Dual-energy micro-computed tomography imaging of radiation-induced vascular changes in primary mouse sarcomas.

PURPOSE To evaluate the effects of radiation therapy on primary tumor vasculature using dual-energy (DE) micro-computed tomography (micro-CT). METHODS AND MATERIALS Primary sarcomas were generated with mutant Kras and p53. Unirradiated tumors were compared with tumors irradiated with 20 Gy. A liposomal-iodinated contrast agent was administered 1 day after treatment, and mice were imaged immediately after injection (day 1) and 3 days later (day 4) with DE micro-CT. CT-derived tumor sizes were used to assess tumor growth. After DE decomposition, iodine maps were used to assess tumor fractional blood volume (FBV) at day 1 and tumor vascular permeability at day 4. For comparison, tumor vascularity and vascular permeability were also evaluated histologically by use of CD31 immunofluorescence and fluorescently-labeled dextrans. RESULTS Radiation treatment significantly decreased tumor growth from day 1 to day 4 (P<.05). There was a positive correlation between CT measurement of tumor FBV on day 1 and extravasated iodine on day 4 with microvascular density (MVD) on day 4 (R(2)=0.53) and dextran accumulation (R(2)=0.63) on day 4, respectively. Despite no change in MVD measured by histology, tumor FBV significantly increased after irradiation as measured by DE micro-CT (0.070 vs 0.091, P<.05). Both dextran and liposomal-iodine accumulation in tumors increased significantly after irradiation, with dextran fractional area increasing 5.2-fold and liposomal-iodine concentration increasing 4.0-fold. CONCLUSIONS DE micro-CT is an effective tool for noninvasive assessment of vascular changes in primary tumors. Tumor blood volume and vascular permeability increased after a single therapeutic dose of radiation treatment.

[1]  Frank Bergner,et al.  Low-dose cardio-respiratory phase-correlated cone-beam micro-CT of small animals. , 2011, Medical physics.

[2]  Cristian T. Badea,et al.  Dual-energy micro-CT imaging for differentiation of iodine- and gold-based nanoparticles , 2011, Medical Imaging.

[3]  V. Goh,et al.  Imaging tumor angiogenesis: functional assessment using MDCT or MRI? , 2006, Abdominal Imaging.

[4]  James Ze Wang,et al.  Stereotactic body radiation therapy: a novel treatment modality , 2010, Nature Reviews Clinical Oncology.

[5]  M. Kaag,et al.  Endothelial Membrane Remodeling Is Obligate for Anti-Angiogenic Radiosensitization during Tumor Radiosurgery , 2010, PloS one.

[6]  Gerald Antoch,et al.  Dual-energy-CT of hypervascular liver lesions in patients with HCC: investigation of image quality and sensitivity , 2011, European Radiology.

[7]  Thomas Henzler,et al.  Contrast-Enhanced Dual-Energy CT of Gastrointestinal Stromal Tumors: Is Iodine-Related Attenuation a Potential Indicator of Tumor Response? , 2012, Investigative radiology.

[8]  R. Myers,et al.  Radiation-induced modification of blood flow distribution in a rat fibrosarcoma. , 1991, International journal of radiation biology.

[9]  J R Griffiths,et al.  Phosphorus-31 magnetic resonance spectroscopy and blood perfusion of the RIF-1 tumor following X-irradiation. , 1989, International journal of radiation oncology, biology, physics.

[10]  G. Allan Johnson,et al.  Denoising of 4D cardiac micro-CT data using median-centric bilateral filtration , 2012, Medical Imaging.

[11]  Ananth Annapragada,et al.  Evaluation of tumor microenvironment in an animal model using a nanoparticle contrast agent in computed tomography imaging. , 2011, Academic radiology.

[12]  R. Timmerman,et al.  Stereotactic Body Radiation Therapy: A Comprehensive Review , 2007, American journal of clinical oncology.

[13]  Jan Grimm,et al.  A spatially and temporally restricted mouse model of soft tissue sarcoma , 2007, Nature Medicine.

[14]  M. Reiser,et al.  Material differentiation by dual energy CT: initial experience , 2007, European Radiology.

[15]  P Jack Hoopes,et al.  Ionizing radiation increases systemic nanoparticle tumor accumulation. , 2012, Nanomedicine : nanotechnology, biology, and medicine.

[16]  C T Badea,et al.  A dual micro-CT system for small animal imaging , 2008, SPIE Medical Imaging.

[17]  Olivier D. Faugeras,et al.  Variational Methods for Multimodal Image Matching , 2002, International Journal of Computer Vision.

[18]  L. Feldkamp,et al.  Practical cone-beam algorithm , 1984 .

[19]  R. Brasch,et al.  Contrast-enhanced MR imaging assessment of tumor capillary permeability: effect of irradiation on delivery of chemotherapy. , 1996, Radiology.

[20]  Mark W. Dewhirst,et al.  Cycling hypoxia and free radicals regulate angiogenesis and radiotherapy response , 2008, Nature Reviews Cancer.

[21]  M. Krause,et al.  Cancer stem cells at the crossroads of current cancer therapy failures--radiation oncology perspective. , 2010, Seminars in cancer biology.

[22]  M. Graham,et al.  Blood flow changes following 137Cs irradiation in a rat glioma model. , 1988, Radiation research.

[23]  R. Jain,et al.  Neovascularization after irradiation: what is the source of newly formed vessels in recurring tumors? , 2012, Journal of the National Cancer Institute.

[24]  Fiona A. Stewart,et al.  Strategies to improve radiotherapy with targeted drugs , 2011, Nature Reviews Cancer.

[25]  S M Johnston,et al.  Dual-energy micro-CT of the rodent lung. , 2012, American journal of physiology. Lung cellular and molecular physiology.