Accurate survival prediction for Non-Small Cell Lung Cancer (NSCLC) patients remains a significant challenge for the scientific and clinical community despite decades of advanced analytics. Addressing this challenge not only helps inform the critical aspects of clinical study design and biomarker discovery but also ensures that the 'right patient' receives the 'right treatment'. However, survival prediction is a highly complex task, given the large number of 'omics; and clinical features, as well as the high degree of freedom that drive patient survival. Prior knowledge could play a critical role in uncovering the complexity of a disease and understanding the driving factors affecting a patient's survival. We introduce a methodology for incorporating prior knowledge into machine learning-based models for prediction of patient survival through Knowledge Graphs, demonstrating the advantage of such an approach for NSCLC patients. Using data from patients treated with immuno-oncologic therapies in the POPLAR (NCT01903993) and OAK (NCT02008227) clinical trials, we found that the use of knowledge graphs yielded significantly improved hazard ratios, including in the POPLAR cohort, for models based on biomarker tumor mutation burden compared with those based on knowledge graphs. Use of a model-defined mutational 10-gene signature led to significant overall survival differentiation for both trials. We provide parameterized code for incorporating knowledge graphs into survival analyses for use by the wider scientific community.
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http://dx.doi.org/10.1186/s12967-024-05509-9 | DOI Listing |
Sci Data
January 2025
Jozef Stefan Institute, Ljubljana, 1000, Slovenia.
Due to growing population and technological advances, global electricity consumption is increasing. Although CO emissions are projected to plateau or slightly decrease by 2025 due to the adoption of clean energy sources, they are still not decreasing enough to mitigate climate change. The residential sector makes up 25% of global electricity consumption and has potential to improve efficiency and reduce CO footprint without sacrificing comfort.
View Article and Find Full Text PDFComput Med Imaging Graph
January 2025
The Department of Computer and Data Science, Case Western Reserve University, Cleveland, OH, USA; The Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, USA.
A generic and versatile CT Image Reconstruction (CTIR) scheme can efficiently mitigate imaging noise resulting from inherent physical limitations, substantially bolstering the dependability of CT imaging diagnostics across a wider spectrum of patient cases. Current CTIR techniques often concentrate on distinct areas such as Low-Dose CT denoising (LDCTD), Sparse-View CT reconstruction (SVCTR), and Metal Artifact Reduction (MAR). Nevertheless, due to the intricate nature of multi-scenario CTIR, these techniques frequently narrow their focus to specific tasks, resulting in limited generalization capabilities for diverse scenarios.
View Article and Find Full Text PDFComput Med Imaging Graph
January 2025
College of Medicine and Biological Information Engineering, Northeastern University, 110819, China. Electronic address:
With the increasing popularity of medical imaging and its expanding applications, posing significant challenges for radiologists. Radiologists need to spend substantial time and effort to review images and manually writing reports every day. To address these challenges and speed up the process of patient care, researchers have employed deep learning methods to automatically generate medical reports.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Background: The structural characteristics of the brain, specifically the decrease of individual gray (or white) matter volumes, provide valuable insights into brain function and cognitive decline, including the development of Alzheimer's disease (AD). In addition, genetic factors can play a significant role in changes in brain volumes, influencing biological activities and interacting in complex ways. In this study, we aim to investigate the relationship between genetic factors, structural brain volume, and the risk of AD.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
The University of Texas Health Science Center at Houston, Houston, TX, USA.
Background: Developing drugs for treating Alzheimer's disease (AD) has been extremely challenging and costly due to limited knowledge on underlying biological mechanisms and therapeutic targets. Repurposing drugs or their combination has shown potential in accelerating drug development due to the reduced drug toxicity while targeting multiple pathologies.
Method: To address the challenge in AD drug development, we developed a multi-task machine learning pipeline to integrate a comprehensive knowledge graph on biological/pharmacological interactions and multi-level evidence on drug efficacy, to identify repurposable drugs and their combination candidates RESULT: Using the drug embedding from the heterogeneous graph representation model, we ranked drug candidates based on evidence from post-treatment transcriptomic patterns, mechanistic efficacy in preclinical models, population-based treatment effect, and Phase 2/3 clinical trials.
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