GLORIA

GEOMAR Library Ocean Research Information Access

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    In: Neuro-Oncology, Oxford University Press (OUP), Vol. 22, No. Supplement_2 ( 2020-11-09), p. ii229-ii229
    Abstract: Glioblastomas are arguably the most aggressive, infiltrative, and heterogeneous adult brain tumor. Biophysical modeling of glioblastoma growth has shown its predictive value towards clinical endpoints, enabling more informed decision-making. However, the mathematically rigorous formulations of biophysical modeling come with a large computational footprint, hindering their application to clinical studies. METHODS We present a deep learning (DL)-based logistical regression model, to estimate in seconds glioblastoma biophysical growth, defined through three tumor-specific parameters: 1) diffusion coefficient of white matter (Dw), which describes how easily the tumor can infiltrate through the white matter, 2) mass-effect parameter (Mp), which defines the average tumor expansion, and 3) estimated time (T) in number of days that the tumor has been growing. Pre-operative multi-parametric MRI (mpMRI) structural scans (T1, T1-Gd, T1, T2-FLAIR) from 135 subjects of the TCGA-GBM imaging collection are used to quantitatively evaluate our approach. We consider the mpMRI intensities within the region defined by the abnormal T2-FLAIR signal envelope, for training three DL models for the three tumor-specific parameters. Each of our DL models consist of two sets of convolution layers followed by a single max-pooling layer, with a normalized root mean squared error as the minimization metric and evaluated using 10-fold cross validation. We train and validate the DL-based predictions against parameters derived from biophysical inversion models. RESULTS Pearson correlation coefficients between our DL-based estimations and the biophysical parameters were equal to 0.85 for Dw, 0.90 for Mp, and 0.94 for T. CONCLUSION This study unlocks the power of tumor-specific parameters from biophysical tumor growth estimation, paving the way towards their utilization in more clinical studies, while opening the door for leveraging advanced radiomic descriptors in future studies, as well as allowing for significantly faster parameter reconstruction compared to biophysical growth modeling approaches. *denotes equal senior authorship.
    Type of Medium: Online Resource
    ISSN: 1522-8517 , 1523-5866
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2020
    detail.hit.zdb_id: 2094060-9
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    In: Medical Physics, Wiley, Vol. 47, No. 12 ( 2020-12), p. 6039-6052
    Abstract: The availability of radiographic magnetic resonance imaging (MRI) scans for the Ivy Glioblastoma Atlas Project (Ivy GAP) has opened up opportunities for development of radiomic markers for prognostic/predictive applications in glioblastoma (GBM). In this work, we address two critical challenges with regard to developing robust radiomic approaches: (a) the lack of availability of reliable segmentation labels for glioblastoma tumor sub‐compartments (i.e., enhancing tumor, non‐enhancing tumor core, peritumoral edematous/infiltrated tissue) and (b) identifying “reproducible” radiomic features that are robust to segmentation variability across readers/sites. Acquisition and validation methods From TCIA’s Ivy GAP cohort, we obtained a paired set (n = 31) of expert annotations approved by two board‐certified neuroradiologists at the Hospital of the University of Pennsylvania (UPenn) and at Case Western Reserve University (CWRU). For these studies, we performed a reproducibility study that assessed the variability in (a) segmentation labels and (b) radiomic features, between these paired annotations. The radiomic variability was assessed on a comprehensive panel of 11 700 radiomic features including intensity, volumetric, morphologic, histogram‐based, and textural parameters, extracted for each of the paired sets of annotations. Our results demonstrated (a) a high level of inter‐rater agreement (median value of DICE ≥0.8 for all sub‐compartments), and (b) ≈24% of the extracted radiomic features being highly correlated (based on Spearman’s rank correlation coefficient) to annotation variations. These robust features largely belonged to morphology (describing shape characteristics), intensity (capturing intensity profile statistics), and COLLAGE (capturing heterogeneity in gradient orientations) feature families. Data format and usage notes We make publicly available on TCIA’s Analysis Results Directory (https://doi.org/10.7937/9j41‐7d44), the complete set of (a) multi‐institutional expert annotations for the tumor sub‐compartments, (b) 11 700 radiomic features, and (c) the associated reproducibility meta‐analysis. Potential applications The annotations and the associated meta‐data for Ivy GAP are released with the purpose of enabling researchers toward developing image‐based biomarkers for prognostic/predictive applications in GBM.
    Type of Medium: Online Resource
    ISSN: 0094-2405 , 2473-4209
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 1466421-5
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    In: NeuroImage, Elsevier BV, Vol. 220 ( 2020-10), p. 117081-
    Type of Medium: Online Resource
    ISSN: 1053-8119
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2020
    detail.hit.zdb_id: 1471418-8
    SSG: 5,2
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    In: Neuro-Oncology, Oxford University Press (OUP), Vol. 24, No. Supplement_7 ( 2022-11-14), p. vii167-vii167
    Abstract: Diffuse astrocytic glioma are common and aggressive malignant primary brain tumors with grim prognosis. Artificial intelligence (AI) has shown promise across predictive, prognostic, and diagnostic neuro-oncology applications, towards improving patient management. However, clinical translation and deployment are hampered by AI models’ requirements for explicit acceleration cards, which are not typically considered in clinical environments. Here, we seek the execution of AI models in such clinical/low-resource environments, facilitated by mathematical optimizations rather than investing in acceleration cards, and focus on the use case of delineating clinically-relevant regions, namely the entire tumor burden (ETB) and tumor core (TC). METHODS We identified the BraTS20 retrospective cohort of 369 glioma cases, each described by 4 structural multi-parametric MRI (mpMRI) scans (T1,T1Gd,T2,T2-FLAIR). The Generally Nuanced Deep Learning Framework (GaNDLFv0.0.14/PyTorchv1.8.2) was used to train the original AI model (ResUNet), by randomly sampling 40 643 patches from each mpMRI scan. We then investigate the contributions of post-training mathematical optimizations. Quantitative performance evaluation of the original and optimized (GaNDLFv0.0.14/OpenVINOTM-INT8-v2022.1.0) models were based on 125 unseen hold-out cases (BraTS20 validation dataset), using the dice similarity coefficient (DSC), while profiling in a consumer-grade workstation, i.e., typical clinical hardware configuration. RESULTS Negligible delineation performance differences were observed between the original and optimized AI models, for both ETB (DSCoriginal/DSCoptimized= 0.877/0.876) and TC (DSCoriginal/DSCoptimized= 0.773/0.772). However, the optimized model yielded substantial improvements in latency (up to 5.4x faster inference) and 53% less memory footprint. CONCLUSIONS Post-training mathematical optimization of AI models yields substantial gains in latency and memory usage, while maintaining their accuracy. Although we focused on delineation, we anticipate these mathematical optimizations to be applicable in other AI models. Post-training optimization is a promising approach for deploying AI models on consumer-grade CPUs, and hence facilitating their translation in low-resource/clinical environments, potentially contributing to improved patient management, treatment decisions, and response assessment. *author Siddhesh Thakur is an equal contributing first author.
    Type of Medium: Online Resource
    ISSN: 1522-8517 , 1523-5866
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2022
    detail.hit.zdb_id: 2094060-9
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    In: Neuro-Oncology, Oxford University Press (OUP), Vol. 23, No. Supplement_6 ( 2021-11-12), p. vi135-vi136
    Abstract: Robustness and generalizability of artificial intelligent (AI) methods is reliant on the training data size and diversity, which are currently hindered in multi-institutional healthcare collaborations by data ownership and legal concerns. To address these, we introduce the Federated Tumor Segmentation (FeTS) Initiative, as an international consortium using federated learning (FL) for data-private multi-institutional collaborations, where AI models leverage data at participating institutions, without sharing data between them. The initial FeTS use-case focused on detecting brain tumor boundaries in MRI. METHODS The FeTS tool incorporates: 1) MRI pre-processing, including image registration and brain extraction; 2) automatic delineation of tumor sub-regions, by label fusion of pretrained top-performing BraTS methods; 3) tools for manual delineation refinements; 4) model training. 55 international institutions identified local retrospective cohorts of glioblastoma patients. Ground truth was generated using the first 3 FeTS functionality modes as mentioned earlier. Finally, the FL training mode comprises of i) an AI model trained on local data, ii) local model updates shared with an aggregator, which iii) combines updates from all collaborators to generate a consensus model, and iv) circulates the consensus model back to all collaborators for iterative performance improvements. RESULTS The first FeTS consensus model, from 23 institutions with data of 2,200 patients, showed an average improvement of 11.1% in the performance of the model on each collaborator’s validation data, when compared to a model trained on the publicly available BraTS data (n=231). CONCLUSION Our findings support that data increase alone would lead to AI performance improvements without any algorithmic development, hence indicating that the model performance would improve further when trained with all 55 collaborating institutions. FL enables AI model training with knowledge from data of geographically-distinct collaborators, without ever having to share any data, hence overcoming hurdles relating to legal, ownership, and technical concerns of data sharing.
    Type of Medium: Online Resource
    ISSN: 1522-8517 , 1523-5866
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2021
    detail.hit.zdb_id: 2094060-9
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    In: Physics in Medicine & Biology, IOP Publishing, Vol. 67, No. 20 ( 2022-10-21), p. 204002-
    Abstract: Objective. De-centralized data analysis becomes an increasingly preferred option in the healthcare domain, as it alleviates the need for sharing primary patient data across collaborating institutions. This highlights the need for consistent harmonized data curation, pre-processing, and identification of regions of interest based on uniform criteria. Approach. Towards this end, this manuscript describes the Fe derated T umor S egmentation (FeTS) tool, in terms of software architecture and functionality. Main results. The primary aim of the FeTS tool is to facilitate this harmonized processing and the generation of gold standard reference labels for tumor sub-compartments on brain magnetic resonance imaging, and further enable federated training of a tumor sub-compartment delineation model across numerous sites distributed across the globe, without the need to share patient data. Significance. Building upon existing open-source tools such as the Insight Toolkit and Qt, the FeTS tool is designed to enable training deep learning models targeting tumor delineation in either centralized or federated settings. The target audience of the FeTS tool is primarily the computational researcher interested in developing federated learning models, and interested in joining a global federation towards this effort. The tool is open sourced at https://github.com/FETS-AI/Front-End .
    Type of Medium: Online Resource
    ISSN: 0031-9155 , 1361-6560
    RVK:
    Language: Unknown
    Publisher: IOP Publishing
    Publication Date: 2022
    detail.hit.zdb_id: 1473501-5
    SSG: 12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...