Evidence map›Paper›PMID 40469212›Full record

ArticleGE Portuguese journal of gastroenterology2025

Prediction of Hepatocellular Carcinoma in a Portuguese Population after Hepatitis C Cure: Comparative Accuracy of Noninvasive Tests (Transient Elastography, FIB-4, and aMAP).

André Mascarenhas, Juliana Serrazina, Sérgio Bronze, Helena Cortez-Pinto, José Presa, Ana Barreira, Paulo Carrola, Francisco Vara-Luiz, Alexandra Rosu-Pires, Pedro Lages Martins and 18 more

Abstract read
In one paragraph

Article in GE Portuguese journal of gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors.

André MascarenhasDepartment of Gastroenterology, Unidade Local de Saúde Lisboa Ocidental, Lisbon, Portugal.
Juliana SerrazinaDepartment of Gastroenterology and Hepatology, Unidade Local de Saúde Santa Maria, Lisbon, Portugal.
Sérgio BronzeDepartment of Gastroenterology and Hepatology, Unidade Local de Saúde Santa Maria, Lisbon, Portugal.
Helena Cortez-PintoDepartment of Gastroenterology and Hepatology, Unidade Local de Saúde Santa Maria, Lisbon, Portugal.
José PresaDepartment of Internal Medicine, Unidade Local de Saúde Trás-os-Montes e Alto Douro, Vila Real, Portugal.
Ana BarreiraDepartment of Internal Medicine, Unidade Local de Saúde Trás-os-Montes e Alto Douro, Vila Real, Portugal.
Paulo CarrolaDepartment of Internal Medicine, Unidade Local de Saúde Trás-os-Montes e Alto Douro, Vila Real, Portugal.
Francisco Vara-LuizDepartment of Gastroenterology, Unidade Local de Saúde de Almada-Seixal, Almada, Portugal.
Alexandra Rosu-PiresDepartment of Gastroenterology, Unidade Local de Saúde de Almada-Seixal, Almada, Portugal.
Pedro Lages MartinsDepartment of Gastroenterology, Unidade Local de Saúde São José, Lisbon, Portugal.
Rita PrataDepartment of Gastroenterology, Unidade Local de Saúde São José, Lisbon, Portugal.
Joana RevésDepartment of Gastroenterology, Unidade Local de Saúde de Loures-Odivelas, Loures, Portugal.
Catarina BravoDepartment of Gastroenterology, Unidade Local de Saúde de Loures-Odivelas, Loures, Portugal.
Catarina NascimentoDepartment of Gastroenterology, Unidade Local de Saúde de Loures-Odivelas, Loures, Portugal.
Catarina GouveiaDepartment of Gastroenterology, Unidade Local de Saúde de Loures-Odivelas, Loures, Portugal.
Ana Rita FrancoDepartment of Gastroenterology, Unidade Local de Saúde Lisboa Ocidental, Lisbon, Portugal.
Pedro LimaDepartment of Gastroenterology, Unidade Local de Saúde Lisboa Ocidental, Lisbon, Portugal.
Catarina O'NeillDepartment of Gastroenterology, Unidade Local de Saúde Lisboa Ocidental, Lisbon, Portugal.
Raquel R MendesDepartment of Gastroenterology, Unidade Local de Saúde Lisboa Ocidental, Lisbon, Portugal.
Inês Rodrigues SimãoDepartment of Gastroenterology, Unidade Local de Saúde Lisboa Ocidental, Lisbon, Portugal.
Inês Costa SantosDepartment of Gastroenterology, Unidade Local de Saúde da Arrábida, Setúbal, Portugal.
André Ruge GonçalvesDepartment of Gastroenterology, Unidade Local de Saúde da Região de Leiria, Leiria, Portugal.
Pedro BarreiroDepartment of Gastroenterology, Unidade Local de Saúde Lisboa Ocidental, Lisbon, Portugal.
Rui MendoDepartment of Gastroenterology, Unidade Local de Saúde Lisboa Ocidental, Lisbon, Portugal.
Rita BarosaDepartment of Gastroenterology, Unidade Local de Saúde Lisboa Ocidental, Lisbon, Portugal.
Pedro FigueiredoDepartment of Gastroenterology, Unidade Local de Saúde Lisboa Ocidental, Lisbon, Portugal.
Cristina ChagasDepartment of Gastroenterology, Unidade Local de Saúde Lisboa Ocidental, Lisbon, Portugal.
“Hepatologia em Rede”

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Chronic infection with hepatitis C virus (HCV) causes 25% of hepatocellular carcinoma (HCC) cases worldwide, a major cause of morbimortality even after sustained virologic response (SVR). Universal screening to all patients with advanced liver fibrosis is currently recommended. A risk-based strategy could improve the detection rate of early HCC and diminish the surveillance burden. Although several risk prediction models exist, exclusion of a subgroup of patients from surveillance has not yet been recommended. The objective of this study was the comparison of the predictive accuracy of transient elastography, FIB-4, and aMAP for HCC in HCV patients after SVR in Portugal. Methods: This was a multicentric retrospective study including patients with HCV after SVR. Comparative, univariate, multivariate, area under the ROC (receiver-operating characteristic) curve (AUC), and Youden's J-statistic analysis were performed. Results: HCC incidence was 4.2% (1.3/100 patient-years) after a median follow-up of 31 months with inclusion of 337 patients. All patients had a liver stiffness measurement (LSM) before SVR (considered the baseline), but only 148 (43.9%) had a transient elastography after SVR. FIB-4 and aMAP post-SVR were calculated in all patients. Multiple parameters positively correlated with HCC, but only age and baseline transient elastography remained as independent predictors in the multivariate analysis. The optimal cutoffs for prediction of HCC were baseline transient elastography 13.7 kPa, post-SVR transient elastography 16.5 and 15.8 kPa (first and last measurements, respectively), FIB-4 1.6, and aMAP 58. Baseline transient elastography revealed a fair accuracy in predicting HCC (AUC 0.776, Conclusion: Transient elastography (FibroScan) before SVR was a fair predictor of HCC, being more accurate than FIB-4 and aMAP. Transient elastography values ≤13.7 kPa at baseline, FIB-4 ≤1.6 and aMAP ≤58 were the cutoffs considered of low risk for HCC in a Portuguese cohort of HCV patients after SVR with advanced fibrosis. aMAP score is a risk-based surveillance tool that could improve the current HCC screening strategy, but further validation is needed.

Indexed as

Chronic hepatitis CHepatocellular carcinomaRisk assessmentScreeningSustained virologic response

Identifiers

PMID40469212
PMCPMC12133121

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.