Evidence map›Paper›PMID 42787171›Full record

ArticleFrontiers in oncology2026

Nomograms and an inflammation model predict immunotherapy prognosis in unresectable hepatocellular carcinoma: from survival and response.

Er-Lei Zhang, Peng Ma, Wen-Jun Zhao, Jia-Jia Du

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Article in Frontiers in oncology, 2026. 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Er-Lei ZhangHepatic Surgery Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Peng MaShanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Third Hospital of Shanxi Medical University, Tongji Shanxi Hospital, Taiyuan, China.
Wen-Jun ZhaoShanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Third Hospital of Shanxi Medical University, Tongji Shanxi Hospital, Taiyuan, China.
Jia-Jia DuShanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Third Hospital of Shanxi Medical University, Tongji Shanxi Hospital, Taiyuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Screening out individuals who could benefit from immunotherapy is important in clinical practice. Methods: Clinical records of 199 individuals with unresectable HCC who underwent immunotherapy were retrospectively analyzed. Based on the effect of treatment, individuals were classified into two groups: the response group and the non-response group. NLR, LMR, and CAR were obtained before treatment. Kaplan-Meier method and Cox proportional risk regression model were used for survival analysis, and nomograms were established. A clinical prediction model was developed using logistic regression. Results: The cutoff values of NLR, LMR, and CAR were 5, 1.8, and 0.105, respectively. Individuals with NLR <5, LMR ≥1.8, and CAR <0.105 had higher ORR (43.09% vs. 13.16%, p < 0.001; 57.89% vs. 25.47%, p < 0.001; 41.49% vs. 22.86%, p < 0.01). In the multivariate analysis, it was determined that NLR and CAR independently served as prognostic factors for both PFS and OS. A combined parameter derived from these independent prognostic factors for ORR yielded an area under the curve (AUC) value of prediction probability of 0.825. Notably, the predictive performance of the model surpassed that of NLR (AUC = 0.794), LMR (AUC = 0.732), and CAR (AUC = 0.774). Conclusion: NLR, LMR, and CAR are potential predictive biomarkers of immunotherapy efficacy in individuals with advanced HCC.

Indexed as

CARhepatocellular carcinomaimmunotherapyNLRobjective response rate

Identifiers

PMID42787171
PMCPMC13600908

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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.