Aumiller Maximilian, Heckl Christian, Quach Stefanie, Stepp Herbert, Ertl-Wagner Birgit, Sroka Ronald, Thon Niklas, Rühm Adrian
Laser-Forschungslabor, LIFE Center, University Hospital, LMU Munich, 82152 Planegg, Germany.
Department of Urology, University Hospital, LMU Munich, 81377 Munich, Germany.
Cancers (Basel). 2021 Dec 27;14(1):120. doi: 10.3390/cancers14010120.
In a former study, interstitial photodynamic therapy (iPDT) was performed on patients suffering from newly diagnosed glioblastoma ( = 11; 8/3 male/female; median age: 68, range: 40-76). The procedure includes the application of 5-ALA to selectively metabolize protoporphyrin IX (PpIX) in tumor cells and illumination utilizing interstitially positioned optical cylindrical diffuser fibers (CDF) (2-10 CDFs, 2-3 cm diffusor length, 200 mW/cm, 635 nm, 60 min irradiation). Intraoperative spectral online monitoring (SOM) was employed to monitor treatment light transmission and PpIX fluorescence during iPDT. MRI was used for treatment planning and outcome assessment. Case-dependent observations included intraoperative reduction of treatment light transmission and local intrinsic T1 hyperintensity in non-contrast-enhanced T1-weighted MRI acquired within one day after iPDT. Intrinsic T1 hyperintensity was observed and found to be associated with the treatment volume, which indicates the presence of methemoglobin, possibly induced by iPDT. Based on SOM data, the optical absorption coefficient and its change during iPDT were estimated for the target tissue volumes interjacent between evaluable CDF-pairs at the treatment wavelength of 635 nm. By spatial comparison and statistical analysis, it was found that observed increases of the absorption coefficient during iPDT were larger in or near regions of intrinsic T1 hyperintensity ( = 0.003). In cases where PpIX-fluorescence was undetectable before iPDT, the increase in optical absorption and intrinsic T1 hyperintensity tended to be less. The observations are consistent with in vitro experiments and indicate PDT-induced deoxygenation of hemoglobin and methemoglobin formation. Further investigations are needed to provide more data on the time course of the observed changes, thus paving the way for optimized iPDT irradiation protocols.
在一项先前的研究中,对新诊断的胶质母细胞瘤患者( = 11;男/女比例为8/3;中位年龄:68岁,范围:40 - 76岁)进行了间质光动力疗法(iPDT)。该 procedure 包括应用5 - 氨基乙酰丙酸(5 - ALA)以选择性地使肿瘤细胞中的原卟啉IX(PpIX)代谢,并利用间质放置的光学圆柱形扩散光纤(CDF)进行照射(2 - 10根CDF,扩散器长度2 - 3 cm,200 mW/cm,635 nm,照射60分钟)。术中采用光谱在线监测(SOM)来监测iPDT期间的治疗光传输和PpIX荧光。MRI用于治疗计划和结果评估。病例相关观察包括术中治疗光传输的降低以及在iPDT后一天内获取的非增强T1加权MRI中局部固有T1高信号强度。观察到固有T1高信号强度并发现其与治疗体积相关,这表明可能由iPDT诱导的高铁血红蛋白的存在。基于SOM数据,在635 nm治疗波长下,对可评估的CDF对之间的目标组织体积估计了光吸收系数及其在iPDT期间的变化。通过空间比较和统计分析,发现在固有T1高信号强度区域或其附近,iPDT期间观察到的吸收系数增加更大( = 0.003)。在iPDT前未检测到PpIX荧光的情况下,光吸收和固有T1高信号强度的增加往往较小。这些观察结果与体外实验一致,并表明PDT诱导血红蛋白脱氧和高铁血红蛋白形成。需要进一步研究以提供关于观察到的变化的时间进程的更多数据,从而为优化的iPDT照射方案铺平道路。