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[Cancer Research 43, 2018-2022, May 1, 1983]
© 1983 American Association for Cancer Research

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Preclinical Trial of a Radiant Heat Device for Whole-Body Hyperthermia Using a Porcine Model1

H. Ian Robins2, Jeffrey Grossman, Thomas E. Davis, James P. AuBuchon and Warren Dennis

Departments of Human Oncology [H. I. R., T. E. D.], Medicine [J. G.], Physiology [W. D.], and Pathology and Laboratory Medicine [J. P. A.], University of Wisconsin Clinical Science Center, Madison, Wisconsin 53792

After review of the published clinical experience with systemic hyperthermia, we concluded that a simple system which controls radiant heat balance to supplement metabolic heat might provide several advantages, including: (a) decreased morbidity; (b) elimination of the requirement for general anesthesia; (c) improved patient comfort; and (d) favorable cost-benefit considerations. We have tested a prototype radiant heat device for whole-body hyperthermia (WBH) in patients with disseminated cancer. From preclinical evaluation of this device, the lightly anesthetized pig was found to be an ideal model for WBH. This species has physiological characteristics closely resembling those of humans. The pig's core, pulmonary artery, liver, rectal, and esophageal temperatures were raised to 41.8° in 80 to 90 min. The air temperatures near the chamber wall never exceeded 65° while the air temperature adjacent to the animal was 46°. Skin temperatures were approximately 42.5° at a core temperature of 41.8°. Once the core temperature is raised to 41.8°, this temperature is maintainable for ~3.5 hr without additional external heating if evaporative losses are controlled.

Prolonged WBH was accomplished with light sedation and without the requirement for endotracheal intubation. No significant acute toxicity was encountered in a series of 6 pigs undergoing 9 separate exposures to WBH. From these results, we conclude that our radiant heat apparatus is feasible for clinical trials. Additionally, the use of the pig as an appropriate animal model for further physiological and pharmacological WBH studies is strongly recommended.

1 Supported in part by NIH Grants R01-CA-24872, R25-CA-18397, and P30-CA-14520 and by the American Cancer Society. Presented in part, American Association of Cancer Research, Washington, D. C., April 1981 (17); Radiation Research Society, Minneapolis, Minn., June 1981 (16).

2 To whom requests for reprints should be addressed.

Received 9/27/82. Accepted 2/ 4/83.




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A. Bakhshandeh, V. Bath, G. J Wiedemann, W. Longo, B. M Lerner, C. L Tiggelaar, and H I. Robins
Year 2000 guidelines for clinical practice of whole body hyperthermia combined with cytotoxic drugs from the University of Lubeck and the University of Wisconsin
Journal of Oncology Pharmacy Practice, September 1, 1999; 5(3): 131 - 134.
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Copyright © 1983 by the American Association for Cancer Research.