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      Dyslipidemia causes overestimation of plasma mitotane measurements

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          Summary

          Mitotane ( o,p′-DDD) is the standard treatment for advanced adrenocortical carcinoma (ACC). Monitoring of plasma mitotane levels is recommended to look for a therapeutic window between 14 and 20mg/L, but its positive predictive value requires optimization. We report the case of an ACC patient with a history of dyslipidemia treated with mitotane in whom several plasma mitotane levels >30mg/L were found together with an excellent neurological tolerance. This observation led us to compare theoretical or measured o,p′-DDD and o,p′-DDE levels in a series of normolipidemic and dyslipidemic plasma samples to explore potential analytical issues responsible for an overestimation of plasma mitotane levels. We demonstrate an overestimation of mitotane measurements in dyslipidemic patients. Mitotane and o,p′-DDE measurements showed a mean 20% overestimation in hypercholesterolemic and hypertriglyceridemic plasma, compared with normolipidemic plasma. The internal standard p,p′-DDE measurements showed a parallel decrease in hypercholesterolemic and hypertriglyceridemic plasma, suggesting a matrix effect. Finally, diluting plasma samples and/or using phospholipid removal cartridges allowed correcting such interference.

          Learning points

          • Hypercholesterolemia (HCH) and hypertriglyceridemia (HTG) induce an overestimation of plasma mitotane measurements.

          • We propose a routine monitoring of lipidemic status.

          • We propose optimized methodology of measurement before interpreting high plasma mitotane levels.

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          Most cited references6

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          Adrenal cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.

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            Lipoprotein-Free Mitotane Exerts High Cytotoxic Activity in Adrenocortical Carcinoma.

            Mitotane (o,p'-DDD), the only approved drug for advanced adrenocortical carcinoma (ACC), is a lipophilic agent that accumulates into circulating lipoprotein fractions and high-lipid-containing tissues.
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              Possible mechanism and treatment of o,p'DDD-induced hypercholesterolaemia.

              Ortho,para,dichlorodiphenyl dichloroethane (o,p'DDD, Mitotane (Roussell)) is used as an adrenolytic drug to reduce adrenocortical mass and circulating cortisol levels in Cushing's syndrome but has the unwanted side-effect of inducing hypercholesterolaemia. This paper examined the mechanism of that effect in 30 patients with Cushing's syndrome treated with o,p'DDD during the past 10 years. o,p'DDD increased serum cholesterol by 68 per cent, mainly by increasing LDL-cholesterol. The latter effect was not due to impaired binding of LDL to its receptor, as shown in vitro using cultured fibroblasts. Increases in plasma mevalonic acid during o,p'DDD administration were suggestive of increased cholesterol synthesis, this effect being reversed by simvastatin. These findings suggest that o,p'DDD causes hypercholesterolaemia by increasing cholesterol synthesis. It is proposed that this effect is due to the drug's known ability to block cytochrome P450-mediated reactions, thus impairing the formation of oxysterols responsible for down-regulating hepatic cholesterol synthesis. Treatment with simvastatin, an inhibitor of cholesterol synthesis, reverses the hyperlipidaemia and enables o,p'DDD therapy to be maintained without increasing cardiovascular risk.
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                Author and article information

                Journal
                Endocrinol Diabetes Metab Case Rep
                Endocrinol Diabetes Metab Case Rep
                edm
                EDM Case Reports
                Endocrinology, Diabetes & Metabolism Case Reports
                Bioscientifica Ltd (Bristol )
                2052-0573
                10 June 2016
                2016
                : 2016
                : 150135
                Affiliations
                [1 ]Pharmacology and Drug Analysis Department , Gustave Roussy, Villejuif, France
                [2 ]INSERM U1185, Fac Med Paris Sud , Le Kremlin-Bicêtre, France
                [3 ]Nuclear Medicine and Endocrine Oncology Department , Gustave Roussy, Villejuif, France
                [4 ]Assistance Publique-Hôpitaux de Paris, La Pitié-Salpetriere Hospital, Department of Endocrinology , Paris, France
                [5 ]CHU Larrey, Department of Endocrinology , Toulouse, France
                [6 ]CHU Nantes, Department of Endocrinology , Nantes, France
                [7 ]Endocrinology in Charlottenburg , Berlin, Germany
                [8 ]Endocrine and Diabetes Unit, Department of Medicine 1, University Hospital, University of Würzburg , Würzburg, Germany
                Author notes
                Correspondence should be addressed to E Baudin Email: eric.baudin@ 123456gustaveroussy.fr
                [*]

                (A Paci and S Hescot contributed equally to this work)

                Article
                EDM150135
                10.1530/EDM-15-0135
                4901334
                27298727
                7e40876b-0c8b-4a48-aad4-ae9f7bdd7a4e
                © 2016 The authors

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.

                History
                : 29 April 2016
                : 12 May 2016
                Categories
                Error in Diagnosis/Pitfalls and Caveats

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