Florida International University, College of Medicine, Miami, Florida 33199, USA.
J Nucl Med. 2010 Feb;51(2):301-10. doi: 10.2967/jnumed.109.069278. Epub 2010 Jan 15.
Selective internal radiation treatment (SIRT) via intrahepatic arterial administration of (90)Y microspheres is an effective therapeutic modality. The conventional and generally applied MIRD schema is based on the premise that the distribution of microspheres in the liver parenchyma is uniform. In reality, however, the distribution of the microspheres follows a distinct pattern, requiring that a model be developed to more appropriately estimate radiation absorbed doses to the different structural/functional elements of the hepatic microanatomy.
A systematic investigation was performed encompassing a conventional average absorbed dose assessment, a compartmental macrodosimetric approach that accounts for the anticipated higher tumor-to-normal liver activity concentration ratio, dose point-kernel convolution-derived estimates, and Monte Carlo dose estimates employing a spherical and 3-dimensional hexagonal liver model, including various subunits of the hepatic anatomy, down to the micrometer level.
Detailed specifics of the radiation dose deposition of (90)Y microspheres demonstrated a rapid decrease in absorbed dose in and around the portal tracts where the microspheres are deposited. The model also demonstrated that the hepatocellular parenchymal and central vein doses could be at significant levels because of a cross-fire effect.
The reported microstructural dosimetry models can help in the detailed assessment of the dose distributions in the hepatic functional subunits and in relating these doses to their effects. These models have also revealed that the there is a consistent relationship between the average liver dose as calculated by MIRD macrodosimetry and the structural dosimetry estimates in support of the clinical utility of the MIRD methodology. This relationship could be used to more realistically assess patterns of hepatic toxicity associated with the (90)Y SIRT treatment.
经肝动脉内注射(90)Y 微球的选择性内放射治疗(SIRT)是一种有效的治疗方法。传统的和通常应用的 MIRD 方案基于微球在肝实质中的分布均匀的前提。然而,实际上,微球的分布遵循明显的模式,需要开发一种模型来更恰当地估计肝微血管解剖结构/功能元素的不同吸收剂量。
进行了系统的研究,包括常规的平均吸收剂量评估、考虑到预期更高的肿瘤-正常肝活性浓度比的房室宏观剂量学方法、剂量点核卷积衍生估计以及使用球形和三维六方肝模型的蒙特卡罗剂量估计,包括肝解剖学的各种亚单位,直至微米级。
(90)Y 微球的辐射剂量沉积的详细细节表明,在门静脉轨道内和周围的吸收剂量迅速下降,微球沉积于此。该模型还表明,由于交叉火力效应,肝细胞实质和中央静脉的剂量可能达到显著水平。
所报道的微结构剂量学模型有助于详细评估肝功能亚单位的剂量分布,并将这些剂量与其效应联系起来。这些模型还表明,MIRD 宏观剂量学计算的平均肝剂量与结构剂量学估计之间存在一致的关系,支持 MIRD 方法的临床实用性。这种关系可用于更真实地评估与(90)Y SIRT 治疗相关的肝毒性模式。