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dc.contributor.authorChisholm, J
dc.contributor.authorMandeville, H
dc.contributor.authorAdams, M
dc.contributor.authorMinard-Collin, V
dc.contributor.authorRogers, T
dc.contributor.authorKelsey, A
dc.contributor.authorShipley, J
dc.contributor.authorvan Rijn, RR
dc.contributor.authorde Vries, I
dc.contributor.authorvan Ewijk, R
dc.contributor.authorde Keizer, B
dc.contributor.authorGatz, SA
dc.contributor.authorCasanova, M
dc.contributor.authorHjalgrim, LL
dc.contributor.authorFirth, C
dc.contributor.authorWheatley, K
dc.contributor.authorKearns, P
dc.contributor.authorLiu, W
dc.contributor.authorKirkham, A
dc.contributor.authorRees, H
dc.contributor.authorBisogno, G
dc.contributor.authorWasti, A
dc.contributor.authorWakeling, S
dc.contributor.authorHeenen, D
dc.contributor.authorTweddle, DA
dc.contributor.authorMerks, JHM
dc.contributor.authorJenney, M
dc.date.accessioned2024-03-07T11:33:12Z
dc.date.available2024-03-07T11:33:12Z
dc.date.issued2024-02-29
dc.identifier.citationCancers, 2024, 16 (5), pp. 998 - 998
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/6174
dc.identifier.eissn2072-6694
dc.identifier.eissn2072-6694
dc.identifier.doi10.3390/cancers16050998
dc.identifier.doi10.3390/cancers16050998
dc.description.abstractThe Frontline and Relapsed Rhabdomyosarcoma (FaR-RMS) clinical trial is an overarching, multinational study for children and adults with rhabdomyosarcoma (RMS). The trial, developed by the European Soft Tissue Sarcoma Study Group (EpSSG), incorporates multiple different research questions within a multistage design with a focus on (i) novel regimens for poor prognostic subgroups, (ii) optimal duration of maintenance chemotherapy, and (iii) optimal use of radiotherapy for local control and widespread metastatic disease. Additional sub-studies focusing on biological risk stratification, use of imaging modalities, including [18F]FDG PET-CT and diffusion-weighted MRI imaging (DWI) as prognostic markers, and impact of therapy on quality of life are described. This paper forms part of a Special Issue on rhabdomyosarcoma and outlines the study background, rationale for randomisations and sub-studies, design, and plans for utilisation and dissemination of results.
dc.format.extent998 - 998
dc.languageen
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofCancers
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleFrontline and Relapsed Rhabdomyosarcoma (FAR-RMS) Clinical Trial: A Report from the European Paediatric Soft Tissue Sarcoma Study Group (EpSSG).
dc.typeJournal Article
dcterms.dateAccepted2024-02-26
dc.date.updated2024-03-01T20:48:42Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.3390/cancers16050998
rioxxterms.licenseref.startdate2024-02-29
rioxxterms.typeJournal Article/Review
pubs.issue5
pubs.organisational-groupICR
pubs.organisational-groupICR/Primary Group
pubs.organisational-groupICR/Primary Group/ICR Divisions
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies/Sarcoma Clinical Trials in Children and Young People
pubs.organisational-groupICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-groupICR/Primary Group/ICR Divisions/Molecular Pathology/Sarcoma Clinical Trials in children and young people
pubs.organisational-groupICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-groupICR/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-groupICR/Primary Group/ICR Divisions/Molecular Pathology/Sarcoma Clinical Trials in children and young people/Sarcoma Clinical Trials in Children and Young People (hon.)
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.3390/cancers16050998
pubs.volume16
dc.contributor.icrauthorShipley, Janet
icr.provenanceDeposited by Dr Julia Chisholm on 2024-03-01. Deposit type is initial. No. of files: 1. Files: cancers-16-00998FaR-RMS.pdf


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