Evidence map›Paper›PMID 40520859›Full record

ArticleAmerican journal of cancer research2025

Clinical predictors for liver function impairment and post-embolization syndrome following transcatheter arterial chemoembolization in primary hepatic carcinoma patients: a retrospective study.

Jieqiong Zhao, Zhihui Zou, Qin Zheng, Caifeng Liu

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Article in American journal of cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

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3citing papers in PubMed, 1 pooled it
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1 · What the graph read from it

What it found

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3 · Its place in the literature

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3 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Jieqiong ZhaoDepartment of Outpatient, Eastern Hepatobiliary Surgery Hospital, Naval Military Medical University Shanghai 201805, China.
Zhihui ZouDepartment of Hepatobiliary Surgery VI, Eastern Hepatobiliary Surgery Hospital, Naval Military Medical University Shanghai 201805, China.
Qin ZhengDepartment of Nursing, Eastern Hepatobiliary Surgery Hospital, Naval Military Medical University Shanghai 201805, China.
Caifeng LiuDepartment of Biliary Surgery VI, Eastern Hepatobiliary Surgery Hospital, Naval Military Medical University Shanghai 200438, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo identify clinical predictors of liver function impairment and post-embolization syndrome (PES) following transcatheter arterial chemoembolization (TACE) in patients with primary hepatic carcinoma (PHC), to facilitate risk stratification and improve clinical outcomes.

methodsA retrospective study was conducted on 549 PHC patients who underwent TACE at Eastern Hepatobiliary Surgery Hospital, Naval Military Medical University from June 2020 to January 2024. Data on demographics, liver function, imaging findings, and TACE regimens were collected. Multivariate Logistic regression analysis was employed to identify the independent risk factors for liver function impairment and PES. The predictive performance of these factors was evaluated using receiver operating characteristic (ROC) curve analysis.

resultsAmong the 549 PHC, 61.93% (340/549) developed liver function impairment and 26.96% (148/549) experienced PES after TACE. ROC analysis indicated that alcohol consumption, cirrhosis, liver function grade, and TACE frequency demonstrated predicted value for liver impairment (AUCs: 0.565-0.619) and PES (AUCs: 0.581-0.656). Multivariate logistic regression identified neutrophils (OR=2.349, P=0.001), prealbumin (PA) (OR=1.674, P=0.028), liver function grade (OR=3.135, P<0.001), alcohol consumption (OR=0.296, P<0.001), cirrhosis (OR=0.528, P=0.005), and TACE frequency (OR=0.482, P=0.001) as independent predictors for liver impairment; For PES, alcohol consumption (OR=1.959, P=0.003), body mass index (BMI) (OR=0.288, P<0.001), albumin (ALB) (OR=0.384, P=0.005), PA (OR=0.288, P<0.001), and ECOG score (OR=0.527, P=0.006) were identified as the independent predictors, whereas liver function grade (P=0.287) and TACE frequency (P=0.634) were not. Nomograms based on these predictors demonstrated good discriminative ability (AUC=0.854 for liver impairment; AUC=0.826 for PES) and satisfactory calibration (P>0.05), with consistent performance in both training and validation cohorts (AUC: 0.852-0.854 for liver impairment; 0.820-0.843 for PES).

conclusionKey clinical variables, including alcohol consumption, cirrhosis, and specific biochemical markers, are significantly associated with liver function impairment and PES following TACE in PHC patients. These findings support the development of individualized treatment strategies to improve patient outcomes.

Indexed as

clinical predictorsliver function impairmentpost-embolization syndromePrimary hepatic carcinomaretrospective studyTACE

Identifiers

PMID40520859
PMCPMC12163436

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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.