Guest guest Posted November 15, 2001 Report Share Posted November 15, 2001 Hi, Here are some references to support the use of active oxygen in cancer therapy, as suggested in Protocol 1. 1: Natl Cancer Inst Monogr 1977 Dec;46:163-9 Hyperbaric oxygen and radiation therapy in the management of glioblastoma. Chang CH A pilot clinical trial on radiotherapy of glioblastoma with and without hyperbaric oxygen was performed at the Columbia-Presbyterian Medical Center. Eighty previously untreated patients with histologically proved glioblastoma were evaluated; 38 were irradiated under hyperbaric oxygen and 42 (controls) in atmospheric air. The survival rates were calculated according to the actuarial analysis method. At the end of 18 months, the survival rate appeared considerably higher in the oxygen group (28%) than in the controls (10%). At the end of 36 months, no patients in the control group survived, whereas 2 patients in the oxygen group were alive beyond 45 and 48 months, respectively. PMID: 206835, UI: 78177153 ------------------------------------------------------------- TI Ozone and gynecologic radiotherapy AU Hernuss-P; Muller-Tyl-E; Wicke-L SO Strahlentherapie. 1975 Nov; 150(5): 493-9 ISSN 0039-2073 LA GERMAN CP GERMANY,-WEST PT JOURNAL-ARTICLE UI 76130722 Abstract Ozone is used in medicine as well as in other spheres. Papers reporting good results of ozone treatment in carcinoma seemed of particular interest. The efficacy of ozone as an adjuvant to the irradiation of carcinosarcomas of rats was confirmed by us. On account of this fact ozone was introduced by us as an adjuvant to the irradiation of women with gynaecological cancer and appeared to give good results. The mechanism of action of ozone is not yet fully clarified and several theories are discussed. Investigations are currently being undertaken in respect to the behaviour of several substances in the organism during ozone therapy. --------------------------------------------------------------------------------\ ----- TI: Antitumor Effects of Hydrogen Peroxide in vivo. DT: July 9, 1981 AU: C.F. and Z.A. Cohn SO: J. Exp. Med, Vol. 154, November 1981, pp 1539-1553 AB: Hydrogen peroxide, a secretory product of mononuclear phagocytes, accounts for a considerable portion of their nonphagocytic lysis of tumor cells in at least three circumstances: when certain secretagogues are added, when antitumor antibody is present, or when the tumor cells are coated with eosinophil peroxidase. Granulocytes also secrete H2O2, which may participate in their cytotoxic effects in a variety of situations. In the present study we sought to devise a nontoxic way to deliver hydrogen peroxide to sites of malignancy in vivo and to test its antitumor efficacy. Finally, preformed or enzymatically generated H2O2, with or without a peroxidase, lyses tumor cells. ------------------------------------------------------------------------------- TI: Rationale For Treatment of Cancer with Ozone DT: 1988 AU: Boguslaw Lipinski, Ph.D. SO: Boston Cardiovascular Health Center and Tufts University School of Medicine One Washington Street, Wellesley, MA. 02181 AB: In cancer there is an abnormally high concentration of artificial, food-derived AOs and low oxygen supply. Under such conditions there is no lipid peroxidation products formed and thus no inhibitors are present to control cell division. This situation, similar to that occurring in the anaerobic cells can be reversed by introduction of strong oxidants such as oxygen or ozone in the presence of sufficient concentration of natural antioxidants (vitamin C and E). Intraarterial administration of ozone might, therefore, prove to be an effective treatment for many types of cancer. --------------------------------------------------------------------------------\ ----- Ozone Selectively Inhibits Growth of Human Cancer Cells Science Vol. 209, 22 Aug 1980, pp. 931-933 Abstract: The growth of human cancer cells from lung, breast, and uterine tumors was selectively inhibited in a dose-dependent manner by ozone at 0.3 to 0.8 part per million of ozone in ambient air during 8 days of culture. Human lung diploid fibroblasts served as noncancerous control cells. The presence of ozone at 0.3 to 0.5 part per million inhibited cancer cell growth 40 and 60 percent, respectively. The non-cancerous lung cells were unaffected at these levels. Exposure to ozone at 0.8 part per million inhibited cancer cell growth more than 90 percent and control cell growth less than 50 percent. Evidently, the mechanisms for defense against ozone damage are impaired in human cancer cells. --------------------------------------------------------------------------------\ -- Adv Exp Med Biol 1984;169:613-9 Effectiveness of respiratory hyperoxia, of normobaric and of hyperbaric oxygen atmospheres in improving tumor oxygenation. Mueller-Klieser W, Vaupel P, Manz R Tumor oxygenation during respiratory hyperoxia is dependent on the tumor growth site, on the growth stage, and hence on the vascular pattern. Diffusion of O2 from the surrounding atmosphere contributes considerably to the oxygenation of subcutaneous tumors during normobaric exposure to a pure O2 atmosphere. However, hypoxia (lack of oxygen) is still present in the tumor core under these conditions, and pressurization up to 4 bar is required to completely eradicate these hypoxic areas, thus enhancing the radiosensitivity of the tumors. PMID: 6731116, UI: 84227650 --------------------------------------------------------- Aronoff, B. L. (1965) " " Regional Oxygenation in Neoplasm. " Cancer. Vol 18. Gerson, Max. (1990) A Cancer Therapy. Bonita, CA: Gerson Institute/Pulse. Samoszuk, M.K. et.al. (1989) " In Vitro Sensitivity of Hodgkins Disease to Hydrogen Peroxide, " Cancer. Vol. 63. Sasaki, H., et. al. (1967) " Application of Hydrogen Peroxide to Maxillary Cancer, " Yonago Acta Medica Vol. 11/3. 109. Sweet, F. et. a;. (1980) " Ozone Selectivity Inhibits Growth of Cancer Cells. " Science. Aug 22. 931-932. Varro, J. (1983) " Ozone Apllications in Cancer Cases, " Medical Applications of Ozone. Norwalk, Conn: International Ozone Association, Pan American Committee. Warburg, Otto.(1966) The Prime Cause and Prevention of Cancer. Wurzburg: K. Triltsch. Grunder, H.G., E. Bauer, G. Tramer, E. Utesch. (1976) " Intravenous Ozone in Irradiated and Non-Irradiated Tumors in Mice. " Strahlenther, Vol151. 151-154, 480-486,522-529. Hernuss, P. (1973) " The Effects of Ozone in RadioTherapy for Tumors in Animal Experiments. " Fortschr auf dem Geb der Roentgenstr und der Nuklearned.Suppl. 196. , C.F. and Z. A. Cohn. (1981) " Antitumor Effects of Hydrogen Peroxide in Vivo, " Journal of Experimental Medicine. Vol. 149. esu, L., Luzzi, E., Bocci, V., (1990) " Studies on the Biological Effects of Ozone: Induction of Tumor Necrosis Factor (TNF-a) on Human Leukocytes. Lymphokine and Cytokine Research. Vol. 10.5: 409-412. Teske, H.J., J. Haller, B. Badenber, G. Hoppe (1972) " Studies of the Effect of Ozone on Tumor Growth and the Action of Irradiation. " Deutschr. Roentgenkongr. (Stuttgart) TI Regional hyperoxygenation: an important factor in the potentiation of antineoplastic chemotherapy AU Nervi-C; Casale-C; Cortese-M SO Tumori. 1969 May-Jun; 55(3): 153-9 ISSN 0300-8916 LA ITALIAN CP ITALY PT JOURNAL-ARTICLE UI 70281300 TI Combined therapy of intra-arterial injection of hydrogen peroxide solution and irradiations in maxillary cancer AU Sasaki-H; Wakuya-T; Oda-K; Yamazaki-Y SO Nippon-Jibiinkoka-Gakkai-Kaiho. 1971 Feb; 74(2): 398-9 ISSN 0030-6622 LA JAPANESE CP JAPAN PT JOURNAL-ARTICLE UI 72003396 TI Studies on the effect of ozone on tumor growth and radiation effect (animal experiments) AU Teske-HJ; Haller-J; Badenberg-B; Hoppe-G SO Fortschr-Geb-Rontgenstr-Nuklearmed. 1972: Suppl:12-4 ISSN 0015-8151 LA GERMAN CP GERMANY,-WEST PT JOURNAL-ARTICLE UI 73053628 moonbeam Quote Link to comment Share on other sites More sharing options...
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