Abstract
The aim of this study was to evaluate the benefit of a volumetric AI-based body composition analysis (BCA) algorithm in multiple myeloma (MM). Therefore, a retrospective monocentric cohort of 91 MM patients was analyzed. The BCA algorithm, powered by a convolutional neural network, quantified tissue compartments and bone density based on routine CT scans. Correlations between BCA data and demographic/clinical parameters were investigated. BCA-endotypes were identified and survival rates were compared between BCA-derived patient clusters. Patients with high-risk cytogenetics exhibited elevated cardiac marker index values. Across Revised-International Staging System (R-ISS) categories, BCA parameters did not show significant differences. However, both subcutaneous and total adipose tissue volumes were significantly lower in patients with progressive disease or death during follow-up compared to patients without progression. Cluster analysis revealed two distinct BCA-endotypes, with one group displaying significantly better survival. Furthermore, a combined model composed of clinical parameters and BCA data demonstrated a higher predictive capability for disease progression compared to models based solely on high-risk cytogenetics or R-ISS. These findings underscore the potential of BCA to improve patient stratification and refining prognostic models in MM.
| Original language | English |
|---|---|
| Article number | 26455 |
| Journal | Scientific Reports |
| Volume | 15 |
| Issue number | 1 |
| ISSN | 2045-2322 |
| DOIs | |
| Publication status | Published - 12.2025 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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SDG 9 Industry, Innovation, and Infrastructure
Research Areas and Centers
- Centers: Center for Artificial Intelligence Luebeck (ZKIL)
- Academic Focus: Center for Infection and Inflammation Research (ZIEL)
- Academic Focus: Biomedical Engineering
- Research Area: Luebeck Integrated Oncology Network (LION)
DFG Research Classification Scheme
- 2.21-05 Immunology
- 2.22-07 Medical Informatics and Medical Bioinformatics
- 2.22-32 Medical Physics, Biomedical Technology
- 2.22-18 Rheumatology
- 2.22-14 Hematology, Oncology
- 4.43-04 Artificial Intelligence and Machine Learning Methods
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