Evidence map›Paper›PMID 27396951›Full record

ArticleMolecular oncology2016

A validated microRNA profile with predictive potential in glioblastoma patients treated with bevacizumab.

Josie Hayes, Helene Thygesen, Walter Gregory, David R Westhead, Pim J French, Martin J Van Den Bent, Sean E Lawler, Susan C Short

Open access · bronzeAbstract read
In one paragraph

Article in Molecular oncology, 2016. 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
2.1field-weighted citation impact, top 14% 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, 23 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

8 authors at 5 institutions in 3 countries.

Josie HayesLeeds Institute of Cancer and Pathology, St James's University Hospital, Leeds LS9 7TF, UK. Electronic address: Josielouise.hayes@ucsf.edu.
Helene ThygesenNetherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.
Walter GregoryClinical Trials Research Unit (CTRU), University of Leeds, 71-75 Clarendon Road, Leeds, West Yorkshire LS2 9JT, UK.
David R WestheadInstitute of Molecular and Cellular Biology, Faculty of Biological Sciences and Institute of Membrane and Systems Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK.
Pim J FrenchDepartment of Neurology, Brain Tumor Center, Erasmus MC Cancer Institute, Wytemaweg 80, 3015 CN Rotterdam, The Netherlands.
Martin J Van Den BentDepartment of Neurology, Brain Tumor Center, Erasmus MC Cancer Institute, Groene Hilledijk 301, 3075 EA Rotterdam, The Netherlands.
Sean E LawlerDepartment of Neurosurgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Susan C ShortLeeds Institute of Cancer and Pathology, St James's University Hospital, Leeds LS9 7TF, UK.
Erasmus MC Cancer Institute · NLSt James's University Hospital · GBUniversity of Leeds · GBBrigham and Women's Hospital · USThe Netherlands Cancer Institute · NL

Funding

Cancer Research UK 10065
6 · The paper itself

Abstract

purposeWe investigated whether microRNA expression data from glioblastoma could be used to produce a profile that defines a bevacizumab responsive group of patients. PATIENTS AND

methodsTCGA microRNA expression data from tumors resected at first diagnosis of glioblastoma in patients treated with bevacizumab at any time during the course of their disease were randomly separated into training (n = 50) and test (n = 37) groups for model generation. MicroRNA-seq data for 51 patients whose treatment included bevacizumab in the BELOB trial were used as an independent validation cohort.

resultsUsing penalized regression we identified 8 microRNAs as potential predictors of overall survival in the training set. We dichotomized the response score based on the most prognostic minimum of a density plot of the response scores (log-rank HR = 0.16, p = 1.2e(-5)) and validated the profile in the test cohort (one-sided log-rank HR = 0.34, p = 0.026). Analysis of the profile using all samples in the TCGA glioblastoma dataset, regardless of treatment received, (n = 473) showed that the prediction of patient benefit was not significant (HR = 0.84, p = 0.083) suggesting the profile is specific to bevacizumab. Further independent validation of our microRNA profile in RNA-seq data from patients treated with bevacizumab (alone or in combination with CCNU) at glioblastoma recurrence in the BELOB trial confirmed that our microRNA profile predicted patient benefit from bevacizumab (HR = 0.59, p = 0.043).

conclusionWe have identified and validated an 8-microRNA profile that predicts overall survival in patients with glioblastoma treated with bevacizumab. This may be useful for identifying patients who are likely to benefit from this agent.

Indexed as

Gene Expression ProfilingBevacizumabBrain NeoplasmsClinical Trials as TopicDisease-Free SurvivalFemaleGene Expression Regulation, NeoplasticGlioblastomaHumansMaleMicroRNAsMiddle AgedMultivariate AnalysisPrognosisReproducibility of ResultsSignal TransductionBevacizumabMicroRNAsBevacizumabGlioblastomaGliomamicroRNAPrediction

Identifiers

PMID27396951
PMCPMC5423205
OpenAlexW2474823095

What OpenQuestion holds

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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.