Mostrar el registro sencillo del ítem

dc.creatorFan R., Papatheodoridis G., Sun J., Innes H., Toyoda H., Xie Q., Mo S., Sypsa V., Guha I.N., Kumada T., Niu J., Dalekos G., Yasuda S., Barnes E., Lian J., Suri V., Idilman R., Barclay S.T., Dou X., Berg T., Hayes P.C., Flaherty J.F., Zhou Y., Zhang Z., Buti M., Hutchinson S.J., Guo Y., Calleja J.L., Lin L., Zhao L., Chen Y., Janssen H.L.A., Zhu C., Shi L., Tang X., Gaggar A., Wei L., Jia J., Irving W.L., Johnson P.J., Lampertico P., Hou J.en
dc.date.accessioned2023-01-31T07:37:36Z
dc.date.available2023-01-31T07:37:36Z
dc.date.issued2020
dc.identifier10.1016/j.jhep.2020.07.025
dc.identifier.issn01688278
dc.identifier.urihttp://hdl.handle.net/11615/71451
dc.description.abstractBackground & Aims: Hepatocellular carcinoma (HCC) is the leading cause of death in patients with chronic hepatitis. In this international collaboration, we sought to develop a global universal HCC risk score to predict the HCC development for patients with chronic hepatitis. Methods: A total of 17,374 patients, comprising 10,578 treated Asian patients with chronic hepatitis B (CHB), 2,510 treated Caucasian patients with CHB, 3,566 treated patients with hepatitis C virus (including 2,489 patients with cirrhosis achieving a sustained virological response) and 720 patients with non-viral hepatitis (NVH) from 11 international prospective observational cohorts or randomised controlled trials, were divided into a training cohort (3,688 Asian patients with CHB) and 9 validation cohorts with different aetiologies and ethnicities (n = 13,686). Results: We developed an HCC risk score, called the aMAP score (ranging from 0 to 100), that involves only age, male, albumin–bilirubin and platelets. This metric performed excellently in assessing HCC risk not only in patients with hepatitis of different aetiologies, but also in those with different ethnicities (C-index: 0.82–0.87). Cut-off values of 50 and 60 were best for discriminating HCC risk. The 3- or 5-year cumulative incidences of HCC were 0–0.8%, 1.5–4.8%, and 8.1–19.9% in the low- (n = 7,413, 43.6%), medium- (n = 6,529, 38.4%), and high-risk (n = 3,044, 17.9%) groups, respectively. The cut-off value of 50 was associated with a sensitivity of 85.7–100% and a negative predictive value of 99.3–100%. The cut-off value of 60 resulted in a specificity of 56.6–95.8% and a positive predictive value of 6.6–15.7%. Conclusions: This objective, simple, reliable risk score based on 5 common parameters accurately predicted HCC development, regardless of aetiology and ethnicity, which could help to establish a risk score-guided HCC surveillance strategy worldwide. Lay summary: In this international collaboration, we developed and externally validated a simple, objective and accurate prognostic tool (called the aMAP score), that involves only age, male, albumin–bilirubin and platelets. The aMAP score (ranged from 0 to 100) satisfactorily predicted the risk of hepatocellular carcinoma (HCC) development among over 17,000 patients with viral and non-viral hepatitis from 11 global prospective studies. Our findings show that the aMAP score had excellent discrimination and calibration in assessing the 5-year HCC risk among all the cohorts irrespective of aetiology and ethnicity. © 2020 European Association for the Study of the Liveren
dc.language.isoenen
dc.sourceJournal of Hepatologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85091689047&doi=10.1016%2fj.jhep.2020.07.025&partnerID=40&md5=202d1fe113ac7b4ab5df112e1a7ef7ac
dc.subjectalbuminen
dc.subjectbilirubinen
dc.subjectantivirus agenten
dc.subjectbilirubinen
dc.subjectserum albuminen
dc.subjectadulten
dc.subjectArticleen
dc.subjectcancer diagnosisen
dc.subjectcancer patienten
dc.subjectcancer prognosisen
dc.subjectchronic hepatitis Ben
dc.subjectcohort analysisen
dc.subjectcontrolled studyen
dc.subjectethnicityen
dc.subjectfemaleen
dc.subjectHepatitis B virusen
dc.subjectHepatitis C virusen
dc.subjecthumanen
dc.subjecthuman cellen
dc.subjectincidenceen
dc.subjectliver cell carcinomaen
dc.subjectliver cirrhosisen
dc.subjectmajor clinical studyen
dc.subjectmaleen
dc.subjectnonalcoholic fatty liveren
dc.subjectpredictive valueen
dc.subjectpriority journalen
dc.subjectprospective studyen
dc.subjectrandomized controlled trialen
dc.subjectrisk assessmenten
dc.subjectscoring systemen
dc.subjectsustained virologic responseen
dc.subjectthrombocyteen
dc.subjectAsian continental ancestry groupen
dc.subjectblooden
dc.subjectCaucasianen
dc.subjectchronic hepatitisen
dc.subjectcomplicationen
dc.subjectethnologyen
dc.subjectglobal healthen
dc.subjectliver cell carcinomaen
dc.subjectliver tumoren
dc.subjectmiddle ageden
dc.subjectpathologyen
dc.subjectproceduresen
dc.subjectprognosisen
dc.subjectrisk factoren
dc.subjectAntiviral Agentsen
dc.subjectAsian Continental Ancestry Groupen
dc.subjectBilirubinen
dc.subjectBlood Plateletsen
dc.subjectCarcinoma, Hepatocellularen
dc.subjectEuropean Continental Ancestry Groupen
dc.subjectFemaleen
dc.subjectGlobal Healthen
dc.subjectHepatitis, Chronicen
dc.subjectHumansen
dc.subjectLiver Neoplasmsen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectPredictive Value of Testsen
dc.subjectPrognosisen
dc.subjectRisk Assessmenten
dc.subjectRisk Factorsen
dc.subjectSerum Albuminen
dc.subjectElsevier B.V.en
dc.titleaMAP risk score predicts hepatocellular carcinoma development in patients with chronic hepatitisen
dc.typejournalArticleen


Ficheros en el ítem

FicherosTamañoFormatoVer

No hay ficheros asociados a este ítem.

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem