Abstract
Cis-Diamminodichloroplatinum (II), or DDP, has been shown to be an effective agent in the treament of various neoplastic diseases. The drug has been usually administered in high intravenous (IV) bolus dose, or rapid infusion. By these schedules, the toxicity of DDP included severe nausea and vomiting, nephrotoxicity, mild to moderate myelosuppression, and hearing loss1. Renal and gastrointestinal toxicities were dose-limiting and constituted major obstacles to prlonged therapy. Although nephrotoxicity was partially ameliorated by fluid and mannitol diuresis2, it remains a major impediment of long-term treatment. Also, in several studies, nausea and vomiting were so severe that many patients refused to continue treatment.
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References
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© 1986 Plenum Press, New York
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Salem, P., Khalyl, M., Jabboury, K., Hashimi, L. (1986). The 5-Day Continuous Infusion of Cis-Platinum: An Update on Toxicity Pattern. In: Rosenthal, C.J., Rotman, M. (eds) Clinical Applications of Continuous Infusion Chemotherapy and Concomitant Radiation Therapy. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-2197-2_13
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DOI: https://doi.org/10.1007/978-1-4613-2197-2_13
Publisher Name: Springer, Boston, MA
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