Considerable evidence exists to indicate that local hyperthermia, alone, or with radiation or drugs, is of value in the therapy of localized malignant tumors. Uniformity of temperature in the treatment field is, however, necessary to establish accurate temperature-duration relationships for tumor response and elucidation of underlying biological mechanisms. A technique for production of such hyperthermia restricted to the treatment volume, superficial or deep, with sparing of normal tissues was developed utilizing steered, focused ultrasound and was evaluated in experimental animals, and canine and human patients. The results were remarkable in the absence of toxicity and high response rates at heat-dose levels lower than those reported in the literature. The research program proposed represents a multidisciplinary, but orchestrated effort for further evaluation and refinement of different aspects of local hyperthermia as a modality in cancer therapy. Phase I and II trials will be continued in patients with superficial and deep tumors, using hyperthermia alone, or with radiation or drugs. The studies will be extended to genitourinary and other intra-abdominal tumors, and to glioblastoma multiforme after the safety of the procedure is established in animal experiments. Effects of known levels of tumor hyperthermia in situ, such as changes in tumor and tumor-bed blood perfusion, and effects on different cytological parameters will be studied using sensitive techniques and will be correlated with the clinical results. The ultrasponic technique for generation of hyperthermia will be refined for easier clinical use, and alternative approaches using electromagnetic energy will be explored to supplement or complement the ultrasonic technique. Non-invasive methods for measurement of temperature in the target tissue will be evaluated, and a predictive computer model of tissue temperature distribution resulting from a known energy input in tissues of known thermo-physical characteristics will be developed. These developments are expected to make a definitive, long term contribution to the science of local hyperthermia for tumor therapy.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA031303-03
Application #
3093419
Study Section
Clinical Cancer Program Project Review Committee (CCP)
Project Start
1982-07-01
Project End
1988-03-31
Budget Start
1985-07-01
Budget End
1988-03-31
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Type
DUNS #
City
Cambridge
State
MA
Country
United States
Zip Code
Hurwitz, Mark D; Hansen, Jorgen L; Prokopios-Davos, Savina et al. (2011) Hyperthermia combined with radiation for the treatment of locally advanced prostate cancer: long-term results from Dana-Farber Cancer Institute study 94-153. Cancer 117:510-6
Wang, XiaoZhe; Khaleque, Md Abdul; Zhao, Mei Juan et al. (2006) Phosphorylation of HSF1 by MAPK-activated protein kinase 2 on serine 121, inhibits transcriptional activity and promotes HSP90 binding. J Biol Chem 281:782-91
Hurwitz, Mark D; Kaplan, Irving D; Hansen, Jorgen L et al. (2005) Hyperthermia combined with radiation in treatment of locally advanced prostate cancer is associated with a favourable toxicity profile. Int J Hyperthermia 21:649-56
Calderwood, Stuart K (2005) Regulatory interfaces between the stress protein response and other gene expression programs in the cell. Methods 35:139-48
Calderwood, Stuart K; Theriault, Jimmy R; Gong, Jianlin (2005) How is the immune response affected by hyperthermia and heat shock proteins? Int J Hyperthermia 21:713-6
Calderwood, S K (2005) Evolving connections between molecular chaperones and neuronal function. Int J Hyperthermia 21:375-8
Tang, Dan; Khaleque, Md Abdul; Jones, Ellen L et al. (2005) Expression of heat shock proteins and heat shock protein messenger ribonucleic acid in human prostate carcinoma in vitro and in tumors in vivo. Cell Stress Chaperones 10:46-58
Calderwood, Stuart K; Theriault, Jimmy R; Gong, Jianlin (2005) Message in a bottle: role of the 70-kDa heat shock protein family in anti-tumor immunity. Eur J Immunol 35:2518-27
Ciocca, Daniel R; Calderwood, Stuart K (2005) Heat shock proteins in cancer: diagnostic, prognostic, predictive, and treatment implications. Cell Stress Chaperones 10:86-103
Tonkiss, J; Calderwood, S K (2005) Regulation of heat shock gene transcription in neuronal cells. Int J Hyperthermia 21:433-44

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