Prideaux Andrew R, Song Hong, Hobbs Robert F, He Bin, Frey Eric C, Ladenson Paul W, Wahl Richard L, Sgouros George
Russell H. Morgan Department of Radiology and Radiological Sciences, School of Medicine, Johns Hopkins University, Baltimore, Maryland 21231, USA.
J Nucl Med. 2007 Jun;48(6):1008-16. doi: 10.2967/jnumed.106.038000. Epub 2007 May 15.
Phantom-based and patient-specific imaging-based dosimetry methodologies have traditionally yielded mean organ-absorbed doses or spatial dose distributions over tumors and normal organs. In this work, radiobiologic modeling is introduced to convert the spatial distribution of absorbed dose into biologically effective dose and equivalent uniform dose parameters. The methodology is illustrated using data from a thyroid cancer patient treated with radioiodine.
Three registered SPECT/CT scans were used to generate 3-dimensional images of radionuclide kinetics (clearance rate) and cumulated activity. The cumulated activity image and corresponding CT scan were provided as input into an EGSnrc-based Monte Carlo calculation: The cumulated activity image was used to define the distribution of decays, and an attenuation image derived from CT was used to define the corresponding spatial tissue density and composition distribution. The rate images were used to convert the spatial absorbed dose distribution to a biologically effective dose distribution, which was then used to estimate a single equivalent uniform dose for segmented volumes of interest. Equivalent uniform dose was also calculated from the absorbed dose distribution directly.
We validate the method using simple models; compare the dose-volume histogram with a previously analyzed clinical case; and give the mean absorbed dose, mean biologically effective dose, and equivalent uniform dose for an illustrative case of a pediatric thyroid cancer patient with diffuse lung metastases. The mean absorbed dose, mean biologically effective dose, and equivalent uniform dose for the tumor were 57.7, 58.5, and 25.0 Gy, respectively. Corresponding values for normal lung tissue were 9.5, 9.8, and 8.3 Gy, respectively.
The analysis demonstrates the impact of radiobiologic modeling on response prediction. The 57% reduction in the equivalent dose value for the tumor reflects a high level of dose nonuniformity in the tumor and a corresponding reduced likelihood of achieving a tumor response. Such analyses are expected to be useful in treatment planning for radionuclide therapy.
传统上,基于体模和基于患者特定影像的剂量测定方法可得出肿瘤和正常器官的平均器官吸收剂量或空间剂量分布。在本研究中,引入了放射生物学建模,以将吸收剂量的空间分布转换为生物有效剂量和等效均匀剂量参数。使用来自接受放射性碘治疗的甲状腺癌患者的数据对该方法进行了说明。
使用三次配准的SPECT/CT扫描生成放射性核素动力学(清除率)和累积活度的三维图像。将累积活度图像和相应的CT扫描作为输入提供给基于EGSnrc的蒙特卡罗计算:累积活度图像用于定义衰变分布,从CT得出的衰减图像用于定义相应的空间组织密度和成分分布。速率图像用于将空间吸收剂量分布转换为生物有效剂量分布,然后用于估计感兴趣的分割体积的单个等效均匀剂量。等效均匀剂量也直接从吸收剂量分布计算得出。
我们使用简单模型验证了该方法;将剂量体积直方图与先前分析的临床病例进行了比较;并给出了一名患有弥漫性肺转移的小儿甲状腺癌患者的示例病例的平均吸收剂量、平均生物有效剂量和等效均匀剂量。肿瘤的平均吸收剂量、平均生物有效剂量和等效均匀剂量分别为57.7、58.5和25.0 Gy。正常肺组织的相应值分别为9.5、9.8和8.3 Gy。
分析证明了放射生物学建模对反应预测的影响。肿瘤等效剂量值降低57%反映了肿瘤中高水平的剂量不均匀性以及实现肿瘤反应的相应可能性降低。预计此类分析将有助于放射性核素治疗的治疗计划。