A study of MRI-guided diffuse fluorescence molecular tomography for monitoring PDT effects in pancreas cancer

K. Samkoe, S. Davis, S. Srinivasan, J. O’Hara, T. Hasan, B. Pogue
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引用次数: 7

Abstract

Over the last several decades little progress has been made in the therapy and treatment monitoring of pancreas adenocarcinoma, a devastating and aggressive form of cancer that has a 5-year patient survival rate of 3%. Currently, investigations for the use of interstitial Verteporfin photodynamic therapy (PDT) are being undertaken in both orthotopic xenograft mouse models and in human clinical trials. In the mouse models, magnetic resonance (MR) imaging has been used as a measure of surrogate response to Verteporfin PDT; however, MR imaging alone lacks the molecular information required to assess the metabolic function and growth rates of the tumor immediately after treatment. We propose the implementation of MR-guided fluorescence tomography in conjunction with a fluorescently labeled (IR-Dye 800 CW, LI-COR) epidermal growth factor (EGF) as a molecular measure of surrogate response. To demonstrate the effectiveness of MR-guided diffuse fluorescence tomography for molecular imaging, we have used the AsPC-1 (+EGFR) human pancreatic adenocarcinoma in an orthotopic mouse model. EGF IRDye 800CW was injected 48 hours prior to imaging. MR image sequences were collected simultaneously with the fluorescence data using a MR-coupled diffuse optical tomography system. Image reconstruction was performed multiple times with varying abdominal organ segmentation in order to obtain a optimal tomographic image. It is shown that diffuse fluorescence tomography of the orthotopic pancreas model is feasible, with consideration of confounding fluorescence signals from the multiple organs and tissues surrounding the pancreas. MR-guided diffuse fluorescence tomography will be used to monitor EGF response after photodynamic therapy. Additionally, it provide the opportunity to individualize subsequent therapies based on response to PDT as well as to evaluate the success of combination therapies, such as PDT with chemotherapy, antibody therapy or even radiation.
mri引导下弥漫荧光分子断层扫描监测胰腺癌PDT效果的研究
在过去的几十年里,胰腺腺癌的治疗和治疗监测几乎没有取得进展,这是一种破坏性和侵袭性的癌症,患者的5年生存率为3%。目前,间质性维替波芬光动力疗法(PDT)的研究正在原位异种移植小鼠模型和人类临床试验中进行。在小鼠模型中,磁共振(MR)成像已被用作对维替波芬PDT的替代反应的测量;然而,单独的磁共振成像缺乏评估治疗后肿瘤代谢功能和生长速度所需的分子信息。我们建议将核磁共振引导下的荧光断层扫描与荧光标记(IR-Dye 800 CW, LI-COR)表皮生长因子(EGF)结合使用,作为替代反应的分子测量方法。为了证明磁共振引导的弥漫荧光断层扫描在分子成像中的有效性,我们在原位小鼠模型中使用了AsPC-1 (+EGFR)人胰腺腺癌。成像前48小时注射EGF IRDye 800CW。使用磁共振耦合漫射光学层析成像系统同时收集磁共振图像序列和荧光数据。通过不同的腹部器官分割进行多次图像重建,以获得最佳的层析图像。结果表明,考虑到胰腺周围多器官和组织的混杂荧光信号,对正位胰腺模型进行弥漫性荧光断层扫描是可行的。mri引导的漫射荧光断层扫描将用于监测光动力治疗后的EGF反应。此外,它提供了基于PDT反应的个性化后续治疗的机会,以及评估联合治疗的成功,例如PDT与化疗,抗体治疗甚至放射治疗。
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