Evidence map›Paper›PMID 29600296›Full record

ArticleJournal of neuroimaging in psychiatry & neurology2016

Assessing the Effects of Software Platforms on Volumetric Segmentation of Glioblastoma.

William D Dunn, Hugo J W L Aerts, Lee A Cooper, Chad A Holder, Scott N Hwang, Carle C Jaffe, Daniel J Brat, Rajan Jain, Adam E Flanders, Pascal O Zinn and 2 more

Abstract read
In one paragraph

Article in Journal of neuroimaging in psychiatry & neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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.

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

2 citing papers in PubMed.

  1. Review
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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

12 authors.

William D DunnDepartments of Biomedical Informatics and Neurology, Emory University School of Medicine, Atlanta, GA, USA.
Hugo J W L AertsDepartments of Radiation Oncology and Radiology, Dana-Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Lee A CooperDepartments of Biomedical Informatics and Neurology, Emory University School of Medicine, Atlanta, GA, USA.
Chad A HolderDepartment of Radiology and Imaging Sciences, Emory University School of Medicine, Atlanta, GA, USA.
Scott N HwangDepartment of Diagnostic Imaging Department, St. Jude Children's Research Hospital, Memphis, TN, USA.
Carle C JaffeDepartment of Radiology, Boston University School of Medicine, Boston, MA, USA.
Daniel J BratDepartment of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, USA.
Rajan JainDepartments of Radiology and Neurosurgery, NYU School of Medicine, New York, NY, USA.
Adam E FlandersDepartment of Neuroradiology, Thomas Jefferson University Hospitals, Philadelphia, PA, USA.
Pascal O ZinnDepartment of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Rivka R ColenDepartment of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
David A GutmanDepartments of Biomedical Informatics and Neurology, Emory University School of Medicine, Atlanta, GA, USA.

Funding

Advanced Development of an Open-source Platform for Web-based Integrative Digital Image Analysis in CancerU24CA194362 · NCI · EMORY UNIVERSITY · PI COOPER, LEE, GUTMAN, DAVID ANDREW · 2015 to 2019
$3.6M
Quantitative Radiomics System Decoding the Tumor PhenotypeU24CA194354 · NCI · DANA-FARBER CANCER INST · PI AERTS, HUGO, QUACKENBUSH, JOHN · 2015 to 2019
$3.5M
NCI NIH HHS U24 CA194354NCI NIH HHS U24 CA194362
6 · The paper itself

Abstract

backgroundRadiological assessments of biologically relevant regions in glioblastoma have been associated with genotypic characteristics, implying a potential role in personalized medicine. Here, we assess the reproducibility and association with survival of two volumetric segmentation platforms and explore how methodology could impact subsequent interpretation and analysis.

methodsPost-contrast T1- and T2-weighted FLAIR MR images of 67 TCGA patients were segmented into five distinct compartments (necrosis, contrast-enhancement, FLAIR, post contrast abnormal, and total abnormal tumor volumes) by two quantitative image segmentation platforms - 3D Slicer and a method based on Velocity AI and FSL. We investigated the internal consistency of each platform by correlation statistics, association with survival, and concordance with consensus neuroradiologist ratings using ordinal logistic regression.

resultsWe found high correlations between the two platforms for FLAIR, post contrast abnormal, and total abnormal tumor volumes (spearman's r(67) = 0.952, 0.959, and 0.969 respectively). Only modest agreement was observed for necrosis and contrast-enhancement volumes (r(67) = 0.693 and 0.773 respectively), likely arising from differences in manual and automated segmentation methods of these regions by 3D Slicer and Velocity AI/FSL, respectively. Survival analysis based on AUC revealed significant predictive power of both platforms for the following volumes: contrast-enhancement, post contrast abnormal, and total abnormal tumor volumes. Finally, ordinal logistic regression demonstrated correspondence to manual ratings for several features.

conclusionTumor volume measurements from both volumetric platforms produced highly concordant and reproducible estimates across platforms for general features. As automated or semi-automated volumetric measurements replace manual linear or area measurements, it will become increasingly important to keep in mind that measurement differences between segmentation platforms for more detailed features could influence downstream survival or radio genomic analyses.

Indexed as

3D SlicerCancerComputational scienceGBMImaging-genomicsMRI

Identifiers

PMID29600296
PMCPMC5870135

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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.