Evidence map›Paper›PMID 30094067›Full record

ArticleESMO open2018

CSF-1 and Ang-2 serum levels - prognostic and diagnostic partners in non-small cell lung cancer.

Ana Luísa Coelho, Mónica Patrícia Gomes, Raquel Jorge Catarino, Christian Rolfo, Rui Manuel Medeiros, António Manuel Araújo

Open access · goldAbstract read
In one paragraph

Article in ESMO open, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 15 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

6 authors at 4 institutions in 2 countries.

Ana Luísa CoelhoMolecular Oncology and Viral Pathology Group, IPO-Porto Research Centre (CI-IPOP), Porto, Portugal; Faculty of Medicine, University of Porto, Porto, Portugal; LPCC Research Department, Portuguese League Against Cancer (NRNorte), Porto, Portugal; Oncology Research Group, UMIB-Unit for Multidisciplinary Research in Biomedicine, Porto, Portugal.
Mónica Patrícia GomesMolecular Oncology and Viral Pathology Group, IPO-Porto Research Centre (CI-IPOP), Porto, Portugal; LPCC Research Department, Portuguese League Against Cancer (NRNorte), Porto, Portugal; Oncology Research Group, UMIB-Unit for Multidisciplinary Research in Biomedicine, Porto, Portugal.
Raquel Jorge CatarinoMolecular Oncology and Viral Pathology Group, IPO-Porto Research Centre (CI-IPOP), Porto, Portugal; Oncology Research Group, UMIB-Unit for Multidisciplinary Research in Biomedicine, Porto, Portugal.
Christian RolfoUniversity of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center, Antwerp University Hospital, Edegem, Belgium; Centre of Oncological Research (CORE), Antwerp University, Edegem, Belgium.
Rui Manuel MedeirosMolecular Oncology and Viral Pathology Group, IPO-Porto Research Centre (CI-IPOP), Porto, Portugal; Faculty of Medicine, University of Porto, Porto, Portugal; LPCC Research Department, Portuguese League Against Cancer (NRNorte), Porto, Portugal.
António Manuel AraújoOncology Research Group, UMIB-Unit for Multidisciplinary Research in Biomedicine, Porto, Portugal; Department of Medical Oncology, Centro Hospitalar do Porto, Porto, Portugal; ICBAS-UP-Instituto de Ciências Biomédicas Abel Salazar, University of Porto, Porto, Portugal. Electronic address: antonio.araujo@chporto.min-saude.pt.
Universidade do Porto · PTAntwerp University Hospital · BEInstituto Português de Oncologia Francisco Gentil · PTPortuguese League Against Epilepsy · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung cancer is the most incident and lethal form of cancer, with late diagnosis as a major determinant of its bad prognosis. Immunotherapies targeting immune checkpoints improve survival, but positive results encompass only 30%-40% of the patients, possibly due to alternative pathways to immunosuppression, including tumour-associated macrophages (TAM). Colony stimulating factor-1 (CSF-1) is implicated in TAM differentiation and recruitment to tumours and in tumour angiogenesis, through a special setting of Tie-2-expressing macrophages, which respond to angiopoietin-2 (Ang-2). We evaluated the role of serum levels of CSF-1 in non-small cell lung cancer (NSCLC) prognosis and whether these could serve as biomarkers for NSCLC detection, along with Ang-2. PARTICIPANTS AND

methodsWe prospectively studied an unselected cohort of 145 patients with NSCLC and a group of 30 control individuals. Serum levels of Ang-2 and CSF-1 were measured by ELISA prior to treatment.

resultsSerum levels of CSF-1 and Ang-2 are positively correlated (p<0.000001). Individuals with high serum levels of CSF-1 have a 17-fold risk for NSCLC presence and patients with combined High Ang-2/CSF-1 serum levels present a 5-fold increased risk of having NSCLC. High Ang-2/CSF-1 phenotype is also associated with worst prognosis in NSCLC.

conclusionsCombined expression of CSF-1 and Ang-2 seems to contribute to worst prognosis in NSCLC and it is worthy to understand the basis of this unexplored partnership. Moreover, we think CSF-1 could be included as a biomarker in NSCLC screening protocols that can improve the positive predictive value of the current screening modalities, increase overall cost effectiveness and potentially improve lung cancer survival.

Indexed as

ANG-2CSF-1non-small cell lung cancer

Identifiers

PMID30094067
PMCPMC6069916
OpenAlexW2884582508

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.