Background: The presence of cytotoxic drug residues in urine of dogs may represent an exposure risk for pet owners and other people as well as a potential environmental contaminant. However, studies on cytotoxic drug residues in excretions of clinical patients are lacking in veterinary oncology. Hypothesis: Variable concentrations of cytotoxic residues are present in urine samples, depending on sampling time and substance. Animals: Client-owned dogs with lymphoma or mast cell tumors treated with standard chemotherapy protocols. Methods: Urine samples were collected before, directly after, and on days after administration of chemotherapy. Measurement of vincristine, vinblastine, cyclophosphamide, and doxorubicin residues in canine urine was performed by a quantitative liquid chromatography tandem mass spectrometry (LC/MS/MS) method. Results: Median cyclophosphamide residue concentration was 398.2mg/L directly after treatment (d0) and was below the level of detection on days 1-3 (d1, d2, d3). Median vincristine residue concentration was 53.8mg/L directly after treatment and was 20.2,11.4, and 6.6mg/L on days 1, 2, and 3. Median vinblastine residues were 144.9 (d0), 70.8 (d1), 35.6 (d2), and 18.7mg/L (d3) with low concentrations detectable for 7 days after treatment. Median urine doxorubicin concentrations were 354.0 (d0), 165.6 (d1), 156.9 (d2), and 158.2mg/L (d3). Low concentrations of doxorubicin were measurable up to 21 days after administration. Conclusions and Clinical Importance: Variable concentrations of chemotherapeutics were measured in urine samples, de-pending on sampling time point and drug. Findings may inform current chemoprotection guidelines and help minimize exposure risks. © 2010 by the American College of Veterinary Internal Medicine.
CITATION STYLE
Knobloch, A., Mohring, S. A. I., Eberle, N., Nolte, I., Hamscher, G., & Simon, D. (2010). Cytotoxic drug residues in urine of dogs receiving anticancer chemotherapy. Journal of Veterinary Internal Medicine, 24(2), 384–390. https://doi.org/10.1111/j.1939-1676.2009.0453.x
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