BMIT research group, School of Information Technologies, The University of Sydney, Sydney, Australia.
The Radiation Oncology Department of Shandong Cancer Hospital, Affiliated to Shandong University, Jinan, China.
Sci Rep. 2018 Jul 13;8(1):10649. doi: 10.1038/s41598-018-28818-8.
Quantitative measurement and analysis of tumor metabolic activities could provide a more optimal solution to personalized accurate dose painting. We collected PET images of 58 lung cancer patients, in which the tumor exhibits heterogeneous FDG uptake. We design an automated delineation and quantitative heterogeneity measurement of the lung tumor for dose-escalation. For tumor delineation, our algorithm firstly separates the tumor from its adjacent high-uptake tissues using 3D projection masks; then the tumor boundary is delineated with our stopping criterion of joint gradient and intensity affinities. For dose-escalation, tumor sub-volumes with low, moderate and high metabolic activities are extracted and measured. Based on our quantitative heterogeneity measurement, a sub-volume oriented dose-escalation plan is implemented in intensity modulated radiation therapy (IMRT) planning system. With respect to manual tumor delineations by two radiation oncologists, the paired t-test demonstrated our model outperformed the other computational methods in comparison (p < 0.05) and reduced the variability between inter-observers. Compared to standard uniform dose prescription, the dosimetry results demonstrated that the dose-escalation plan statistically boosted the dose delivered to high metabolic tumor sub-volumes (p < 0.05). Meanwhile, the doses received by organs-at-risk (OAR) including the heart, ipsilateral lung and contralateral lung were not statistically different (p > 0.05).
肿瘤代谢活性的定量测量和分析可为个性化精确剂量描绘提供更优的解决方案。我们收集了 58 例肺癌患者的 PET 图像,这些肿瘤表现出不均匀的 FDG 摄取。我们设计了一种自动勾画和定量分析肺肿瘤异质性的方法,以进行剂量递增。对于肿瘤勾画,我们的算法首先使用 3D 投影掩模将肿瘤与其相邻的高摄取组织分离;然后,我们使用联合梯度和强度亲和力的停止准则来勾画肿瘤边界。对于剂量递增,提取和测量低、中、高代谢活性的肿瘤亚体积。基于我们的定量异质性测量,在强度调制放射治疗(IMRT)计划系统中实现了基于亚体积的剂量递增计划。与两名放射肿瘤学家的手动肿瘤勾画相比,配对 t 检验表明,我们的模型在比较中优于其他计算方法(p<0.05),并减少了观察者之间的变异性。与标准均匀剂量处方相比,剂量学结果表明,剂量递增计划在统计学上增加了高代谢肿瘤亚体积的剂量(p<0.05)。同时,心脏、同侧肺和对侧肺等危及器官(OAR)的剂量没有统计学差异(p>0.05)。