Evidence map›Paper›PMID 33400009›Full record

ArticleJournal of neuro-oncology2021

Low MGMT digital expression is associated with a better outcome of IDH1 wildtype glioblastomas treated with temozolomide.

Isabella Gomes, Daniel Antunes Moreno, Mariana Bisarro Dos Reis, Luciane Sussuchi da Silva, Letícia Ferro Leal, Gisele Melo Gonçalves, Caio Augusto Pereira, Marco Antônio Oliveira, Marcus de Medeiros Matsushita, Rui Manuel Reis

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neuro-oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

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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 1 institution in 2 countries.

Isabella GomesMolecular Oncology Research Center, Barretos Cancer Hospital (BCH), Rua Antenor Duarte Villela, 1331, Barretos, SP, CEP 14784 400, Brazil.
Daniel Antunes MorenoMolecular Oncology Research Center, Barretos Cancer Hospital (BCH), Rua Antenor Duarte Villela, 1331, Barretos, SP, CEP 14784 400, Brazil.
Mariana Bisarro Dos ReisMolecular Oncology Research Center, Barretos Cancer Hospital (BCH), Rua Antenor Duarte Villela, 1331, Barretos, SP, CEP 14784 400, Brazil.
Luciane Sussuchi da SilvaMolecular Oncology Research Center, Barretos Cancer Hospital (BCH), Rua Antenor Duarte Villela, 1331, Barretos, SP, CEP 14784 400, Brazil.
Letícia Ferro LealMolecular Oncology Research Center, Barretos Cancer Hospital (BCH), Rua Antenor Duarte Villela, 1331, Barretos, SP, CEP 14784 400, Brazil.
Gisele Melo GonçalvesDepartment of Medical Oncology, BCH, Barretos, SP, Brazil.
Caio Augusto PereiraDepartment of Medical Oncology, BCH, Barretos, SP, Brazil.
Marco Antônio OliveiraNucleus of Epidemiology and Statistics, BCH, Barretos, SP, Brazil.
Marcus de Medeiros MatsushitaPathology Department, BCH, Barretos, SP, Brazil.
Rui Manuel ReisMolecular Oncology Research Center, Barretos Cancer Hospital (BCH), Rua Antenor Duarte Villela, 1331, Barretos, SP, CEP 14784 400, Brazil. ruireis.hcb@gmail.com.ORCID http://orcid.org/0000-0002-9639-7940
Hospital de Câncer de Barretos · BR

Funding

FAPESP 2018/ 10511-6Public Ministry of Labor Campinas (Research, Prevention, and Education of Occupational Cancer) 2015
6 · The paper itself

Abstract

introductionGlioblastoma (GBM) is the deadliest primary brain tumor. The standard treatment consists of surgery, radiotherapy, and temozolomide (TMZ). TMZ response is heterogeneous, and MGMT promoter (MGMTp) methylation has been the major predictive biomarker. We aimed to describe the clinical and molecular data of GBMs treated with TMZ, compare MGMT methylation with MGMT expression, and further associate with patient's outcome.

methodsWe evaluate 112 FFPE adult GBM cases. IDH1 and ATRX expression was analyzed by immunohistochemistry, hotspot TERT promoter (TERTp) mutations were evaluated by Sanger or pyrosequencing, and MGMTp methylation was assessed by pyrosequencing and MGMT mRNA expression using the nCounter® Vantage 3D™ DNA damage and repair panel.

resultsOf the 112 GBMs, 96 were IDH1

conclusionsMGMT mRNA levels evaluated by digital expression were associated with the outcome of TMZ-treated GBM patients. The combination of MGMT methylation and mRNA expression may provide a more accurate prediction of TMZ response in GBM patients.

Indexed as

MutationAdultAgedAntineoplastic Agents, AlkylatingBiomarkers, TumorBrain NeoplasmsDNA Modification MethylasesDNA Repair EnzymesFemaleFollow-Up StudiesGlioblastomaHumansIsocitrate DehydrogenaseMaleMiddle AgedPrognosisAntineoplastic Agents, AlkylatingBiomarkers, TumorDNA Modification MethylasesDNA Repair EnzymesIDH1 protein, humanIsocitrate DehydrogenaseMGMT protein, humanTemozolomideTumor Suppressor ProteinsBiomarkersBrazilGlioblastomaIDHMethylationMGMTNanoStringTemozolomide

Identifiers

PMID33400009
OpenAlexW3120996230

What OpenQuestion holds

Textmetadata
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.