Mitotane is the only drug currently available which is effective in the treatment of metastatic adrenal carcinoma. In the doses generally recommended for this purpose, the drug causes severe side effects which ultimately limit its use. Low doses of Mitotane are better tolerated and have been used effectively as adjuvant therapy in the treatment of adrenal carcinoma as well as in the medical treatment of nonneoplastic forms of Cushing's syndrome. Toxic side effects, however, still occur with low doses. The major metabolite of Mitotane is DDA, an inactive diphenylacetic acid derivative. It had been proposed that the efficacy of Mitotane could be enhanced if the metabolic formation of this metabolite could be reduced. Recently, a methylated analog of Mitotane (Mitometh) has been synthesized. The methyl group blocks the formation of DDA. Preliminary biological studies in the guinea pig have shown that Mitometh has adrenolytic activity essentially equivalent to that of Mitotane but with much less toxicity. The main objective of the proposed study is to investigate Mitometh as an adrenolytic drug and to determine its therapeutic effectiveness on adrenal cancer and other non-neoplastic adrenocortical diseases. We propose to: 1) Prepare sufficient quantities of Mitometh for toxicological studies and, if indicated, for subsequent clinical trial; 2) Formulate the drug for oral administration and carry out quality control procedures; 3) Study its pharmacokinetics and organ concentration in the rat, guinea pig and dog; and 4) Conduct clinical trials in patients with functioning and nonfunctioning adrenal carcinoma who have developed metastases or in whom Mitotane had been used as adjuvant therapy following resection of the primary tumor. If effective and with lower toxicity than Mitotane, Mitometh will be tried as an adrenolytic drug in the therapy of nonneoplastic types of adrenal hyperfunction. These studies with Mitometh should disclose whether this compound will offer improved therapy and prognosis with adrenal carcinoma. If effective, this drug may be important in the medical treatment of nonneoplastic types of adrenal hyperfunction.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA037794-02
Application #
3175626
Study Section
Experimental Therapeutics Subcommittee 2 (ET)
Project Start
1984-08-01
Project End
1987-07-31
Budget Start
1985-08-01
Budget End
1986-07-31
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Schteingart, David E; Sinsheimer, Joseph E; Benitez, Ricardo S et al. (2012) Structural requirements for mitotane activity: development of analogs for treatment of adrenal cancer. Anticancer Res 32:2711-20
Cai, W; Counsell, R E; Schteingart, D E et al. (1997) Adrenal proteins bound by a reactive intermediate of mitotane. Cancer Chemother Pharmacol 39:537-40
Sinsheimer, J E; Counsell, R E; Cai, W et al. (1996) Gas chromatographic-electron capture determination of 2,4'-dichlorodiphenylacetic acid from in-vitro adrenal transformations of mitotane and its analogs. J Pharm Biomed Anal 14:861-6
Cai, W; Counsell, R E; Djanegara, T et al. (1995) Metabolic activation and binding of mitotane in adrenal cortex homogenates. J Pharm Sci 84:134-8
Cai, W; Benitez, R; Counsell, R E et al. (1995) Bovine adrenal cortex transformations of mitotane [1-(2-chlorophenyl)-1-(4-chlorophenyl)-2,2-dichloroethane;o,p'-DDD] and its p,p'- and m,p'-isomers. Biochem Pharmacol 49:1483-9
Schteingart, D E; Sinsheimer, J E; Counsell, R E et al. (1993) Comparison of the adrenalytic activity of mitotane and a methylated homolog on normal adrenal cortex and adrenal cortical carcinoma. Cancer Chemother Pharmacol 31:459-66
Sinsheimer, J E; Freeman, C J (1987) Mitotane (1-(o-chlorophenyl)-1-(p-chlorophenyl)-2,2-dichloroethane) metabolism in perfusion studies with dog adrenal glands. Drug Metab Dispos 15:267-9
Musial, S P; Freeman, C J; Sinsheimer, J E (1985) Mitotane (o,p'-DDD) emulsion and tablet analysis by high-performance liquid chromatography. J Chromatogr 319:467-70