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Purpose: The present study aimed to investigate the role of body composition as an independent image-derived biomarker for clinical outcome prediction in a clinical trial cohort of patients with relapsed or refractory (rel/ref) diffuse large B-cell lymphoma (DLBCL) treated with loncastuximab tesirine.
Materials And Methods: The imaging cohort consisted of positron emission tomography/computed tomography scans of 140 patients with rel/ref DLBCL treated with loncastuximab tesirine in the LOTIS-2 (ClinicalTrials.gov identifier: NCT03589469) trial. Body composition analysis was conducted using both manual and deep learning-based segmentation of three primary tissue compartments-skeletal muscle (SM), subcutaneous fat (SF), and visceral fat (VF)-at the L3 level from baseline CT scans. From these segmented compartments, body composition ratio indices, including SM*/VF*, SF*/VF*, and SM*/(VF*+SF*), were derived. Pearson's correlation analysis was used to examine the agreement between manual and automated segmentation. Logistic regression analyses were used to assess the association between the derived indices and treatment response. Cox regression analyses were used to determine the effect of body composition indices on time-to-event outcomes. Body composition indices were considered as continuous and binary variables defined by cut points. The Kaplan-Meier method was used to estimate progression-free survival (PFS) and overall survival (OS).
Results: The manual and automated SM*/VF* indices, as dichotomized, were significant predictors in univariable and multivariable logistic models for failure to achieve complete metabolic response. The manual SM*/VF* index as dichotomized was significantly associated with PFS, but not OS, in univariable and multivariable Cox models.
Conclusion: The pretreatment SM*/VF* body composition index shows promise as a biomarker for patients with rel/ref DLBCL undergoing treatment with loncastuximab tesirine. The proposed deep learning-based approach for body composition analysis demonstrated comparable performance to the manual process, presenting a more cost-effective alternative to conventional methods.
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http://dx.doi.org/10.1200/CCI-25-00051 | DOI Listing |
Abdom Radiol (NY)
September 2025
Research Centre for Optimal Health, School of Life Sciences, University of Westminster, London, UK.
Objectives: The escalating global incidence of obesity, cardiometabolic disease and sarcopenia necessitates reliable body composition measurement tools. MRI-based assessment is the gold standard, with utility in both clinical and drug trial settings. This study aims to validate a new automated volumetric MRI method by comparing with manual ground truth, prior volumetric measurements, and against a new method for semi-automated single-slice area measurements.
View Article and Find Full Text PDFEur J Heart Fail
September 2025
Institute for Exercise and Environmental Medicine, Texas Health Presbyterian Hospital Dallas, Dallas, TX, USA.
Aims: Obesity is commonly hypothesized to lead to the development of heart failure (HF) in part due to increases in blood volume (BV) and left ventricular (LV) remodelling. Whether adiposity and obesity severity are associated with BV expansion and subsequent LV remodelling in middle-aged individuals at increased risk (IR) prior to the onset of HF is unknown.
Methods And Results: We analysed data from 96 middle-aged (40-64 years) non-obese (25.
Pediatr Pulmonol
September 2025
Department of Medicine, Division of Diabetes, Endocrinology and Metabolism, University of Minnesota, Minneapolis, Minnesota, USA.
Background: The approval of cystic fibrosis transmembrane conductance regulator modulators elexacaftor/tezacaftor/ivacaftor (ETI), has significantly improved pulmonary function for people with cystic fibrosis (pwCF). However, the effects on CF-related bone disease and body composition remain unclear.
Methods: This retrospective real-world study examined adults with CF who received ETI treatment.
Int J Environ Health Res
September 2025
Unidad Interinstitucional de Investigación Clínica y Epidemiológica, Facultad de Medicina, Universidad Autónoma de Yucatán, Mérida, México.
The human microbiota consists of millions of microorganisms, predominantly bacteria, that inhabit the body and form communities. Each human body site has a unique population that is specifically adapted to complement the metabolic functions of the environments in which they are present. These microbial communities begin to form at birth, with their primary establishment occurring during the early years of childhood and persisting in adulthood.
View Article and Find Full Text PDFJ Obes
September 2025
School of Natural Sciences, University of Lincoln, Lincoln, UK.
To investigate the genetic determinants of fat distribution across anatomical sites and their implications for health outcomes. We analyzed neck-to-knee MRI data from the UK Biobank ( = 37,589) to measure fat at various locations and used Mendelian randomization to assess effects on 26 obesity-related diseases and 94 biomarkers from FinnGen and other consortia. We identified genetic loci associated with 10 fat depots: abdominal subcutaneous adipose tissue ( = 2 loci), thigh subcutaneous adipose tissue (25), thigh intermuscular adipose tissue (15), visceral adipose tissue (7), liver proton density fat fraction (PDFF) (8), pancreas PDFF (11), paraspinal adipose tissue (9), pelvic bone marrow fat (28), thigh bone marrow fat (27), and vertebrae bone marrow fat (5).
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