Spitz, Irving M., Steven M. Grunberg, Nathalie Chabbert-Buffet,
Tzina Lindenberg, Hadassa Gelber, and Régine Sitruk-Ware. 2005.
"Management of patients receiving long-term treatment with mifepristone,"
Fertility and Sterility 84(6): 1719–1726.
Objective
To determine clinical side effects and biochemical and hematological
abnormalities in patients with nonresectable meningioma on long-term
mifepristone (RU 486) therapy.
Design
Long-term mifepristone administration in patients with meningioma.
Setting
Outpatient clinic of a university hospital.
Patients
Sixteen women and nine men aged 22–80 years with nonresectable meningioma.
Intervention
Mifepristone (200 mg daily). One patient received treatment for more than 13
years; six received treatment for 10–12 years; five received treatment for
4–9 years; eight received treatment for 1–4 years; and the remainder
received treatment for 4–10 months.
Main outcome measures
Evaluation of side effects and of hematological and biochemical
abnormalities.
Results
Fatigue was observed in 22 of 25 patients. Endometrial hyperplasia occurred
in one premenopausal woman and one postmenopausal woman. Another two women
had endometrial thickening without hyperplasia. There were no consistent
abnormalities in liver or renal function or in any other biochemical or
hematological parameters. One subject (on long-term dexamethasone) developed
hypoadrenalism, which responded to treatment.
Conclusions
Mifepristone can be administered for prolonged periods. Ultrasound should be
performed if irregular vaginal bleeding occurs. In asymptomatic women, it
should be performed annually. If endometrial thickening is observed, then
endometrial biopsy is recommended. Because biochemical hypothyroidism has
been reported during long-term mifepristone therapy, thyroid function tests
should be performed annually.
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