Evidence map›Paper›PMID 40859162›Full record

ArticleBMC gastroenterology2025

Prognostic comparison between LNM and MaVI of hepatocellular carcinoma: a multicenter population-based propensity scores matching study.

Jinyu Zhang, Yifan Chen, Peng Ye, Qionglan Wu, Jingfeng Liu, Jianxing Zeng

Abstract readComparative StudyMulticenter Study
In one paragraph

Article in BMC 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.

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5 · Who and what money

Authors and funding

6 authors.

Jinyu Zhang *Department of Hepatobiliary Surgery, Mengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou, 350025, China.
Yifan Chen *Department of Gastrointestinal Surgery, Fujian Provincial Hospital, Fuzhou, 350001, China.
Peng Ye *Department of Anesthesiology, Shengli Clinical Medical College of Fujian Medical University, Fuzhou, 350001, China.
Qionglan WuDepartment of Pathology, Mengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou, 350025, China.
Jingfeng LiuDepartment of Hepatobiliary Surgery, Mengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou, 350025, China.
Jianxing ZengDepartment of Hepatobiliary Surgery, Mengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou, 350025, China. zjx_20051@163.com.

Funding

the Medical Innovation Project of Fujian Province 2020CXA055the Natural Science Foundation of Fujian Province 2020J011160the Scientific Foundation of Fuzhou Municipal Health commission 2021-S-wp1the Startup Fund for scientific research, Fujian Medical University 2021QH1159
6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) with lymph node metastases (LNM) is an uncommon neoplasm and has an ambivalent prognosis compared to the common type of HCC with macrovascular invasion (MaVI).

methodsIn this study, the clinical data of patients were extracted from Surveillance, Epidemiology, and End Results (SEER) and Southeast Big Data Institute of Hepatobiliary Health, Mengchao Hepatobiliary Hospital of Fujian Medical University. The K-M survival curve described overall survival (OS), cancer-specific survival (CSS), and recurrence-free survival (RFS) between LNM and MaVI. Prognostic factors were identified by univariate and multivariate Cox regression analysis. Additionally, propensity score matching (PSM) was performed to minimize the potential confounding factors to facilitate a more reliable conclusion.

resultsA total of 3,326 HCC patients were included in our study. In the SEER cohort, after PSM, the 1-, 3-, and 5-year OS rates were 41.1%, 13.8%, and 8.8% in Group LNM and 28.3%, 11.0%, and 7.1% in Group MaVI (p < 0.001). The 1-, 3-, and 5-year CSS rates were 46.5%, 17.6%, and 12.0% in Group LNM and 32.2%, 14.3%, and 9.7% in Group MaVI (p < 0.001). Multivariate Cox analysis showed that LNM had better OS (HR = 0.79, 95% CI = 0.71-0.89, p < 0.001) and CSS (HR = 0.78, 95% CI = 0.70-0.88, p < 0.001) compared to MaVI. In the hospital cohort, the 1-, 3-, and 5-year OS rates were 57.5%, 42.6%, and 36.3% in Group LNM and 56.3%, 27.4%, and 14.3% in Group MaVI (p = 0.038). The 1-, 3-, and 5-year RFS rates were 40.7%, 32.3%, and 23.5% in Group LNM and 28.9%, 13.0%, and 5.7% in Group MaVI (p = 0.015). Multivariate Cox analysis revealed similar OS (HR = 0.83, 95% CI = 0.57-1.23, p = 0.361) and CSS (HR = 0.76, 95% CI = 0.53-1.10, p = 0.142) between LNM and MaVI.

conclusionThis study found that the current HCC AJCC TNM staging system cannot accurately distinguish the prognosis of LNM and MaVI patients. For patients undergoing hepatectomy, HCC with LNM may obtain a better prognosis than that of HCC with MaVI. Future research requires additional clinical data to further corroborate this finding.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsAdultAgedChinaFemaleHumansLymphatic MetastasisMaleMiddle AgedNeoplasm InvasivenessPrognosisPropensity ScoreProportional Hazards ModelsSEER ProgramSurvival RateAJCC TNM stagingHepatocellular carcinomaLymph node metastasesMacrovascular invasionPrognosis

Identifiers

PMID40859162
PMCPMC12379393

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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.