Evidence map›Paper›PMID 41703499›Full record

ArticleBMC cancer2026

Prognostic significance of the pan-immune-inflammatory value (PIV) in gastric cancer: a retrospective cohort study.

Didar Senocak, Mina Karakullukcu, Eris Ozkan, Oguz Bilgi, M Alpaslan Ozgun

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Article in BMC cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Didar SenocakDepartment of Medical Oncology, Sultan Abdulhamid Han Training and Research Hospital, University of Health Sciences, Istanbul, Türkiye. ddrsnck@gmail.com.
Mina KarakullukcuDepartment of Medical Oncology, Sultan Abdulhamid Han Training and Research Hospital, University of Health Sciences, Istanbul, Türkiye.
Eris OzkanDepartment of Medical Oncology, Sultan Abdulhamid Han Training and Research Hospital, University of Health Sciences, Istanbul, Türkiye.
Oguz BilgiDepartment of Medical Oncology, Sultan Abdulhamid Han Training and Research Hospital, University of Health Sciences, Istanbul, Türkiye.
M Alpaslan OzgunDepartment of Medical Oncology, Sultan Abdulhamid Han Training and Research Hospital, University of Health Sciences, Istanbul, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesPeripheral blood cell parameters are used as prognostic markers in gastric cancer. In this study, we evaluated the prognostic significance of the Pan-Immune-Inflammatory Value (PIV), calculated as (neutrophil × platelet × monocyte) / lymphocyte counts, in patients with gastric cancer.

methodsThe study included 120 patients with gastric adenocarcinoma who were followed at the Department of Medical Oncology, Sultan Abdulhamid Han Training and Research Hospital, University of Health Sciences, between September 2017 and December 2024. PIV was calculated from pre-treatment complete blood counts. Associations between PIV and overall survival (OS), progression-free survival (PFS), and treatment response were analyzed. In our study, receiver operating characteristic (ROC) analysis was performed to determine the optimal cut-off value for PIV to achieve prognostic discrimination. Survival analyses were performed using the Kaplan-Meier method, and differences between groups were compared with the log-rank test. Univariate and multivariate Cox proportional hazards regression models were used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs). Logistic regression analysis was performed to identify independent predictors of treatment response.

resultsThe optimal cut-off value for PIV was 334.8, and 49.2% of patients had a PIV above this value. Patients with a high PIV (≥ 334.8) had significantly poorer PFS (HR = 1.975; 95% CI: 1.046-3.730; p = 0.036) and OS (HR = 2.286; 95% CI: 1.332-3.924; p = 0.003) compared with those in the low PIV group. A significant association was observed between PIV and treatment response. Patients with low PIV had significantly higher response rates than those with high PIV.

conclusionsOur study suggests that PIV can be considered a prognostic parameter for overall survival in patients with gastric adenocarcinoma.

Indexed as

AdenocarcinomaStomach NeoplasmsAgedBiomarkers, TumorBlood PlateletsFemaleHumansKaplan-Meier EstimateLymphocyte CountLymphocytesMaleMiddle AgedMonocytesNeutrophilsPrognosisRetrospective StudiesBiomarkers, TumorGastric cancerInflammatory biomarkersPan-immune-inflammation valuePathological responsePrognosis

Identifiers

PMID41703499
PMCPMC13019817

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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.