Kawakubo Masayoshi, Eguchi Keisuke, Arai Tsunenori, Kobayashi Koichi, Hamblin Michael R
Department of Thoracic Surgery, School of Medicine, Keio University, Tokyo, Japan.
Lasers Surg Med. 2012 Aug;44(6):500-7. doi: 10.1002/lsm.22046. Epub 2012 Jun 29.
Photodynamic therapy (PDT) may be a less invasive treatment for lung cancer. Our newly developed surface layer-preserving PDT (SPPDT) technique enables us to irradiate deep tumor while preserving the overlying tissue. The aim of this basic study was to verify that the SPPDT technique might be applied to lung cancer.
STUDY DESIGN/MATERIALS AND METHODS: PDT with talaporfin sodium was performed using a pulsed laser with different pulse dose rates (PDRs, 2.5-20.0 mJ/cm(2) /pulse) in a mouse model of subcutaneous tumor. To mimic the tracheal wall structure and a thoracic tumor in the tracheobronchus, we also made a mouse model in which a piece of swine cartilage was placed between the dermis and the tumor, and PDT was carried out 2 weeks after implantation. In both experiments, the tissue samples were collected 48 hours after PDT and evaluated microscopically.
SPPDT using a high-PDR laser damaged the underlying tissue but left the superficial tissue intact in the mouse subcutaneous tumor model. In SPPDT, a higher PDR produced a thicker layer of intact superficial tissue than a lower PDR, while a lower PDR produced a deeper layer of damaged tissue than a higher PDR. SPPDT was also able to preserve the superficial tissue and to damage the tumor tissue beneath the cartilage implant.
SPPDT was able to damage tumor beneath the superficial normal tissue layer, which included tracheal cartilage in the mouse model. The thickness control of SPPDT was provided by controlling laser pulse intensity. SPPDT is a new technology, whose future potential is unknown. The initial clinical application of this technology could be endoscopic treatment (e.g., palliative therapy of thoracic malignancies via bronchoscopy).
光动力疗法(PDT)可能是一种侵入性较小的肺癌治疗方法。我们新开发的保留表层光动力疗法(SPPDT)技术使我们能够在保留覆盖组织的同时照射深部肿瘤。这项基础研究的目的是验证SPPDT技术是否可应用于肺癌。
研究设计/材料与方法:在皮下肿瘤小鼠模型中,使用不同脉冲剂量率(PDRs,2.5 - 20.0 mJ/cm²/脉冲)的脉冲激光进行用替莫泊芬钠的PDT。为模拟气管壁结构和气管支气管内的胸部肿瘤,我们还制作了一个小鼠模型,其中在真皮和肿瘤之间放置一块猪软骨,并在植入后2周进行PDT。在两个实验中,PDT后48小时收集组织样本并进行显微镜评估。
在小鼠皮下肿瘤模型中,使用高PDR激光的SPPDT损伤了深层组织,但表层组织保持完整。在SPPDT中,较高的PDR比较低的PDR产生更厚的完整表层组织层,而较低的PDR比较高的PDR产生更深层的受损组织。SPPDT还能够保留表层组织并损伤软骨植入物下方的肿瘤组织。
SPPDT能够损伤表层正常组织层下方的肿瘤,在小鼠模型中这包括气管软骨。通过控制激光脉冲强度可实现SPPDT的厚度控制。SPPDT是一项新技术,其未来潜力未知。该技术的初步临床应用可能是内镜治疗(例如,通过支气管镜对胸部恶性肿瘤进行姑息治疗)。