Evidence map›Paper›PMID 33001310›Full record

ArticleEuropean radiology2021

MGMT methylation may benefit overall survival in patients with moderately vascularized glioblastomas.

Elies Fuster-Garcia, David Lorente Estellés, María Del Mar Álvarez-Torres, Javier Juan-Albarracín, Eduard Chelebian, Alex Rovira, Cristina Auger Acosta, Jose Pineda, Laura Oleaga, Enrique Mollá-Olmos and 5 more

Registry-linked trialAbstract read
In one paragraph

Article in European radiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03439332 (Multicentre Validation of Hemodynamic Multiparametric Tissue Signature), which is not on this map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT03439332 completednot on this map

Multicentre Validation of Hemodynamic Multiparametric Tissue Signature (MTS) Biomarkers From Preoperative and Postradiotherapy MRI in Patients With Glioblastoma: Predictors of Overall Survival

TypeobservationalSponsorJuan M Garcia-GomezRan2018 to 2019Enrolled305ConditionsGlioblastoma
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Radiomics for precision medicine in glioblastoma.Journal of neuro-oncology · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

15 authors.

Elies Fuster-GarciaDepartment of Diagnostic Physics, Oslo University Hospital, Sognsvannsveien 20, 0372, Oslo, Norway. elies.fuster@gliohab.eu.ORCID http://orcid.org/0000-0002-0716-8960
David Lorente EstellésMedical Oncology Service, Hospital Provinicial de Castellón, Castellón de La Plana, Castellón, Spain.
María Del Mar Álvarez-TorresInstituto Universitario de Tecnologías de la Información y Comunicaciones, Universitat Politècnica de València, València, Spain.
Javier Juan-AlbarracínInstituto Universitario de Tecnologías de la Información y Comunicaciones, Universitat Politècnica de València, València, Spain.
Eduard ChelebianInstituto Universitario de Tecnologías de la Información y Comunicaciones, Universitat Politècnica de València, València, Spain.
Alex RoviraSection of Neuroradiology, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Cristina Auger AcostaSection of Neuroradiology, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Jose PinedaHospital Clínic, Barcelona, Spain.
Laura OleagaHospital Clínic, Barcelona, Spain.
Enrique Mollá-OlmosHospital Universitario de La Ribera, València, Spain.
Silvano FiliceDepartment of Medical Physics, University Hospital of Parma, Parma, Italy.
Paulina Due-TønnessenDepartment of Radiology, Oslo University Hospital, Oslo, Norway.
Torstein R MelingDepartment of Neurosurgery, Oslo University Hospital, Oslo, Norway.
Kyrre E EmblemDepartment of Diagnostic Physics, Oslo University Hospital, Sognsvannsveien 20, 0372, Oslo, Norway.
Juan M García-GómezInstituto Universitario de Tecnologías de la Información y Comunicaciones, Universitat Politècnica de València, València, Spain.

Funding

H2020 European Research Council 758657H2020 Health 727560H2020 Health 825750H2020 Marie Skłodowska-Curie Actions 844646Helse Sør-Øst RHF 2013069Helse Sør-Øst RHF 2017073Programa Estatal de Promoción del Talento y su Empleabilidad en I+D+I DPI2016-80054-RSecretaría de Estado de Investigación, Desarrollo e Innovación DPI2016-80054-R
6 · The paper itself

Abstract

objectivesTo assess the combined role of tumor vascularity, estimated from perfusion MRI, and MGMT methylation status on overall survival (OS) in patients with glioblastoma.

methodsA multicentric international dataset including 96 patients from NCT03439332 clinical study were used to study the prognostic relationships between MGMT and perfusion markers. Relative cerebral blood volume (rCBV) in the most vascularized tumor regions was automatically obtained from preoperative MRIs using ONCOhabitats online analysis service. Cox survival regression models and stratification strategies were conducted to define a subpopulation that is particularly favored by MGMT methylation in terms of OS.

resultsrCBV distributions did not differ significantly (p > 0.05) in the methylated and the non-methylated subpopulations. In patients with moderately vascularized tumors (rCBV < 10.73), MGMT methylation was a positive predictive factor for OS (HR = 2.73, p = 0.003, AUC = 0.70). In patients with highly vascularized tumors (rCBV > 10.73), however, there was no significant effect of MGMT methylation (HR = 1.72, p = 0.10, AUC = 0.56).

conclusionsOur results indicate the existence of complementary prognostic information provided by MGMT methylation and rCBV. Perfusion markers could identify a subpopulation of patients who will benefit the most from MGMT methylation. Not considering this information may lead to bias in the interpretation of clinical studies. KEY POINTS: • MRI perfusion provides complementary prognostic information to MGMT methylation. • MGMT methylation improves prognosis in glioblastoma patients with moderate vascular profile. • Failure to consider these relations may lead to bias in the interpretation of clinical studies.

Indexed as

Brain NeoplasmsGlioblastomaAntineoplastic Agents, AlkylatingDNA MethylationDNA Modification MethylasesDNA Repair EnzymesHumansPrognosisPromoter Regions, GeneticTemozolomideTumor Suppressor ProteinsAntineoplastic Agents, AlkylatingDNA Modification MethylasesDNA Repair EnzymesMGMT protein, humanTemozolomideTumor Suppressor ProteinsGlioblastomaO(6)-Methylguanine-DNA methyltransferasePerfusion imagingPrognostic factorsTemozolomide

Identifiers

PMID33001310
PMCPMC7880975

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.