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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorde Vries, Isabelle S. A.
dc.contributor.authorZanetti, Ilaria
dc.contributor.authorMorosi, Carlo
dc.contributor.authorBisogno, Gianni
dc.contributor.authorMinard-Colin, Veronique
dc.contributor.authorCoppadoro, Beatrice
dc.contributor.authorGuillén Burrieza, Gabriela
dc.date.accessioned2025-10-31T07:25:50Z
dc.date.available2025-10-31T07:25:50Z
dc.date.issued2025-09
dc.identifier.citationde Vries ISA, Morosi C, Bisogno G, Minard-Colin V, Coppadoro B, Zanetti I, et al. Early radiologic tumour volume response in non-metastatic rhabdomyosarcoma is not predictive for survival. Pediatr Radiol. 2025 Sep;55:2160–70.
dc.identifier.issn1432-1998
dc.identifier.urihttp://hdl.handle.net/11351/13989
dc.descriptionPaediatric oncology; Radiological response assessment; Rhabdomyosarcoma
dc.description.abstractBackground There is an urgent need for early radiological markers predicting survival in paediatric rhabdomyosarcoma patients. Objective To analyse the predictive value of early radiological tumour volume response to chemotherapy in non-metastatic rhabdomyosarcoma patients. Methods The 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. Results Of 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. Conclusion Early radiological tumour volume response after the third cycle of neoadjuvant chemotherapy, with exclusion of progressive disease, does not predict survival in paediatric rhabdomyosarcoma patients.
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofseriesPediatric Radiology;55
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectTumors de parts toves - Quimioteràpia
dc.subjectTumors de parts toves - Radioteràpia
dc.subjectTumors de parts toves - Prognosi
dc.subject.meshRhabdomyosarcoma
dc.subject.mesh/drug therapy
dc.subject.meshTumor Burden
dc.subject.meshRadiotherapy
dc.subject.meshPrognosis
dc.titleEarly radiologic tumour volume response in non-metastatic rhabdomyosarcoma is not predictive for survival
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1007/s00247-025-06359-3
dc.subject.decsrabdomiosarcoma
dc.subject.decs/farmacoterapia
dc.subject.decscarga tumoral
dc.subject.decsradioterapia
dc.subject.decspronóstico
dc.relation.publishversionhttps://doi.org/10.1007/s00247-025-06359-3
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[de Vries ISA] Princess Máxima Center for Pediatric Oncology, CS Utrecht, Netherlands. [Morosi C] Department of Radiology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy. [Bisogno G] Department of Women’s and Children’s Health, University of Padua, Padua, Italy. Pediatric Hematology Oncology Division, University Hospital of Padua, Padua, Italy. [Minard Colin V] Department of Pediatric and Adolescent Oncology, Gustave-Roussy, Université Paris-Saclay, Villejuif, France. [Coppadoro B] Department of Women’s and Children’s Health, University of Padua, Padua, Italy. [Zanetti I] Pediatric Hematology Oncology Division, University Hospital of Padua, Padua, Italy. [Guillen G] Servei de Cirurgia Pediàtrica, Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid40810863
dc.identifier.wos001551367000001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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