Weizman Lior, Sira Liat Ben, Joskowicz Leo, Rubin Daniel L, Yeom Kristen W, Constantini Shlomi, Shofty Ben, Bashat Dafna Ben
School of Engineering and Computer Science, The Hebrew University of Jerusalem, Jerusalem 91904, Israel.
Department of Radiology, Tel Aviv Medical Center, Tel Aviv University, Tel Aviv 64239, Israel.
Med Phys. 2014 May;41(5):052303. doi: 10.1118/1.4871040.
Tracking the progression of low grade tumors (LGTs) is a challenging task, due to their slow growth rate and associated complex internal tumor components, such as heterogeneous enhancement, hemorrhage, and cysts. In this paper, the authors show a semiautomatic method to reliably track the volume of LGTs and the evolution of their internal components in longitudinal MRI scans.
The authors' method utilizes a spatiotemporal evolution modeling of the tumor and its internal components. Tumor components gray level parameters are estimated from the follow-up scan itself, obviating temporal normalization of gray levels. The tumor delineation procedure effectively incorporates internal classification of the baseline scan in the time-series as prior data to segment and classify a series of follow-up scans. The authors applied their method to 40 MRI scans of ten patients, acquired at two different institutions. Two types of LGTs were included: Optic pathway gliomas and thalamic astrocytomas. For each scan, a "gold standard" was obtained manually by experienced radiologists. The method is evaluated versus the gold standard with three measures: gross total volume error, total surface distance, and reliability of tracking tumor components evolution.
Compared to the gold standard the authors' method exhibits a mean Dice similarity volumetric measure of 86.58% and a mean surface distance error of 0.25 mm. In terms of its reliability in tracking the evolution of the internal components, the method exhibits strong positive correlation with the gold standard.
The authors' method provides accurate and repeatable delineation of the tumor and its internal components, which is essential for therapy assessment of LGTs. Reliable tracking of internal tumor components over time is novel and potentially will be useful to streamline and improve follow-up of brain tumors, with indolent growth and behavior.
由于低级别肿瘤(LGTs)生长速度缓慢且具有复杂的内部肿瘤成分,如不均匀强化、出血和囊肿,追踪其进展是一项具有挑战性的任务。在本文中,作者展示了一种半自动方法,可在纵向MRI扫描中可靠地追踪LGTs的体积及其内部成分的演变。
作者的方法利用了肿瘤及其内部成分的时空演变模型。肿瘤成分的灰度参数由随访扫描本身估计,无需进行灰度的时间归一化。肿瘤勾勒程序有效地将基线扫描的内部分类作为先验数据纳入时间序列,以分割和分类一系列随访扫描。作者将他们的方法应用于在两个不同机构获取的10名患者的40次MRI扫描。包括两种类型的LGTs:视神经通路胶质瘤和丘脑星形细胞瘤。对于每次扫描,由经验丰富的放射科医生手动获得“金标准”。该方法与金标准进行了三项指标的评估:总体积误差、总表面距离以及追踪肿瘤成分演变的可靠性。
与金标准相比,作者的方法表现出平均Dice相似性体积测量值为86.58%,平均表面距离误差为0.25毫米。在追踪内部成分演变的可靠性方面,该方法与金标准表现出强正相关。
作者的方法提供了对肿瘤及其内部成分的准确且可重复的勾勒,这对于LGTs的治疗评估至关重要。随着时间的推移可靠地追踪肿瘤内部成分是新颖的,并且可能有助于简化和改善对生长缓慢且行为惰性的脑肿瘤的随访。