Clinical Trial Details
— Status: Active, not recruiting
Administrative data
NCT number |
NCT06036381 |
Other study ID # |
4146 |
Secondary ID |
|
Status |
Active, not recruiting |
Phase |
|
First received |
|
Last updated |
|
Start date |
February 15, 2024 |
Est. completion date |
December 2026 |
Study information
Verified date |
April 2024 |
Source |
Tata Memorial Centre |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
Glioma are type of primary brain tumors arising within the substance of brain. Different type
of gliomas are seen which are classified depending upon pathological examination and advanced
molecular techniques, which help to determine the aggressiveness of the tumor and outcomes.
Artificial intelligence uses advanced analytical process aided by computer which can be
undertaken on the medical images. We plan to use artificial intelligence techniques to
identify the abnormal areas within the brain representing tumor from the radiological images.
Also, similar approach will be undertaken to classify gliomas with good or bad prognosis, to
differentiate glioma from other type of brain tumors, and to detect response after treatment.
Description:
In the proposed retrospective study, images (MRI, CT, or PET) undertaken as part of standard
of care (pre-treatment, post-operative, response assessment, and surveillance) will be
analyzed. The DMG database maintaining records of patients registered in TMC neuro-oncology
DMG will be screened to identify the patients eligible for the study. With approximately
500-600 gliomas seen annually and approximately 80-100 patients/year having pre-treatment
imaging, we expect a ceiling of 1000 patients during 2010-2022, which will be the maximum
number of patients used for the analysis. All the images will be downloaded from the PACS
applying anonymization filters, with clinical records extracted by review of electronic
medical records and radiation plans. Imaging pre-processing will be done, which will include
skull stripping and registration across different modalities (e.g., MRI and CT) or different
sequences (e.g., T1C, T2W, ADC) will be done using rigid or deformable algorithms as suited
best for the modality. Image segmentation to classify the region of interest will be done and
verified individually by a neuro-radiologist or nuclear medicine physician as appropriate.
The segmentations will be done to identify T1-contrast enhancing region (CE), non-enhancing
regions (NE), and necrosis (NEC) guided by T1-C, T2W, and T2-FLAIR areas. The contours and
the images will be resampled to a uniform resolution for different sequences or modalities
(e.g., T2W/ ADC/ PET) to match either with the 3D sequence (e.g., FSPGR sequence) or
available images with the least slice thickness. Subsequently, normalization techniques
(e.g., histogram normalization/ Z-score normalization) will be undertaken within the
individual images and across the entire dataset to account or image heterogeneity, including
field strength for MRI and different image acquisition parameters. For auto segmentation,
both supervised and unsupervised machine learning algorithms will be applied. For the
supervised model, the entire database will be split into training and test cohorts for the
model and application development, respectively. The effectiveness of the automated model
will be tested using the dice similarity coefficient between manually segmentation regions
and AI-based segments. For prognostication of gliomas, the next step will include feature
extraction, which will consist of first-order (including shape, histogram), second-order or
higher-order (e.g., different texture features like GLCM, GLDM, GLSZM, etc.), or deep
learning techniques will be employed. Delta-radiomics will include temporal changes in the
radiomic features from different time points for the same patient within the entire volume
and individual regions. Subsequently, feature reduction and selection techniques like LASSO,
recursive feature elimination will be used to shortlist the number of features depending on
the sample size. The outputs will be decided based on the modeling defined for specific class
problems (e.g., tumor vs. edema, recurrence vs. pseudo progression, outcomes, tumor region of
interest vs. non-tumoral area) as obtained from the clinical information. Any class imbalance
will be addressed using methods like random subset sampling or SMOTE analysis for data
augmentation of the minority class. Machine learning algorithms like LDA, k-NN, SVM, random
forest, AdaBoost, etc., will be applied singularly or in combination as an ensembled
classifier to find the model with best performance. Deep learning classifiers will be used
along with feature-based modeling and compared to test the classifier's applicability.
Validation techniques like leave-one-out validation, k-fold validation, and split (into
training and test cohort) will be used to assess the stability of the machine learning model.
Radiomic analysis will be done by data scientist/ study investigators with expertise in data
analytics. All segmentations will be done on open-source software like ITK snap (itksnap.org)
or 3D Slicer (slicer.org). Feature extraction and modeling will be done using open-source
software like Python (python.org). With continuous advancements in computational science,
available newer analytical techniques and platforms will be applied as appropriate by
collaborators from Indian Statistical Institute, Kolkata, Machine Intelligence Unit by
sharing of the anonymized data.