Evidence map›Paper›PMID 40705262›Full record

ArticleAnnals of surgical oncology2025

Surgical Lymph Node Staging in Extremity Rhabdomyosarcoma: The EpSSG RMS 2005 Trial Experience.

Sheila Terwisscha van Scheltinga, Johannes H M Merks, Florent Guerin, Timothy Rogers, Ross J Craigie, Gabriela Guillén, Federica De Corti, Patrizia Dall'Igna, Raquel Dávila Fajardo, Gianni Bisogno and 13 more

Abstract read
In one paragraph

Article in Annals of surgical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Observational
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

23 authors.

Sheila Terwisscha van ScheltingaPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands. s.terwisscha@prinsesmaximacentrum.nl.ORCID http://orcid.org/0000-0001-7993-0208
Johannes H M MerksPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Florent GuerinDepartment of Pediatric Surgery, Assistance Publique Hôpitaux de Paris, University Paris-Saclay, Le Kremlin Bicêtre, France.
Timothy RogersUniversity Hospitals Bristol and Weston NHS Foundation Trust, Bristol, UK.
Ross J CraigieDepartment of Pediatric Surgery, Royal Manchester Children's Hospital, Manchester, UK.
Gabriela GuillénDepartment of Pediatric Surgery, Pediatric Surgical Oncology Unit, Hospital Vall d'Hebron, Barcelona, Spain.
Federica De CortiPediatric Surgery, Women's and Children's Health Department, University Hospital of Padua, Padua, Italy.
Patrizia Dall'IgnaPediatric Surgery, Women's and Children's Health Department, University Hospital of Padua, Padua, Italy.
Raquel Dávila FajardoPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Gianni BisognoDepartment of Women's and Children's Health, Pediatric Hematology Oncology Division, University Hospital of Padua, University of Padua, Padua, Italy.
Andrea FerrariDepartment of Pediatric Oncology, National Tumour Institute, Milan, Italy.
Daniel OrbachSIREDO Oncology Center (Care, Innovation and Research for Children, Adolescents and Young Adults with Cancer), Institut Curie, PSL University, Paris, France.
Meriel JenneyDepartment of Pediatric Oncology, University Hospital of Wales, Cardiff, UK.
Julia C ChisholmChildren and Young People's Unit, Royal Marsden Hospital and Institute of Cancer Research, Sutton, UK.
Véronique Minard-ColinDepartment of Pediatric and Adolescent Oncology, Gustave Roussy, Villejuif, France.
Maya CesenPediatric Hematology and Oncology Department, University Children's Hospital, Ljubliana, Slovenia.
Nina JehannoDepartment of Nuclear Medicine, Institut Curie, Paris, France.
Laura S Hiemcke-JiwaPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Ilaria ZanettiDepartment of Women's and Children's Health, Pediatric Hematology Oncology Division, University Hospital of Padua, University of Padua, Padua, Italy.
Beatrice CoppadoroDepartment of Women's and Children's Health, Pediatric Hematology Oncology Division, University Hospital of Padua, University of Padua, Padua, Italy.
Alida F W van der SteegPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Max M van NoeselPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Marc H W A WijnenPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe European pediatric soft tissue Sarcoma Study Group (EpSSG) RMS 2005 study recommends a lymph node biopsy for extremity rhabdomyosarcoma (RMS). The aim of our study was to analyze the results of the lymph node sampling strategies used, such as sentinel node biopsy (SNB) and nodal sampling (NS), and compare the outcome of patients undergoing different nodal staging techniques.

methodsAll non-metastatic (M0) patients registered in the EpSSG RMS 2005 study with an RMS of the extremity, presenting between 2005 and 2016, were included for analysis of the lymph node sampling techniques used. The secondary objective was to compare the results and outcome for the different sampling procedures.

resultsOf 198 patients, 144 had clinically/radiologically negative nodes (cN0), and 72/144 underwent a biopsy (26 SNB/46 NS). Final nodal status was upstaged to pN1 in 11/72 (15.3%) patients-6 after SNB and 5 after NS. In 54 radiologically malignant/suspicious-appearing nodes, 34 NS biopsies were performed, resulting in downstaging to N0 in 9/34 (26.5%) patients. 5-years overall survival (OS) of N0 patients versus N1 patients was 82.5% (95% confidence interval CI 74.7-88.0) versus 46.5% (95% CI 32.2-59.7). 5-years OS in N0 patients was not significantly different in biopsied and non-biopsied patients (p = 0.88). However, in N1 patients, survival was significantly better in biopsied compared with non-biopsied patients (p = 0.006).

conclusionLymph node staging plays a crucial role in determining appropriate treatment strategies. Pathology of sampled lymph nodes can upstage or downstage the lymph node status, guiding treatment decisions based on the stage.

Indexed as

ExtremitiesLymph Node ExcisionLymph NodesRhabdomyosarcomaSentinel Lymph Node BiopsyAdolescentChildChild, PreschoolFemaleFollow-Up StudiesHumansInfantLymphatic MetastasisMaleNeoplasm StagingPrognosisBiopsyExtremityLymph nodesPediatricRhabdomyosarcomaSentinel nodeStaging

Identifiers

PMID40705262
PMCPMC12454586

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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.