Evidence map›Paper›PMID 30523141›Full record

ArticleAJNR. American journal of neuroradiology2019

MR Imaging-Based Radiomic Signatures of Distinct Molecular Subgroups of Medulloblastoma.

M Iv, M Zhou, K Shpanskaya, S Perreault, Z Wang, E Tranvinh, B Lanzman, S Vajapeyam, N A Vitanza, P G Fisher and 9 more

Abstract readMulticenter Study
In one paragraph

Article in AJNR. American journal of neuroradiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 4 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.

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

80 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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20 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

M IvFrom the Department of Radiology (M.I., M.Z., K.S., E.T., B.L., K.W.Y.).ORCID 0000-0001-6794-7213
M ZhouFrom the Department of Radiology (M.I., M.Z., K.S., E.T., B.L., K.W.Y.).ORCID 0000-0001-5072-5630
K ShpanskayaFrom the Department of Radiology (M.I., M.Z., K.S., E.T., B.L., K.W.Y.).ORCID 0000-0003-2741-4046
S PerreaultDepartment of Pediatrics (S.P.), Pediatric Neurology, Centre Hospitalier Universitaire Sainte Justine, University of Montréal, Montreal, Quebec, Canada.ORCID 0000-0002-4417-7698
Z WangStanford Center for Biomedical Informatics (M.Z., O.G., Z.W.).ORCID 0000-0002-2532-4816
E TranvinhFrom the Department of Radiology (M.I., M.Z., K.S., E.T., B.L., K.W.Y.).ORCID 0000-0002-2063-6634
B LanzmanFrom the Department of Radiology (M.I., M.Z., K.S., E.T., B.L., K.W.Y.).ORCID 0000-0002-6580-8540
S VajapeyamDepartment of Radiology (S.V., T.Y.P.), Boston Children's Hospital, Harvard University, Boston, Massachusetts.ORCID 0000-0002-1782-1919
N A VitanzaDepartment Pediatrics Hematology-Oncology (N.A.V.), Seattle Children's Hospital, University of Washington, Seattle, Washington.ORCID 0000-0002-3966-4985
P G FisherDepartment of Pediatrics (P.G.F.), Pediatric Neurology.ORCID 0000-0002-1196-1590
Y J ChoDepartment of Pediatrics (Y.J.C.), Pediatric Neurology, Oregon Health & Science University, Portland, Oregon.ORCID 0000-0003-2710-9631
S LaughlinDepartments of Radiology, Neuro-Oncology, and Neurosurgery (S.L., V.R., M.D.T.), Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0002-9972-5858
V RamaswamyDepartments of Radiology, Neuro-Oncology, and Neurosurgery (S.L., V.R., M.D.T.), Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0002-6557-895X
M D TaylorDepartments of Radiology, Neuro-Oncology, and Neurosurgery (S.L., V.R., M.D.T.), Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0001-7009-3466
S H CheshierDepartment of Neurosurgery (S.H.C.), Pediatric Neurosurgery, University of Utah, Salt Lake City, Utah.ORCID 0000-0003-4983-6610
G A GrantDepartment of Neurosurgery (G.A.G.), Pediatric Neurosurgery, Lucile Packard Children's Hospital, Stanford University, Palo Alto, California.ORCID 0000-0002-2651-4603
T Young PoussaintDepartment of Radiology (S.V., T.Y.P.), Boston Children's Hospital, Harvard University, Boston, Massachusetts.ORCID 0000-0002-0814-0791
O GevaertStanford Center for Biomedical Informatics (M.Z., O.G., Z.W.).ORCID 0000-0002-9965-5466
K W YeomFrom the Department of Radiology (M.I., M.Z., K.S., E.T., B.L., K.W.Y.) kyeom@stanford.edu.ORCID 0000-0001-9860-3368

Funding

Radiogenomics Framework for Non-Invasive Personalized MedicineR01EB020527 · NIBIB · STANFORD UNIVERSITY · PI GEVAERT, OLIVIER · 2015 to 2018
$2.3M
Radiogenomics framework for non-invasive personalized medicineR56EB020527 · NIBIB · STANFORD UNIVERSITY · PI GEVAERT, OLIVIER · 2019 to 2019
$444k
NIBIB NIH HHS R01 EB020527NIBIB NIH HHS R56 EB020527
6 · The paper itself

Abstract

background and purposeDistinct molecular subgroups of pediatric medulloblastoma confer important differences in prognosis and therapy. Currently, tissue sampling is the only method to obtain information for classification. Our goal was to develop and validate radiomic and machine learning approaches for predicting molecular subgroups of pediatric medulloblastoma. MATERIALS AND

methodsIn this multi-institutional retrospective study, we evaluated MR imaging datasets of 109 pediatric patients with medulloblastoma from 3 children's hospitals from January 2001 to January 2014. A computational framework was developed to extract MR imaging-based radiomic features from tumor segmentations, and we tested 2 predictive models: a double 10-fold cross-validation using a combined dataset consisting of all 3 patient cohorts and a 3-dataset cross-validation, in which training was performed on 2 cohorts and testing was performed on the third independent cohort. We used the Wilcoxon rank sum test for feature selection with assessment of area under the receiver operating characteristic curve to evaluate model performance.

resultsOf 590 MR imaging-derived radiomic features, including intensity-based histograms, tumor edge-sharpness, Gabor features, and local area integral invariant features, extracted from imaging-derived tumor segmentations, tumor edge-sharpness was most useful for predicting sonic hedgehog and group 4 tumors. Receiver operating characteristic analysis revealed superior performance of the double 10-fold cross-validation model for predicting sonic hedgehog, group 3, and group 4 tumors when using combined T1- and T2-weighted images (area under the curve = 0.79, 0.70, and 0.83, respectively). With the independent 3-dataset cross-validation strategy, select radiomic features were predictive of sonic hedgehog (area under the curve = 0.70-0.73) and group 4 (area under the curve = 0.76-0.80) medulloblastoma.

conclusionsThis study provides proof-of-concept results for the application of radiomic and machine learning approaches to a multi-institutional dataset for the prediction of medulloblastoma subgroups.

Indexed as

AdolescentCerebellar NeoplasmsChildChild, PreschoolCohort StudiesDatabases, FactualFemaleHedgehog ProteinsHumansImage Processing, Computer-AssistedMachine LearningMagnetic Resonance ImagingMaleMedulloblastomaPredictive Value of TestsPrognosisHedgehog ProteinsSHH protein, human

Identifiers

PMID30523141
PMCPMC6330121

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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.