Evidence map›Paper›PMID 42168526›Full record

ArticleNPJ digital medicine2026

Machine learning based hepatic safety score predicts decompensation in hepatocellular carcinoma systemic therapy.

Ji Won Han, Jaejun Lee, Keungmo Yang, Kwon Yong Tak, Hyun Yang, Si Hyun Bae, Hee Sun Cho, Heechul Nam, Chang Wook Kim, Hae Lim Lee and 11 more

Abstract read
In one paragraph

Article in NPJ digital medicine, 2026. 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

21 authors.

Ji Won HanThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea. tmznjf@catholic.ac.kr.ORCID http://orcid.org/0000-0003-1456-1450
Jaejun LeeThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Keungmo YangThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Kwon Yong TakThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Hyun YangThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Si Hyun BaeThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Hee Sun ChoThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Heechul NamThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Chang Wook KimThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Hae Lim LeeThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Hee Yeon KimThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Sung Won LeeThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Ahlim LeeThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Do Seon SongThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Seok Hwan KimThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Myeong Jun SongThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Soon Woo NamThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Soon Kyu LeeThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Jung Hyun KwonThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Pil Soo SungThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Jeong Won JangThe Catholic University Liver Research Center, Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.

Funding

Korea Health Industry Development Institute RS-2024-00406716
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) frequently coexists with portal hypertension, significantly increasing the risk of hepatic decompensation (HD) and variceal bleeding during systemic therapy. We developed a machine learning based hepatic safety score (MHSS) using data from 2026 patients with unresectable HCC to predict clinically significant portal hypertension (CSPH) and prognosis. A random forest model was trained in a derivation cohort (n = 1262) and validated in an independent cohort (n = 764). The MHSS demonstrated robust performance (AUROC 0.840) in CSPH and predicting HD. Stratification revealed that high MHSS patients faced significantly elevated risks of HD (HR 3.25), variceal bleeding (VB, HR 4.90), and mortality (HR 2.21). Crucially, while atezolizumab-bevacizumab offered a survival advantage in low MHSS patients, it was associated with high bleeding risk and no survival benefit in the high MHSS group compared to other regimens. A simulation of MHSS guided treatment selection demonstrated a 24% reduction in HD, a 40% reduction in VB, and a 26% reduction in mortality. In conclusion, the MHSS effectively predicts CSPH, decompensation, and survival in patients with HCC prior to systemic therapy. By enabling individualized risk stratification, the MHSS may guide personalized treatment selection between bevacizumab-containing and alternative regimens, ultimately improving patient outcomes. Clinical trial number: not applicable.

Identifiers

PMID42168526
PMCPMC13470065

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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.