A phase I trial of tocoferol monoglucoside in patients undergoing hemi-body radiation.
dc.contributor.author | Huilgol, N G | en_US |
dc.contributor.author | Nair, C K K | en_US |
dc.contributor.author | Merhotra, P | en_US |
dc.contributor.author | Kagiya, V T | en_US |
dc.date.accessioned | 2005-01-14 | en_US |
dc.date.accessioned | 2009-06-01T16:13:51Z | |
dc.date.available | 2005-01-14 | en_US |
dc.date.available | 2009-06-01T16:13:51Z | |
dc.date.issued | 2005-01-14 | en_US |
dc.description.abstract | PURPOSE: To evaluate Tocoferol monoglucoside (TMG), a water soluble vit. E. in a phase I trial, as a radiation protector in those undergoing hemi-body radiation for disseminated disease. MATERIALS AND METHODS: Patients scheduled to receive modified hemi-body radiation were accrued for the study. Patients not only had disseminated skeletal disease but, were heavily pretreated Seven patients were accrued for the study. Patients received 1 and 2 gms of TMG. 30-40 minutes before hemibody radiation. A dose of 600 cGy was delivered on telecobalt equipment at mid plane. Immediate Toxicities were evaluated as well as response to pain. RESULTS: All the seven patients underwent radiation uneventfully. There was no drug related toxicity. Pain relief was adequate. CONCLUSION: Tocoferol monoglucoside an effective antioxidant with no significant acute toxicity, when administered in a dose of 1 or 2 gms per oral route. TMG being water-soluble can have global antioxidant and radio protective effects. This needs further clinical evaluation. | en_US |
dc.description.affiliation | Division of Radiation Oncology, Nanavati Hospital, Vile Parle (W), Mumbai, India. nagrajh@vsnl.net | en_US |
dc.identifier.citation | Huilgol NG, Nair CK, Merhotra P, Kagiya VT. A phase I trial of tocoferol monoglucoside in patients undergoing hemi-body radiation. Journal of Cancer Research and Therapeutics. 2005 Jan-Mar; 1(1): 38-40 | en_US |
dc.identifier.uri | https://imsear.searo.who.int/handle/123456789/111401 | |
dc.language.iso | eng | en_US |
dc.source.uri | https://www.cancerjournal.net | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Breast Neoplasms --radiotherapy | en_US |
dc.subject.mesh | Glucosides --adverse effects | en_US |
dc.subject.mesh | Hemibody Irradiation | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Prostatic Neoplasms --radiotherapy | en_US |
dc.subject.mesh | Radiation-Protective Agents --adverse effects | en_US |
dc.subject.mesh | Tocopherols --adverse effects | en_US |
dc.title | A phase I trial of tocoferol monoglucoside in patients undergoing hemi-body radiation. | en_US |
dc.type | Clinical Trial, Phase I | en_US |
dc.type | Journal Article | en_US |
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