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dc.contributor.authorRothermundt, C
dc.contributor.authorAndreou, D
dc.contributor.authorBlay, J-Y
dc.contributor.authorBrodowicz, T
dc.contributor.authorDesar, IME
dc.contributor.authorDileo, P
dc.contributor.authorGelderblom, H
dc.contributor.authorHaas, R
dc.contributor.authorJakob, J
dc.contributor.authorJones, RL
dc.contributor.authorJudson, I
dc.contributor.authorKunz, WG
dc.contributor.authorLiegl-Atzwanger, B
dc.contributor.authorLindner, LH
dc.contributor.authorMessiou, C
dc.contributor.authorMiah, AB
dc.contributor.authorReichardt, P
dc.contributor.authorSzkandera, J
dc.contributor.authorvan der Graaf, WTA
dc.contributor.authorvan Houdt, WJ
dc.contributor.authorWardelmann, E
dc.contributor.authorHofer, S
dc.contributor.authorWriting committee on behalf of CSSS panellists,
dc.coverage.spatialEngland
dc.date.accessioned2023-02-06T16:28:35Z
dc.date.available2023-02-06T16:28:35Z
dc.date.issued2022-11-16
dc.identifierS0959-8049(22)01344-2
dc.identifier.citationEuropean Journal of Cancer, 2022, 180 pp. 158 - 179
dc.identifier.issn0959-8049
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5677
dc.identifier.eissn1879-0852
dc.identifier.eissn1879-0852
dc.identifier.doi10.1016/j.ejca.2022.11.008
dc.description.abstractBACKGROUND: Owing to the rarity and heterogeneity in biology and presentation, there are multiple areas in the diagnosis, treatment and follow-up of soft tissue sarcoma (STS), with no, low-level or conflicting evidence. METHODS: During the first Consensus Conference on the State of Science in Sarcoma (CSSS), we used a modified Delphi process to identify areas of controversy in the field of sarcoma, to name topics with limited evidence-based data in which a scientific and knowledge gap may remain and a consensus statement will help to guide patient management. We determined scientific questions which need to be addressed in the future in order to generate evidence and to inform physicians and caregivers in daily clinical practice in order to improve the outcomes of patients with sarcoma. We conducted a vote on STS key questions and controversies prior to the CSSS meeting, which took place in May 2022. RESULTS: Sixty-two European sarcoma experts participated in the survey. Sixteen strong consensus (≥95%) items were identified by the experts, as well as 30 items with a ≥75% consensus on diagnostic and therapeutic questions. Ultimately, many controversy topics remained without consensus. CONCLUSIONS: In this manuscript, we summarise the voting results and the discussion during the CSSS meeting. Future scientific questions, priorities for clinical trials, registries, quality assurance, and action by stakeholders are proposed. Platforms and partnerships can support innovative approaches to improve management and clinical research in STS.
dc.formatPrint-Electronic
dc.format.extent158 - 179
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER SCI LTD
dc.relation.ispartofEuropean Journal of Cancer
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectConsensus
dc.subjectDiagnosis
dc.subjectImaging
dc.subjectMultimodal treatment
dc.subjectPeri-operative management
dc.subjectPolicy
dc.subjectSoft tissue sarcoma
dc.subjectSurveillance
dc.subjectTreatment of advanced disease
dc.titleControversies in the management of patients with soft tissue sarcoma: Recommendations of the Conference on State of Science in Sarcoma 2022.
dc.typeJournal Article
dcterms.dateAccepted2022-11-04
dc.date.updated2023-02-02T16:06:36Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1016/j.ejca.2022.11.008
rioxxterms.licenseref.startdate2022-11-16
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/36599184
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
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Sarcoma Clinical Trials (R Jones)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Sarcoma Clinical Trials (R Jones)/Sarcoma Clinical Trials (R Jones) (hon.)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Molecular and Systems Oncology
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.1016/j.ejca.2022.11.008
pubs.volume180
icr.researchteamSarcoma Clinical Trials
dc.contributor.icrauthorJones, Robin
dc.contributor.icrauthorJudson, Ian
dc.contributor.icrauthorMessiou, Christina
icr.provenanceDeposited by Mr Arek Surman on 2023-02-02. Deposit type is initial. No. of files: 1. Files: 1-s2.0-S0959804922013442-main.pdf


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