Population Pharmacokinetic and Pharmacogenetic Analysis of Mitotane in Patients with Adrenocortical Carcinoma: Towards Individualized Dosing
Author:
Funder
HRA Pharma
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Pharmacology
Link
http://link.springer.com/content/pdf/10.1007/s40262-020-00913-y.pdf
Reference30 articles.
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2. Moolenaar AJ, van Slooten H, van Seters AP, Smeenk D. Blood levels of o, p’-DDD following administration in various vehicles after a single dose and during long-term treatment. Cancer Chemother Pharmacol. 1981;7(1):51–4. https://doi.org/10.1007/bf00258213.
3. Arshad U, Taubert M, Kurlbaum M, Frechen S, Herterich S, Megerle F, et al. Enzyme autoinduction by mitotane supported by population pharmacokinetic modelling in a large cohort of adrenocortical carcinoma patients. Eur J Endocrinol. 2018;179(5):287–97. https://doi.org/10.1530/EJE-18-0342.
4. Vanslooten H, Vanseters AP, Smeenk D, Moolenaar AJ. O, P’-Ddd (Mitotane) levels in plasma and tissues during chemotherapy and at autopsy. Cancer Chemoth Pharm. 1982;9(2):85–8. https://doi.org/10.1007/bf00265384.
5. Kerkhofs TM, Baudin E, Terzolo M, Allolio B, Chadarevian R, Mueller HH, et al. Comparison of two mitotane starting dose regimens in patients with advanced adrenocortical carcinoma. J Clin Endocrinol Metab. 2013;98(12):4759–67. https://doi.org/10.1210/jc.2013-2281.
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