Evidence map›Paper›PMID 30977010›Full record

ArticleAngiogenesis2019

Prognostic effect of VEGF gene variants in metastatic non-small-cell lung cancer patients.

Ivana Sullivan, Pau Riera, Marta Andrés, Albert Altés, Margarita Majem, Remei Blanco, Laia Capdevila, Andrés Barba, Agustí Barnadas, Juliana Salazar

Abstract read
PubMed Publisher
In one paragraph

Article in Angiogenesis, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 53 citations in OpenAlex.

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  10. p38β - MAPK11 and its role in female cancers.Journal of ovarian research · 2021
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  15. p38β and Cancer: The Beginning of the Road.International journal of molecular sciences · 2020
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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 4 institutions in 1 country.

Ivana Sullivan *Medical Oncology Department, Hospital de la Santa Creu i Sant Pau, Sant Quintí, 89, 08041, Barcelona, Spain. isullivan@santpau.cat.
Pau Riera *Genetics Department, Hospital de la Santa Creu i Sant Pau, Sant Quintí, 89, 08041, Barcelona, Spain.ORCID http://orcid.org/0000-0002-3074-3927
Marta AndrésMedical Oncology Department, Hospital de la Santa Creu i Sant Pau, Sant Quintí, 89, 08041, Barcelona, Spain.
Albert AltésHematology Department, Fundació Althaia, C/Dr. Joan Soler, 1-3, 08243, Manresa, Barcelona, Spain.
Margarita MajemMedical Oncology Department, Hospital de la Santa Creu i Sant Pau, Sant Quintí, 89, 08041, Barcelona, Spain.
Remei BlancoMedical Oncology Department, Consorci Sanitari de Terrassa, Carretera de Torrebonica, S/N, 08227, Terrassa, Spain.
Laia CapdevilaMedical Oncology Department, Hospital de Sant Pau i Santa Tecla, Rambla Vella, 14, 43003, Tarragona, Spain.
Andrés BarbaMedical Oncology Department, Hospital de la Santa Creu i Sant Pau, Sant Quintí, 89, 08041, Barcelona, Spain.
Agustí BarnadasMedical Oncology Department, Hospital de la Santa Creu i Sant Pau, Sant Quintí, 89, 08041, Barcelona, Spain.
Juliana SalazarGenetics Department, Hospital de la Santa Creu i Sant Pau, Sant Quintí, 89, 08041, Barcelona, Spain. jsalazar@santpau.cat.ORCID http://orcid.org/0000-0002-3581-4499
Hospital de Sant Pau · ESAlthaia · ESConsorci Sanitari de Terrassa · ESUniversitat Autònoma de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionClinical and pathological characteristics are still considered prognostic markers in metastatic non-small-cell lung cancer (NSCLC) patients but they cannot explain all interindividual variability. Tumoral angiogenesis mediated by the vascular endothelial growth factor (VEGF) is critical for the progression and metastasis of the disease. We aimed to investigate the prognostic role of genetic variants within the VEGF pathway in patients with metastatic NSCLC. MATERIALS AND

methodsWe prospectively included 170 patients with metastatic NSCLC treated with first-line platinum-based chemotherapy. A comprehensive panel of single-nucleotide polymorphisms (SNPs) in genes belonging to the VEGF pathway (VEGFA, VEGFR1/FLT1, VEGFR2/KDR, GRB2, ITGAV, KISS1, KRAS, PRKCE, HIF1α, MAP2K4, MAP2K6, and MAPK11) were genotyped in blood DNA samples. SNPs were evaluated for association with overall survival (OS) and progression-free survival (PFS).

resultsIn multivariate analyses adjusted for patient characteristics, we found that VEGFA rs2010963 and VEGFR2 rs2071559 were significantly associated with OS [Hazard Ratio (HR) 0.7 (0.5-0.9); p = 0.026 and HR 1.5 (1.1-2.3); p = 0.025, respectively]. Additionally, ITGAV rs35251833 and MAPK11 rs2076139 were significantly associated with PFS [HR 2.5 (1.4-4.3; p = 0.002 and HR 0.6 (0.5-0.9); p = 0.013, respectively].

conclusionOur findings reinforce the potential clinical value of germline variants in VEGFA and VEGFR2 and show for the first time variants in ITGAV and MAPK11 as promising prognostic markers in metastatic NSCLC patients receiving platinum-based chemotherapy.

Indexed as

Genetic VariationAdultAgedAged, 80 and overCarcinoma, Non-Small-Cell LungDisease-Free SurvivalFemaleGenetic Predisposition to DiseaseHumansLung NeoplasmsMaleMiddle AgedPolymorphism, Single NucleotidePrognosisSurvival AnalysisVascular Endothelial Growth Factor AVascular Endothelial Growth Factor AGenetic variantsMetastatic NSCLCPrognostic factorsVEGF

Identifiers

PMID30977010
OpenAlexW2937901763

What OpenQuestion holds

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Read underepoch 390

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.