EORTC Radiation Oncology Group quality assurance platform: Establishment of a digital central review facility

被引:34
作者
Fairchild, Alysa [1 ,2 ]
Aird, Edwin [3 ]
Fenton, Paul A. [4 ]
Gregoire, Vincent
Gulyban, Akos
Lacombe, Denis [1 ]
Matzinger, Oscar [5 ]
Poortmans, Philip [6 ]
Ruyskart, Pascal [1 ]
Weber, Damien C. [7 ]
Hurkmans, Coen W. [8 ]
机构
[1] EORTC Headquartes, Brussels, Belgium
[2] Cross Canc Inst, Edmonton, AB T6G 1Z2, Canada
[3] Mt Vernon Hosp, Northwood HA6 2RN, Middx, England
[4] Southampton Univ Hosp NHS Trust, Southampton, Hants, England
[5] CHU Vaudois, CH-1011 Lausanne, Switzerland
[6] Inst Verbeeten, Tilburg, Netherlands
[7] Univ Hosp Geneva, Geneva, Switzerland
[8] Catharina Hosp, Eindhoven, Netherlands
关键词
Quality assurance; Radiotherapy; Clinical trial; Platform; Central review; RANDOMIZED CONTROLLED-TRIAL; TECHNOLOGY CLINICAL-TRIALS; DUMMY RUN; PROSTATE-CANCER; CONFORMAL RADIOTHERAPY; INTERNAL MAMMARY; PHASE-III; MRC RT01; IRRADIATION; CHALLENGES;
D O I
10.1016/j.radonc.2012.04.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Quality assurance (QA) in clinical trials is essential to ensure treatment is safely and effectively delivered. As QA requirements have increased in complexity in parallel with evolution of radiation therapy (RT) delivery, a need to facilitate digital data exchange emerged. Our objective is to present the platform developed for the integration and standardization of QART activities across all EORTC trials involving RT. Methods: The following essential requirements were identified: secure and easy access without on-site software installation; integration within the existing EORTC clinical remote data capture system; and the ability to both customize the platform to specific studies and adapt to future needs. After retrospective testing within several clinical trials, the platform was introduced in phases to participating sites and QART study reviewers. Results: The resulting QA platform, integrating RT analysis software installed at EORTC Headquarters, permits timely, secure, and fully digital central DICOM-RT based data review. Participating sites submit data through a standard secure upload webpage. Supplemental information is submitted in parallel through web-based forms. An internal quality check by the QART office verifies data consistency, formatting, and anonymization. QART reviewers have remote access through a terminal server. Reviewers evaluate submissions for protocol compliance through an online evaluation matrix. Comments are collected by the coordinating centre and institutions are informed of the results. Conclusions: This web-based central review platform facilitates rapid, extensive, and prospective QART review. This reduces the risk that trial outcomes are compromised through inadequate radiotherapy and facilitates correlation of results with clinical outcomes. (C) 2012 Elsevier Ireland Ltd. All rights reserved. Radiotherapy and Oncology 103 (2012) 279-286
引用
收藏
页码:279 / 286
页数:8
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