Evidence map›Paper›PMID 38097343›Full record

ArticleJournal for immunotherapy of cancer2023

Early kinetics of C reactive protein for cancer-agnostic prediction of therapy response and mortality in patients treated with immune checkpoint inhibitors: a multicenter cohort study.

Dominik A Barth, Florian Moik, Sarah Steinlechner, Florian Posch, Marie-Christina Mayer, Amelie M Sandner, Franziska Berton, Verena Schlintl, Lukas Koch, Nikolaus John and 13 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Journal for immunotherapy of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
4.4field-weighted citation impact, top 5% of its field
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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 19 citations in OpenAlex.

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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

23 authors at 3 institutions in 3 countries.

Dominik A BarthDivision of Oncology; Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Florian MoikDivision of Oncology; Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Sarah SteinlechnerDivision of Oncology; Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Florian PoschDivision of Hematology; Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Marie-Christina MayerDivision of Oncology; Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Amelie M SandnerDivision of Oncology; Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Franziska BertonDivision of Oncology; Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Verena SchlintlDivision of Oncology; Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Lukas KochDepartment of Dermatology, Medical University of Graz, Graz, Austria.
Nikolaus JohnDivision of Pulmonology; Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Robert WurmDivision of Pulmonology; Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Martin PichlerDivision of Oncology; Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Thomas BauernhoferDivision of Oncology; Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Patrick ReimannInternal Medicine II, Department of Hematology, Oncology, Gastroenterology and Infectiology, Landeskrankenhaus Feldkirch, Feldkirch, Austria.
Christoph WohlkönigDivision of Pulmonology; Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Erika RichtigDepartment of Dermatology, Medical University of Graz, Graz, Austria.
Thomas WinderInternal Medicine II, Department of Hematology, Oncology, Gastroenterology and Infectiology, Landeskrankenhaus Feldkirch, Feldkirch, Austria.
Matthias PreusserDivision of Oncology, Department of Medicine 1, Medizinische Universitat Wien, Wien, Austria.
Philipp J JostDivision of Oncology; Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Cihan AyClinical Division of Hematology and Hemostaseology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Armin GergerDivision of Oncology; Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Angelika TerbuchDivision of Oncology; Department of Internal Medicine, Medical University of Graz, Graz, Austria j.riedl@medunigraz.at angelika.terbuch@medunigraz.at.
Jakob Michael RiedlDivision of Oncology; Department of Internal Medicine, Medical University of Graz, Graz, Austria j.riedl@medunigraz.at angelika.terbuch@medunigraz.at.ORCID 0000-0002-5144-4715
Medical University of Graz · ATLandeskrankenhaus Feldkirch · ATMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundC reactive protein (CRP) kinetics have recently been suggested as predictive biomarkers for the efficacy of immune checkpoint inhibitor (ICI) therapy in selected cancer types. The aim of this study was to characterize early CRP kinetics as a tumor-agnostic biomarker for ICI treatment outcomes.

methodsIn this multicenter retrospective cohort study, two independent cohorts of patients with various cancer types undergoing palliative ICI treatment at Austrian academic centers served as the discovery (n=562) and validation cohort (n=474). Four different patterns of CRP kinetics in the first 3 months of ICI therapy were defined (CRP-flare responders, CRP-responders, CRP non-responders, patients with all-normal CRP). Objective response rate (ORR), progression-free survival (PFS) and overall survival (OS) were defined as coprimary endpoints. Univariable and multivariable logistic regression, landmark analysis and Cox regression including CRP kinetics as time-dependent variable were performed.

resultsThe ORR in patients with all-normal CRP, CRP responders, CRP flare-responders and CRP non-responders was 41%, 38%, 31% and 12%, respectively. The median OS and PFS estimates were 24.5 months (95% CI 18.5 to not reached) and 8.2 months (95% CI 5.9 to 12.0) in patients with all-normal CRP, 16.1 months (95% CI 12.6 to 19-8) and 6.1 months (95% CI 4.9 to 7.2) in CRP-responders, 14.0 months (95% CI 8.5 to 19.4) and 5.7 months (95% CI 4.1 to 8.5) in CRP flare-responders and 8.1 months (95% CI 5.8 to 9.9) and 2.3 months (95% CI 2.2 to 2.8) in CRP non-responders (log-rank p for PFS and OS<0.001). These findings prevailed in multivariable analysis and could be fully confirmed in our validation cohort. Pooled subgroup analysis suggested a consistent predictive significance of early CRP kinetics for treatment efficacy and outcome independent of cancer type.

conclusionEarly CRP kinetics represent a tumor-agnostic predictor for treatment response, progression risk and mortality in patients with cancer undergoing ICI therapy.

Indexed as

C-Reactive ProteinNeoplasmsBiomarkers, TumorHumansImmune Checkpoint InhibitorsRetrospective StudiesBiomarkers, TumorC-Reactive ProteinImmune Checkpoint InhibitorsBiomarkers, TumorImmune Checkpoint Inhibitors

Identifiers

PMID38097343
PMCPMC10729183
OpenAlexW4389744395

What OpenQuestion holds

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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.