Evidence map›Paper›PMID 40810863›Full record

ArticlePediatric radiology2025

Early radiologic tumour volume response in non-metastatic rhabdomyosarcoma is not predictive for survival.

Isabelle S A de Vries, Carlo Morosi, Gianni Bisogno, Veronique Minard-Colin, Beatrice Coppadoro, Ilaria Zanetti, Andrea Ferrari, Daniel Orbach, Salma Moalla, Myriam Ben-Arush and 9 more

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Article in Pediatric radiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

19 authors.

Isabelle S A de VriesPrincess Máxima Center for Pediatric Oncology, Heidelberglaan 25, 3584 CS, Utrecht, Netherlands. i.s.a.devries-10@prinsesmaximacentrum.nl.
Carlo MorosiDepartment of Radiology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Gianni BisognoDepartment of Women's and Children's Health, University of Padua, Padua, Italy.
Veronique Minard-ColinDepartment of Pediatric and Adolescent Oncology, Gustave-Roussy, Université Paris-Saclay, Villejuif, France.
Beatrice CoppadoroDepartment of Women's and Children's Health, University of Padua, Padua, Italy.
Ilaria ZanettiPediatric Hematology Oncology Division, University Hospital of Padua, Padua, Italy.
Andrea FerrariPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Daniel OrbachSIREDO Oncology Center (Care, Innovation and Research for Children, Adolescents and Young Adults with Cancer), PSL University, Institut Curie, Paris, France.
Salma MoallaDepartment of Pediatric and Adolescent Oncology, Gustave-Roussy, Université Paris-Saclay, Villejuif, France.
Myriam Ben-ArushRambam Medical Center, Joan and Sanford Weill Pediatric Hematology Oncology and Bone Marrow Transplantation Division, Ruth Rappaport Children's Hospital, Haifa, Israel.
Christine DevalckDepartment Hematology Oncology, HUDERF, ULB, HUB, Brussels, Belgium.
Roelof van EwijkPrincess Máxima Center for Pediatric Oncology, Heidelberglaan 25, 3584 CS, Utrecht, Netherlands.
Kieran McHughDepartment of Radiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.
Meriel JenneyDepartment of Paediatric Oncology, Children's Hospital for Wales, Heath Park, Cardiff, United Kingdom.
Julia ChisholmChildren and Young Peoples Unit, Royal Marsden Hospital and Institute of Cancer Research, Sutton, United Kingdom.
Gabriela GuillenDepartment of Pediatric Surgery, Hospital Infantil Universitari Vall d'Hebron, Barcelona, Spain.
Henry MandevilleDepartment of Radiotherapy, Royal Marsden Hospital and The Institute of Cancer Research, Sutton, United Kingdom.
Johannes H M MerksPrincess Máxima Center for Pediatric Oncology, Heidelberglaan 25, 3584 CS, Utrecht, Netherlands.
Rick R Van RijnDepartment of Radiology and Nuclear Medicine, Amsterdam UMC - Emma Children's Hospital, University of Amsterdam, Amsterdam, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is an urgent need for early radiological markers predicting survival in paediatric rhabdomyosarcoma patients.

objectiveTo analyse the predictive value of early radiological tumour volume response to chemotherapy in non-metastatic rhabdomyosarcoma patients.

methodsThe European paediatric Soft tissue sarcoma Study Group (EpSSG) RMS 2005 study prospectively included non-metastatic rhabdomyosarcoma patients. Patients with Intergroup Rhabdomyosarcoma Studies (IRS) postsurgical Group III (i.e. measurable disease) at diagnosis, with three tumour diameters available at diagnosis and following three cycles of chemotherapy, were included. Tumour response was categorized as complete response, partial response, minor partial response, stable disease, or progressive disease. Patients with progressive disease were excluded from analyses. Failure-free survival and overall survival were estimated with Kaplan-Meier using a landmark analysis. Prognostic factors were assessed using Cox proportional hazards analyses.

resultsOf 1,674 patients aged < 18 years at diagnosis included in the EpSSG RMS 2005 study, 613 patients (median age 4.2 years, interquartile range 2.2-8.0, 346 males) were eligible for analysis. After three cycles of chemotherapy, 48 patients reached complete response, 371 partial response, 139 minor partial response, 48 stable disease, and seven patients progressive disease. Univariate Cox proportional hazards model showed no significant difference between response groups for failure-free survival or overall survival. In multivariate Cox regression analysis, tumour volume response was not an independent prognostic factor for failure-free survival or overall survival.

conclusionEarly radiological tumour volume response after the third cycle of neoadjuvant chemotherapy, with exclusion of progressive disease, does not predict survival in paediatric rhabdomyosarcoma patients.

Indexed as

RhabdomyosarcomaAdolescentChildChild, PreschoolFemaleHumansInfantMalePredictive Value of TestsPrognosisProspective StudiesSurvival RateTreatment OutcomeTumor BurdenPaediatric oncologyRadiological response assessmentRhabdomyosarcomaTumour volume

Identifiers

PMID40810863
PMCPMC12513956

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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.