Evidence map›Paper›PMID 42870461›Full record

Observational studyCancer2026

Evaluation of early C-reactive protein kinetics as an early response marker in biliary tract cancer treated with combined chemoimmunotherapy: A multicenter observational study.

Gabriel Allo, Joshua Leutiger, Catherine Leyh, Christian Möhring, Ann-Kristin Zöller, Vera Himmelsbach, Gianluca Ciarlo, Maryam Barsch, Christoph Neumann-Haefelin, Bertram Bengsch and 10 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Observational
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

20 authors.

Gabriel AlloDepartment for Gastroenterology and Hepatology, Faculty of Medicine, University Hospital of Cologne, University of Cologne, Cologne, Germany.ORCID https://orcid.org/0000-0001-7568-7431
Joshua LeutigerDepartment for Gastroenterology and Hepatology, Faculty of Medicine, University Hospital of Cologne, University of Cologne, Cologne, Germany.
Catherine LeyhClinic for Gastroenterology, Hepatology, and Infectious Diseases, University Hospital Dusseldorf, Dusseldorf, Germany.
Christian MöhringDepartment of Medicine I, University Hospital of Bonn, Bonn, Germany.
Ann-Kristin ZöllerDepartment of Gastroenterology, Hepatology, Infectious Diseases, and Endocrinology, Hannover Medical School, Hannover, Germany.
Vera HimmelsbachDepartment of Gastroenterology, Medical Clinic 1, University Hospital Frankfurt, Frankfurt am Main, Germany.
Gianluca CiarloDepartment of Gastroenterology, Medical Clinic 1, University Hospital Frankfurt, Frankfurt am Main, Germany.
Maryam BarschClinic for Internal Medicine II, University Hospital Freiburg, Freiburg, Germany.
Christoph Neumann-HaefelinDepartment for Gastroenterology and Hepatology, Faculty of Medicine, University Hospital of Cologne, University of Cologne, Cologne, Germany.ORCID https://orcid.org/0000-0001-7351-1387
Bertram BengschClinic for Internal Medicine II, University Hospital Freiburg, Freiburg, Germany.
Fabian FinkelmeierDepartment of Gastroenterology, Medical Clinic 1, University Hospital Frankfurt, Frankfurt am Main, Germany.
Mohamad MuradMedical Department III, University Hospital, Rhenisch-Westphalian Technical University Aachen, Aachen, Germany.
Cennet SahinMedical Department III, University Hospital, Rhenisch-Westphalian Technical University Aachen, Aachen, Germany.
Marie-Luise BerresMedical Department III, University Hospital, Rhenisch-Westphalian Technical University Aachen, Aachen, Germany.
Maria A Gonzalez-CarmonaDepartment of Medicine I, University Hospital of Bonn, Bonn, Germany.
Christoph RoderburgClinic for Gastroenterology, Hepatology, and Infectious Diseases, University Hospital Dusseldorf, Dusseldorf, Germany.
Arndt WeinmannFirst Department of Medicine, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Anna SaborowskiDepartment of Gastroenterology, Hepatology, Infectious Diseases, and Endocrinology, Hannover Medical School, Hannover, Germany.
Arndt VogelDepartment of Gastroenterology, Hepatology, Infectious Diseases, and Endocrinology, Hannover Medical School, Hannover, Germany.
Dirk WaldschmidtDepartment for Gastroenterology and Hepatology, Faculty of Medicine, University Hospital of Cologne, University of Cologne, Cologne, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundReliable prognostic biomarkers for treatment response in patients with biliary tract cancer (BTC) who receive chemoimmunotherapy are still lacking. The objective of this study was to evaluate the potential of early C-reactive protein (CRP) kinetics as a tool for predicting survival in these patients.

methodsThe authors retrospectively analyzed patients with BTC who received chemoimmunotherapy at eight tertiary centers and evaluated CRP kinetic models with regard of their prognostic ability within the first 3 months of treatment.

resultsProgression-free survival (PFS) and overall survival (OS) differed according to CRP dynamics. The median PFS was not reached (95% confidence interval [CI], not reached to not reached) for patients with consistently normal CRP, 11.0 months (95% CI, 6.7-15.3 months) for those with initially normal CRP, 6.0 months (95% CI, 3.6-8.4 months) for those with subsequent CRP normalization, and 2.0 months (95% CI, 0.9-3.1 months) for those with persistently elevated CRP. The corresponding median OS was not reached (95% CI, not reached to not reached) for patients with consistently normal CRP, 26 months (95% CI,15.5-36.5 months) for those with initially normal CRP, 23 months (95% CI, 12.0-34.0 months) for those with subsequent normalization, and 9.0 months (95% CI, 6.3-11.7 months) for those with persistently elevated CRP (PFS, log-rank p < .001; OS, p = .005). The overall response rates were 50%, 33.3%, 36.0%, and 21.2%, respectively. The prognostic performance of this model remained stable when subgroup definitions were based on 6-week cutoffs.

conclusionsCRP kinetics may be a valuable prognostic tool for early response assessment in patients with BTC who receive chemoimmunotherapy. However, these findings require prospective external validation in larger cohorts.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBiliary Tract NeoplasmsBiomarkers, TumorC-Reactive ProteinAgedAged, 80 and overFemaleHumansImmunotherapyKineticsMaleMiddle AgedPrognosisProgression-Free SurvivalRetrospective StudiesBiomarkers, TumorC-Reactive Proteinbiliary tract neoplasmscholangiocarcinomaC‐reactive proteindurvalumabimmune checkpoint inhibitors

Identifiers

PMID42870461
PMCPMC13662409

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.