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  1. Article ; Online: T2-FLAIR mismatch sign and machine learning-based multiparametric MRI radiomics in predicting IDH mutant 1p/19q non-co-deleted diffuse lower-grade gliomas.

    Tang, W-T / Su, C-Q / Lin, J / Xia, Z-W / Lu, S-S / Hong, X-N

    Clinical radiology

    2024  Volume 79, Issue 5, Page(s) e750–e758

    Abstract: Aim: To investigate the application of the T2-weighted (T2)-fluid-attenuated inversion recovery (FLAIR) mismatch sign and machine learning-based multiparametric magnetic resonance imaging (MRI) radiomics in predicting 1p/19q non-co-deletion of lower- ... ...

    Abstract Aim: To investigate the application of the T2-weighted (T2)-fluid-attenuated inversion recovery (FLAIR) mismatch sign and machine learning-based multiparametric magnetic resonance imaging (MRI) radiomics in predicting 1p/19q non-co-deletion of lower-grade gliomas (LGGs).
    Materials and methods: One hundred and forty-six patients, who had pathologically confirmed isocitrate dehydrogenase (IDH) mutant LGGs were assigned randomly to the training cohort (n=102) and the testing cohort (n=44) at a ratio of 7:3. The T2-FLAIR mismatch sign and conventional MRI features were evaluated. Radiomics features extracted from T1-weighted imaging (T1WI), T2-weighted imaging (T2WI), FLAIR, apparent diffusion coefficient (ADC), and contrast-enhanced T1WI images (CE-T1WI). The models that displayed the best performance of each sequence were selected, and their predicted values as well as the T2-FLAIR mismatch sign data were collected to establish a final stacking model. Receiver operating characteristic curve (ROC) analyses and area under the curve (AUC) values were applied to evaluate and compare the performance of the models.
    Results: The T2-FLAIR mismatch sign was more common in the IDH mutant 1p/19q non-co-deleted group (p<0.05) and the area under the curve (AUC) value was 0.692 with sensitivity 0.397, specificity 0.987, and accuracy 0.712, respectively. The stacking model showed a favourable performance with an AUC of 0.925 and accuracy of 0.882 in the training cohort and an AUC of 0.886 and accuracy of 0.864 in the testing cohort.
    Conclusion: The stacking model based on multiparametric MRI can serve as a supplementary tool for pathological diagnosis, offering valuable guidance for clinical practice.
    MeSH term(s) Humans ; Multiparametric Magnetic Resonance Imaging ; Isocitrate Dehydrogenase/genetics ; Radiomics ; Brain Neoplasms/diagnostic imaging ; Brain Neoplasms/genetics ; Brain Neoplasms/pathology ; Mutation/genetics ; Glioma/diagnostic imaging ; Glioma/genetics ; Glioma/pathology ; Magnetic Resonance Imaging/methods ; Machine Learning ; Retrospective Studies
    Chemical Substances Isocitrate Dehydrogenase (EC 1.1.1.41)
    Language English
    Publishing date 2024-02-02
    Publishing country England
    Document type Randomized Controlled Trial ; Journal Article
    ZDB-ID 391227-9
    ISSN 1365-229X ; 0009-9260
    ISSN (online) 1365-229X
    ISSN 0009-9260
    DOI 10.1016/j.crad.2024.01.021
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: A radiomics-based model to differentiate glioblastoma from solitary brain metastases.

    Su, C-Q / Chen, X-T / Duan, S-F / Zhang, J-X / You, Y-P / Lu, S-S / Hong, X-N

    Clinical radiology

    2021  Volume 76, Issue 8, Page(s) 629.e11–629.e18

    Abstract: Aim: To differentiate glioblastoma (GBM) from solitary brain metastases (MET) using radiomic analysis.: Materials and methods: Two hundred and fifty-three patients with solitary brain tumours (157 GBM and 98 solitary brain MET) were split into a ... ...

    Abstract Aim: To differentiate glioblastoma (GBM) from solitary brain metastases (MET) using radiomic analysis.
    Materials and methods: Two hundred and fifty-three patients with solitary brain tumours (157 GBM and 98 solitary brain MET) were split into a training cohort (n=178) and a validation cohort (n=77) by stratified sampling using computer-generated random numbers at a ratio of 7:3. After feature extraction, minimum redundancy maximum relevance (mRMR) and the least absolute shrinkage and selection operator (LASSO) were used to build the radiomics signature on the training cohort and validation cohort. Performance was assessed by radiomics score (Rad-score), receiver operating characteristic (ROC) curve, calibration, and clinical usefulness.
    Results: Eleven radiomic features were selected as significant features in the training cohort. The Rad-score was significantly associated with the differentiation between GBM and solitary brain MET (p<0.001) both in the training and validation cohorts. The radiomics signature yielded area under the curve (AUC) values of 0.82 and 0.81 in the training and validation cohorts to distinguish between GBM and solitary brain MET.
    Conclusions: The radiomics model might be a useful supporting tool for the preoperative differentiation of GBM from solitary brain MET, which could aid pretreatment decision-making.
    MeSH term(s) Brain/diagnostic imaging ; Brain/pathology ; Brain Neoplasms/diagnostic imaging ; Brain Neoplasms/pathology ; Brain Neoplasms/secondary ; Cohort Studies ; Diagnosis, Differential ; Glioblastoma/diagnostic imaging ; Glioblastoma/pathology ; Humans ; Magnetic Resonance Imaging/methods ; Reproducibility of Results ; Retrospective Studies
    Language English
    Publishing date 2021-06-04
    Publishing country England
    Document type Journal Article
    ZDB-ID 391227-9
    ISSN 1365-229X ; 0009-9260
    ISSN (online) 1365-229X
    ISSN 0009-9260
    DOI 10.1016/j.crad.2021.04.012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Combined texture analysis of diffusion-weighted imaging with conventional MRI for non-invasive assessment of IDH1 mutation in anaplastic gliomas.

    Su, C-Q / Lu, S-S / Zhou, M-D / Shen, H / Shi, H-B / Hong, X-N

    Clinical radiology

    2018  Volume 74, Issue 2, Page(s) 154–160

    Abstract: Aim: To examine whether texture analysis (TA) of diffusion-weighted imaging (DWI) combined with conventional magnetic resonance imaging (MRI) could non-invasively predict isocitrate dehydrogenase 1 (IDH1) mutational status in anaplastic gliomas.: ... ...

    Abstract Aim: To examine whether texture analysis (TA) of diffusion-weighted imaging (DWI) combined with conventional magnetic resonance imaging (MRI) could non-invasively predict isocitrate dehydrogenase 1 (IDH1) mutational status in anaplastic gliomas.
    Materials and methods: Fifty-two patients with histologically confirmed anaplastic glioma was reviewed retrospectively. Conventional MRI was evaluated using the Visually Accessible Rembrandt Images (VASARI) scoring system. TA of DWI based on the entire tumour volume was compared between IDH1-mutant and wild-type tumours by using unpaired Student's t-test. Receiver operating characteristic curve (ROC) and logistic regression were used to assess their diagnostic performance.
    Results: Significant statistical differences in VASARI features and TA of DWI were observed between IDH1-mutant and wild-type tumours (all p<0.05). Using multivariable logistic regression, the proportion of the tumour that was non-enhancing and the entropy of apparent diffusion coefficient (ADC) were found to possess higher prediction potential for IDH1 mutation with areas under the ROC curve (AUC) of 0.918 and 0.724, respectively. A combination of these for the identification of IDH1 mutations improved the AUC to 0.954, with a sensitivity and a specificity of 81% and 96%.
    Conclusions: The combined assessment of the conventional MRI and TA of DWI were useful for predicting IDH1 mutation in anaplastic gliomas.
    MeSH term(s) Brain/diagnostic imaging ; Brain Neoplasms/diagnostic imaging ; Brain Neoplasms/genetics ; Diffusion Magnetic Resonance Imaging/methods ; Female ; Glioma/diagnostic imaging ; Glioma/genetics ; Humans ; Image Interpretation, Computer-Assisted/methods ; Isocitrate Dehydrogenase/genetics ; Magnetic Resonance Imaging/methods ; Male ; Middle Aged ; Mutation/genetics ; Reproducibility of Results ; Retrospective Studies ; Sensitivity and Specificity
    Chemical Substances Isocitrate Dehydrogenase (EC 1.1.1.41) ; IDH1 protein, human (EC 1.1.1.42.)
    Language English
    Publishing date 2018-11-01
    Publishing country England
    Document type Journal Article
    ZDB-ID 391227-9
    ISSN 1365-229X ; 0009-9260
    ISSN (online) 1365-229X
    ISSN 0009-9260
    DOI 10.1016/j.crad.2018.10.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Clinical Evaluation of Highly Accelerated Compressed Sensing Time-of-Flight MR Angiography for Intracranial Arterial Stenosis.

    Lu, S S / Qi, M / Zhang, X / Mu, X H / Schmidt, M / Sun, Y / Forman, C / Speier, P / Hong, X N

    AJNR. American journal of neuroradiology

    2018  Volume 39, Issue 10, Page(s) 1833–1838

    Abstract: Background and purpose: Time-of-flight MR angiography is the preferred imaging technique to assess intracranial arterial stenosis but is limited by a relatively long acquisition time. Compressed sensing provides an innovative approach in undersampling !# ...

    Abstract Background and purpose: Time-of-flight MR angiography is the preferred imaging technique to assess intracranial arterial stenosis but is limited by a relatively long acquisition time. Compressed sensing provides an innovative approach in undersampling
    Materials and methods: Compressed sensing TOF and parallel imaging TOF were performed in 22 patients with intracranial arterial stenosis. The MRA scan times were 2 minutes and 31 seconds and 4 minutes and 48 seconds for compressed sensing TOF and parallel imaging TOF, respectively. The reconstructed resolutions were 0.4 × 0.4 × 0.4 and 0.4 × 0.4 × 0.6 mm
    Results: The interrater agreement was good to excellent. Compressed sensing TOF resulted in image quality comparable with that of parallel imaging TOF but boosted confidence in diagnosing arterial stenoses (
    Conclusions: Compressed sensing TOF both remarkably reduced the scan time and provided adequate image quality for the diagnosis of intracranial arterial stenosis.
    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; Constriction, Pathologic/diagnostic imaging ; Female ; Humans ; Intracranial Arterial Diseases/diagnostic imaging ; Magnetic Resonance Angiography/methods ; Male ; Middle Aged ; Sensitivity and Specificity
    Language English
    Publishing date 2018-09-13
    Publishing country United States
    Document type Journal Article
    ZDB-ID 603808-6
    ISSN 1936-959X ; 0195-6108
    ISSN (online) 1936-959X
    ISSN 0195-6108
    DOI 10.3174/ajnr.A5786
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: [A phase Ⅰ dose-escalating trial of pegylated liposomal doxorubicin in combination with cyclophosphamide, vincristine and prednisone for aggressive non-Hodgkin lymphoma].

    Shen, W N / Ji, D M / Xue, K / Zhang, Q L / Lyu, F F / Hong, X N / Cao, J N / Guo, Y

    Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi

    2017  Volume 37, Issue 12, Page(s) 1044–1048

    Abstract: Objective: ...

    Abstract Objective:
    MeSH term(s) Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols/administration & dosage ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Cyclophosphamide/administration & dosage ; Doxorubicin/administration & dosage ; Doxorubicin/analogs & derivatives ; Female ; Humans ; Lymphoma, B-Cell ; Lymphoma, Non-Hodgkin ; Lymphoma, T-Cell ; Male ; Middle Aged ; Neutropenia ; Polyethylene Glycols/administration & dosage ; Prednisolone/administration & dosage ; Prednisone ; Treatment Outcome ; Vincristine/administration & dosage
    Chemical Substances liposomal doxorubicin ; Polyethylene Glycols (3WJQ0SDW1A) ; Vincristine (5J49Q6B70F) ; Doxorubicin (80168379AG) ; Cyclophosphamide (8N3DW7272P) ; Prednisolone (9PHQ9Y1OLM) ; Prednisone (VB0R961HZT)
    Language Chinese
    Publishing date 2017-01-05
    Publishing country China
    Document type Clinical Trial, Phase I ; Journal Article
    ISSN 0253-2727
    ISSN 0253-2727
    DOI 10.3760/cma.j.issn.0253-2727.2016.12.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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