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dc.contributor.authorGallego, S
dc.contributor.authorChi, Y-Y
dc.contributor.authorDe Salvo, GL
dc.contributor.authorLi, M
dc.contributor.authorMerks, JHM
dc.contributor.authorRodeberg, DA
dc.contributor.authorvan Scheltinga, ST
dc.contributor.authorMascarenhas, L
dc.contributor.authorOrbach, D
dc.contributor.authorJenney, M
dc.contributor.authorMillion, L
dc.contributor.authorMinard-Colin, V
dc.contributor.authorWolden, S
dc.contributor.authorZanetti, I
dc.contributor.authorParham, DM
dc.contributor.authorMandeville, H
dc.contributor.authorVenkatramani, R
dc.contributor.authorBisogno, G
dc.contributor.authorHawkins, DS
dc.contributor.authorEuropean paediatric Soft tissue sarcoma Study Group and Children's Oncology Group
dc.coverage.spatialUnited States
dc.date.accessioned2024-04-30T15:55:03Z
dc.date.available2024-04-30T15:55:03Z
dc.date.issued2021-03-01
dc.identifierARTN e28832
dc.identifier.citationPediatric Blood and Cancer, 2021, 68 (3), pp. e28832 -
dc.identifier.issn1545-5009
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/6213
dc.identifier.eissn1545-5017
dc.identifier.eissn1545-5017
dc.identifier.doi10.1002/pbc.28832
dc.identifier.doi10.1002/pbc.28832
dc.description.abstractBACKGROUND: Treatment of children and adolescents with alveolar rhabdomyosarcoma (ARMS) and regional nodal involvement (N1) have been approached differently by North American and European cooperative groups. In order to define a better therapeutic strategy, we analyzed two studies conducted between 2005 and 2016 by the European paediatric Soft tissue sarcoma Study Group (EpSSG) and Children's Oncology Group (COG). METHODS: We retrospectively identified patients with ARMS N1 enrolled in either EpSSG RMS2005 or in COG ARST0531. Chemotherapy in RMS2005 comprised ifosfamide + vincristine + dactinomycin + doxorubicin (IVADo), IVA and maintenance (vinorelbine, cyclophosphamide); in ARST0531, it consisted of either vincristine + dactinomycin + cyclophosphamide (VAC) or VAC alternating with vincristine + irinotecan (VI). Local treatment was similar in both protocols. RESULTS: The analysis of the clinical characteristics of 239 patients showed some differences between study groups: in RMS2005, advanced Intergroup Rhabdomyosarcoma Study Group (IRS) and large tumors predominated. There were no differences in outcomes between the two groups: 5-year event-free survival (EFS), 49% (95% confidence interval [CI]: 39-59) and 44% (95% CI: 30-58), and overall survival (OS), 51% (95% CI: 41-61) and 53.6% (95% CI: 40-68) in RMS2005 and ARST0531, respectively. In RMS2005, EFS of patients with FOXO1-positive tumors was significantly inferior to those with FOXO1-negative (49.3% vs 73%, P = .034). In contrast, in ARST0531, EFS of patients with FOXO1-positive tumors was 45% compared with 43.8% for those with FOXO1-negative. CONCLUSIONS: The outcome of patients with ARMS N1 was similar in both protocols. However, patients with FOXO1 fusion-negative tumors enrolled in RMS2005 showed a significantly better outcome, suggesting that different strategies of chemotherapy may have an impact in the outcome of this subgroup of patients.
dc.formatPrint-Electronic
dc.format.extente28832 -
dc.languageeng
dc.language.isoeng
dc.publisherWILEY
dc.relation.ispartofPediatric Blood and Cancer
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectalveolar rhabdomyosarcoma
dc.subjectchemotherapy
dc.subjectnodal involvement
dc.subjectprognostic factors
dc.subjectrhabdomyosarcoma
dc.subjectAntineoplastic Combined Chemotherapy Protocols
dc.subjectChild
dc.subjectChild, Preschool
dc.subjectFemale
dc.subjectFollow-Up Studies
dc.subjectHumans
dc.subjectInfant
dc.subjectInfant, Newborn
dc.subjectLymph Nodes
dc.subjectMale
dc.subjectPrognosis
dc.subjectRetrospective Studies
dc.subjectRhabdomyosarcoma, Alveolar
dc.subjectSurvival Rate
dc.titleAlveolar rhabdomyosarcoma with regional nodal involvement: Results of a combined analysis from two cooperative groups.
dc.typeJournal Article
dcterms.dateAccepted2020-11-08
dc.date.updated2024-04-16T14:46:24Z
rioxxterms.versionAM
rioxxterms.versionofrecord10.1002/pbc.28832
rioxxterms.licenseref.startdate2021-03-01
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/33245207
pubs.issue3
pubs.organisational-groupICR
pubs.organisational-groupICR/Primary Group
pubs.organisational-groupICR/Primary Group/ICR Divisions
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-groupICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Paediatric and Adolescent Radiotherapy
pubs.publication-statusPublished
pubs.publisher-urlhttp://dx.doi.org/10.1002/pbc.28832
pubs.volume68
icr.researchteamPaed & Adolesc Radiother
dc.contributor.icrauthorMandeville, Henry
icr.provenanceDeposited by Henry Mandeville on 2024-04-16. Deposit type is initial. No. of files: 1. Files: Alveolar rhabdomyosarcoma with regional nodal involvement Results of a combined analysis from two cooperative groups.pdf


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