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Update to the study protocol, including statistical analysis plan, for the multicentre, randomised controlled OuTSMART trial: a combined screening/treatment programme to prevent premature failure of renal transplants due to chronic rejection in patients with HLA antibodies

Stringer, D; Gardner, LM; Peacock, JL; Rebollo-Mesa, I; Hilton, R; Shaw, O; Baker, R; Clark, B; Thuraisingham, RC; Buckland, M; et al. Stringer, D; Gardner, LM; Peacock, JL; Rebollo-Mesa, I; Hilton, R; Shaw, O; Baker, R; Clark, B; Thuraisingham, RC; Buckland, M; Picton, M; Worthington, J; Borrows, R; Briggs, D; Shah, S; Shiu, KY; McCullough, K; Phanish, M; Hegarty, J; Stoves, J; Ahmed, A; Ayub, W; Horne, R; McCrone, P; Kelly, J; Murphy, C; Dorling, A (2019) Update to the study protocol, including statistical analysis plan, for the multicentre, randomised controlled OuTSMART trial: a combined screening/treatment programme to prevent premature failure of renal transplants due to chronic rejection in patients with HLA antibodies. Trials, 20 (1). p. 476. ISSN 1745-6215 https://doi.org/10.1186/s13063-019-3602-2
SGUL Authors: Peacock, Janet Lesley Phanish, Mysore

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Abstract

BACKGROUND: Chronic rejection is the single biggest cause of premature kidney graft failure. HLA antibodies (Ab) are an established prognostic biomarker for premature graft failure so there is a need to test whether treatment decisions based on the presence of the biomarker can alter prognosis. The Optimised TacrolimuS and MMF for HLA Antibodies after Renal Transplantation (OuTSMART) trial combines two elements. Firstly, testing whether a routine screening programme for HLA Ab in all kidney transplant recipients is useful by comparing blinding versus unblinding of HLA Ab status. Secondly, for those found to be HLA Ab+, testing whether the introduction of a standard optimisation treatment protocol can reduce graft failure rates. METHODS: OuTSMART is a prospective, open-labelled, randomised biomarker-based strategy (hybrid) trial, with two arms stratified by biomarker (HLA Ab) status. The primary outcome was amended from graft failure rates at 3 years to time to graft failure to increase power and require fewer participants to be recruited. Length of follow-up subsequently is variable, with all participants followed up for at least 43 months up to a maximum of 89 months. The primary outcome will be analysed using Cox regression adjusting for stratification factors. Analyses will be according to the intention-to-treat using all participants as randomised. Outcomes will be analysed comparing standard care versus biomarker-led care groups within the HLA Ab+ participants (including those who become HLA Ab+ through re-screening) as well as between HLA-Ab-unblinded and HLA-Ab-blinded groups using all participants. DISCUSSION: Changes to the primary outcome permit recruitment of fewer participants to achieve the same statistical power. Pre-stating the statistical analysis plan guards against changes to the analysis methods at the point of analysis that might otherwise introduce bias through knowledge of the data. Any deviations from the analysis plan will be justified in the final report. TRIAL REGISTRATION: ISRCTN registry, ID: ISRCTN46157828 . Registered on 26 March 2013; EudraCT 2012-004308-36 . Registered on 10 December 2012.

Item Type: Article
Additional Information: © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Keywords: Graft failure, Human leucocyte antigen antibodies, Immunosuppression, Randomised controlled trial, Renal transplantation, Statistical analysis plan, Time-to-event, Chronic Disease, Data Interpretation, Statistical, Graft Rejection, HLA Antigens, Humans, Isoantibodies, Kidney Transplantation, Multicenter Studies as Topic, Outcome Assessment, Health Care, Prospective Studies, Randomized Controlled Trials as Topic, Research Design, Sample Size
SGUL Research Institute / Research Centre: Academic Structure > Institute of Medical, Biomedical and Allied Health Education (IMBE)
Academic Structure > Population Health Research Institute (INPH)
Journal or Publication Title: Trials
ISSN: 1745-6215
Language: en
Media of Output: Electronic
Related URLs:
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
11/100/34Efficacy and Mechanism Evaluation programmehttp://dx.doi.org/10.13039/501100001922
Dates:
Date Event
2019-08-05 Published
2019-07-19 Accepted
URI: https://openaccess.sgul.ac.uk/id/eprint/118494
Publisher's version: https://doi.org/10.1186/s13063-019-3602-2

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