1. Feasibility of using intraperitoneal epinephrine and cisplatin in patients with advanced peritoneal carcinomatosis.
- Author
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Molucon-Chabrot C, Isambert N, Benoit L, Zanetta S, Fraisse J, Guilland JC, Royer B, Monin-Baroille P, Flesch M, Fargeot P, Coudert B, Mayer F, Fumoleau P, and Chauffert B
- Subjects
- Aged, Antineoplastic Combined Chemotherapy Protocols adverse effects, Carcinoma pathology, Cisplatin adverse effects, Cisplatin pharmacokinetics, Epinephrine adverse effects, Epinephrine pharmacokinetics, Feasibility Studies, Female, Humans, Infusions, Parenteral adverse effects, Male, Middle Aged, Peritoneal Neoplasms pathology, Treatment Outcome, Antineoplastic Combined Chemotherapy Protocols administration & dosage, Carcinoma drug therapy, Cisplatin administration & dosage, Epinephrine administration & dosage, Ovarian Neoplasms drug therapy, Ovarian Neoplasms pathology, Peritoneal Neoplasms drug therapy, Peritoneal Neoplasms secondary
- Abstract
Intraperitoneal epinephrine above 1 mg/l concentration has been shown to enhance the intratumoral accumulation and antitumor activity of intraperitoneal cisplatin in rats with advanced peritoneal carcinomatosis. The aim of this study was to determine the tolerance of intraperitoneal epinephrine combined with intraperitoneal cisplatin in patients with advanced peritoneal carcinomatosis (17 ovarian cancers, one peritoneal mesothelioma). Intraperitoneal epinephrine (1-5 mg/l) and cisplatin (50 mg/l; 100 mg total dose) were infused in 2 l of saline solution over 2 h. The maximal tolerated concentration of intraperitoneal epinephrine was not reached at 5 mg/l. Cardiovascular symptoms were infrequent and not strictly related to the epinephrine concentration. Tumor responses were obtained in some patients with disease resistant to intravenous platinum compounds. This work demonstrates for the first time that intraperitoneal epinephrine at sufficient concentration enhances the cisplatin effect and can be safely infused into the peritoneal cavity of patients with peritoneal carcinomatosis. The greatest limitation was abdominal pain and limited intraperitoneal distribution of the peritoneal fluid in this closed-abdomen procedure.
- Published
- 2006
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