Evidence map›Paper›PMID 42068148›Full record

ArticleJournal of clinical laboratory analysis2026

Association Between Multi-Laboratory Parameters Pre- and Post-Treatment and Pathological Features and Their Values in Clinical Decision in Primary Hepatic Carcinoma.

Xiaowei Chi, Weifang Liu, Zihan Liu, Jie Liu

Abstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

4 authors.

Xiaowei ChiDepartment of Laboratory Medicine, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, China.ORCID https://orcid.org/0000-0002-1195-805X
Weifang LiuDepartment of Laboratory Medicine, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, China.
Zihan LiuUniversity of Washington at Seattle, Seattle, Washington, USA.
Jie LiuShandong Province Health Precision Medicine Industry Technology Research Institute, Jinan, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrimary hepatic cancer (PHC) is still a significant burden worldwide. The efficacy of diagnosis, treatment response monitoring, and prognostication using laboratory biomarkers is still a challenge. This study analyzed multi-laboratory parameters pre- and post-treatment and their associations with clinical and pathological features and clinical decisions in PHC patients to evaluate their clinical usefulness.

methodsThis study analyzed laboratory data from PHC patients by comparing changes between pre- and post-treatment and the efficacy of commonly used tumor markers and their associations with clinical and pathological features. Data from 441 PHC patients were analyzed.

resultsSerum alpha-fetoprotein (AFP) and alpha-L-fucosidase (AFU), alanine aminotransferase (ALT), aspartate aminotransferase (AST), gamma-glutamyltransferase (γ-GT), indirect bilirubin (IBIL), and hepatitis B virus DNA (HBV DNA) were reduced after treatment; AFP, carcinoembryonic antigen (CEA), and cancer antigen 19-9 (CA-199) showed value in assisting the judgment of surgical resection; serum ferritin increased significantly along with stage advanced. AFP, CEA, CA-199, and ferritin were lower in surgical resection patients than non-surgical patients. A significant association was displayed between AFP levels and multiple biomarkers and clinical features when AFP cut-off was adjusted to 140 ng/mL. AFP was increased in PHC patients with chronic hepatitis B infection and liver cirrhosis, while CA-199 was decreased in both situations.

conclusionsTumor marker AFP, CEA, CA-199, serum chemistry test panel AFU, ALT, AST, γ-GT, bilirubin, protein, and HBV DNA are useful indicators in monitoring therapeutic response and disease progression and may be used as indicators in assisting the judgment of surgical resection of PHC.

Indexed as

Biomarkers, TumorCarcinoma, HepatocellularClinical Decision-MakingLiver NeoplasmsAdultAgedalpha-FetoproteinsFemaleHumansMaleMiddle Agedalpha-FetoproteinsBiomarkers, Tumorcholangiocarcinomaclinical and pathological featureshepatocellular carcinomaprimary hepatic carcinomatumor marker

Identifiers

PMID42068148
PMCPMC13267153

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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.