Bérard Véronique, Rousseau Jacques A, Cadorette Jules, Hubert Laurent, Bentourkia M'hamed, van Lier Johan E, Lecomte Roger
Sherbrooke Molecular Imaging Centre, Etienne-LeBel Clinical Research Centre, Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Quebec, Canada.
J Nucl Med. 2006 Jul;47(7):1119-26.
This study evaluated the potential use of dynamic PET to monitor transient metabolic processes and to investigate the mechanisms of action of new photosensitizing drugs in the photodynamic therapy (PDT) of cancer.
Rats bearing 2 mammary tumors received different phthalocyanine-based photosensitizers. The following day, the animals were positioned in a Sherbrooke small-animal PET scanner and continuously infused with 18F-FDG while dynamic images were acquired for 2 h. During that period, one of the 2 tumors was exposed for 30 min to red light delivered by a small diode laser to activate PDT.
18F-FDG time-activity curves during PDT showed distinct transient patterns characterized by a drop and subsequent recovery of tumor 18F-FDG uptake rates. Variations in these rates and response delay parameters revealed tumoral and systemic metabolic processes that correlated with differences in mechanism of action between drugs, that is, direct tumor cell kill or initial vascular shutdown.
Real-time follow-up of tumor response to PDT as monitored by dynamic 18F-FDG PET has been shown to correlate with the mechanisms of action of photosensitizing drugs in vivo. This new imaging paradigm can be exploited to monitor a variety of transient cellular and molecular processes as they occur in vivo, enabling the mechanisms of action of therapeutic interventions to be scrutinized and their efficacy predicted in real time.
本研究评估了动态正电子发射断层扫描(PET)在监测短暂代谢过程以及研究新型光敏药物在癌症光动力疗法(PDT)中的作用机制方面的潜在用途。
患有两个乳腺肿瘤的大鼠接受了不同的基于酞菁的光敏剂。第二天,将动物置于舍布鲁克小动物PET扫描仪中,并持续输注18F-氟代脱氧葡萄糖(18F-FDG),同时采集2小时的动态图像。在此期间,两个肿瘤中的一个暴露于小型二极管激光器发出的红光下30分钟以激活PDT。
PDT期间的18F-FDG时间-活性曲线显示出明显的短暂模式,其特征是肿瘤18F-FDG摄取率下降并随后恢复。这些速率和反应延迟参数的变化揭示了肿瘤和全身代谢过程,这些过程与药物之间作用机制的差异相关,即直接杀死肿瘤细胞或最初的血管关闭。
动态18F-FDG PET监测的肿瘤对PDT反应的实时随访已被证明与体内光敏药物的作用机制相关。这种新的成像模式可用于监测体内发生的各种短暂细胞和分子过程,从而能够仔细研究治疗干预的作用机制并实时预测其疗效。