Evidence map›Paper›PMID 31308421›Full record

ArticleScientific reports2019

Differential prognostic impact of platelet-derived growth factor receptor expression in NSCLC.

Thomas Karsten Kilvaer, Mehrdad Rakaee, Turid Hellevik, Jørg Vik, Luigi De Petris, Tom Donnem, Carina Strell, Arne Ostman, Lill-Tove Rasmussen Busund, Inigo Martinez-Zubiaurre

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. PDGFR-βAging · 2021
    Pooled it
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  13. [Research Progress of Cancer-associated Fibroblasts in Lung Cancer].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2020
    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

10 authors at 3 institutions in 2 countries.

Thomas Karsten KilvaerDepartment of Oncology, University Hospital of North Norway, Tromso, Norway. kilvaer@gmail.com.
Mehrdad RakaeeInstitute of Clinical Medicine, UiT The Arctic University of Norway, Tromso, Norway.
Turid HellevikDepartment of Oncology, University Hospital of North Norway, Tromso, Norway.
Jørg VikInstitute of Clinical Medicine, UiT The Arctic University of Norway, Tromso, Norway.
Luigi De PetrisDepartment of Oncology-Pathology Cancer Center Karolinska, Karolinska Institutet, Stockholm, Sweden.
Tom DonnemDepartment of Oncology, University Hospital of North Norway, Tromso, Norway.
Carina StrellDepartment of Oncology-Pathology Cancer Center Karolinska, Karolinska Institutet, Stockholm, Sweden.
Arne OstmanDepartment of Oncology-Pathology Cancer Center Karolinska, Karolinska Institutet, Stockholm, Sweden.
Lill-Tove Rasmussen BusundInstitute of Medical Biology, UiT The Arctic University of Norway, Tromso, Norway.
Inigo Martinez-ZubiaurreInstitute of Clinical Medicine, UiT The Arctic University of Norway, Tromso, Norway.
University Hospital of North Norway · NOKarolinska Institutet · SEUiT The Arctic University of Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preclinical evidence suggests that stromal expression of platelet-derived growth factor receptors (PDGFRs) stimulates tumor development and diminishes intratumoral drug uptake. In non-small cell lung cancer (NSCLC), the clinical relevance of stromal PDGFR expression remains uncertain. Tumor specimens from 553 patients with primary operable stage I-IIIB NSCLC was obtained and tissue micro-arrays (TMA) were constructed (Norwegian cohort). Immunohistochemistry (IHC) was used to evaluate the expression of PDGFRα and -β in stromal cells and to explore their impact on patient survival. Results were validated in a non-related cohort consisting of TMAs of 367 stage I (A and B) NSCLC patients (Swedish cohort). High stromal PDGFRα expression was an independent predictor of increased survival in the overall populations and SCC (squamous cell carcinoma) subgroups of both investigated cohorts. PDGFRβ was an independent predictor of poor survival in the overall Norwegian cohort and an independent predictor of increased survival in the ADC (adenocarcinoma) subgroup of the Swedish cohort. Tumors displaying the combination PDGFRα-low/PDGFRβ-high exhibited inferior survival according to increasing stage in the Norwegian cohort. This study confirms that high stromal expression of PDGFRα is a predictor of increased survival in NSCLC. Further exploration of the prognostic impact of PDGFRβ and the relationship between PDGFRα and -β is warranted.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCarcinoma, Non-Small-Cell LungCarcinoma, Squamous CellFemaleHumansImmunohistochemistryLung NeoplasmsMaleMiddle AgedPlatelet-Derived Growth FactorPrognosisReceptor, Platelet-Derived Growth Factor alphaReceptor, Platelet-Derived Growth Factor betaBiomarkers, TumorPlatelet-Derived Growth FactorReceptor, Platelet-Derived Growth Factor alphaReceptor, Platelet-Derived Growth Factor betaReceptors, Platelet-Derived Growth Factor

Identifiers

PMID31308421
PMCPMC6629689
OpenAlexW2960044684

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.