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dc.contributor.authorSelby, PJ
dc.contributor.authorBanks, RE
dc.contributor.authorGregory, W
dc.contributor.authorHewison, J
dc.contributor.authorRosenberg, W
dc.contributor.authorAltman, DG
dc.contributor.authorDeeks, JJ
dc.contributor.authorMcCabe, C
dc.contributor.authorParkes, J
dc.contributor.authorSturgeon, C
dc.contributor.authorThompson, D
dc.contributor.authorTwiddy, M
dc.contributor.authorBestall, J
dc.contributor.authorBedlington, J
dc.contributor.authorHale, T
dc.contributor.authorDinnes, J
dc.contributor.authorJones, M
dc.contributor.authorLewington, A
dc.contributor.authorMessenger, MP
dc.contributor.authorNapp, V
dc.contributor.authorSitch, A
dc.contributor.authorTanwar, S
dc.contributor.authorVasudev, NS
dc.contributor.authorBaxter, P
dc.contributor.authorBell, S
dc.contributor.authorCairns, DA
dc.contributor.authorCalder, N
dc.contributor.authorCorrigan, N
dc.contributor.authorDel Galdo, F
dc.contributor.authorHeudtlass, P
dc.contributor.authorHornigold, N
dc.contributor.authorHulme, C
dc.contributor.authorHutchinson, M
dc.contributor.authorLippiatt, C
dc.contributor.authorLivingstone, T
dc.contributor.authorLongo, R
dc.contributor.authorPotton, M
dc.contributor.authorRoberts, S
dc.contributor.authorSim, S
dc.contributor.authorTrainor, S
dc.contributor.authorWelberry Smith, M
dc.contributor.authorNeuberger, J
dc.contributor.authorThorburn, D
dc.contributor.authorRichardson, P
dc.contributor.authorChristie, J
dc.contributor.authorSheerin, N
dc.contributor.authorMcKane, W
dc.contributor.authorGibbs, P
dc.contributor.authorEdwards, A
dc.contributor.authorSoomro, N
dc.contributor.authorAdeyoju, A
dc.contributor.authorStewart, GD
dc.contributor.authorHrouda, D
dc.date.accessioned2019-06-25T14:27:59Z
dc.date.issued2018-07-31
dc.description.abstractBackground: Protein biomarkers with associations with the activity and outcomes of diseases are being identified by modern proteomic technologies. They may be simple, accessible, cheap and safe tests that can inform diagnosis, prognosis, treatment selection, monitoring of disease activity and therapy and may substitute for complex, invasive and expensive tests. However, their potential is not yet being realised. Design and methods: The study consisted of three workstreams to create a framework for research: workstream 1, methodology – to define current practice and explore methodology innovations for biomarkers for monitoring disease; workstream 2, clinical translation – to create a framework of research practice, high-quality samples and related clinical data to evaluate the validity and clinical utility of protein biomarkers; and workstream 3, the ELF to Uncover Cirrhosis as an Indication for Diagnosis and Action for Treatable Event (ELUCIDATE) randomised controlled trial (RCT) – an exemplar RCT of an established test, the ADVIA Centaur® Enhanced Liver Fibrosis (ELF) test (Siemens Healthcare Diagnostics Ltd, Camberley, UK) [consisting of a panel of three markers – (1) serum hyaluronic acid, (2) amino-terminal propeptide of type III procollagen and (3) tissue inhibitor of metalloproteinase 1], for liver cirrhosis to determine its impact on diagnostic timing and the management of cirrhosis and the process of care and improving outcomes. Results: The methodology workstream evaluated the quality of recommendations for using prostate-specific antigen to monitor patients, systematically reviewed RCTs of monitoring strategies and reviewed the monitoring biomarker literature and how monitoring can have an impact on outcomes. Simulation studies were conducted to evaluate monitoring and improve the merits of health care. The monitoring biomarker literature is modest and robust conclusions are infrequent. We recommend improvements in research practice. Patients strongly endorsed the need for robust and conclusive research in this area. The clinical translation workstream focused on analytical and clinical validity. Cohorts were established for renal cell carcinoma (RCC) and renal transplantation (RT), with samples and patient data from multiple centres, as a rapid-access resource to evaluate the validity of biomarkers. Candidate biomarkers for RCC and RT were identified from the literature and their quality was evaluated and selected biomarkers were prioritised. The duration of follow-up was a limitation but biomarkers were identified that may be taken forward for clinical utility. In the third workstream, the ELUCIDATE trial registered 1303 patients and randomised 878 patients out of a target of 1000. The trial started late and recruited slowly initially but ultimately recruited with good statistical power to answer the key questions. ELF monitoring altered the patient process of care and may show benefits from the early introduction of interventions with further follow-up. The ELUCIDATE trial was an ‘exemplar’ trial that has demonstrated the challenges of evaluating biomarker strategies in ‘end-to-end’ RCTs and will inform future study designs. Conclusions: The limitations in the programme were principally that, during the collection and curation of the cohorts of patients with RCC and RT, the pace of discovery of new biomarkers in commercial and non-commercial research was slower than anticipated and so conclusive evaluations using the cohorts are few; however, access to the cohorts will be sustained for future new biomarkers. The ELUCIDATE trial was slow to start and recruit to, with a late surge of recruitment, and so final conclusions about the impact of the ELF test on long-term outcomes await further follow-up. The findings from the three workstreams were used to synthesise a strategy and framework for future biomarker evaluations incorporating innovations in study design, health economics and health informatics.en_GB
dc.description.sponsorshipNational Institute for Health Research (NIHR)en_GB
dc.identifier.citationVol. 6 (3), pp. 1 - 528en_GB
dc.identifier.doi10.3310/pgfar06030
dc.identifier.grantnumberGrants for Applied Research programmeen_GB
dc.identifier.urihttp://hdl.handle.net/10871/37669
dc.language.isoenen_GB
dc.publisherNIHR Journals Libraryen_GB
dc.rights© Queen’s Printer and Controller of HMSO 2018. This work was produced by Selby et al. under the terms of a commissioning contract issued by the Secretary of State for Health and Social Care. This issue may be freely reproduced for the purposes of private research and study and extracts (or indeed, the full report) may be included in professional journals provided that suitable acknowledgement is made and the reproduction is not associated with any form of advertising.en_GB
dc.titleMethods for the evaluation of biomarkers in patients with kidney and liver diseases: multicentre research programme including ELUCIDATE RCTen_GB
dc.typeArticleen_GB
dc.date.available2019-06-25T14:27:59Z
dc.identifier.issn2050-4322
dc.descriptionThis is the final version, also available from NIHR Journals Library via the DOI in this record.en_GB
dc.identifier.journalProgramme Grants for Applied Researchen_GB
dc.rights.urihttp://www.rioxx.net/licenses/all-rights-reserveden_GB
dcterms.dateAccepted2017-06-30
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2017-06-30
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2019-06-25T14:22:25Z
refterms.versionFCDVoR
refterms.dateFOA2019-06-25T14:28:03Z
refterms.panelAen_GB


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