Photodynamic Therapy Center at the Department of Cell Stress Biology, Roswell Park Comprehensive Cancer Center (Roswell Park), Buffalo, NY, USA.
Laboratory Animals Shared Resources, Roswell Park, Buffalo, NY, USA.
Methods Mol Biol. 2022;2451:151-162. doi: 10.1007/978-1-0716-2099-1_11.
Interstitial photodynamic therapy (I-PDT) is a promising therapy considered for patients with locally advanced cancer. In I-PDT, laser fibers are inserted into the tumor for effective illumination and activation of the photosensitizer in a large tumor. The intratumoral light irradiance and fluence are critical parameters that affect the response to I-PDT. In vivo animal models are required to conduct light dose studies, to define optimal irradiance and fluence for I-PDT. Here we describe two animal models with locally advanced tumors that can be used to evaluate the response to I-PDT. One model is the C3H mouse bearing large subcutaneous SCCVII carcinoma (400-600 mm). Using this murine model, multiple light regimens with one or two optical fibers with cylindrical diffuser ends (cylindrical diffuser fiber, CDF) can be used to study tumor response to I-PDT. However, tissue heating may occur when 630 nm therapeutic light is delivered through CDF at an intensity ≥60 mW/cm and energy ≥100 J/cm. These thermal effects can impact tumor response while treating locally advanced mice tumors. Magnetic resonance imaging and thermometry can be used to study these thermal effects. A larger animal model, New Zealand White rabbit with VX2 carcinoma (~5000 mm) implanted in either the sternomastoid (neck implantation model) or the biceps femoris muscle (thigh implantation model), can be used to study I-PDT with image-based pretreatment planning using computed tomography. In the VX2 model, the light delivery can include the use of multiple laser fibers to test light dosimetry and delivery that are relevant for clinical use of I-PDT.
间质光动力疗法(I-PDT)是一种有前途的治疗方法,适用于局部晚期癌症患者。在 I-PDT 中,激光纤维插入肿瘤中,以有效照亮和激活大肿瘤中的光敏剂。肿瘤内的光辐照度和剂量是影响 I-PDT 反应的关键参数。需要进行活体动物模型的光剂量研究,以确定 I-PDT 的最佳辐照度和剂量。本文介绍了两种具有局部晚期肿瘤的动物模型,可用于评估 I-PDT 的反应。一种模型是携带大的皮下 SCCVII 癌(400-600mm)的 C3H 小鼠。使用这种鼠模型,可以使用一个或两个带有圆柱形扩散器末端的光纤(圆柱形扩散光纤,CDF)的多种光方案来研究肿瘤对 I-PDT 的反应。然而,当 630nm 治疗光以≥60mW/cm 的强度和≥100J/cm 的能量通过 CDF 传输时,可能会发生组织加热。这些热效应会影响治疗局部晚期小鼠肿瘤时的肿瘤反应。磁共振成像和测温仪可用于研究这些热效应。一种更大的动物模型,即新西兰白兔,在胸锁乳突肌(颈部植入模型)或股二头肌(大腿植入模型)中植入 VX2 癌(约 5000mm),可用于使用计算机断层扫描进行基于图像的预处理规划来研究 I-PDT。在 VX2 模型中,光传递可以包括使用多个激光纤维来测试与 I-PDT 的临床应用相关的光剂量学和传递。