Author/Editor     Plaxe, SC; Christen, RD; O'Quigley, J; Braly, PS; Freddo, JL; McClay, E; Heath, D; Howell, SB
Title     Phase I and pharmacokinetic study of intraperitoneal topotecan
Type     članek
Source     Invest New Drugs
Vol. and No.     Letnik 16, št. 2
Publication year     1998
Volume     str. 147-53
Language     eng
Abstract     Objective: To determine the maximum tolerated dose and pharmacokinetics of topotecan when administered by the intraperitoneal route. Methods: A dose-escalating Phase I trial was conducted in which fifteen % of the total dose was given as an intraperitoneal bolus in two litres of D5W and the remainder was given as a continuous intraperitoneal infusion over 24 hours. Treatments were given every 21 days. Pharmacokinetic analyses were performed at the recommended phase II dose. Results: Seventeen patients received a total of 43 cycles at 21-day intervals. The maximum tolerated dose was 4 mg/m2 and acute dose-limiting toxicity was neutropenia. Other toxicities included leukopenia, anemia, emesis, fever, and abdominal pain. Although no objective responses were achieved, five of ten patients with ascites had a decrease in fluid accumulation with administration of intraperitoneal topotecan. The recommended phase II dose is 3 mg/m2. Pharmacokinetic analysis performed at a dose of 3 mg/m2 demonstrated that elimination from the peritoneal cavity followed second-order kinetics with k1 = 1.6 hr(-1), k2 = 0.3 hr(-1) and first and second-phase half-lives of 0.49 and 2.7 hours, respectively. Plasma pharmacokinetic behavior was best described by first-order kinetics with k = 0.5 hr(-1) and a half-life of 3.9 hours. The pharmacologic advantage, expressed as the peritoneal to plasma AUC ratio was 31.2. Conclusion: Intraperitoneal administration of topotecan at 3 mg/m2 results in a substantial increase in drug exposure for the peritoneal cavity without compromising systemic exposure; this may be beneficial for the treatment of patients with ovarian cancer or intraperitoneal carcinomatosis.
Descriptors     ANTINEOPLASTIC AGENTS
AGE FACTORS
INFUSIONS, PARENTERAL