TY - JOUR
T1 - Addition of MR imaging features and genetic biomarkers strengthens glioblastoma survival prediction in TCGA patients
AU - on behalf of the TCGA Glioma Phenotype Research Group
AU - Nicolasjilwan, Manal
AU - Hu, Ying
AU - Yan, Chunhua
AU - Meerzaman, Daoud
AU - Holder, Chad A.
AU - Gutman, David
AU - Jain, Rajan
AU - Colen, Rivka
AU - Rubin, Daniel L.
AU - Zinn, Pascal O.
AU - Hwang, Scott N.
AU - Raghavan, Prashant
AU - Hammoud, Dima A.
AU - Scarpace, Lisa M.
AU - Mikkelsen, Tom
AU - Chen, James
AU - Gevaert, Olivier
AU - Buetow, Kenneth
AU - Freymann, John
AU - Kirby, Justin
AU - Flanders, Adam E.
AU - Wintermark, Max
N1 - Publisher Copyright:
© 2014 Elsevier Masson SAS.
PY - 2015/7/1
Y1 - 2015/7/1
N2 - Purpose: The purpose of our study was to assess whether a model combining clinical factors, MR imaging features, and genomics would better predict overall survival of patients with glioblastoma (GBM) than either individual data type. Methods: The study was conducted leveraging The Cancer Genome Atlas (TCGA) effort supported by the National Institutes of Health. Six neuroradiologists reviewed MRI images from The Cancer Imaging Archive (http://cancerimagingarchive.net) of 102 GBM patients using the VASARI scoring system. The patients' clinical and genetic data were obtained from the TCGA website (http://www.cancergenome.nih.gov/). Patient outcome was measured in terms of overall survival time. The association between different categories of biomarkers and survival was evaluated using Cox analysis. Results: The features that were significantly associated with survival were: (1) clinical factors: chemotherapy; (2) imaging: proportion of tumor contrast enhancement on MRI; and (3) genomics: HRAS copy number variation. The combination of these three biomarkers resulted in an incremental increase in the strength of prediction of survival, with the model that included clinical, imaging, and genetic variables having the highest predictive accuracy (area under the curve 0.679 ± 0.068, Akaike's information criterion 566.7, P< 0.001). Conclusion: A combination of clinical factors, imaging features, and HRAS copy number variation best predicts survival of patients with GBM.
AB - Purpose: The purpose of our study was to assess whether a model combining clinical factors, MR imaging features, and genomics would better predict overall survival of patients with glioblastoma (GBM) than either individual data type. Methods: The study was conducted leveraging The Cancer Genome Atlas (TCGA) effort supported by the National Institutes of Health. Six neuroradiologists reviewed MRI images from The Cancer Imaging Archive (http://cancerimagingarchive.net) of 102 GBM patients using the VASARI scoring system. The patients' clinical and genetic data were obtained from the TCGA website (http://www.cancergenome.nih.gov/). Patient outcome was measured in terms of overall survival time. The association between different categories of biomarkers and survival was evaluated using Cox analysis. Results: The features that were significantly associated with survival were: (1) clinical factors: chemotherapy; (2) imaging: proportion of tumor contrast enhancement on MRI; and (3) genomics: HRAS copy number variation. The combination of these three biomarkers resulted in an incremental increase in the strength of prediction of survival, with the model that included clinical, imaging, and genetic variables having the highest predictive accuracy (area under the curve 0.679 ± 0.068, Akaike's information criterion 566.7, P< 0.001). Conclusion: A combination of clinical factors, imaging features, and HRAS copy number variation best predicts survival of patients with GBM.
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U2 - 10.1016/j.neurad.2014.02.006
DO - 10.1016/j.neurad.2014.02.006
M3 - Article
C2 - 24997477
AN - SCOPUS:84937640437
SN - 0150-9861
VL - 42
SP - 212
EP - 221
JO - Journal of Neuroradiology
JF - Journal of Neuroradiology
IS - 4
ER -