Questionnaire based quality assurance for the RT01 trial of dose escalation in conformal radiotherapy for prostate cancer (ISRCTN 47772397)

被引:20
作者
Mayles, WPM [1 ]
Moore, AR
Aird, EGA
Bidmead, AM
Dearnaley, DP
Griffiths, SE
Stephens, RJ
Warrington, APJ
机构
[1] Clatterbridge Ctr Oncol, Dept Phys, Wirral CH63 4JY, Merseyside, England
[2] Mt Vernon Hosp, Dept Phys Med, Northwood HA6 2RN, Middx, England
[3] Royal Marsden Hosp, NHS Trust, Joint Dept Phys, London SW3 6JJ, England
[4] Royal Marsden Hosp, Sutton SM2 5PT, Surrey, England
[5] Inst Canc Res, Sutton SM2 5PT, Surrey, England
[6] Cookridge Hosp, Leeds Teaching Hosp, NHS Trust, Dept Radiotherapy, Leeds LS16 6QB, W Yorkshire, England
[7] MRC Clin Trials Unit 222, London NW1 2DA, England
[8] Royal Marsden Hosp, NHS Trust, Joint Dept Phys, Sutton SM2 5PT, Surrey, England
关键词
clinical trials; prostate; quality assurance; questionnaires;
D O I
10.1016/j.radonc.2004.08.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and purpose: In order to ensure the validity of the outcome of the Medical Research Council's 'RT01 trial' of dose escalation in conformal radiotherapy for prostate cancer it was considered important that the quality of treatment delivery should meet an adequate standard across all contributing centres. A questionnaire was therefore devised to ensure that all aspects of the planning and delivery process were adequately covered. Patients and methods: The questionnaire considered each step in the planning and delivery process and drew the attention of the participants to the specific requirements of the trial. Before entering patients into the trial each participating centre had to complete the questionnaire and an outlining exercise (reported elsewhere). Results: It was not practicable to define a detailed universally acceptable protocol for the whole process of delivery of conformal radiotherapy, not least because of the different equipment available for planning and treatment in different centres. The questionnaire identified some areas of difference in practice between centres where there may be a need for the development of a consensus as to best practice, particularly in the area of patient set-up. Occasionally it was necessary to follow up responses to questions that had been misunderstood or inadequately answered, but in most cases these issues proved to be easily resolved. Conclusions: The questionnaire proved to be a useful self-assessment tool as well as enabling the quality assurance group to ensure that the standards of the trial were being met. Subsequent follow-up visits confirmed the usefulness and validity of this self assessment process. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:199 / 207
页数:9
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