Related Experiment Video
Updated: Jan 11, 2026

Predictive Immune Modeling of Solid Tumors
Published on: February 25, 2020
A prognostic index integrating deep learning baseline PET/CT biomarkers and multi-omics profiling in diffuse large B
Yue Wang1, Xue Wang2, Xin-Yun Huang3
1Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics, National Research Center for Translational Medicine at Shanghai, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
None:
[18F]-Fluorodeoxyglucose (FDG)-positron emission tomography (PET)/computed tomography (CT) is essential for disease staging and treatment response evaluation in diffuse large B cell lymphoma (DLBCL). In this study, we analyze 18F-FDG-PET scans from 1,024 newly diagnosed DLBCL patients, integrating with DNA and RNA sequencing data. Using the nnUNet deep learning framework and training on both AutoPET public and in-house datasets, we identify key baseline biomarkers-including total metabolic tumor volume (TMTV), Max MTV, and the standardized tumor dissemination biomarker-that demonstrate significant prognostic value. Further integrating PET biomarkers with clinical factors and LymphPlex genetic subtypes, we develop high TMTV, elevated lactate dehydrogenase (LDH), and EZB-like MYC+, MCD-like, and TP53Mut subtypes as risk factors to form the ClinicalPET LymphPlex model, efficiently distinguishing patient outcomes across different treatments. Notably, high TMTV correlates with an immunosuppressive tumor microenvironment, while elevated LDH is linked to increased metabolic activity and tumor proliferation. Collectively, our findings necessitate multimodal integration to enhance prognostic precision and advance personalized therapy in DLBCL.

