van Wijk Yvonka, Vanneste Ben G L, Walsh Sean, van der Meer Skadi, Ramaekers Bram, van Elmpt Wouter, Pinkawa Michael, Lambin Philippe
Department of Radiation Oncology (MAASTRO, D-lab), GROW - School for Oncology and Developmental Biology, Maastricht University Medical Center, The Netherlands.
Department of Radiation Oncology (MAASTRO, D-lab), GROW - School for Oncology and Developmental Biology, Maastricht University Medical Center, The Netherlands.
Radiother Oncol. 2017 Oct;125(1):107-112. doi: 10.1016/j.radonc.2017.07.026. Epub 2017 Aug 16.
Previous studies have shown that the implantable rectum spacer (IRS) is not beneficial for all patients. A virtual IRS (V-IRS) was constructed to help identify the patients for whom it is cost-effective to implant an IRS, and its viability as a tool to tailor the decision of an IRS implantation to be beneficial for the specified patient was assessed. Please watch animation: (https://www.youtube.com/watch?v=tDlagSXMKqw) MATERIALS AND METHODS: The V-IRS was tested on 16 patients: 8 with a rectal balloon implant (RBI) and 8 with a hydrogel spacer. A V-IRS was developed using 7 computed tomography (CT) scans of patients with a RBI. To examine the V-IRS, CT scans before and after the implantation of an IRS were used. IMRT plans were made based on CT scans before the IRS, after IRS and with the V-IRS, prescribing 70 Gray (Gy) to the planning target volume. Toxicity was accessed using externally validated normal tissue complication probability (NTCP) models, and the Cost-effectiveness was analyzed using a published Markov model.
The rectum volume receiving 75Gy (V75) were improved by both the IRS and the V-IRS with on average 4.2% and 4.3% respectively. The largest NTCP reduction resulting from the IRS and the V-IRS was 4.0% and 3.9% respectively. The RBI was cost-effective for 1 out of 8 patients, and the hydrogel was effective for 2 out of 8 patients, and close to effective for a third patient. The classification accuracy of the model, regarding cost-effectiveness, was 100%.
The V-IRS approach in combination with a toxicity prediction model and a cost-effectiveness analyses is a promising basis for a decision support tool for the implantation of either a hydrogel spacer or a rectum balloon implant.
先前的研究表明,可植入直肠间隔器(IRS)并非对所有患者都有益。构建了虚拟IRS(V-IRS)以帮助识别植入IRS具有成本效益的患者,并评估其作为一种工具的可行性,该工具可使IRS植入决策适合特定患者并使其受益。请观看动画:(https://www.youtube.com/watch?v=tDlagSXMKqw)
对16例患者进行了V-IRS测试:8例使用直肠球囊植入物(RBI),8例使用水凝胶间隔器。利用7例RBI患者的计算机断层扫描(CT)扫描数据开发了V-IRS。为了检验V-IRS,使用了IRS植入前后的CT扫描。基于IRS植入前、植入后以及使用V-IRS后的CT扫描制定调强放疗计划,向计划靶体积处方70格雷(Gy)剂量。使用外部验证的正常组织并发症概率(NTCP)模型评估毒性,并使用已发表的马尔可夫模型分析成本效益。
接受75Gy剂量的直肠体积(V75)在IRS和V-IRS作用下均得到改善,平均分别提高了4.2%和4.3%。IRS和V-IRS导致的最大NTCP降低分别为4.0%和3.9%。8例患者中,RBI对1例具有成本效益,水凝胶对8例中的2例有效,对第3例接近有效。该模型在成本效益方面的分类准确率为100%。
V-IRS方法结合毒性预测模型和成本效益分析,有望成为水凝胶间隔器或直肠球囊植入物植入决策支持工具的基础。