The long term objective of this research is to provide information on the type and expected frequency of injury to normal periaortic tissues following intraoperative irradiation (IORT). There is great interest in IORT for improving control of tumors located near radiosensitive structures or involving large vessels or nerves.
A specific aim of this study is to determine the effect of the volume of normal tissue irradiated. As the major advantage of IORT is to restrict the irradiated volume as much as possible, information concerning dose volume relationships is most important. Another objective of the volume study is to determine the progression and pathogenesis of slowly developing lesions in canine periaortic tissues at variable intervals following IORT. This will be done primarily with specialized histologic techniques including ultrastructural studies. Of particular interest is the cellular response near the periphery of the irradiated field as migration from non-irradiated tissue may modify the tissue response depending on volume irradiated.
A second aim of this is to estimate the amount and rate of repair of periaortic tissues using split dose techniques with variable intervals between the first and second dose. Sequential functional examinations will include aortagrams and aortic pressure measurements, observations for peripheral nerve injury, electrophysiologic measurements, intravenous urography, and blood and urine chemistries. Other functional examinations include ureteral electromyography and pressure measurements. Necropsies of dogs three years following treatment will provide tissues for morphometric analysis of the aorta, arteries, microvasculature, peripheral nerves, muscles, ureters, and lumbar vertebrae. Of special interest will be the percentage volume changes in parenchyma, stroma and microvasculature. Development of thrombi and aneurysms in vessels, neuropathies, structures of ureters and bone necrosis will be evaluated. This information will provide guidance to those using IORT so that the risk of late developing serious normal tissue complications can be reduced. The questions asked are of more general interest in radiation therapy than just for intraoperative radiation therapy. The tissues evaluated are the entire vascular tree from aorta to capillaries, peripheral nerves, muscle, bone and ureters. There is little research specifically directed at those tissues even though they include the most common tissues at risk in radiation therapy and in many cases are dose limiting. Because of the size of the dog, they can all be studied in the same animal and the same field of irradiation. Questions concerning radiation repair by these late responding tissues and volume effects have not been answered and are of major concern in radiation therapy. Another important attribute of the animal model proposed is that functional and histologic studies can be done on the same animal. The functional studies are clinically relevant, the end points of paralysis, ureteral structure, aneurysm, thrombosis, bone necrosis and muscle atrophy are obviously important clinical consequences of radiation. Careful histologic evaluations permit dose response comparisons and insight into the basic mechanisms and cellular interactions leading to late consequences of irradiation.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA029117-13
Application #
2087875
Study Section
Surgery and Bioengineering Study Section (SB)
Project Start
1981-01-01
Project End
1995-12-31
Budget Start
1994-03-01
Budget End
1995-12-31
Support Year
13
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Colorado State University-Fort Collins
Department
Radiation-Diagnostic/Oncology
Type
Schools of Veterinary Medicine
DUNS #
112617480
City
Fort Collins
State
CO
Country
United States
Zip Code
80523
Powers, B E; Thames, H D; Gillette, E L (1999) Long-term adverse effects of radiation inhibition of restenosis: radiation injury to the aorta and branch arteries in a canine model. Int J Radiat Oncol Biol Phys 45:753-9
Gillette, S M; Gillette, E L; LaRue, S M et al. (1998) Effects of volume irradiated on the function of the canine ureter. Radiat Res 150:436-41
Gillette, E L; Mahler, P A; Powers, B E et al. (1995) Late radiation injury to muscle and peripheral nerves. Int J Radiat Oncol Biol Phys 31:1309-18
Gillette, E L; LaRue, S M; Gillette, S M (1995) Normal tissue tolerance and management of radiation injury. Semin Vet Med Surg (Small Anim) 10:209-13
LaRue, S M; Gillette, S M; Poulson, J M (1995) Radiation therapy of thoracic and abdominal tumors. Semin Vet Med Surg (Small Anim) 10:190-6
Gillette, E L; Powers, B E; Gillette, S M et al. (1993) Muscle injury in experimental intraoperative irradiation. Recent Results Cancer Res 130:79-87
Powers, B E; Gillette, E L; Gillette, S L et al. (1991) Muscle injury following experimental intraoperative irradiation. Int J Radiat Oncol Biol Phys 20:463-71
Gillette, S M; Gillette, E L; Powers, B E et al. (1990) Radiation-induced osteosarcoma in dogs after external beam or intraoperative radiation therapy. Cancer Res 50:54-7
Powers, B E; Gillette, E L; McChesney, S L et al. (1989) Bone necrosis and tumor induction following experimental intraoperative irradiation. Int J Radiat Oncol Biol Phys 17:559-67
Gillette, E L; Powers, B E; McChesney, S L et al. (1989) Response of aorta and branch arteries to experimental intraoperative irradiation. Int J Radiat Oncol Biol Phys 17:1247-55

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