Show simple item record

dc.contributor.authorVaarwerk, B
dc.contributor.authorMallebranche, C
dc.contributor.authorAffinita, MC
dc.contributor.authorvan der Lee, JH
dc.contributor.authorFerrari, A
dc.contributor.authorChisholm, JC
dc.contributor.authorDefachelles, A-S
dc.contributor.authorDe Salvo, GL
dc.contributor.authorCorradini, N
dc.contributor.authorMinard-Colin, V
dc.contributor.authorMorosi, C
dc.contributor.authorBrisse, HJ
dc.contributor.authorMcHugh, K
dc.contributor.authorBisogno, G
dc.contributor.authorvan Rijn, RR
dc.contributor.authorOrbach, D
dc.contributor.authorMerks, JHM
dc.date.accessioned2021-12-07T09:27:11Z
dc.date.available2021-12-07T09:27:11Z
dc.identifier.citationCancer, 2020, 126 (4), pp. 823 - 831
dc.identifier.issn0008-543X
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4911
dc.identifier.eissn1097-0142
dc.identifier.doi10.1002/cncr.32603
dc.description.abstractBackground After the completion of therapy, patients with localized rhabdomyosarcoma (RMS) are subjected to intensive radiological tumor surveillance. However, the clinical benefit of this surveillance is unclear. This study retrospectively analyzed the value of off-therapy surveillance by comparing the survival of patients in whom relapse was detected by routine imaging (the imaging group) and patients in whom relapse was first suspected by symptoms (the symptom group). Methods This study included patients with relapsed RMS after the completion of therapy for localized RMS who were treated in large pediatric oncology hospitals in France, the United Kingdom, Italy, and the Netherlands and who were enrolled in the International Society of Paediatric Oncology Malignant Mesenchymal Tumor 95 (1995-2004) study, the Italian Paediatric Soft Tissue Sarcoma Committee Rhabdomyosarcoma 96 (1996-2004) study, or the European Paediatric Soft Tissue Sarcoma Study Group Rhabdomyosarcoma 2005 (2005-2013) study. The survival times after relapse were compared with a log-rank test between patients in the imaging group and patients in the symptom group. Results In total, 199 patients with relapsed RMS were included: 78 patients (39.2%) in the imaging group and 121 patients (60.8%) in the symptom group. The median follow-up time after relapse was 7.4 years (interquartile range, 3.9-11.5 years) for survivors (n = 86); the 3-year postrelapse survival rate was 50% (95% confidence interval [CI], 38%-61%) for the imaging group and 46% (95% CI, 37%-55%) for the symptom group (P = .7). Conclusions Although systematic routine imaging is the standard of care after RMS therapy, the majority of relapses were detected as a result of clinical symptoms. This study found no survival advantage for patients whose relapse was detected before the emergence of clinical symptoms. These results show that the value of off-therapy surveillance is controversial, particularly because repeated imaging may also entail potential harm.
dc.formatPrint-Electronic
dc.format.extent823 - 831
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0
dc.subjectHumans
dc.subjectRhabdomyosarcoma
dc.subjectNeoplasm Recurrence, Local
dc.subjectDiagnostic Imaging
dc.subjectTomography, X-Ray Computed
dc.subjectMagnetic Resonance Imaging
dc.subjectMonitoring, Physiologic
dc.subjectDisease-Free Survival
dc.subjectRetrospective Studies
dc.subjectFollow-Up Studies
dc.subjectChild
dc.subjectChild, Preschool
dc.subjectFrance
dc.subjectItaly
dc.subjectNetherlands
dc.subjectFemale
dc.subjectMale
dc.subjectUnited Kingdom
dc.titleIs surveillance imaging in pediatric patients treated for localized rhabdomyosarcoma useful? The European experience.
dc.typeJournal Article
dcterms.dateAccepted2019-09-30
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1002/cncr.32603
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc/4.0
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfCancer
pubs.issue4
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/Royal Marsden Clinical Units
pubs.publication-statusPublished
pubs.volume126
pubs.embargo.termsNo embargo
icr.researchteamSarcoma Clinical Trials in children and young people
dc.contributor.icrauthorChisholm, Julia


Files in this item

Thumbnail

This item appears in the following collection(s)

Show simple item record

https://creativecommons.org/licenses/by-nc-nd/4.0
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by-nc-nd/4.0