Evidence map›Paper›PMID 42131343›Full record

ArticleFrontiers in immunology2026

Prognostic significance of neutrophil-to-lymphocyte and platelet-to-lymphocyte ratios in hepatocellular carcinoma: a retrospective multicenter study on overall and recurrence-free survival following liver resection or liver transplantation.

Konstantinos Arvanitakis, Spyridon Pantzios, Chrysanthos Christou, Vasileios Papadopoulos, Eleni Theocharidou, Christos Topalidis, Georgios Kalopitas, Orestis Sidiropoulos, Antonios Chatzigeorgiou, Ioannis Mitroulis and 6 more

Abstract readMulticenter Study
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

Konstantinos ArvanitakisDivision of Gastroenterology and Hepatology, First Department of Internal Medicine, AHEPA University Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Spyridon PantziosAcademic Department of Internal Medicine-Hepatogastroenterology Unit, General Oncology Hospital of Kifissia, National and Kapodistrian University of Athens, Athens, Greece.
Chrysanthos ChristouDepartment of Transplantation Surgery, Hippokration General Hospital, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Vasileios PapadopoulosLaboratory of Anatomy, Medical School, Democritus University of Thrace, Alexandroupolis, Greece.
Eleni TheocharidouSecond Department of Internal Medicine, Hippokration General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Christos TopalidisDepartment of Pathology, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Georgios KalopitasDivision of Gastroenterology and Hepatology, First Department of Internal Medicine, AHEPA University Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Orestis SidiropoulosAcademic Department of Internal Medicine-Hepatogastroenterology Unit, General Oncology Hospital of Kifissia, National and Kapodistrian University of Athens, Athens, Greece.
Antonios ChatzigeorgiouDepartment of Physiology, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Ioannis MitroulisFirst Department of Internal Medicine, University Hospital of Alexandroupolis, Democritus University of Thrace, Alexandroupolis, Greece.
Triantafyllia KoletsaDepartment of Pathology, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Prodromos HytiroglouDepartment of Pathology, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Georgios KatsanosDepartment of Transplantation Surgery, Hippokration General Hospital, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Ioannis ElefsiniotisAcademic Department of Internal Medicine-Hepatogastroenterology Unit, General Oncology Hospital of Kifissia, National and Kapodistrian University of Athens, Athens, Greece.
Georgios TsoulfasDepartment of Transplantation Surgery, Hippokration General Hospital, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Georgios GermanidisDivision of Gastroenterology and Hepatology, First Department of Internal Medicine, AHEPA University Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Systemic inflammation plays a critical role in hepatocellular carcinoma (HCC) progression and postoperative outcomes. This study assessed the prognostic value of the neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) for overall (OS) and recurrence-free survival (RFS) in patients undergoing curative hepatectomy or orthotopic liver transplantation (OLT). Methods: In this multicenter retrospective cohort of 74 HCC patients (86.5% male; median age 68.0 years), NLR and PLR were evaluated preoperatively and at 1-, 3-, 6-, and 12-months post-surgery. Associations with OS and RFS were evaluated using univariate, multivariable, and Cox proportional hazards models with time-varying covariates, while model discrimination was assessed using Harrell's concordance index. Results: Elevated preoperative PLR predicted major postoperative complications (AUROC = 0.667, p = 0.030). The 3-month NLR demonstrated strong discriminative performance for OS (C-index 0.79). In time-varying Cox models, postoperative NLR emerged as a robust, time-independent predictor of OS (HR 1.35; p = 0.033), independent of the surgical procedure and Barcelona Clinic Liver Cancer stage. Multivariable analyses demonstrated that elevated NLR at 3-, 6-, and 12-months and PLR at 12 months independently predicted reduced OS. Hepatectomy was the dominant determinant of reduced RFS compared with OLT (p < 0.001), while an NLR threshold >2.5 identified a subgroup at markedly increased mortality risk, particularly following hepatectomy. Conclusions: Postoperative NLR is a powerful, time-independent prognostic biomarker for OS in surgically treated HCC, especially after liver resection, while PLR provides complementary prognostic information. These findings support the clinical integration of inflammation-based biomarkers into postoperative risk stratification and surveillance strategies.

Indexed as

Blood PlateletsCarcinoma, HepatocellularHepatectomyLiver NeoplasmsLiver TransplantationLymphocytesNeutrophilsAgedFemaleHumansLymphocyte CountMaleMiddle AgedNeoplasm Recurrence, LocalPlatelet CountPrognosishepatocellular carcinomaneutrophil-to-lymphocyte ratiooverall survivalplatelet-to-lymphocyte ratioprognostic biomarkersrecurrence-free survivalsystemic inflammation

Identifiers

PMID42131343
PMCPMC13161088

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