Malignant lymphomas encompass a range of malignancies with incidence rising globally, particularly with age. In younger populations, Hodgkin and Burkitt lymphomas predominate, while older populations more commonly experience subtypes such as diffuse large B-cell, follicular, marginal zone, and mantle cell lymphomas. Positron emission tomography/computed tomography (PET/CT) using [F] fluorodeoxyglucose (FDG) is the gold standard for staging, treatment response assessment, and prognostication in lymphoma. However, interpretation of PET/CT is complex, time-consuming, and reliant on expert imaging specialists, exacerbating challenges associated with workforce shortages worldwide. Artificial intelligence (AI) offers transformative potential across multiple aspects of PET/CT imaging in this setting. AI applications in appointment planning have demonstrated utility in reducing nonattendance rates and improving departmental efficiency. Advanced reconstruction techniques leveraging convolutional neural networks (CNNs) enable reduced injected activities of radiopharmaceutical and patient dose whilst maintaining diagnostic accuracy, particularly benefiting younger patients requiring multiple scans. Automated segmentation tools, predominantly using 3D U-Net architectures, have improved quantification of metrics such as total metabolic tumour volume (TMTV) and total lesion glycolysis (TLG), facilitating prognostication and treatment stratification. Despite these advancements, challenges remain, including variability in segmentation performance, impact on Deauville Score interpretation, and standardization of TMTV/TLG measurements. Emerging large language models (LLMs) also show promise in enhancing PET/CT reporting, converting free-text reports into structured formats, and improving patient communication. Further research is required to address limitations such as AI-induced errors, physiological uptake differentiation, and the integration of AI models into clinical workflows. With robust validation and harmonization, AI integration could significantly enhance lymphoma care, improving diagnostic precision, workflow efficiency, and patient outcomes.
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http://dx.doi.org/10.1053/j.semnuclmed.2025.02.007 | DOI Listing |
J Cutan Med Surg
March 2025
Department of Dermatology, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Mycosis fungoides (MF) and Sézary syndrome (SS) are subtypes of cutaneous T-cell lymphoma with numerous topical and systemic therapies. Early-stage MF can be managed with topical corticosteroids, mechlorethamine, and phototherapy. However, patients are often non-responsive to topical therapies, thus requiring systemic therapies.
View Article and Find Full Text PDFFront Immunol
March 2025
Department of Immunology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Recent studies have highlighted the potential contribution of CD4 T cells with cytotoxic activity (CD4 CTLs) to anti-tumor immunity. However, their precise roles remain elusive, partly due to the absence of specific markers defining CD4 CTLs with target-killing potential in humans. We previously demonstrated that Epstein-Barr virus (EBV)-driven immortalized B cell lines efficiently induce human CD4 CTLs with cytotoxic functions comparable to cytotoxic CD8 T cells (CD8 CTLs).
View Article and Find Full Text PDFJ Biochem Mol Toxicol
March 2025
Biochemistry Department, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, Egypt.
Colorectal cancer (CRC) is a multicomponent disease and the second most frequent root of cancer-related deaths globally. Linagliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor. It has been repurposed in recent experimental studies due to its marked anti-inflammatory activities.
View Article and Find Full Text PDFJ Hematol Oncol
March 2025
Department of Hematology, The First Hospital of China Medical University, Shenyang, 110001, Liaoning Province, China.
Lymphoma, a malignant tumor derived from lymphocytes and lymphoid tissues, presents with complex and heterogeneous clinical manifestations, requiring accurate patient classification for appropriate treatment. While invasive pathological examination of lymph nodes or lymphoid tissue remains the gold standard for lymphoma diagnosis, its utility is limited in cases of deep-seated tumors such as intraperitoneal and central nervous system lymphomas. In addition, biopsy procedures carry an inherent risk of complications.
View Article and Find Full Text PDFSemin Nucl Med
March 2025
Faculty of Medicine, University of Leeds, Leeds LS2 9JT, England; Department of Radiology, St James's University Hospital, Leeds Teaching Hospitals NHS Trust, Leeds, LS9 7TF, England. Electronic address:
Malignant lymphomas encompass a range of malignancies with incidence rising globally, particularly with age. In younger populations, Hodgkin and Burkitt lymphomas predominate, while older populations more commonly experience subtypes such as diffuse large B-cell, follicular, marginal zone, and mantle cell lymphomas. Positron emission tomography/computed tomography (PET/CT) using [F] fluorodeoxyglucose (FDG) is the gold standard for staging, treatment response assessment, and prognostication in lymphoma.
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