Evidence map›Paper›PMID 38421522›Full record

ArticleClinical & experimental metastasis2024

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 and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical & experimental metastasis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Advances inWorld journal of radiology · 2025
    Review
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 1 country.

Anton Burkhard-MeierDepartment of Medicine III, University Hospital, LMU Munich, Munich, Germany. anton.burkhardmeier@med.uni-muenchen.de.
Vindi JurinovicDepartment of Medicine III, University Hospital, LMU Munich, Munich, Germany.
Luc M BerclazDepartment of Medicine III, University Hospital, LMU Munich, Munich, Germany.
Markus AlbertsmeierDepartment of General, Visceral and Transplantation Surgery, University Hospital, LMU Munich, Munich, Germany.
Hans Roland DürrDepartment of Orthopedics and Trauma Surgery, University Hospital, LMU Munich, Munich, Germany.
Alexander KleinDepartment of Orthopedics and Trauma Surgery, University Hospital, LMU Munich, Munich, Germany.
Thomas KnöselInstitute of Pathology, University Hospital, LMU Munich, Munich, Germany.
Dorit Di GioiaDepartment of Medicine III, University Hospital, LMU Munich, Munich, Germany.
Lena M UnterrainerDepartment of Nuclear Medicine, University Hospital, LMU Munich, Munich, Germany.
Nina-Sophie Schmidt-HegemannDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Jens RickeDepartment of Radiology, University Hospital, LMU Munich, Munich, Germany.
Michael von Bergwelt-BaildonDepartment of Medicine III, University Hospital, LMU Munich, Munich, Germany.
Wolfgang G Kunz *Department of Radiology, University Hospital, LMU Munich, Munich, Germany.
Lars H Lindner *Department of Medicine III, University Hospital, LMU Munich, Munich, Germany.
LMU Klinikum · DELudwig-Maximilians-Universität München · DEZimmer Biomet (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

SarcomaSoft Tissue NeoplasmsFluorodeoxyglucose F18HumansLymphatic MetastasisLymph NodesNecrosisPositron Emission Tomography Computed TomographyRetrospective StudiesFluorodeoxyglucose F18Lymph node metastasisPredictive parametersSoft tissue sarcomaStaging imaging

Identifiers

PMID38421522
PMCPMC10973039
OpenAlexW4392295203

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.