Evidence map›Paper›PMID 37190125›Full record

ArticleCancers2023

High VEGFA Expression Is Associated with Improved Progression-Free Survival after Bevacizumab Treatment in Recurrent Glioblastoma.

Bárbara Alves, Joana Peixoto, Sofia Macedo, Jorge Pinheiro, Bruno Carvalho, Paula Soares, Jorge Lima, Raquel T Lima

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. 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

8 authors at 2 institutions in 1 country.

Bárbara Alvesi3S-Instituto de Investigação e Inovação em Saúde, 4200 Porto, Portugal.ORCID 0000-0003-1743-6022
Joana Peixotoi3S-Instituto de Investigação e Inovação em Saúde, 4200 Porto, Portugal.ORCID 0000-0001-9469-5680
Sofia Macedoi3S-Instituto de Investigação e Inovação em Saúde, 4200 Porto, Portugal.ORCID 0000-0001-7752-998X
Jorge PinheiroDepartment of Pathology, Centro Hospitalar Universitário S. João, 4200 Porto, Portugal.
Bruno CarvalhoDepartment of Neurosurgery, Centro Hospitalar Universitário S. João, 4200 Porto, Portugal.ORCID 0000-0002-3972-7544
Paula Soaresi3S-Instituto de Investigação e Inovação em Saúde, 4200 Porto, Portugal.ORCID 0000-0001-9607-6998
Jorge Limai3S-Instituto de Investigação e Inovação em Saúde, 4200 Porto, Portugal.ORCID 0000-0001-7780-0901
Raquel T Limai3S-Instituto de Investigação e Inovação em Saúde, 4200 Porto, Portugal.ORCID 0000-0002-5838-9659
Universidade do Porto · PTHospital de São João · PT

Funding

European Regional Development Fund project "The Porto Comprehensive Cancer Center" with the reference NORTE-01-0145-FEDER-072678 - Consórcio PORTO.CCC - Porto.Comprehensive Cancer Center Raquel Seruca.Fundação para a Ciência e Tecnologia project "Institute for Research and Innovation in Health Sciences" (UID/BIM/04293/2019)Fundação para a Ciência e Tecnologia project POCI-01-0145-FEDER-028779 (PTDC/BIA-MIC/28779/2017Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF) the project "Cancer Research on Therapy Resistance: From Basic Mechanisms to Novel Tar-gets"-NORTE-01-0145-FEDER-000051
6 · The paper itself

Abstract

Glioblastoma (GB) is one of the deadliest human cancers. Many GB patients do not respond to treatment, and inevitably die within a median of 15-18 months post-diagnosis, highlighting the need for reliable biomarkers to aid clinical management and treatment evaluation. The GB microenvironment holds tremendous potential as a source of biomarkers; several proteins such as MMP-2, MMP-9, YKL40, and VEGFA have been identified as being differentially expressed in GB patient samples. Still to date, none of these proteins have been translated into relevant clinical biomarkers. This study evaluated the expression of MMP-2, MMP-9, YKL40, and VEGFA in a series of GBs and their impact on patient outcome. High levels of VEGFA expression were significantly associated with improved progression-free survival after bevacizumab treatment, thus having potential as a tissue biomarker for predicting patients' response to bevacizumab. Noteworthily, VEGFA expression was not associated with patient outcome after temozolomide treatment. To a lesser extent, YKL40 also provided significant information regarding the extent of bevacizumab treatment. This study highlights the importance of studying secretome-associated proteins as GB biomarkers and identifies VEGFA as a promising marker for predicting response to bevacizumab.

Indexed as

biomarkersglioblastomaimmunohistochemistryMMP-2MMP-9secretomeVEGFAYKL40

Identifiers

PMID37190125
PMCPMC10136662
OpenAlexW4363675520

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.