Comparative Response of SC CAKI-1 Renal Tumor to Treatment with Doxorubicin HCl and Doxorubicin Orotate
- 1 SavviPharm Inc. and Tactical Therapeutics Inc., New York, USA
- 2 SavviPharm Inc. and Tactical Therapeutics Inc., New York, USA
- 3 Pharmaceutical Sciences Research Institute, Samford University, Birmingham, USA
Abstract
Background: Doxorubicin (DOX) is an effective treatment for many cancers across the age spectrum, but its therapeutic potential is limited because of dose-dependent relation to both progressive and irreversible cardiomyopathy leading to congestive heart failure. While decreases in cardiotoxicity have been reported with liposomal doxorubicin, the long-term cardiac effects are not known. Orotate salts of cytotoxic drugs have been shown to confer antitumor effects with a better safety profile than unconverted drug, and therefore may offer an improved approach to cancer treatment. Materials and Methods: Male, athymic NCr- nu/nu mice with subcutaneously implanted CAKI-1 human renal tumor xenografts were treated with DOX and its orotate salt (DOX-O) to evaluate antitumor activity, measured by median tumor mass doubling time and tumor weight. Nontumored male, athymic NCr- nu/nu mice were treated with DOX, DOX-O and liposomal doxorubicin formulations to determine DOX concentration in liver and heart; and to evaluate their effect on body weight. Non-tumored female, athymic NCr- nu/nu mice were treated with daunorubicin and daunorubicin orotate to evaluate tolerance. Results: DOX and DOX-O exhibited significant, similar levels of antitumor activity. Mice treated with DOX-O had a lower percentage body weight loss. In the animals treated with DOX, DOX-O, or liposomal doxorubicin, liposomal doxorubicin was associated with the lowest percentage of body weight loss, but the highest concentration of DOX in heart. In daunorubicin tolerance experiments, animals showed a better tolerance for daunorubicin orotate as measured by a smaller percentage change in body weight. Conclusions: DOX-O is effective as an antitumor therapy and may offer a less toxic alternative to DOX for maintaining therapy. The lower percentage of body weight loss in animals treated with DOX-O and daunorubicin orotate is a measure of improved tolerance and may translate into better patient outcomes.
- Ali, M., Kamjoo, M., Thomas, H.D., Kyle, S., Pavlovska, I., Babur, M., Telfer, B.A., et al. (2011) The Clinically Active PARP Inhibitor AG014699 Ameliorates Cardiotoxicity but Does Not Enhance the Efficacy of Doxorubicin, Despite Improving Tumor Perfusion and Radiation Response in Mice. Molecular Cancer Therapeutics, 10, 2320-2329. http://dx.doi.org/10.1158/1535-7163.MCT-11-0356
- Burstein, H.J., Piccart-Gebhart, M.J., Perez, E.A., Hortobagyi, G.N., Wolmark, N., Albain, K.S., et al. (2012) Choosing the Best Trastuzumab-Based Adjuvant Chemotherapy Regimen: Should We Abandon Anthracyclines? Journal of Clinical Oncology, 30, 2179-2182. http://dx.doi.org/10.1200/JCO.2012.42.0695
- Healy-Bird, B.R. and Swain, S.M. (2008) Cardiac Toxicity in Breast Cancer Survivors: Review of Potential Cardiac Problems. Clinical Cancer Research, 14, 14-24. http://dx.doi.org/10.1158/1078-0432.CCR-07-1033
- Zoeller, L.S. (2012) Cardiotoxicity in Cancer Patients: Often More Malignant than Cancer. Interview. Oncology Statistics, 24.
- Lebrecht, D., Setzer, B., Ketelsen, U.P., Haberstroh, J. and Walker, U.A. (2003) Time-Dependent and Tissue-Specific Accumulation of mtDNA and Respiratory Chain Defects in Chronic Doxorubicin Cardiomyopathy. Circulation, 108, 2423-2429. http://dx.doi.org/10.1161/01.CIR.0000093196.59829. DF
- Volkova, M. and Russell, R. (2011) Anthracycline Cardiotoxicity: Prevalence, Pathogenesis and Treatment. Current Cardiology Reviews, 7, 214-2120. http://dx.doi.org/10.2174/1573403117999 60645
- Lenihan, D.J. and Cardinale, D.M. (2012) Late Cardiac Effects of Cancer Treatment. Journal of Clinical Oncology. 30(30), 3657-3664. Epub 2012 Sep 24. http://dx.doi.org/10.1200/JCO.2012.45.2938
- Cardinale, D., Sandri, M.T., Martinoni, A., Borghini, E., Civelli, M., Lamantia, G., et al. (2002) Myocardial Injury Revealed by Plasma Troponin I in Breast Cancer Treated with High-Dose Chemotherapy. Annals of Oncology, 13, 710-715. http://dx.doi.org/10.1093/annonc/mdf170
- Giordano, S.H., Lin, Y.L., Kuo, Y.F., Hortobagyi, G.N. and Goodwin, J.S. (2012) Decline in the Use of Anthracyclines for Breast Cancer. Journal of Clinical Oncology, 30, 2232-2239. http://dx.doi.org/10.1200/JCO.2011.40.1273
- Wang, X., Liu, W., Sun, C.L., Armenian, S.H., Hakonarson, H., Hageman, L., et al. (2014) Hyaluronan Synthase 3 Variant and Anthracycline-Related Cardiomyopathy: A Report from the Children’s Oncology Group. Journal of Clinical Oncology, 32, 647-653. http://dx.doi.org/10.1200/JCO.2013. 50.3557