Cavin Sabrina, Wang Xingyu, Zellweger Matthieu, Gonzalez Michel, Bensimon Michaël, Wagnières Georges, Krueger Thorsten, Ris Hans-Beat, Gronchi Fabrizio, Perentes Jean Y
Division of Thoracic Surgery, Centre Hospitalier Universitaire Vaudois, Lausanne, Vaud, Switzerland.
Central Environmental Laboratory, Swiss Federal Institute of Technology, Centre Hospitalier Universitaire Vaudois, Lausanne, Vaud, Switzerland.
Lasers Surg Med. 2017 Oct;49(8):773-780. doi: 10.1002/lsm.22687. Epub 2017 May 22.
Low-dose photodynamic therapy PDT (photoinduction) can modulate tumor vessels and enhance the uptake of liposomal cisplatin (Lipoplatin®) in pleural malignancies. However, the photo-induction conditions must be tightly controlled as overtreatment shuts down tumor vessels and enhances normal tissue drug uptake.
In a pleural sarcoma and adenocarcinoma rat model (n = 12/group), we applied photoinduction (0.0625 mg/kg Visudyne®, 10 J/cm ) followed by intravenous Lipoplatin® (5 mg/kg) administration. Tumor and normal tissue IFP were assessed before and up to 1 hour following photoinduction. Lipoplatin® uptake was determined 60 minutes following photoinduction. We then treated the pleura of tumor-free minipigs with high dose photodynamic therapy (PDT) (0.0625 mg/kg Visudyne®, 30 J/cm , n = 5) followed by Lipoplatin (5 mg/kg) administration.
In rodents, photoinduction resulted in a significant decrease of IFP (P < 0.05) in both tumor types but not in the surrounding normal lung, equally exposed to light. Also, photoinduction resulted in a significant increase of Lipoplatin® uptake in both tumor types (P < 0.05) but not in normal lung. Tumor IFP variation and Lipoplatin® uptake fitted an inverted parabola. In minipigs, high dose photodynamic treatment resulted in pleural IFP increase of some animals which predicted higher Lipoplatin® uptake levels.
Normal and tumor vasculatures react differently to PDT. Continuous IFP monitoring in normal and tumor tissues is a promising biomarker of vessel photoinduction. Moderate drop in tumor with no change in normal tissue IFP are predictive of specific Lipoplatin® uptake by cancer following PDT. Lasers Surg. Med. 49:773-780, 2017. © 2017 Wiley Periodicals, Inc.
低剂量光动力疗法(PDT,光诱导)可调节肿瘤血管,并增强胸膜恶性肿瘤中脂质体顺铂(力扑素®)的摄取。然而,光诱导条件必须严格控制,因为过度治疗会导致肿瘤血管关闭,并增强正常组织对药物的摄取。
在胸膜肉瘤和腺癌大鼠模型(每组n = 12只)中,我们先进行光诱导(0.0625mg/kg维速达尔®,10J/cm²),随后静脉注射力扑素®(5mg/kg)。在光诱导前及诱导后1小时内评估肿瘤和正常组织的组织间液静水压(IFP)。在光诱导60分钟后测定力扑素®的摄取情况。然后,我们对无肿瘤小型猪的胸膜进行高剂量光动力疗法(PDT)(0.0625mg/kg维速达尔®,30J/cm²,n = 5),随后给予力扑素(5mg/kg)。
在啮齿动物中,光诱导导致两种肿瘤类型的IFP均显著降低(P < 0.05),但在同样暴露于光线下的周围正常肺组织中未出现这种情况。此外,光诱导导致两种肿瘤类型的力扑素®摄取均显著增加(P < 0.05),但正常肺组织中未出现这种情况。肿瘤IFP变化和力扑素®摄取呈倒抛物线关系。在小型猪中,高剂量光动力治疗导致一些动物的胸膜IFP升高,这预示着力扑素®摄取水平更高。
正常血管和肿瘤血管对PDT的反应不同。对正常组织和肿瘤组织进行连续的IFP监测是血管光诱导的一个有前景的生物标志物。肿瘤中IFP适度下降而正常组织IFP无变化可预测PDT后癌症对力扑素®的特异性摄取。《激光外科与医学》49:773 - 780,2017年。©2017威利期刊公司