Evidence map›Paper›PMID 42448748›Full record

ArticleScientific reports2026

Evaluating the clinical significance of tumor-expressed C-reactive protein in chromophobe renal cell carcinoma.

Marie Mikuteit, Stefanie Zschäbitz, Michael Autenrieth, Wilko Weichert, Arndt Hartmann, Sandra Steffens, Franziska Erlmeier

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Article in Scientific reports, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

7 authors.

Marie MikuteitDepartment for Dermatology and Allergy, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany. mikuteit.marie@mh-hannover.de.ORCID 0000-0001-8546-0548
Stefanie ZschäbitzDepartment of Medical Oncology, National Center of Tumor Diseases, University Hospital Heidelberg, 69120, Heidelberg, Germany.
Michael AutenriethDepartment of Urology, Technical University of Munich, Klinikum Rechts Der Isar, München, Germany.
Wilko WeichertInstitute for Pathology and Pathological Anatomy, Technical University Munich, Munich, Germany.
Arndt HartmannInstitute of Pathology, University Hospital of Erlangen, Erlangen, Germany.
Sandra SteffensDepartment of Medical Education, Hannover Medical School, Hannover, Germany.
Franziska ErlmeierInstitute for Pathology and Pathological Anatomy, Technical University Munich, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

C-reactive Protein (CRP) has been established as a prognostic biomarker in various malignancies, with elevated serum levels correlating with poorer outcomes. However, the significance of tissue-based CRP expression specifically in chromophobe renal cell carcinoma (chRCC), remains inadequately characterized. This study investigates the potential prognostic relevance of intratumoral CRP expression from a substantial cohort of chRCC patients. We conducted a retrospective analysis of patients who underwent surgical intervention for chRCC. Comprehensive clinical data was collected, and immunohistochemical evaluation of tumor specimens was performed to assess intratumoral CRP expression patterns. The study included 81 chRCC patients, with intratumoral CRP expression identified in 35 cases (43.2%). Statistical analysis revealed no significant correlation between CRP expression status and clinical parameters. While 5-year overall survival (OS) analysis showed no statistically significant difference between CRP-positive versus CRP-negative tumors (86.4% versus 100.0%; p = 0.106), overall follow-up demonstrated a significantly higher mortality rate in patients with CRP-positive tumors compared to those with CRP-negative tumors (22.9% vs. 2.2%; p = 0.013). Our findings suggest that intratumoral CRP expression in chRCC is not clearly associated with parameters of aggressiveness or survival. Further studies should assess the possible correlation between CRP tissue expression and blood levels. However, these findings should be interpreted with caution given the limited sample size, low event rate, and high loss to follow-up, and are best considered hypothesis-generating.

Indexed as

Biomarkers, TumorCarcinoma, Renal CellC-Reactive ProteinKidney NeoplasmsAdultAgedFemaleHumansImmunohistochemistryMaleMiddle AgedPrognosisRetrospective StudiesBiomarkers, TumorC-Reactive ProteinChromophobe histologyCRPRenal cell carcinomaSurvival

Identifiers

PMID42448748
PMCPMC13370012

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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.