Evidence map›Paper›PMID 42694061›Full record

ArticleFrontiers in oncology2026

Early C-reactive protein kinetics predict outcomes in unresectable hepatocellular carcinoma treated with immune checkpoint inhibitors: a multicenter, observational study comparing different C-reactive protein kinetic definitions.

Joshua Leutiger, Melanie Bathon, Christian Möhring, Max Ole Hubert, Catherine Leyh, Alexandra Emilia Schlaak, Katharina Mitzlaff, Laurenz Krämer, Christoph Neumann-Haefelin, Carolin Zimpel and 11 more

Abstract read
In one paragraph

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.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Joshua LeutigerDepartment of Gastroenterology and Hepatology, University Hospital Cologne, Faculty of Medicine, University of Cologne, Cologne, Germany.
Melanie BathonDepartment of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany.
Christian MöhringDepartment I of Internal Medicine, University Hospital of Bonn, Bonn, Germany.
Max Ole HubertDepartment of Medicine II, University Hospital, Ludwig Maximilian University Munich, Munich, Germany.
Catherine LeyhClinic for Gastroenterology, Hepatology and Infectious Diseases, University Hospital Düsseldorf, Medical Faculty of Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Alexandra Emilia SchlaakDepartment of Medicine II, Medical Center University of Freiburg, Freiburg, Germany.
Katharina MitzlaffDepartment of Internal Medicine 1, University Hospital Schleswig-Holstein, Lübeck, Germany.
Laurenz KrämerDepartment of Gastroenterology and Hepatology, University Hospital Cologne, Faculty of Medicine, University of Cologne, Cologne, Germany.
Christoph Neumann-HaefelinDepartment of Gastroenterology and Hepatology, University Hospital Cologne, Faculty of Medicine, University of Cologne, Cologne, Germany.
Carolin ZimpelDepartment of Internal Medicine 1, University Hospital Schleswig-Holstein, Lübeck, Germany.
Bertram BengschDepartment of Medicine II, Medical Center University of Freiburg, Freiburg, Germany.
Christoph RoderburgClinic for Gastroenterology, Hepatology and Infectious Diseases, University Hospital Düsseldorf, Medical Faculty of Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Najib Ben KhaledDepartment of Medicine II, University Hospital, Ludwig Maximilian University Munich, Munich, Germany.
Cennet SahinMedical Department III, University Hospital Rheinisch-Westfälische Technische Hochschule Aachen (RWTH) Aachen, Aachen, Germany.
Marie-Luise BerresMedical Department III, University Hospital Rheinisch-Westfälische Technische Hochschule Aachen (RWTH) Aachen, Aachen, Germany.
Maria A Gonzalez-CarmonaDepartment I of Internal Medicine, University Hospital of Bonn, Bonn, Germany.
Anna Lena SaborowskiDepartment of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany.
Arndt VogelDepartment of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany.
Arndt WeinmannDepartment of Internal Medicine I, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Dirk WaldschmidtDepartment of Gastroenterology and Hepatology, University Hospital Cologne, Faculty of Medicine, University of Cologne, Cologne, Germany.
Gabriel AlloDepartment of Gastroenterology and Hepatology, University Hospital Cologne, Faculty of Medicine, University of Cologne, Cologne, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and aims: Immune checkpoint inhibitors (ICIs) have become the standard therapy for unresectable hepatocellular carcinoma (HCC). However, reliable prognostic biomarkers for treatment response remain warranted. This study assessed the prognostic value of early C-reactive protein (CRP) kinetics as an on-treatment biomarker in patients with hepatocellular carcinoma receiving ICIs. Methods: In this multicenter retrospective study, 289 patients with HCC treated with ICIs between 2019 and 2023 were analyzed. Patients were stratified using two established CRP kinetic models. The Fukuda model classified patients as flare responders, responders, or non-responders based on early CRP kinetics after treatment initiation. The Ishihara model categorized patients as "normal", "normalized", or "non-normalized" according to baseline and on-treatment CRP levels. Both models were additionally evaluated at eight weeks for earlier risk stratification. Results: According to the Fukuda model, flare responders demonstrated significantly prolonged median overall survival (34.5 vs 12.7 months), progression-free survival (12.42 vs 5.32 months), and higher objective response rates (53.7% vs 25.2%) compared with non-responders. In the Ishihara model, the normalized and normal groups showed significantly improved outcomes with median overall survival of 28.35 and 25.1 months, progression-free survival of 12.48 and 9.89 months, and objective response rates of 54.2% and 43.4%, respectively, compared with the non-normalized group (7.46 months; 3.35 months; 18.8%). The adapted 8-week Ishihara model enabled earlier risk stratification prior to first radiologic staging. Conclusions: Early C-reactive protein kinetics provide robust prognostic information in patients with HCC treated with ICIs. Both CRP-based models identify subgroups with significantly improved outcomes, with the Ishihara model enabling earlier identification of patients at high risk of treatment failure and thereby supporting earlier risk stratification during immunotherapy.

Indexed as

biomarkersC-reactive proteinhepatocellular carcinomaimmune checkpoint inhibitorsimmuno-oncologyliver cancer

Identifiers

PMID42694061
PMCPMC13537936

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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.