Evidence map›Paper›PMID 40961812›Full record

ArticleEuropean journal of cancer (Oxford, England : 1990)2025

Single site metastatic rhabdomyosarcoma: An INternational Soft Tissue saRcoma ConsorTium (INSTRuCT) pooled analysis.

Federico Mercolini, Monika Sparber-Sauer, Leo Mascarenhas, Johannes H M Merks, Ewa Koscielniak, Christine M Heske, Julia Chisholm, Beatrice Coppadoro, Semi Harrabi, Dana L Casey and 4 more

Abstract read
In one paragraph

Article in European journal of cancer (Oxford, England : 1990), 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. 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.

Federico MercoliniPediatric Hematology and Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy. Electronic address: federico.mercolini@aosp.bo.it.
Monika Sparber-SauerDepartment of Pediatric Hematology and Oncology, University Children´s Hospital Tuebingen, Tuebingen, Germany; Stuttgart Cancer Center, Zentrum für Kinder-, Jugend, und Frauenmedizin (Olgahospital), Pädiatrie 5 (Pädiatrische Onkologie, Hämatologie, Immunologie), Klinikum der Landeshauptstadt Stuttgart, Stuttgart, Germany.
Leo MascarenhasCedars-Sinai Medical Center, Los Angeles, California, USA.
Johannes H M MerksPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Division of Imaging and Oncology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Ewa KoscielniakStuttgart Cancer Center, Zentrum für Kinder-, Jugend, und Frauenmedizin (Olgahospital), Pädiatrie 5 (Pädiatrische Onkologie, Hämatologie, Immunologie), Klinikum der Landeshauptstadt Stuttgart, Stuttgart, Germany; University of Tübingen, Medical Faculty, Germany.
Christine M HeskePediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
Julia ChisholmChildren and Young People's Unit, Royal Marsden Hospital and Institute of Cancer Research, Sutton, UK.
Beatrice CoppadoroDepartment of Women and Children's Health, University of Padova, Padova, Italy.
Semi HarrabiHeidelberg Ion Beam Therapy Center (HIT), Dept. of Radiation Oncology, Heidelberg University Hospital, Germany.
Dana L CaseyDepartment of Radiation Oncology, University of North Carolina School of Medicine, Chapel Hill, NC, USA.
Guido SeitzDepartment of Pediatric Surgery and Urology, Centre of Pediatric Surgery, University Hospital Giessen-Marburg, Marburg, Germany; Department of Pediatric Surgery, Centre of Pediatric Surgery, University Hospital Giessen-Marburg, Giessen, Germany.
Roshni DasguptaDivison of Pediatric General and Thoracic Surgery, Cincinnati Childrens Hospital Medical Center, University of Cincinnati, Cincinnati, OH, USA.
Rajkumar VenkatramaniDepartment of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Gianni BisognoDepartment of Women and Children's Health, University of Padova, Padova, Italy.

Funding

Intramural NIH HHS Z99 CA999999
6 · The paper itself

Abstract

purposeAlthough the prognosis for patients with metastatic rhabdomyosarcoma (RMS) is generally unfavorable, outcomes can vary significantly depending on the extent of metastatic spread. This study focuses on the specific subgroup of patients presenting with a single metastatic site, aiming to better define their clinical characteristics and outcomes.

methodsPatients with a diagnosis of RMS and single-site metastatic involvement, collected in the INSTRuCT database were included. Clinical and pathological data were analyzed, with event-free survival (EFS) and overall survival (OS) as primary outcomes.

resultsOf 1095 metastatic patients, 497 (45.4 %) had single-site metastasis: 187 in lung, 83 in distant lymph nodes, 72 in bone marrow, 53 in bone, and 102 in other sites. Most patients with lung-only metastasis had embryonal histology. Compared to patients with multiple metastatic sites (5-year EFS: 16.4 %, 95 %CI 13.5-19.6; OS: 19.8 %, 95 % CI 16.6-23.2), those with single-site metastasis had better outcomes, showing 5-year EFS of 39.7 % (95 % CI 33.7-42.4) and OS of 47.0 %, (95 % CI 42.4-51.5) with significant site differences: 5-year OS was 53.3 % (95 % CI 45.8-60.3) for lung, 49.2 % (95 %CI 37.2-60.2) for lymph nodes, and 53.0 % (95 %CI 42.6-62.4) for other sites, but only 33.5 % (95 %CI 20.2-47.3) for bone and 28.7 % (95 %CI 18.5-39.7) for bone marrow (p = 0.0006). The presence of a fusion transcript negatively impacted prognosis for distant nodes (5-year EFS: 35.7 % vs. 63.6 %), lungs (10.0 % vs. 49.5 %), and other sites (13.6 % vs. 65.5 %).

conclusionWithin the patients with metastatic RMS, those with distant tumor isolated in lung, lymph node, or 'other' sites are associated with lower risk of events, while bone and bone marrow metastasis indicate poorest prognosis. The fusion transcript plays an important role in specific subgroups.

Indexed as

Bone NeoplasmsLung NeoplasmsRhabdomyosarcomaSoft Tissue NeoplasmsAdolescentAdultAgedChildChild, PreschoolFemaleHumansInfantLymphatic MetastasisMaleMiddle AgedNeoplasm MetastasisFusion transcriptINSTRuCTRhabdomyosarcomaSingle-site metastases

Identifiers

PMID40961812
PMCPMC13215572

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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.