Radiomic signature as a predictive factor for lymph node metastasis in early-stage cervical cancer.


Journal

Journal of magnetic resonance imaging : JMRI
ISSN: 1522-2586
Titre abrégé: J Magn Reson Imaging
Pays: United States
ID NLM: 9105850

Informations de publication

Date de publication:
01 2019
Historique:
received: 08 03 2018
accepted: 12 05 2018
pubmed: 14 8 2018
medline: 24 3 2020
entrez: 14 8 2018
Statut: ppublish

Résumé

Lymph node metastasis (LNM) is the principal risk factor for poor outcomes in early-stage cervical cancer. Radiomics may offer a noninvasive way for predicting the stage of LNM. To evaluate a radiomic signature of LN involvement based on sagittal T Retrospective. In all, 143 patients were randomly divided into two primary and validation cohorts with 100 patients in the primary cohort and 43 patients in the validation cohort. T The gold standard of LN status was based on histologic results. A radiologist with 10 years of experience used the ITK-SNAP software for 3D manual segmentation. A senior radiologist with 15 years of experience validated all segmentations. The area under the receiver operating characteristics curve (ROC AUC), classification accuracy, sensitivity, and specificity were used between LNM and non-LNM groups. A total of 970 radiomic features and seven clinical characteristics were extracted. Minimum redundancy / maximum relevance and support vector machine algorithms were applied to select features and construct a radiomic signature. The Mann-Whitney U-test and the chi-square test were used to test the performance of clinical characteristics and potential prognostic outcomes. The results were used to assess the quantitative discrimination performance of the SVM-based radiomic signature. The radiomic signatures allowed good discrimination between LNM and non-LNM groups. The ROC AUC was 0.753 (95% confidence interval [CI], 0.656-0.850) in the primary cohort and 0.754 (95% CI, 0584-0.924) in the validation cohort. A multiple-sequence MRI radiomic signature can be used as a noninvasive biomarker for preoperative assessment of LN status and potentially influence the therapeutic decision-making in early-stage cervical cancer patients. 3 Technical Efficacy: Stage 2 J. Magn. Reson. Imaging 2019;49:304-310.

Sections du résumé

BACKGROUND
Lymph node metastasis (LNM) is the principal risk factor for poor outcomes in early-stage cervical cancer. Radiomics may offer a noninvasive way for predicting the stage of LNM.
PURPOSE
To evaluate a radiomic signature of LN involvement based on sagittal T
STUDY TYPE
Retrospective.
POPULATION
In all, 143 patients were randomly divided into two primary and validation cohorts with 100 patients in the primary cohort and 43 patients in the validation cohort.
FIELD STRENGTH/SEQUENCE
T
ASSESSMENT
The gold standard of LN status was based on histologic results. A radiologist with 10 years of experience used the ITK-SNAP software for 3D manual segmentation. A senior radiologist with 15 years of experience validated all segmentations. The area under the receiver operating characteristics curve (ROC AUC), classification accuracy, sensitivity, and specificity were used between LNM and non-LNM groups.
STATISTICAL TESTS
A total of 970 radiomic features and seven clinical characteristics were extracted. Minimum redundancy / maximum relevance and support vector machine algorithms were applied to select features and construct a radiomic signature. The Mann-Whitney U-test and the chi-square test were used to test the performance of clinical characteristics and potential prognostic outcomes. The results were used to assess the quantitative discrimination performance of the SVM-based radiomic signature.
RESULTS
The radiomic signatures allowed good discrimination between LNM and non-LNM groups. The ROC AUC was 0.753 (95% confidence interval [CI], 0.656-0.850) in the primary cohort and 0.754 (95% CI, 0584-0.924) in the validation cohort.
DATA CONCLUSIONS
A multiple-sequence MRI radiomic signature can be used as a noninvasive biomarker for preoperative assessment of LN status and potentially influence the therapeutic decision-making in early-stage cervical cancer patients.
LEVEL OF EVIDENCE
3 Technical Efficacy: Stage 2 J. Magn. Reson. Imaging 2019;49:304-310.

Identifiants

pubmed: 30102438
doi: 10.1002/jmri.26209
doi:

Substances chimiques

Contrast Media 0

Types de publication

Journal Article Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

304-310

Subventions

Organisme : National Natural Science Foundation of China
ID : 81771924
Pays : International
Organisme : National Natural Science Foundation of China
ID : 81501616
Pays : International
Organisme : National Natural Science Foundation of China
ID : 81671851
Pays : International
Organisme : National Natural Science Foundation of China
ID : 81527805
Pays : International
Organisme : National Natural Science Foundation of China
ID : 81601492
Pays : International
Organisme : National Key R&D Program of China
ID : 2017YFA0205200
Pays : International
Organisme : National Key R&D Program of China
ID : 2017YFC1308700
Pays : International
Organisme : National Key R&D Program of China
ID : 2017YFC1308701
Pays : International
Organisme : National Key R&D Program of China
ID : 2017YFC1309100
Pays : International
Organisme : Science and Technology Service Network Initiative of the Chinese Academy of Sciences
ID : KFJ-SW-STS-160
Pays : International
Organisme : Instrument Developing Project of the Chinese Academy of Sciences
ID : YZ201502
Pays : International
Organisme : Beijing Municipal Science and Technology Commission
ID : Z161100002616022
Pays : International
Organisme : Youth Innovation Promotion Association CAS, and Special Fund for Research in the Public Interest of China
ID : 201402020
Pays : International

Informations de copyright

© 2018 International Society for Magnetic Resonance in Medicine.

Auteurs

Yangyang Kan (Y)

Dalian Medical University, Dalian, P.R. China.
Cancer Hospital of China Medical University, Shenyang, P.R. China.
Liaoning Cancer Hospital & Institute, Shenyang, P.R. China.

Di Dong (D)

CAS Key Laboratory of Molecular Imaging, Institute of Automation, Chinese Academy of Sciences, Beijing, P.R. China.
University of Chinese Academy of Sciences, Beijing, P.R. China.

Yuchen Zhang (Y)

University of Electronic Science and Technology of China, Chengdu, Sichuan, P.R. China.

Wenyan Jiang (W)

Cancer Hospital of China Medical University, Shenyang, P.R. China.
Liaoning Cancer Hospital & Institute, Shenyang, P.R. China.

Nannan Zhao (N)

Cancer Hospital of China Medical University, Shenyang, P.R. China.
Liaoning Cancer Hospital & Institute, Shenyang, P.R. China.

Lu Han (L)

Cancer Hospital of China Medical University, Shenyang, P.R. China.
Liaoning Cancer Hospital & Institute, Shenyang, P.R. China.

Mengjie Fang (M)

CAS Key Laboratory of Molecular Imaging, Institute of Automation, Chinese Academy of Sciences, Beijing, P.R. China.
University of Chinese Academy of Sciences, Beijing, P.R. China.

Yali Zang (Y)

CAS Key Laboratory of Molecular Imaging, Institute of Automation, Chinese Academy of Sciences, Beijing, P.R. China.
University of Chinese Academy of Sciences, Beijing, P.R. China.

Chaoen Hu (C)

CAS Key Laboratory of Molecular Imaging, Institute of Automation, Chinese Academy of Sciences, Beijing, P.R. China.
University of Chinese Academy of Sciences, Beijing, P.R. China.

Jie Tian (J)

CAS Key Laboratory of Molecular Imaging, Institute of Automation, Chinese Academy of Sciences, Beijing, P.R. China.
University of Chinese Academy of Sciences, Beijing, P.R. China.

Chunming Li (C)

University of Electronic Science and Technology of China, Chengdu, Sichuan, P.R. China.

Yahong Luo (Y)

Dalian Medical University, Dalian, P.R. China.
Cancer Hospital of China Medical University, Shenyang, P.R. China.
Liaoning Cancer Hospital & Institute, Shenyang, P.R. China.

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