dc.contributor.author | Daye, Dania | |
dc.contributor.author | Tabari, Azadeh | |
dc.contributor.author | Kim, Hyunji | |
dc.contributor.author | Chang, Ken | |
dc.contributor.author | Kamran, Sophia C. | |
dc.contributor.author | Hong, Theodore S. | |
dc.contributor.author | Kalpathy-Cramer, Jayashree | |
dc.contributor.author | Gee, Michael S. | |
dc.date.accessioned | 2022-02-07T15:51:11Z | |
dc.date.available | 2021-11-01T14:33:57Z | |
dc.date.available | 2022-02-07T15:51:11Z | |
dc.date.issued | 2021-01 | |
dc.date.submitted | 2020-11 | |
dc.identifier.issn | 0938-7994 | |
dc.identifier.issn | 1432-1084 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/136879.2 | |
dc.description.abstract | Abstract
Objectives
Intra-tumor heterogeneity has been previously shown to be an independent predictor of patient survival. The goal of this study is to assess the role of quantitative MRI-based measures of intra-tumor heterogeneity as predictors of survival in patients with metastatic colorectal cancer.
Methods
In this IRB-approved retrospective study, we identified 55 patients with stage 4 colon cancer with known hepatic metastasis on MRI. Ninety-four metastatic hepatic lesions were identified on post-contrast images and manually volumetrically segmented. A heterogeneity phenotype vector was extracted from each lesion. Univariate regression analysis was used to assess the contribution of 110 extracted features to survival prediction. A random forest–based machine learning technique was applied to the feature vector and to the standard prognostic clinical and pathologic variables. The dataset was divided into a training and test set at a ratio of 4:1. ROC analysis and confusion matrix analysis were used to assess classification performance.
Results
Mean survival time was 39 ± 3.9 months for the study population. A total of 22 texture features were associated with patient survival (p < 0.05). The trained random forest machine learning model that included standard clinical and pathological prognostic variables resulted in an area under the ROC curve of 0.83. A model that adds imaging-based heterogeneity features to the clinical and pathological variables resulted in improved model performance for survival prediction with an AUC of 0.94.
Conclusions
MRI-based texture features are associated with patient outcomes and improve the performance of standard clinical and pathological variables for predicting patient survival in metastatic colorectal cancer.
Key Points
• MRI-based tumor heterogeneity texture features are associated with patient survival outcomes.
• MRI-based tumor texture features complement standard clinical and pathological variables for prognosis prediction in metastatic colorectal cancer.
• Agglomerative hierarchical clustering shows that patient survival outcomes are associated with different MRI tumor profiles. | en_US |
dc.publisher | Springer Science and Business Media LLC | en_US |
dc.relation.isversionof | https://doi.org/10.1007/s00330-020-07673-0 | en_US |
dc.rights | Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. | en_US |
dc.source | Springer Berlin Heidelberg | en_US |
dc.title | Quantitative tumor heterogeneity MRI profiling improves machine learning–based prognostication in patients with metastatic colon cancer | en_US |
dc.type | Article | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory | |
dc.relation.journal | European Radiology | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dc.date.updated | 2021-07-10T03:17:37Z | |
dc.language.rfc3066 | en | |
dc.rights.holder | European Society of Radiology | |
dspace.embargo.terms | Y | |
dspace.date.submission | 2021-07-10T03:17:37Z | |
mit.journal.volume | 31 | en_US |
mit.journal.issue | 8 | en_US |
mit.license | PUBLISHER_POLICY | |
mit.metadata.status | Authority Work Needed | en_US |