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Radiotherapy trial set-up in the UK: identifying inefficiencies and potential solutions

"V体育安卓版" Hanna, C.R. ORCID logoORCID: https://orcid.org/0000-0002-0907-7747, Lynskey, D.M., Wadsley, J., Appleyard, S.E., Anwar, S., Miles, E., Gower, J., Hall, E., VSports在线直播 - Coles, C.E. and Hanna, G.G. (2020) Radiotherapy trial set-up in the UK: identifying inefficiencies and potential solutions. Clinical Oncology, 32(4), pp. 266-275. (doi: 10.1016/j.clon.2019.10.004) (PMID:31685377)

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Abstract

Aims: Radiotherapy clinical trials are integral to the development of new treatments to improve the outcomes of patients with cancer. A collaborative study by the National Cancer Research Institute Clinical and Translational Radiotherapy Research Working Group and the National Institute for Health Research was carried out to understand better if and why inefficiencies occur in the set-up of radiotherapy trials in the UK. Materials and methods: Two online surveys collected information on the time taken for UK radiotherapy trials to reach key milestones during set-up and the research support currently being provided to radiotherapy centres to enable efficient clinical trial set-up. Semi-structured interviews with project managers and chief investigators identified better ways of working to improve trial set-up in the future. Results: The timelines for the set-up of 39 UK radiotherapy trials were captured in an online survey showing that the median time from grant approval to trial opening was 600 days (range 169–1172). There were 38 responses from radiotherapy centres to a survey asking about the current support provided for radiotherapy research. Most of these centres have more than one type of staff member dedicated to supporting radiotherapy research VSports app下载. The most frequent barrier to radiotherapy trial set-up identified was lack of physicists' time and lack of time for clinical oncologists to carry out research activities. Four main themes around trial set-up were identified from semi-structured interviews: the importance of communication and building relationships, the previous experience of the chief investigator and clinical trials units, a lack of resources and having the time and personnel required to produce trial documentation and to process trial approval requests. Conclusions: This unique, collaborative project has provided up to date information about the current landscape of trial set-up and research support in the UK and identified several avenues on which to focus future efforts in order to support the excellent radiotherapy trial work carried out across the UK.

Item Type:Articles
Additional Information:The authors acknowledge the UK National Cancer Research Institute Clinical and Translational Radiotherapy Research Working Group (CTRad) and the National Institute for Health Research (NIHR), who contributed to the initiation and development of this research. Dr Catherine Hanna is a CRUK Clinical Trials Fellow (Grant ID: 174279-01).
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Hall, Mrs Elizabeth and Hanna, Catherine
Authors: Hanna, C.R., Lynskey, D.M., Wadsley, J., Appleyard, S.E., Anwar, S., Miles, E., Gower, J., Hall, E., Coles, C.E., and Hanna, G.G.
College/School:College of Medical Veterinary and Life Sciences > School of Cancer Sciences
Journal Name:Clinical Oncology
Publisher:Elsevier
ISSN:0936-6555
ISSN (Online):1433-2981
Published Online:01 November 2019
Copyright Holders:Copyright © 2019 The Authors
First Published:First published in Clinical Oncology 32(4): 266-275
Publisher Policy:Reproduced under a Creative Commons License

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Project Code
Award No
Project Name
Principal Investigator
Funder's Name
Funder Ref
Lead Dept
CRUK CTU Glasgow - Clinical Trial Fellowship
Catherine Hanna
C61974/A24293
Institute of Cancer Sciences
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