Evidence map›Paper›PMID 34697170›Full record

ArticleIn vivo (Athens, Greece)

Tumour Markers in the Differential Diagnosis of Patients With Isolated Involuntary Weight Loss.

Jaume Trape, Jordi Aligue, Mireia Vicente, Anna Arnau, Antonio San-Jose, Josep Ordeig, Roser Ordeig, Mariona Bonet, Andres Abril, Omar El-Boutrouki and 6 more

Open access · diamondAbstract read
In one paragraph

Article in In vivo (Athens, Greece). 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
1.0field-weighted citation impact, top 23% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. Article
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

16 authors at 3 institutions in 1 country.

Jaume TrapeLaboratory Medicine Althaia, Xarxa Assistencial Universitària de Manresa, Manresa, Spain; jtrape@althaia.cat.
Jordi AligueFaculty of Medicine, Universitat de Vic, Universitat Central de Catalunya, Vic, Spain.
Mireia VicenteCAP Manresa 2 Institut Catala de la Salut Barcelona, Barcelona, Spain.
Anna ArnauClinical Research Unit, Althaia Xarxa Assistencial Universitària de Manresa, Manresa, Spain.
Antonio San-JoseInternal Medicine, Vall d'Hebron University Hospital, Barcelona, Spain.
Josep OrdeigInternal Medicine Althaia, Xarxa Assistencial Universitària de Manresa, Manresa, Spain.
Roser OrdeigInternal Medicine Althaia, Xarxa Assistencial Universitària de Manresa, Manresa, Spain.
Mariona BonetInternal Medicine Althaia, Xarxa Assistencial Universitària de Manresa, Manresa, Spain.
Andres AbrilInternal Medicine Althaia, Xarxa Assistencial Universitària de Manresa, Manresa, Spain.
Omar El-BoutroukiInternal Medicine Althaia, Xarxa Assistencial Universitària de Manresa, Manresa, Spain.
Carolina Gonzalez-FernandezLaboratory Medicine Althaia, Xarxa Assistencial Universitària de Manresa, Manresa, Spain.
Maria SalaLaboratory Medicine Althaia, Xarxa Assistencial Universitària de Manresa, Manresa, Spain.
Cristina FigolsLaboratory Medicine Althaia, Xarxa Assistencial Universitària de Manresa, Manresa, Spain.
Elisabeth Gonzalez-GarciaCAP Manresa 2 Institut Catala de la Salut Barcelona, Barcelona, Spain.
Lourdes MontsantLaboratory Medicine Althaia, Xarxa Assistencial Universitària de Manresa, Manresa, Spain.
Domingo RuizInternal Medicine Althaia, Xarxa Assistencial Universitària de Manresa, Manresa, Spain.
Althaia · ESInstitut Català de la Salut · ESVall d'Hebron Hospital Universitari · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimParaneoplastic syndrome symptoms include isolated involuntary weight loss (IIWL). The differential diagnosis of cancer from other diseases may require a significant number of tests. Tumour markers (TMs) can be used for the diagnosis and stratification of patients according to cancer risk. PATIENTS AND

methodsThis study included 606 patients (48% females) seen at the rapid diagnostic unit for IIWL. We determined the levels of TMs carcinoembryonic antigen, carbohydrate antigen 19-9, soluble fragments of cytokeratin 19, carbohydrate antigen 15-3, carbohydrate antigen 125, neuron specific enolase, alpha-fetoprotein, prostatic specific antigen using the multiparametric analyser COBAS 601. Two cut-off points were established, the upper reference limit described by the manufacturer and a high cut-off point suggested by Molina et al., to stratify patients according to cancer risk.

resultsPatients were classified according to TM levels as follows: I) all TMs below the upper reference limit; II) highest number of TMs between the two cut-offs; III) at least one TM above the higher cut-off. The odds ratio for malignancy was 4.3 for group II and 248 for group III. These results indicate that when at least one TM is above the higher cut-off, neoplasia is highly probable.

conclusionTM determination allowed to establish cancer risk in patients with IIWL.

Indexed as

Biomarkers, TumorLung NeoplasmsAntigens, NeoplasmCarcinoembryonic AntigenDiagnosis, DifferentialFemaleHumansKeratinsMaleSensitivity and SpecificityWeight LossAntigens, NeoplasmBiomarkers, TumorCarcinoembryonic AntigenKeratinscancerCEACYFRA 21-1differential diagnosistumour markersWeight loss

Identifiers

PMID34697170
PMCPMC8627726
OpenAlexW3208823164

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.