Pharmacokinetics and toxicity of isolated perfusion of lung with doxorubicin

• Published in: The Journal of surgical research Vol. 50; no. 2; p. 124
• Main Authors: Baciewicz, Jr, F A, Arredondo, M, Chaudhuri, B, Crist, K A, Basilius, D, Bandyopadhyah, S, Thomford, N R, Chaudhuri, P K
• Format: Journal Article
• Language: English
• Published: United States 01-02-1991
• Subjects: Animals; Biological Transport; Dogs; Doxorubicin - pharmacokinetics; Doxorubicin - toxicity; In Vitro Techniques; Kinetics; Lung - drug effects; Lung - metabolism; Lung - pathology; Perfusion
• ISSN: 0022-4804
• DOI: 10.1016/0022-4804(91)90234-D

The treatment of pulmonary metastases from soft tissue sarcomas with chemotherapy has an overall response rate of less than 30%, and the majority of these responses are short lived. It is postulated that increased drug delivery to the pulmonary metastases may improve the outcome of these patients. An isolated perfusion system would have the ability of delivering increased levels of drug to target tissue without the systemic toxic effect of the drug. The purpose of this study was to establish the pharmacokinetics of doxorubicin delivery, lung toxicity, and the ideal dose for clinical application in an in vivo isolated perfusion model. Our results suggest that normothermic isolated perfusion of the lung with doxorubicin using a dose level up to 6 micrograms/ml in the perfusate can be accomplished without histologic lung injury, systemic toxicity, or adverse clinical outcome. Perfusate concentration of greater than 7 micrograms/ml caused significant histologic injury and adverse clinical outcome without systemic toxicity. The technique may be utilized in selective settings to improve treatment in mesenchymal tumors metastatic to the lung.