Literature DB >> 16001176

Treatment of anthracycline extravasation in mice with dexrazoxane with or without DMSO and hydrocortisone.

Seppo W Langer1, Annemette V Thougaard, Maxwell Sehested, Peter Buhl Jensen.   

Abstract

Dexrazoxane has been reported to be protective against anthracycline induced subcutaneous ulceration in mice. It is currently under clinical investigation as an acute antidote in accidental anthracycline extravasation, for which indication topical dimethylsulfoxide (DMSO) and intralesional hydrocortisone are used empirically. We studied the effect in 72 mice of monotherapy with and combined therapy of intraperitoneal dexrazoxane, topical DMSO, and intralesional hydrocortisone as acute antidotes against ulceration after subcutaneous daunorubicin. Dexrazoxane completely prevented wounds from occurring, while neither DMSO nor hydrocortisone had any preventive effect. The addition of topical DMSO actually reduced the efficacy of dexrazoxane. In conclusion, the present study does not support the concomitant use of topical DMSO + systemic dexrazoxane or intralesional hydrocortisone + systemic dexrazoxane. Monotherapy with systemic dexrazoxane seems preferable and is highly efficacious in preventing ulceration.

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Year:  2005        PMID: 16001176     DOI: 10.1007/s00280-005-0022-7

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  10 in total

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5.  Outcome of chemotherapy extravasation in a large patient series using a standardised management protocol.

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Review 6.  Management of the extravasation of anti-neoplastic agents.

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Review 7.  Treatment of anthracycline extravasations using dexrazoxane.

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8.  Extravasational side effects of cytotoxic drugs: A preventable catastrophe.

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9.  Anthracycline extravasation injuries: management with dexrazoxane.

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Review 10.  Dexrazoxane for the treatment of chemotherapy-related side effects.

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  10 in total

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