Evidence map›Paper›PMID 28520730›Full record

ArticlePloS one2017

Analysis of heterogeneity in T2-weighted MR images can differentiate pseudoprogression from progression in glioblastoma.

Thomas C Booth, Timothy J Larkin, Yinyin Yuan, Mikko I Kettunen, Sarah N Dawson, Daniel Scoffings, Holly C Canuto, Sarah L Vowler, Heide Kirschenlohr, Michael P Hobson and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 3 pooled it
2.5field-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

31 citing papers in PubMed, 3 syntheses or guidelines pooled it, 46 citations in OpenAlex.

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  9. Magnetic Resonance Imaging Sequences and Technologies in Adaptive Radiation Therapy.International journal of radiation oncology, biology, physics · 2025
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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

13 authors at 3 institutions in 1 country.

Thomas C BoothDepartment of Biochemistry, University of Cambridge, Cambridge, United Kingdom.ORCID http://orcid.org/0000-0003-0984-3998
Timothy J LarkinDepartment of Biochemistry, University of Cambridge, Cambridge, United Kingdom.
Yinyin YuanCancer Research UK Cambridge Institute, University of Cambridge, Li Ka Shing Centre, Cambridge, United Kingdom.
Mikko I KettunenDepartment of Biochemistry, University of Cambridge, Cambridge, United Kingdom.
Sarah N DawsonCambridge Clinical Trials Unit, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
Daniel ScoffingsDepartment of Radiology, Addenbrooke's Hospital, Cambridge, United Kingdom.
Holly C CanutoDepartment of Biochemistry, University of Cambridge, Cambridge, United Kingdom.
Sarah L VowlerCancer Research UK Cambridge Institute, University of Cambridge, Li Ka Shing Centre, Cambridge, United Kingdom.
Heide KirschenlohrDepartment of Biochemistry, University of Cambridge, Cambridge, United Kingdom.
Michael P HobsonBattock Centre for Experimental Astrophysics, Cavendish Laboratory, University of Cambridge, Cambridge, United Kingdom.
Florian MarkowetzCancer Research UK Cambridge Institute, University of Cambridge, Li Ka Shing Centre, Cambridge, United Kingdom.
Sarah JefferiesDepartment of Oncology, Addenbrooke's Hospital, Cambridge, United Kingdom.
Kevin M BrindleDepartment of Biochemistry, University of Cambridge, Cambridge, United Kingdom.
University of Cambridge · GBAddenbrooke's Hospital · GBCambridge University Hospitals NHS Foundation Trust · GB

Funding

Cancer Research UK 16465Cancer Research UK 17242Cancer Research UK 19274Medical Research Council G1000265
6 · The paper itself

Abstract

purposeTo develop an image analysis technique that distinguishes pseudoprogression from true progression by analyzing tumour heterogeneity in T2-weighted images using topological descriptors of image heterogeneity called Minkowski functionals (MFs).

methodsUsing a retrospective patient cohort (n = 50), and blinded to treatment response outcome, unsupervised feature estimation was performed to investigate MFs for the presence of outliers, potential confounders, and sensitivity to treatment response. The progression and pseudoprogression groups were then unblinded and supervised feature selection was performed using MFs, size and signal intensity features. A support vector machine model was obtained and evaluated using a prospective test cohort.

resultsThe model gave a classification accuracy, using a combination of MFs and size features, of more than 85% in both retrospective and prospective datasets. A different feature selection method (Random Forest) and classifier (Lasso) gave the same results. Although not apparent to the reporting radiologist, the T2-weighted hyperintensity phenotype of those patients with progression was heterogeneous, large and frond-like when compared to those with pseudoprogression.

conclusionAnalysis of heterogeneity, in T2-weighted MR images, which are acquired routinely in the clinic, has the potential to detect an earlier treatment response allowing an early change in treatment strategy. Prospective validation of this technique in larger datasets is required.

Indexed as

AdolescentAdultAgedBrain NeoplasmsDiagnosis, DifferentialFemaleGlioblastomaHumansMagnetic Resonance ImagingMaleMiddle AgedReproducibility of Results

Identifiers

PMID28520730
PMCPMC5435159
OpenAlexW2610187756

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.