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dc.contributor.authorTerwisscha van Scheltinga, SEJ
dc.contributor.authorWijnen, MHWA
dc.contributor.authorMartelli, H
dc.contributor.authorRogers, T
dc.contributor.authorMandeville, H
dc.contributor.authorGaze, MN
dc.contributor.authorMcHugh, K
dc.contributor.authorCorradini, N
dc.contributor.authorOrbach, D
dc.contributor.authorJenney, M
dc.contributor.authorKelsey, A
dc.contributor.authorChisholm, J
dc.contributor.authorGallego, S
dc.contributor.authorGlosli, H
dc.contributor.authorFerrari, A
dc.contributor.authorZanetti, I
dc.contributor.authorDe Salvo, GL
dc.contributor.authorMinard-Colin, V
dc.contributor.authorBisogno, G
dc.contributor.authorvan Noesel, MM
dc.contributor.authorMerks, HHM
dc.date.accessioned2021-12-07T09:27:06Z
dc.date.available2021-12-07T09:27:06Z
dc.identifier.citationCancer medicine, 2020, 9 (20), pp. 7580 - 7589
dc.identifier.issn2045-7634
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4910
dc.identifier.eissn2045-7634
dc.identifier.doi10.1002/cam4.3365
dc.description.abstractRhabdomyosarcoma of the extremities present with two main challenges: correct evaluation of initial regional nodal involvement and define adequate local treatment. Methods Pediatric patients with localized rhabdomyosarcoma of the extremity included in the EpSSG-RMS2005 study between 2005 and 2014 were evaluated for staging, treatment, and survival. The outcome was compared to the preceding European SIOP-MMT studies. Results Of the 162 patients included, histology was unfavorable in 113 (70%), 124 (77%) were younger than 10 years, 128 (79%) were IRS III, and 47 (29%) were node-positive. A regional node biopsy was performed in 97 patients (60%) and modified the lymph node stage in 15/97 (16%). Primary and delayed surgery was performed in 155 (96%) and radiotherapy delivered in 118 (73%) patients. Relapse occurred in 61 cases (38%), local in 14 (23%), regional in 13 (21%), distant in 22 (36%), and combined relapse in 12 (20%) with five progressive diseases (8%) and four secondary tumors (7%). Five-year event free (EFS) and overall survival (OS) were 58.4% (95%CI, 50.3-65.7) and 71.7% (63.6-78.4), respectively. In the previous studies MMT89 and MMT95, tumor surgery was performed in 32/53 (60%) and 74/82(90%), respectively, and radiotherapy delivered in 13/53 (25%) and 26/82 (30%), respectively. Five-year EFS and OS were 35.6%, and 50.3% in MMT89 and 54.3% and 68.2% in the MMT95 study. Conclusions Even if the lymph node staging was not always complete according to the RMS2005 protocol, node sampling changed lymph node status in a significant number of patients. Despite the higher rate of patients treated with locoregional radiotherapy, survival in RMS2005 did not improve compared to the previous European SIOP-MMT95 study.
dc.formatPrint-Electronic
dc.format.extent7580 - 7589
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectExtremities
dc.subjectHumans
dc.subjectRhabdomyosarcoma
dc.subjectNeoplasm Metastasis
dc.subjectRecurrence
dc.subjectDiagnostic Imaging
dc.subjectBiopsy
dc.subjectNeoplasm Staging
dc.subjectPrognosis
dc.subjectTreatment Outcome
dc.subjectCombined Modality Therapy
dc.subjectTumor Burden
dc.subjectSurvival Analysis
dc.subjectAdolescent
dc.subjectChild
dc.subjectChild, Preschool
dc.subjectInfant
dc.subjectDisease Management
dc.subjectFemale
dc.subjectMale
dc.subjectClinical Decision-Making
dc.titleLocal staging and treatment in extremity rhabdomyosarcoma. A report from the EpSSG-RMS2005 study.
dc.typeJournal Article
dcterms.dateAccepted2020-07-20
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1002/cam4.3365
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfCancer medicine
pubs.issue20
pubs.notesNo embargo
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Sarcoma Clinical Trials in Children and Young People
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Sarcoma Clinical Trials in Children and Young People/Sarcoma Clinical Trials in Children and Young People (hon.)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Sarcoma Clinical Trials in children and young people
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Sarcoma Clinical Trials in children and young people/Sarcoma Clinical Trials in Children and Young People (hon.)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Paediatric and Adolescent Radiotherapy
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.publication-statusPublished
pubs.volume9
pubs.embargo.termsNo embargo
icr.researchteamSarcoma Clinical Trials in children and young people
icr.researchteamPaediatric and Adolescent Radiotherapy
dc.contributor.icrauthorMandeville, Henryen_US
dc.contributor.icrauthorChisholm, Juliaen_US


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