Abstract
Rosenberg first reported the antitumor activity of cis-diamminedichloroplatinum (II) (DDP) in 1969 and since that time DDP has become one of the most widely used cancer chemotherapeutic drugs in the clinic. DDP has marked activity in several types of tumors including testicular, ovarian and head and neck carcinomas (1–3). In spite of the impressive activity of DDP in selected tumors a number of factors, such as a limited spectrum of responsive tumors, severe host toxicity, the development of resistance by tumor cells and relatively poor water solubility, have hampered the clinical usefulness of this drug.
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Hacker, M.P., Roberts, J.D. (1988). Cisplatin Efficacy and Toxicity: Are they Separable?. In: Nicolini, M. (eds) Platinum and Other Metal Coordination Compounds in Cancer Chemotherapy. Developments in Oncology, vol 54. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-1717-3_19
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DOI: https://doi.org/10.1007/978-1-4613-1717-3_19
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