Evidence map›Paper›PMID 41803760›Full record

ArticleBMC cancer2026

The prognostic value analysis of PIV, PLR, LMR, NPR, and NLR in hilar cholangiocarcinoma.

Hongyang Guo, Xueyan Bai, Jin Shi, Zhen Liu, Zhaoyang Hu

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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 1 paper.

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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Hongyang GuoDepartment of General Surgery, Tai'an City Central Hospital, Tai'an, 271000, Shandong Province, China.
Xueyan BaiDepartment of Gastroenterology, Tai'an City Central Hospital, Tai'an, 271000, Shandong Province, China.
Jin ShiDepartment of Gastroenterology, Tai'an City Central Hospital, Tai'an, 271000, Shandong Province, China.
Zhen LiuDepartment of Hepatobiliary and Pancreatic Medicine, Tai'an City Central Hospital, No.29, Longtan Road, Mount Taishan District, Tai'an, Shandong Province, 271000, China. zhen123hua123@163.com.
Zhaoyang HuDepartment of Emergency Surgery, Tai'an City Central Hospital, No.29, Longtan Road, Mount Taishan District, Tai'an, Shandong Province, 271000, China. 18653735407@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHilar cholangiocarcinoma (HCCA) has a high propensity for early recurrence. We evaluated the prognostic value of preoperative inflammatory biomarkers, Pan‑Immunological Value (PIV), Platelet‑Lymphocyte Ratio (PLR), Lymphocyte‑Monocyte Ratio (LMR), Neutrophil‑Platelet Ratio (NPR), and Neutrophil‑Lymphocyte Ratio (NLR), in resected HCCA.

methodsA retrospective cohort study included 373 HCCA patients undergoing radical resection from January 2017 to May 2022. Patients treated between January 2017 and December 2020 were assigned to the training set (n = 236) for model development. Those treated between January 2021 and May 2022 were assigned to the independent temporal validation set (n = 137), this split approximates a 6:4 ratio. Baseline characteristics were comparable between sets (all P > 0.05). Patients were categorized based on one-year recurrence-free survival (RFS) into early and non-early recurrence groups. Clinical, pathological, and preoperative inflammatory marker data were collected. Statistical analyses included univariate and multivariate Cox proportional hazards regression, Kaplan-Meier curves, and receiver operating characteristic (ROC) curve analysis to assess the prognostic value of the inflammatory markers.

resultsIn univariate analysis, higher PIV, PLR, NLR, NPR and lower LMR were associated with early recurrence (all P < 0.05). To avoid statistical collinearity, separate multivariable Cox models were constructed, each adjusting for clinicopathological factors but including only one inflammatory marker. In these models, PLR (HR = 1.026, P = 0.026), NLR (HR = 1.523, P = 0.011), NPR (HR = 1.831, P = 0.010), and LMR (HR = 0.483, P = 0.001) remained independent predictors of early recurrence; PIV did not (HR = 1.001, P = 0.425). Kaplan‑Meier curves confirmed shorter RFS for patients with high PIV, PLR, NLR, NPR or low LMR (all log‑rank P < 0.001). The combined model integrating all five markers achieved AUCs of 0.857 (training) and 0.908 (validation), outperforming individual markers (AUCs 0.616–0.637).

conclusionThe combined predictive model integrating inflammatory markers PIV, PLR, NLR, NPR, and LMR shows improved prognostic accuracy in HCCA, potentially providing clinically actionable stratification alongside traditional clinical parameters.

Indexed as

Bile Duct NeoplasmsBlood PlateletsKlatskin TumorLymphocytesMonocytesNeutrophilsAgedBiomarkers, TumorFemaleHumansLymphocyte CountMaleMiddle AgedNeoplasm Recurrence, LocalPlatelet CountPrognosisBiomarkers, TumorCholangiocarcinomaInflammatory biomarkersPan-Immunological ValuePredictive modelPrognosisRadical resection

Identifiers

PMID41803760
PMCPMC13054974

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