contributor.author | 김승업 | - |
dc.contributor.author | 박용은 | - |
dc.contributor.author | 박준용 | - |
dc.contributor.author | 박지혜 | - |
dc.contributor.author | 안상훈 | - |
dc.contributor.author | 윤해룡 | - |
dc.contributor.author | 한광협 | - |
dc.contributor.author | 박예현 | - |
dc.date.accessioned | 2017-02-24T03:43:32Z | - |
dc.date.available | 2017-02-24T03:43:32Z | - |
dc.date.issued | 2016 | - |
dc.identifier.issn | 1478-3223 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/146425 | - |
dc.description.abstract | BACKGROUND & AIMS: The hepatoma arterial-embolization prognostic (HAP) score predicts survival outcome in patients with hepatocellular carcinoma (HCC) treated with trans-arterial chemoembolization (TACE). We validated the HAP score in Korean subjects with HCC and investigated whether its prognostic performance is improved with additional parameters. METHODS: A total of 280 patients with HCC treated with TACE between 2003 and 2009 were included. Validation and modification of HAP score were performed based on multivariate Cox regression models. RESULTS: The median age of the study population (211 men, 69 women) was 60 years. Viral etiology of HCC accounted for 80.4% (n = 181 for hepatitis B, 44 for hepatitis C). The median overall survival (OS) was 40.5 months. On multivariate analysis, together with the original components of the HAP score (serum albumin <3.6 g/dl, total bilirubin >0.9 mg/dl, alpha-foetoprotein >400 ng/ml, and tumor size >7 cm), tumor number ≥2 was selected as an independent unfavorable prognostic factor for OS (hazard ratio 2.3; P < 0.001). Accordingly, a modified HAP-II (mHAP-II) score was established by adding tumor number ≥2. Although both HAP and mHAP-II scores discriminated the four different risk groups (log-rank test, all P < 0.001), the mHAP-II score performed significantly better than the HAP score, as per the areas under receiver-operating curves predicting OS at 3 years (0.717 vs. 0.658) and 5 years (0.728 vs. 0.645), respectively (all P < 0.05). CONCLUSIONS: Although the HAP score predicted OS for Korean subjects with HCC undergoing TACE, the addition of tumor number significantly improved the prognostic performance. The mHAP-II score can be used for accurate prognostication and selection of optimal candidates for TACE. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.format.extent | 100~107 | - |
dc.language | English | - |
dc.publisher | Wiley-Blackwell | - |
dc.relation.isPartOf | LIVER INTERNATIONAL | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Biomarkers, Tumor/analysis | - |
dc.subject.MESH | Carcinoma, Hepatocellular*/diagnosis | - |
dc.subject.MESH | Carcinoma, Hepatocellular*/etiology | - |
dc.subject.MESH | Carcinoma, Hepatocellular*/mortality | - |
dc.subject.MESH | Carcinoma, Hepatocellular*/pathology | - |
dc.subject.MESH | Carcinoma, Hepatocellular*/therapy | - |
dc.subject.MESH | Chemoembolization, Therapeutic*/adverse effects | - |
dc.subject.MESH | Chemoembolization, Therapeutic*/methods | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Liver Neoplasms*/diagnosis | - |
dc.subject.MESH | Liver Neoplasms*/etiology | - |
dc.subject.MESH | Liver Neoplasms*/mortality | - |
dc.subject.MESH | Liver Neoplasms*/pathology | - |
dc.subject.MESH | Liver Neoplasms*/therapy | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Neoplasm Staging | - |
dc.subject.MESH | Prognosis | - |
dc.subject.MESH | Proportional Hazards Models | - |
dc.subject.MESH | Republic of Korea | - |
dc.subject.MESH | Research Design/standards | - |
dc.subject.MESH | Risk Assessment/methods* | - |
dc.subject.MESH | Survival Analysis | - |
dc.subject.MESH | Tumor Burden | - |
dc.subject.MESH | alpha-Fetoproteins/analysis | - |
dc.title | Addition of tumor multiplicity improves the prognostic performance of the hepatoma arterial-embolization prognostic score | - |
dc.type | Article | - |
dc.publisher.location | United States | - |
dc.contributor.college | College of Medicine | - |
dc.contributor.department | Dept. of Internal Medicine | - |
dc.contributor.googleauthor | Yehyun Park | - |
dc.contributor.googleauthor | Seung Up Kim | - |
dc.contributor.googleauthor | Beom Kyung Kim | - |
dc.contributor.googleauthor | Jun Yong Park | - |
dc.contributor.googleauthor | Do Young Kim | - |
dc.contributor.googleauthor | Sang Hoon Ahn | - |
dc.contributor.googleauthor | Yong Eun Park | - |
dc.contributor.googleauthor | Ji Hye Park | - |
dc.contributor.googleauthor | Yong Il Lee | - |
dc.contributor.googleauthor | Hae Ryong Yun | - |
dc.contributor.googleauthor | Kwang-Hyub Han | - |
dc.identifier.doi | 10.1111/liv.12878 | - |
dc.contributor.localId | A00385 | - |
dc.contributor.localId | A00487 | - |
dc.contributor.localId | A00654 | - |
dc.contributor.localId | A04571 | - |
dc.contributor.localId | A01675 | - |
dc.contributor.localId | A04575 | - |
dc.contributor.localId | A02226 | - |
dc.contributor.localId | A04617 | - |
dc.contributor.localId | A04268 | - |
dc.contributor.localId | A01575 | - |
dc.relation.journalcode | J02171 | - |
dc.identifier.eissn | 1478-3231 | - |
dc.identifier.pmid | 26013186 | - |
dc.identifier.url | http://onlinelibrary.wiley.com/doi/10.1111/liv.12878/abstract | - |
dc.subject.keyword | hepatocellular carcinoma | - |
dc.subject.keyword | model | - |
dc.subject.keyword | overall survival | - |
dc.subject.keyword | prediction | - |
dc.subject.keyword | prognosis | - |
dc.subject.keyword | trans-arterial chemoembolization | - |
dc.contributor.alternativeName | Kim, Do Young | - |
dc.contributor.alternativeName | Kim, Beom Kyung | - |
dc.contributor.alternativeName | Kim, Seung Up | - |
dc.contributor.alternativeName | Park, Yong Eun | - |
dc.contributor.alternativeName | Park, Jun Yong | - |
dc.contributor.alternativeName | Park, Ji Hye | - |
dc.contributor.alternativeName | Ahn, Sang Hoon | - |
dc.contributor.alternativeName | Yun, Hae Ryong | - |
dc.contributor.alternativeName | Han, Kwang Hyup | - |
dc.contributor.alternativeName | Park, Ye Hyun | - |
dc.contributor.affiliatedAuthor | Kim, Do Young | - |
dc.contributor.affiliatedAuthor | Kim, Beom Kyung | - |
dc.contributor.affiliatedAuthor | Kim, Seung Up | - |
dc.contributor.affiliatedAuthor | Park, Yong Eun | - |
dc.contributor.affiliatedAuthor | Park, Jun Yong | - |
dc.contributor.affiliatedAuthor | Park, Ji Hye | - |
dc.contributor.affiliatedAuthor | Ahn, Sang Hoon | - |
dc.contributor.affiliatedAuthor | Yun, Hae Ryong | - |
dc.contributor.affiliatedAuthor | Han, Kwang Hyup | - |
dc.contributor.affiliatedAuthor | Park, Ye Hyun | - |
dc.citation.volume | 36 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 100 | - |
dc.citation.endPage | 107 | - |
dc.identifier.bibliographicCitation | LIVER INTERNATIONAL, Vol.36(1) : 100-107, 2016 | - |
dc.date.modified | 2017-02-24 | - |
dc.identifier.rimsid | 48413 | - |
dc.type.rims | ART | - |
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