Addition of MR imaging features and genetic biomarkers strengthens glioblastoma survival prediction in TCGA patients.
Addition of MR imaging features and genetic biomarkers strengthens glioblastoma survival prediction in TCGA patients.
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DOI:
10.1016/j.neurad.2014.02.006
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发表时间:
2015-07
期刊:
影响因子:
--
通讯作者:
TCGA Glioma Phenotype Research Group
中科院分区:
文献类型:
--
作者:
Nicolasjilwan M;Hu Y;Yan C;Meerzaman D;Holder CA;Gutman D;Jain R;Colen R;Rubin DL;Zinn PO;Hwang SN;Raghavan P;Hammoud DA;Scarpace LM;Mikkelsen T;Chen J;Gevaert O;Buetow K;Freymann J;Kirby J;Flanders AE;Wintermark M;TCGA Glioma Phenotype Research Group
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. 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. 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). A combination of clinical factors, imaging features, and HRAS copy number variation best predicts survival of patients with GBM.
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影响因子:
2.7
作者:
Serão NV;Delfino KR;Southey BR;Beever JE;Rodriguez-Zas SL
通讯作者:
Rodriguez-Zas SL
影响因子:
50.3
作者:
Phillips, HS;Kharbanda, S;Aldape, K
通讯作者:
Aldape, K
影响因子:
19.7
作者:
Murakami, Ryuji;Sugahara, Takeshi;Yamashita, Yasuyuki
通讯作者:
Yamashita, Yasuyuki
影响因子:
3.5
作者:
Zolal, Amir;Hejcl, Ales;Sames, Martin
通讯作者:
Sames, Martin
DOI:
10.1111/j.2517-6161.1995.tb02031.x
发表时间:
1995-01-01
影响因子:
5.8
作者:
BENJAMINI, Y;HOCHBERG, Y
通讯作者:
HOCHBERG, Y