Evidence map›Paper›PMID 38877146›Full record

ArticleScientific reports2024

C-reactive protein as robust laboratory value associated with prognosis in patients with stage III non-small cell lung cancer (NSCLC) treated with definitive radiochemotherapy.

Cedric Richlitzki, Marcel Wiesweg, Martin Metzenmacher, Nika Guberina, Christoph Pöttgen, Hubertus Hautzel, Wilfried E E Eberhardt, Kaid Darwiche, Dirk Theegarten, Clemens Aigner and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

14 authors.

Cedric RichlitzkiDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Marcel WieswegNational Center for Tumor Diseases (NCT) West, Essen, Germany.
Martin MetzenmacherNational Center for Tumor Diseases (NCT) West, Essen, Germany.
Nika GuberinaDepartment of Radiotherapy, West German Cancer Center, University Hospital Essen, Essen, Germany.
Christoph PöttgenDepartment of Radiotherapy, West German Cancer Center, University Hospital Essen, Essen, Germany.
Hubertus HautzelNational Center for Tumor Diseases (NCT) West, Essen, Germany.
Wilfried E E EberhardtNational Center for Tumor Diseases (NCT) West, Essen, Germany.
Kaid DarwicheDepartment of Pulmonary Medicine, Section of Interventional Pneumology, West German Lung Transplantation Center, University Medicine Essen - Ruhrlandklinik, Essen, Germany.
Dirk TheegartenInstitute of Pathology, University Hospital Essen, Essen, Germany.
Clemens AignerDepartment of Thoracic Surgery, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Servet BölükbasNational Center for Tumor Diseases (NCT) West, Essen, Germany.
Martin SchulerNational Center for Tumor Diseases (NCT) West, Essen, Germany.
Martin StuschkeDepartment of Radiotherapy, West German Cancer Center, University Hospital Essen, Essen, Germany.
Maja GuberinaDepartment of Radiotherapy, West German Cancer Center, University Hospital Essen, Essen, Germany. maja.guberina@uk-essen.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To evaluate the prognostic value of biomarkers from peripheral blood obtained as routine laboratory assessment for overall survival in a cohort of stage III non-small cell lung cancer (NSCLC) patients treated with definitive radiochemotherapy at a high-volume cancer center. Seven blood biomarkers from 160 patients treated with definitive radiochemotherapy for stage III NSCLC were analyzed throughout the course treatment. Parameters were preselected using univariable and multivariable proportional hazards analysis and were assessed for internal validity using leave-one-out cross validation. Cross validated classifiers including biomarkers in addition to important clinical parameters were compared with classifiers containing the clinical parameters alone. An increased C-reactive protein (CRP) value in the final week of radiotherapy was found as a prognostic factor for overall survival, both as a continuous (HR 1.099 (1.038-1.164), p < 0.0012) as well as categorical variable splitting data at the median value of 1.2 mg/dl (HR 2.214 (1.388-3.531), p < 0.0008). In the multivariable analysis, the CRP value-maintained significance with an HR of 1.105 (1.040-1.173) and p-value of 0.0012. The cross validated classifier using CRP at the end of radiotherapy in addition to clinical parameters separated equally sized high and low risk groups more distinctly than a classifier containing the clinical parameters alone (HR = 2.786 (95% CI 1.686-4.605) vs. HR = 2.287 (95% CI 1.407-3.718)). Thus, the CRP value at the end of radiation therapy has successfully passed the crucial cross-validation test. The presented data on CRP levels suggests that inflammatory markers may become increasingly important during definitive radiochemotherapy, particularly with the growing utilization of immunotherapy as a consolidation therapy for stage III NSCLC.

Indexed as

Biomarkers, TumorCarcinoma, Non-Small-Cell LungChemoradiotherapyC-Reactive ProteinLung NeoplasmsNeoplasm StagingAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedPrognosisBiomarkers, TumorC-Reactive ProteinC-reactive protein (CRP)Definitive radiochemotherapyESPATUE trialLaboratory valuesOverall survivalStage III non-small cell lung cancer (NSCLC)

Identifiers

PMID38877146
PMCPMC11178931

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.