Irreversible Ototoxicity Associated with Difluoromethylornithine

Author:

Lao Christopher D.1,Backoff Patricia2,Shotland Lawrence I.3,McCarty Deborah4,Eaton Tracy1,Ondrey Frank G.5,Viner Jaye L.6,Spechler Stuart Jon4,Hawk Ernest T.6,Brenner Dean E.172

Affiliation:

1. 1Departments of Internal Medicine and

2. 3Ann Arbor VA Medical Center, Ann Arbor, Michigan;

3. 4James H. Quillen VA Medical Center, Mountain Home, Tennessee;

4. 5Dallas VA Medical Center, Dallas, Texas;

5. 6Department of Otolaryngology, University of Minnesota, Minneapolis, Minnesota; and

6. 7Division of Cancer Prevention, National Cancer Institute, Bethesda, Maryland

7. 2Pharmacology, University of Michigan Medical Center, Ann Arbor, Michigan;

Abstract

Abstract Difluoromethylornithine (DFMO) is a potent, irreversible inhibitor of ornithine decarboxylase, the rate-limiting enzyme in the synthesis of polyamines that promote cellular proliferation. DFMO has been tested as a potential cancer therapeutic and chemopreventive agent in clinical trials. Reversible hearing loss is a recognized toxicity of DFMO that usually occurs at doses above 2 g/m2/d, and generally when the cumulative dose exceeds 250 g/m2. In a recently completed Barrett's esophagus chemoprevention trial, a participant developed a 15-dB decrease in hearing at frequencies of 250, 2,000, and 3,000 Hz in the right ear and a ≥20-dB decrease in hearing at 4,000 to 6,000 Hz in the left ear after taking 0.5 g/m2/d DFMO for approximately 13 weeks (cumulative dose of 45 g/m2). The threshold shifts persisted 7 months after DFMO was discontinued. There was no obvious impact on the participant's clinical hearing, but these findings were consistent with irreversible hearing loss. This is the first case reported of irreversible ototoxicity in a clinical trial participant receiving DFMO and, thus, trial participants should be made aware of this small but important risk.

Publisher

American Association for Cancer Research (AACR)

Subject

Oncology,Epidemiology

Reference28 articles.

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2. Abeloff MD, Slavik M, Luk GD, et al. Phase I trial and pharmacokinetic studies of α-difluoromethylornithine—an inhibitor of polyamine biosynthesis. J Clin Oncol 1984;2:124-30.

3. Croghan MK, Booth A, Meyskens FL Jr. A phase I trial of recombinant interferon-α and α-difluoromethylornithine in metastatic melanoma. J Biol Response Modif 1988;7:409-15.

4. Meyskens FL, Kingsley EM, Glattke T, Loescher L, Booth A. A phase II study of α-difluoromethylornithine (DFMO) for the treatment of metastatic melanoma. Invest New Drugs 1986;4:257-62.

5. Abeloff MD, Rosen ST, Luk GD, Baylin SB, Zeltzman M, Sjoerdsma A. Phase II trials of α-difluoromethylornithine, an inhibitor of polyamine synthesis, in advanced small cell lung cancer and colon cancer. Cancer Treat Rep 1986;70:843-5.

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