Long-Term Danazol Therapy in Autoimmune Thrombocytopenia: Unmaintained Remission and Age-Dependent Response in Women

Abstract

Study Objective: To assess the long-term benefit and side effects of danazol therapy, and to delineate factors influencing the responses in patients with autoimmune thrombocytopenia.

Design: Before and after trial.

Setting: Referral-based hematology clinics and the University of Miami teaching hospitals.

Patients: Data were collected on 96 patients (60 women and 36 men, 45 of whom had had splenectomies) receiving danazol therapy for autoimmune thrombocytopenia and analyzed.

Intervention: Danazol was added to the previous therapy or begun as an initial therapy. Glucocorticoids were tapered gradually.

Measurements and Main Results: The overall response rate to danazol was 61.4%. Among responders, the platelet counts (mean ± SD) before and after danazol treatment were 36 ± 24 x 109/L and 145 ± 77 x 109/L, respectively, and the time to response was 2.7 ± 3 months. Sex, age, and the status of the spleen (absent or present) influenced the responses to danazol: In women, but not in men, response rates improved with advancing age, especially in the nonsplenectomized women. This may be because estrogen levels are high in younger women and low in older women and men. Danazol, when given longer than a year, induced remissions lasting for years even after its discontinuation, but early relapses were frequent when danazol was administered for less than 6 months. Platelet-associated IgG returned to normal range during unmaintained remission.

Conclusion: Danazol is best suited for long-term medical management of autoimmune thrombocytopenia. It is well tolerated, and lasting, unmaintained remissions often occur after prolonged danazol administration. Age, sex, and the status of the spleen influence the responses. When danazol therapy is used, glucocorticoids can be substantially reduced in dosage or withdrawn. Danazol is a good alternative to splenectomy in elderly persons, especially in women.

Article and Author Information

  • From the University of Miami Hospitals and Clinics, the University of Miami School of Medicine, and the U.S. Veterans Administration Hospital, Miami, Florida. For current author addresses, see end of text.

  • Grant Support: Supported in part by grant 1R01 DK 33813 from the National Institutes of Health, by a Merit Review Award (0215-01), and by the Mary Beth Weiss Research Fund, the Kenneth Chasen Fund, the Friends for Life Fund, and the Cissy and Marvin Friedman Fund.

  • Requests for Reprints: Yeon Soong Ahn, MD, University of Miami Hospitals and Clinics, Center for Blood Diseases (D-1), 1475 NW 12 Avenue, Miami, FL 33136.

  • Current Author Addresses: Drs. Ahn, Mylvaganam, Garcia, and Harrington: University of Miami Hospitals and Clinics, Center for Blood Diseases (D-1), 1475 NW 12 Avenue, Miami, FL 33136.

    Dr. Rocha: Department of Medicine, Lincoln Medical/Mental Health Center, 234 East 149th Street, Bronx, NY 10451.

    Dr. Duncan: Fox Cancer Research Building, University of Miami, Department of Oncology, Division of Biostatistics, P.O. Box 016960, Miami, FL 33101.

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