Evidence map›Paper›PMID 41647967›Full record

ArticleESMO gastrointestinal oncology2025

Novel blood signature for hepatocellular carcinoma screening.

K-M Chueng, K-N Kwok, S J-L Lam, H-S Lam, S-M Yip, S Lam, O-P Chiu, A K-Y Chan, H H-W Liu, S K-K Ng and 6 more

Abstract read
In one paragraph

Article in ESMO gastrointestinal oncology, 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

16 authors.

K-M ChuengDepartment of Clinical Oncology, Queen Elizabeth Hospital, Kowloon, Hong Kong SAR, China.
K-N KwokDepartment of Mechanical and Aerospace Engineering, The Hong Kong University of Science and Technology, Kowloon, Hong Kong SAR, China.
S J-L LamFaculty of Medicine, The Chinese University of Hong Kong, Sha Tin, N.T., Hong Kong SAR, China.
H-S LamDepartment of Medicine, Kwong Wah Hospital, Kowloon, Hong Kong SAR, China.
S-M YipDepartment of Surgery, Kwong Wah Hospital, Yaumatei, Kowloon, Hong Kong SAR, China.
S LamDepartment of Surgery, Addenbrookes Hospital, Cambridge, UK.
O-P ChiuDepartment of Medicine, Kwong Wah Hospital, Kowloon, Hong Kong SAR, China.
A K-Y ChanDepartment of Medicine, Queen Elizabeth Hospital, Kowloon, Hong Kong SAR, China.
H H-W LiuDepartment of Medicine, Queen Elizabeth Hospital, Kowloon, Hong Kong SAR, China.
S K-K NgDepartment of Surgery, Prince of Wales Hospital, Shatin, N.T., Hong Kong SAR, China.
L SutantoDepartment of Clinical Oncology, Queen Elizabeth Hospital, Kowloon, Hong Kong SAR, China.
J C K YungDepartment of Oncology, United Christian Hospital, Kowloon, Hong Kong SAR, China.
H-L LeungDepartment of Oncology, United Christian Hospital, Kowloon, Hong Kong SAR, China.
P Y-M WooDepartment of Neurosurgery, Prince of Wales Hospital, Shatin, N.T., Hong Kong SAR, China.
H H-Y YiuDepartment of Clinical Oncology, Queen Elizabeth Hospital, Kowloon, Hong Kong SAR, China.
D C C LamDepartment of Mechanical and Aerospace Engineering, The Hong Kong University of Science and Technology, Kowloon, Hong Kong SAR, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Alpha-fetoprotein is commonly used for hepatocellular carcinoma (HCC) screening in at-risk populations, but its effectiveness is limited. Routine blood tests offer insights into cancer-related conditions and improve detection in other cancers. This study explores the postulated changes in routine blood tests of HCC patients, allowing the development of routine blood-based artificial intelligence for early HCC detection. Patients and methods: This population-based retrospective study analyzed patient records from 2000 to 2018 from the Hong Kong Hospital Authority Data Collaboration Laboratory. Patients with chronic liver disease (CLD), both with and without HCC, were identified using ICD codes, antiviral drug history, virology tests, and radiology reports. Those with decompensated CLD were excluded. Routine blood tests included complete blood count, liver function test, renal function test, and clotting profiles, with records collected within 1 month before HCC diagnosis. Statistical analyses included descriptive statistics and the Mann-Whitney Results: The cohort comprised 223 862 patients, including 31 149 with HCC (13.9%). Statistical analysis revealed a distinct blood signature for HCC patients, characterized by significant liver function derangement (elevated alanine aminotransferase, alkaline phosphatase, bilirubin, aspartate aminotransferase; decreased albumin), signs of systemic inflammation (lower lymphocyte count, red cell distribution width), bleeding tendencies (prolonged prothrombin time, activated partial thromboplastin time; low platelet count), and indications of cachexia (lower albumin, creatinine, urea)-all statistically significant ( Conclusions: This study presents a novel blood signature for HCC detection based on extensive clinical data. The unique spectral characteristics effectively differentiate HCC from CLD controls, supporting the potential for machine learning models in HCC detection.

Indexed as

big datacancer detectionhepatocellular carcinomaliver cancerroutine blood testtumor marker

Identifiers

PMID41647967
PMCPMC12836581

What OpenQuestion holds

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Registered trials

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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.