Evidence map›Paper›PMID 41142780›Full record

Trial reportFrontiers in immunology2025

On-treatment modified Glasgow Prognostic Score (mGPS) in hepatocellular carcinoma treated with atezolizumab and bevacizumab provides prognostic information.

Tessa Hattenhauer, Rebekka Mispelbaum, Annkristin Heine, Katjana Schwab, Peter Brossart, Niklas Klümper, Jonas Saal

Abstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Frontiers in immunology, 2025. 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

7 authors.

Tessa Hattenhauer *Medical Clinic III for Oncology, Hematology, Immune-Oncology and Rheumatology, University Hospital Bonn (UKB), Bonn, Germany.
Rebekka Mispelbaum *Medical Clinic III for Oncology, Hematology, Immune-Oncology and Rheumatology, University Hospital Bonn (UKB), Bonn, Germany.
Annkristin HeineMedical Clinic III for Oncology, Hematology, Immune-Oncology and Rheumatology, University Hospital Bonn (UKB), Bonn, Germany.
Katjana SchwabMedical Clinic III for Oncology, Hematology, Immune-Oncology and Rheumatology, University Hospital Bonn (UKB), Bonn, Germany.
Peter BrossartMedical Clinic III for Oncology, Hematology, Immune-Oncology and Rheumatology, University Hospital Bonn (UKB), Bonn, Germany.
Niklas KlümperCenter for Integrated Oncology Aachen/Bonn/Cologne/Düsseldorf (CIO-ABCD), Bonn, Germany.
Jonas SaalMedical Clinic III for Oncology, Hematology, Immune-Oncology and Rheumatology, University Hospital Bonn (UKB), Bonn, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & aims: Hepatocellular carcinoma (HCC) is associated with high cancer-specific mortality. While immune-checkpoint inhibitors (ICIs) improved overall survival (OS) compared to tyrosine kinase inhibitors, biomarkers predicting response to ICI in HCC are lacking. This study investigates the prognostic value of serum-based prognostic scores in patients with HCC receiving atezolizumab and bevacizumab. Methods: This Results: The on-treatment mGPS, assessed 9 weeks post-treatment initiation, predicted OS with hazard ratios of 2.31 (95% CI 1.39-3.83, p < 0.001) for intermediate-risk and 3.40 (95% CI 3.07-5.59, p < 0.001) for high-risk, compared to low-risk groups, showing greater accuracy than RECIST imaging. Albumin, CRP, and IL-6 were individually good prognostic indicators, with albumin/CRP (ACR) and albumin/IL-6 (AIR) ratios having the highest prognostic power (c-index: ACR 0.66 (95% CI 0.61-0.71), AIR 0.67 (0.62-0.72), mGPS 0.62 (0.57-0.66)). Multivariable analysis confirmed serum-based scores' prognostic value independent of imaging. Serum-based scores significantly correlated with survival in patients with stable disease (SD, 79% of patients) or progressive disease (PD, 12% of patients). Conclusions: The on-treatment mGPS, as well as ACR and AIR, predicted outcomes in patients with HCC independent of and more accurately than radiological staging. Since, the mGPS is the most cost effective and widely validated score, we consider it best suited for clinical use. Prospective validation is needed to confirm these findings.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsBevacizumabCarcinoma, HepatocellularLiver NeoplasmsAgedBiomarkers, TumorC-Reactive ProteinFemaleHumansInterleukin-6MaleMiddle AgedPrognosisTreatment OutcomeAntibodies, Monoclonal, HumanizedatezolizumabBevacizumabBiomarkers, TumorC-Reactive ProteinInterleukin-6biomarkerscheckpoint-inhibitionHCCimmunotherapymGPS

Identifiers

PMID41142780
PMCPMC12546374

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Registered trials

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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.