Isolated pelvic perfusion: plasma pharmacokinetics depend primarily on drug dosage and not the type of drug

Author:

Belliveau James F.,Arevalo Elisabeth,Griffin Hank,Wanebo Harold J.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Cancer Research,Pharmacology,Toxicology,Oncology

Reference10 articles.

1. Belliveau J, Wanebo H (2003) Clinical experiences and pharmacology with isolated pelvic perfusion (IPP) for lower GI cancers. Proceedings of the 14th International Congress on Anti-Cancer Treatment, Paris (P059) 14:206

2. Creech O, Krementz ET, Ryan RF, Winblad JN (1958) Chemotherapy of cancer: regional perfusion utilizing an extracorporeal circuit. Ann Surg 148:616

3. Darnowski JW, Sawyer RC, Stolfi RL, Martin DS, Lau-Cam CA (1985) Decreased host toxicity in vivo during chronic treatment with 5-fluorouracil. Cancer Chemother Pharmacol 14:63

4. Forastiere AA, Belliveau JF, Goren M, Vogel WC, Posner MC, O?Leary GP (1988) Pharmacokinetic and toxicity evaluation of five-day continuous infusion versus intermittent bolus cis-diamminedichloro-platinum (II) in head and neck cancer patients. Cancer Res 48:3869

5. den Hartigh J, van Oort WJ (1981) High-pressure liquid chromatographic determination of the antitumor agent mitomycin C in human blood plasma. Anal Chim Acta 127:47

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