Evidence map›Paper›PMID 31463975›Full record

ArticleEuropean journal of clinical investigation2019

GDF-15 in solid vs non-solid treatment-naïve malignancies.

Henrike Arfsten, Anna Cho, Claudia Freitag, Markus Raderer, Georg Goliasch, Philipp E Bartko, Raphael Wurm, Guido Strunk, Heinz Gisslinger, Christine Marosi and 4 more

Open access · hybridAbstract read
In one paragraph

Article in European journal of clinical investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

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  13. GDF-15 in solid vs non-solid treatment-naïve malignancies.European journal of clinical investigation · 2019
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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

14 authors at 2 institutions in 2 countries.

Henrike ArfstenDepartment of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0002-5836-7759
Anna ChoDepartment of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Claudia FreitagDepartment of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Markus RadererDepartment of Internal Medicine I, Division of Oncology and Hematology, Medical University of Vienna, Vienna, Austria.
Georg GoliaschDepartment of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Philipp E BartkoDepartment of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Raphael WurmDepartment of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Guido StrunkComplexity Research, Vienna, Austria.
Heinz GisslingerDepartment of Internal Medicine I, Division of Oncology and Hematology, Medical University of Vienna, Vienna, Austria.
Christine MarosiDepartment of Internal Medicine I, Division of Oncology and Hematology, Medical University of Vienna, Vienna, Austria.
Gabriela KornekDepartment of Internal Medicine I, Division of Oncology and Hematology, Medical University of Vienna, Vienna, Austria.
Christoph ZielinskiDepartment of Internal Medicine I, Division of Oncology and Hematology, Medical University of Vienna, Vienna, Austria.
Martin HülsmannDepartment of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0001-7944-7363
Noemi PavoDepartment of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0003-3377-4507
Medical University of Vienna · ATTU Dortmund University · DE

Funding

Thermo Fisher Scientific This study was supported by an unrestricted grant
6 · The paper itself

Abstract

aimGDF-15 is an established cardiovascular risk marker but is equally implicated in tumour biology. Elevated levels of GDF-15 have indeed been observed in distinct tumour entities. This study aimed to explore the relation of GDF-15 to other cardiac biomarkers and the general association of GDF-15 on prognosis in an unselected cohort of treatment-naïve cancer patients.

methodsWe prospectively enrolled 555 consecutive patients at time of diagnosis of malignant disease prior receiving anticancer therapy. Plasma GDF-15 concentrations were determined alongside other cardiac and routine laboratory markers. All-cause mortality was defined as primary endpoint.

resultsGDF-15 levels were 338 ng/L (IQR:205-534) for the total cohort, and values were comparable for different tumour entities except breast cancer. Metastatic disease was characterized by higher plasma GDF-15 [435 ng/L (IQR:279-614) vs 266 ng/L (IQR:175-427), P < .001]. GDF-15 correlated positively with inflammatory status reflected by CRP, SAA and IL-6 [r = .31, P < .001, r = .23, P < .001 and r = .14, P = .002] and cardiac biomarkers as NT-proBNP, hsTnT, MR-proADM and CT-proET-1 [r = .46; r = .46; r = .59 and r = .50; P < .001 for all]. GDF-15 was significantly associated with all-cause mortality after multivariate adjustment [adj.HR for ln(GDF-15) 1.78, 95%CI:1.47-2.16, P < .001]. There was a significant interaction between solid and haematological malignancies with loss of association of GDF-15 with outcome in myelodysplastic and myeloproliferative disease.

conclusionsElevated plasma GDF-15 is associated with progressing disease severity and poor prognosis in solid tumours of treatment-naïve cancer patients. GDF-15 increase is accompanied by worsening systemic inflammation and a subclinical functional impairment of different organs including the heart. GDF-15 represents a promising target for our pathophysiologic understanding in cardio-oncology linking conditions of both cardiac and neoplastic disease.

Indexed as

MortalityAdrenomedullinAgedBreast NeoplasmsCause of DeathC-Reactive ProteinEndothelin-1FemaleGastrointestinal NeoplasmsGlycopeptidesGrowth Differentiation Factor 15HumansInterleukin-6Lung NeoplasmsMaleMiddle AgedAdrenomedullincopeptinsC-Reactive ProteinC-terminal proendothelin-1Endothelin-1GDF15 protein, humanGlycopeptidesGrowth Differentiation Factor 15IL6 protein, humanInterleukin-6mid-regional pro-adrenomedullin, humanNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)Protein PrecursorsSerum Amyloid A ProteinTroponin TbiomarkercancerGDF-15inflammationprognosis

Identifiers

PMID31463975
PMCPMC6899906
OpenAlexW2970485386

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.