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dc.contributor.authorSolovyeva, O
dc.contributor.authorDimairo, M
dc.contributor.authorWeir, CJ
dc.contributor.authorHee, SW
dc.contributor.authorEspinasse, A
dc.contributor.authorUrsino, M
dc.contributor.authorPatel, D
dc.contributor.authorKightley, A
dc.contributor.authorHughes, S
dc.contributor.authorJaki, T
dc.contributor.authorMander, A
dc.contributor.authorEvans, TRJ
dc.contributor.authorLee, S
dc.contributor.authorHopewell, S
dc.contributor.authorRantell, KR
dc.contributor.authorChan, A-W
dc.contributor.authorBedding, A
dc.contributor.authorStephens, R
dc.contributor.authorRichards, D
dc.contributor.authorRoberts, L
dc.contributor.authorKirkpatrick, J
dc.contributor.authorde Bono, J
dc.contributor.authorYap, C
dc.coverage.spatialEngland
dc.date.accessioned2023-09-29T11:35:06Z
dc.date.available2023-09-29T11:35:06Z
dc.date.issued2023-07-05
dc.identifierARTN 246
dc.identifier10.1186/s12916-023-02937-0
dc.identifier.citationBMC Medicine, 2023, 21 (1), pp. 246 -en_US
dc.identifier.issn1741-7015
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5994
dc.identifier.eissn1741-7015
dc.identifier.eissn1741-7015
dc.identifier.doi10.1186/s12916-023-02937-0
dc.description.abstractBACKGROUND: Early phase dose-finding (EPDF) trials are crucial for the development of a new intervention and influence whether it should be investigated in further trials. Guidance exists for clinical trial protocols and completed trial reports in the SPIRIT and CONSORT guidelines, respectively. However, both guidelines and their extensions do not adequately address the characteristics of EPDF trials. Building on the SPIRIT and CONSORT checklists, the DEFINE study aims to develop international consensus-driven guidelines for EPDF trial protocols (SPIRIT-DEFINE) and reports (CONSORT-DEFINE). METHODS: The initial generation of candidate items was informed by reviewing published EPDF trial reports. The early draft items were refined further through a review of the published and grey literature, analysis of real-world examples, citation and reference searches, and expert recommendations, followed by a two-round modified Delphi process. Patient and public involvement and engagement (PPIE) was pursued concurrently with the quantitative and thematic analysis of Delphi participants' feedback. RESULTS: The Delphi survey included 79 new or modified SPIRIT-DEFINE (n = 36) and CONSORT-DEFINE (n = 43) extension candidate items. In Round One, 206 interdisciplinary stakeholders from 24 countries voted and 151 stakeholders voted in Round Two. Following Round One feedback, one item for CONSORT-DEFINE was added in Round Two. Of the 80 items, 60 met the threshold for inclusion (≥ 70% of respondents voted critical: 26 SPIRIT-DEFINE, 34 CONSORT-DEFINE), with the remaining 20 items to be further discussed at the consensus meeting. The parallel PPIE work resulted in the development of an EPDF lay summary toolkit consisting of a template with guidance notes and an exemplar. CONCLUSIONS: By detailing the development journey of the DEFINE study and the decisions undertaken, we envision that this will enhance understanding and help researchers in the development of future guidelines. The SPIRIT-DEFINE and CONSORT-DEFINE guidelines will allow investigators to effectively address essential items that should be present in EPDF trial protocols and reports, thereby promoting transparency, comprehensiveness, and reproducibility. TRIAL REGISTRATION: SPIRIT-DEFINE and CONSORT-DEFINE are registered with the EQUATOR Network ( https://www.equator-network.org/ ).
dc.formatElectronic
dc.format.extent246 -
dc.languageeng
dc.language.isoengen_US
dc.publisherBMCen_US
dc.relation.ispartofBMC Medicine
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectCONSORT guideline
dc.subjectSPIRIT guideline
dc.subjectclinical trials
dc.subjectdose finding
dc.subjectearly phase
dc.subjectHumans
dc.subjectConsensus
dc.subjectReproducibility of Results
dc.subjectResearch Design
dc.subjectChecklist
dc.subjectResearch Report
dc.titleDevelopment of consensus-driven SPIRIT and CONSORT extensions for early phase dose-finding trials: the DEFINE study.en_US
dc.typeJournal Article
dcterms.dateAccepted2023-06-12
dc.date.updated2023-09-29T11:34:10Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1186/s12916-023-02937-0en_US
rioxxterms.licenseref.startdate2023-07-05
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/37408015
pubs.issue1
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/Clinical Trials & Statistics Unit
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies/Prostate Cancer Targeted Therapy Group
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.1186/s12916-023-02937-0
pubs.volume21
icr.researchteamClin Trials & Stats Uniten_US
icr.researchteamPrCa Targeted Therapyen_US
dc.contributor.icrauthorSolovyeva, Olga
dc.contributor.icrauthorDe Bono, Johann
dc.contributor.icrauthorYap, Christina
icr.provenanceDeposited by Mr Arek Surman on 2023-09-29. Deposit type is initial. No. of files: 1. Files: Development of consensus-driven SPIRIT and CONSORT extensions for early phase dose-finding trials the DEFINE study.pdf


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