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Differentiation of benign and metastatic lymph nodes in soft tissue sarcoma

Anton Burkhard-Meier; Vindi Jurinovic; Luc M. Berclaz; Markus Albertsmeier; Hans Roland Dürr; Alexander Klein; Thomas Knösel; Dorit Di Gioia; Lena M. Unterrainer; Nina-Sophie Schmidt-Hegemann; Jens Ricke; Michael von Bergwelt-Baildon; Wolfgang G. Kunz; Lars H. Lindner
Clinical & Experimental Metastasis · Vol. 41, Issue 2 · pp. 131-141 · 2024

Abstract

Lymph node metastasis (LNM) occurs in less than 5% of soft tissue sarcoma (STS) patients and indicates an aggressive course of disease. Suspicious lymph nodes (LN) in staging imaging are a frequent topic of discussion in multidisciplinary tumor boards. Predictive markers are needed to facilitate stratification and improve treatment of STS patients. In this study, 56 STS patients with radiologically suspicious and subsequently histologically examined LN were reviewed. Patients with benign (n = 26) and metastatic (n = 30) LN were analyzed with regard to clinical, laboratory and imaging parameters. Patients with LNM exhibited significantly larger short axis diameter (SAD) and long axis diameter (LAD) vs. patients with benign LN (median 22.5 vs. 14 mm, p < 0.001 and median 29.5 vs. 21 mm, p = 0.003, respectively). Furthermore, the presence of central necrosis and high maximal standardized uptake value (SUVmax) in FDG-PET-CT scans were significantly associated with LNM (60 vs. 11.5% of patients, p < 0.001 and median 8.59 vs. 3.96, p = 0.013, respectively). With systemic therapy, a slight median size regression over time was observed in both metastatic and benign LN. Serum LDH and CRP levels were significantly higher in patients with LNM (median 247 vs. 187.5U/L, p = 0.005 and 1.5 vs. 0.55 mg/dL, p = 0.039, respectively). This study shows significant associations between LNM and imaging features as well as laboratory parameters of STS patients. The largest SAD, SUVmax in FDG-PET-CT scan, the presence of central necrosis, and high serum LDH level are the most important parameters to distinguish benign from metastatic LNs.

Bibliographic Information

JournalClinical & Experimental Metastasis
PublisherSpringer
Publication Date2024-04-01
Publication Year2024
Volume41
Issue2
Pages131-141
Document TypeJournal Article
eISSN1573-7276
DOI10.1007/s10585-024-10273-7

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NARA Access Coverage1983-01-01~Current
Journal Homepagehttps://www.springer.com/journal/10585
Publisher PageOpen Publisher Page
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