Evidence map›Paper›PMID 38622530›Full record

ArticleBMC cancer2024

Relevance of blood tumor markers in inpatients with significant involuntary weight loss and elevated levels of inflammation biomarkers.

Morgane Gronnier, Kaies Hedhli, Chloé Sauzay, Valéry Salle, Pierre Duhaut, Jean Schmidt, Amandine Dernoncourt

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
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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

7 authors at 4 institutions in 1 country.

Morgane GronnierDepartment of Internal Medicine, Amiens-Picardie University Medical Center, Rue du Professeur Christian Cabrol, F-80054, Amiens, France.
Kaies HedhliLaboratory of Hematology, Center of Human Biology, Amiens-Picardie University Medical Center, F-80054, Amiens, France.
Chloé SauzayLaboratory of Biochemistry, Center of Human Biology, Amiens-Picardie University Medical Center, F-80054, Amiens, France.
Valéry SalleDepartment of Internal Medicine, Amiens-Picardie University Medical Center, Rue du Professeur Christian Cabrol, F-80054, Amiens, France.
Pierre DuhautDepartment of Internal Medicine, Amiens-Picardie University Medical Center, Rue du Professeur Christian Cabrol, F-80054, Amiens, France.
Jean SchmidtDepartment of Internal Medicine, Amiens-Picardie University Medical Center, Rue du Professeur Christian Cabrol, F-80054, Amiens, France.
Amandine DernoncourtDepartment of Internal Medicine, Amiens-Picardie University Medical Center, Rue du Professeur Christian Cabrol, F-80054, Amiens, France. dernoncourt.amandine@chu-amiens.fr.
Centre Hospitalier Universitaire Amiens-Picardie · FRSociété Francophone du Diabète · FRUniversité de Picardie Jules Verne · FROncogenesis Stress Signaling · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo assess the diagnostic performance of a panel of standard tumor markers (TMs) in patients hospitalized with significant involuntary weight loss (IWL) and elevated levels of inflammation biomarkers, and a combination of the TM panel and the finding of the computed tomography (CT) scan.

methodsWe conducted a retrospective study in the internal medicine department at Amiens-Picardie University Medical Center (Amiens, France) between January 1st, 2015, and November 1st, 2021. The inclusion criteria were age 18 or over, significant IWL (≥ 5 kg over 6 months), elevated inflammation biomarkers (e.g. C-reactive protein), and assay data on two or more standard TMs (carcinoembryonic antigen (CEA), carbohydrate antigen (CA) 19 - 9, CA 15 - 3, CA 125, neuron-specific enolase (NSE), alpha-fetoprotein (AFP), calcitonin, and prostate-specific antigen (PSA)). The result of each TM assay was interpreted qualitatively (as positive or negative), according to our central laboratory's usual thresholds.

resultsCancer was diagnosed in 50 (37.0%) of the 135 patients included. Positivity for one or more TMs had a positive predictive value (PPV) of 0.55 [0.43-0.66], and a negative predictive value (NPV) of 0.84 [0.75-0.93] for cancer diagnosis. When combined with the presence of suspicious CT findings (e.g. a mass, enlarged lymph nodes and/or effusion), positivity for one or more TMs had a PPV of 0.92 [0.08-0.30]. In the absence of suspicious CT findings, a fully negative TM panel had an NPV of 0.96 [0.89-1.00].

conclusionA negative TM panel argues against the presence of a cancer, especially in the absence of suspicious CT findings.

Indexed as

Biomarkers, TumorNeoplasmsAdolescentCA-125 AntigenCA-19-9 AntigenCarcinoembryonic AntigenHumansInflammationInpatientsMaleMucin-1Retrospective StudiesWeight LossBiomarkers, TumorCA-125 AntigenCA-19-9 AntigenCarcinoembryonic AntigenMucin-1CancerComputed tomographyDiagnostic testInflammationTumor biomarkersWeight loss

Identifiers

PMID38622530
PMCPMC11017702
OpenAlexW4394819727

What OpenQuestion holds

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LicenceCC BY
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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.