Publications by authors named "Colen R"

Background: Glioblastoma is the most aggressive adult primary brain cancer, characterized by significant heterogeneity, posing challenges for patient management, treatment planning, and clinical trial stratification.

Methods: We developed a highly reproducible, personalized prognostication and clinical subgrouping system using machine learning (ML) on routine clinical data, MRI, and molecular measures from 2,838 demographically diverse patients across 22 institutions and 3 continents. Patients were stratified into favorable, intermediate, and poor prognostic subgroups (I, II, III) using Kaplan-Meier analysis (Cox proportional model and hazard ratios [HR]).

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  • Technological advancements are enhancing the use of computational methods in fields like health care, particularly in neuro-oncology, to improve clinical decision-making through various biomarkers.
  • Artificial intelligence (AI) algorithms, including radiomics, are being increasingly integrated, but challenges like generalizability and validation hinder their widespread application.
  • This Policy Review aims to provide recommendations for standardizing AI practices in health care, focusing on neuro-oncology, while discussing the importance of reliable AI for future clinical trials.
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The development, application, and benchmarking of artificial intelligence (AI) tools to improve diagnosis, prognostication, and therapy in neuro-oncology are increasing at a rapid pace. This Policy Review provides an overview and critical assessment of the work to date in this field, focusing on diagnostic AI models of key genomic markers, predictive AI models of response before and after therapy, and differentiation of true disease progression from treatment-related changes, which is a considerable challenge based on current clinical care in neuro-oncology. Furthermore, promising future directions, including the use of AI for automated response assessment in neuro-oncology, are discussed.

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  • The study assessed how radiomics—a method of extracting and analyzing features from medical images—can predict the tumor microenvironment (TME) and response to anti-PD-1 treatment in patients with recurrent/metastatic head and neck squamous cell carcinoma (HNSCC).
  • Using advanced techniques like CT scans and machine learning algorithms, researchers built models to evaluate disease control rates, progression-free survival, and overall survival, alongside assessing tumor characteristics like hypoxia and immune cell presence.
  • Findings indicated that radiomics could accurately predict treatment outcomes and TME features, suggesting its potential as a valuable tool, although more extensive research is needed to confirm these results.
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  • The study investigates the differences in treatment responses among melanoma patients based on tumor characteristics, utilizing radiomic analysis of medical images to identify non-invasive biomarkers.
  • This research involved 291 patients treated with either immune checkpoint inhibitors or BRAF targeted therapy, and 667 tumor lesions were analyzed for treatment outcomes.
  • The findings show significant organ-level differences in treatment response and variability, with specific machine-learning models accurately predicting disease control or progression based on radiomic features, highlighting the potential for personalized treatment strategies.
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  • The study aimed to explore sex-based differences in patients with glioblastoma to enhance personalized treatment and improve outcomes, focusing on differences in tumor parameters and survival.
  • Data from 1832 patients was analyzed, revealing that women were diagnosed at an older median age and had lower tumor volumes compared to men, who generally had higher performance scores.
  • Despite these differences in tumor characteristics, the research found no significant discrepancies in survival outcomes or mortality rates between sexes, although certain factors like age and treatment type influenced mortality risk for both genders.
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Background: Immune-checkpoint inhibitors (ICIs) have showed unprecedent efficacy in the treatment of patients with advanced non-small cell lung cancer (NSCLC). However, not all patients manifest clinical benefit due to the lack of reliable predictive biomarkers. We showed preliminary data on the predictive role of the combination of radiomics and plasma extracellular vesicle (EV) PD-L1 to predict durable response to ICIs.

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Background: Preoperative symptom severity in cervical spondylotic myelopathy (CSM) can be variable. Radiomic signatures could provide an imaging biomarker for symptom severity in CSM. This study utilizes radiomic signatures of T1-weighted and T2-weighted magnetic resonance imaging images to correlate with preoperative symptom severity based on modified Japanese Orthopaedic Association (mJOA) scores for patients with CSM.

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Glioblastoma (GBM) is fatal and the study of therapeutic resistance, disease progression, and drug discovery in GBM or glioma stem cells is often hindered by limited resources. This limitation slows down progress in both drug discovery and patient survival. Here we present a genetically engineered human cerebral organoid model with a cancer-like phenotype that could provide a basis for GBM-like models.

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  • Automated brain tumor segmentation methods have reached a level of performance that is clinically useful, relying on MRI modalities like T1, T2, and FLAIR images.
  • These methods often face challenges due to missing sequences caused by issues like time constraints and patient motion, making it crucial to find ways to substitute missing modalities for better segmentation.
  • The Brain MR Image Synthesis Benchmark (BraSyn) was established to evaluate image synthesis techniques that can generate these missing MRI modalities, aiming to enhance the automation of brain tumor segmentation processes.
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Purpose: While the T2-FLAIR mismatch sign is highly specific for isocitrate dehydrogenase (IDH)-mutant, 1p/19q-noncodeleted astrocytomas among lower-grade gliomas, its utility in WHO grade 4 gliomas is not well-studied. We derived the partial T2-FLAIR mismatch sign as an imaging biomarker for IDH mutation in WHO grade 4 gliomas.

Methods: Preoperative MRI scans of adult WHO grade 4 glioma patients (n = 2165) from the multi-institutional ReSPOND (Radiomics Signatures for PrecisiON Diagnostics) consortium were analyzed.

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Background And Purpose: To determine the incidence of acute neuroimaging (NI) findings and comorbidities in the coronavirus disease of 2019 (COVID-19)-infected subjects in seven U.S. and four European hospitals.

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Taurine is a sulphur-containing amino acid with important physiological roles and a key compound for the synthesis of bile salts, which are essential for the emulsion and absorption of dietary lipids. This study aimed to evaluate the effects of taurine supplementation to low-fishmeal diets on the metabolism of taurine, bile acids, and lipids of Senegalese sole. A fishmeal (FM) and a plant-protein-based (PP0) diet were formulated, and the latter was supplemented with taurine at 0.

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Deep learning (DL) models have provided state-of-the-art performance in various medical imaging benchmarking challenges, including the Brain Tumor Segmentation (BraTS) challenges. However, the task of focal pathology multi-compartment segmentation (e.g.

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Background: Treatment options for patients with melanoma brain metastasis (MBM) have changed significantly in the last decade. Few studies have evaluated changes in outcomes and factors associated with survival in MBM patients over time. The aim of this study is to evaluate changes in clinical features and overall survival (OS) for MBM patients.

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  • Machine learning can work well, but it often struggles to make accurate predictions on new data, which is called out-of-sample generalizability.
  • To solve this problem, researchers are using a method called Federated ML that allows computers to share information about how well they're learning without actually sharing the data itself.
  • In a big study with 71 locations around the world, scientists created a model to help detect brain tumors more accurately, showing a significant improvement compared to older methods and hoping to help with rare illnesses and data sharing in healthcare.
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Purpose: Although glioblastoma (GBM) is the most common primary brain malignancy, few tools exist to pre-operatively risk-stratify patients by overall survival (OS) or common genetic alterations. We developed an MRI-based radiomics model to identify patients with EGFR amplification, MGMT methylation, GBM subtype, and OS greater than 12 months.

Methods: We retrospectively identified 235 patients with pathologically confirmed GBMs from the Cancer Genome Atlas (88; TCGA) and MD Anderson Cancer Center (147; MDACC).

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Accurate skull stripping facilitates following neuro-image analysis. For computer-aided methods, the presence of brain skull in structural magnetic resonance imaging (MRI) impacts brain tissue identification, which could result in serious misjudgments, specifically for patients with brain tumors. Though there are several existing works on skull stripping in literature, most of them either focus on healthy brain MRIs or only apply for a single image modality.

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Introduction: For maximum utility of molecular characterization by next-generation sequencing (NGS) and better understanding of tumor microenvironment with immune correlates analysis, biopsy specimens must yield adequate tumor tissue, and sequential biopsy specimens should sample a consistent site. We developed a web-based lesion selection tool (LST) that enables management and tracking of the biopsy specimen collections.

Methods: Of 145 patients, the LST was used for 88 patients; the other 57 served as controls.

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Background: Immune-checkpoint inhibitors (ICIs) changed the therapeutic landscape of patients with lung cancer. However, only a subset of them derived clinical benefit and evidenced the need to identify reliable predictive biomarkers. Liquid biopsy is the non-invasive and repeatable analysis of biological material in body fluids and a promising tool for cancer biomarkers discovery.

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Accurate glioma subtype classification is critical for the treatment management of patients with brain tumors. Developing an automatically computer-aided algorithm for glioma subtype classification is challenging due to many factors. One of the difficulties is the label constraint.

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Immune therapeutics are revolutionizing cancer treatments. In tandem, new and confounding imaging characteristics have appeared that are distinct from those typically seen with conventional cytotoxic therapies. In fact, only 10% of patients on immunotherapy may show tumor shrinkage, typical of positive responses on conventional therapy.

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