Using 18F-FDG PET/CT-derived body composition features to predict lymphovascular invasion in non-small cell lung cancerPozitron PET/CT Center, Budapest, Hungary.
Department of Biomedical Imaging and Image-Guided Therapy, Division of Nuclear Medicine, Medical University of Vienna, Währinger Gürtel 18-20, Vienna, Austria.
National Koranyi Institute of Pulmonology, Budapest, Hungary.
National Koranyi Institute of Pulmonology, Budapest, Hungary.
National Koranyi Institute of Pulmonology, Budapest, Hungary; Department of Thoracic Surgery, National Institute of Oncology-Semmelweis University, Budapest, Hungary; National Institute of Oncology and National Tumor Biology Laboratory, Budapest, Hungary.
Department of Thoracic Surgery, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
National Koranyi Institute of Pulmonology, Budapest, Hungary; Department of Thoracic Surgery, National Institute of Oncology-Semmelweis University, Budapest, Hungary; Department of Thoracic Surgery, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria; Department of Translational Medicine, Lund University, Lund, Sweden.
Department of Thoracic Surgery, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria; Division of Pulmonology, Department of Medicine II, Medical University of Vienna, Vienna, Austria.
National Koranyi Institute of Pulmonology, Budapest, Hungary; Department of Thoracic Surgery, National Institute of Oncology-Semmelweis University, Budapest, Hungary; Department of Thoracic Surgery, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Department of Biomedical Imaging and Image-Guided Therapy, Division of Nuclear Medicine, Medical University of Vienna, Währinger Gürtel 18-20, Vienna, Austria; Comprehensive Cancer Center, Medical University Vienna, Vienna, Austria.
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2026 (English)In: European Journal of Nuclear Medicine and Molecular Imaging, ISSN 1619-7070, E-ISSN 1619-7089, Vol. 53, no 2, p. 774-785Article in journal (Refereed) Published
Abstract [en]
Abstract: Lymphovascular invasion (LVI) in non-small cell lung cancer (NSCLC) is a critical prognostic marker linked to higher risks of metastasis and recurrence. This study aimed to develop a non-invasive predictive model using body composition features from 18F-FDG PET/CT imaging to assess LVI risk in early-stage NSCLC patients.
Methods: We retrospectively analyzed 248 patients, including 153 from Vienna (training cohort) and 95 from Budapest (validation cohort). Preoperative 18F-FDG PET/CT scans were used to assess tumor metabolic parameters, including standardized uptake values (SUVmax, SUVmean), metabolic tumor volume (MTV), and total lesion glycolysis (TLG), as well as body composition features, including visceral, subcutaneous, and intermuscular adipose tissue, skeletal muscle at L1–L5. LASSO regression identified key body composition features, and a logistic regression-based nomogram was constructed and validated through ROC analysis, calibration, decision curve analysis, and survival analysis.
Results: LVI was present in 66/153 (43.1%) of Vienna and 39/95 (41.1%) of Budapest patients. The nomogram, developed using the Vienna training cohort, incorporating MTV, N stage, and body composition achieved an AUC of 0.839 and 0.790 in the Budapest validation cohort. Statistical tests confirmed that the nomogram significantly outperformed models based on either clinical (p = 7.92e-06) or imaging variables alone (p = 0.0474). Furthermore, LVI predicted by the nomogram was associated with significantly poorer 3-year recurrence-free and 5-year survival.
Conclusion: Integrating body composition with clinical and tumor metabolic features from PET/CT enables preoperative prediction of LVI in NSCLC, supporting improved risk stratification.
Place, publisher, year, edition, pages
Springer Nature, 2026. Vol. 53, no 2, p. 774-785
Keywords [en]
18F-FDG PET/CT, Body composition, Lymphovascular invasion, NSCLC
National Category
Radiology and Medical Imaging
Identifiers
URN: urn:nbn:se:umu:diva-242815DOI: 10.1007/s00259-025-07435-4ISI: 001535241000001PubMedID: 40699302Scopus ID: 2-s2.0-105011285978OAI: oai:DiVA.org:umu-242815DiVA, id: diva2:1987931
2025-08-082025-08-082026-03-31Bibliographically approved