Fertility preservation treatment for young women with autoimmune diseases facing treatment with gonadotoxic agents
Open Access
- 26 July 2008
- journal article
- research article
- Published by Oxford University Press (OUP) in Rheumatology
- Vol. 47 (10) , 1506-1509
Abstract
Objective. To describe a case series of seven women with SLE and other systemic autoimmune rheumatic diseases (SARDs) who required cyclophosphamide therapy and underwent fertility preservation treatments. Methods. Of the seven patients reported here, five women had SLE with nephritis, the sixth had immune thrombocytopenia purpura (ITP) and the seventh had microscopic polyangiitis (MPA) with renal involvement. All women were nulliparous and younger than 35 yrs. Results. Patients with SLE underwent in vitro maturation (IVM) of immature oocytes aspirated during a natural menstrual cycle followed by vitrification of the matured oocytes if a male partner was not available, or vitrification of embryos if one was available. The patient with ITP and the patient with MPA underwent gonadotropin ovarian stimulation followed by oocyte or embryo vitrification. All women completed fertility preservation treatment successfully and mature oocytes or embryos (36 and 13, respectively) were vitrified. No complications were associated with this treatment and cytotoxic therapy was initiated as scheduled in all cases. Conclusions. Oocyte or embryo cryopreservation should be considered for fertility preservation in young women with SARDs who face imminent gonadotoxic treatment. In patients, where gonadotropin ovarian stimulation is deemed unsafe, IVM of immature oocytes, aspirated during a natural menstrual cycle, followed by vitrification or fertilization of the mature oocytes, seems to be safe and feasible. For patients in whom hormonal ovarian stimulation is not contraindicated, this method may be considered depending on the urgency to start cytotoxic therapy.Keywords
This publication has 36 references indexed in Scilit:
- Absence of Conclusive Evidence for the Safety and Efficacy of Gonadotropin-Releasing Hormone Analogue Treatment in Protecting Against Chemotherapy-Induced Gonadal InjuryThe Oncologist, 2007
- The safety profile of cyclophosphamide in multiple sclerosis therapyExpert Opinion on Drug Safety, 2007
- Cyclophosphamide versus Placebo in Scleroderma Lung DiseaseNew England Journal of Medicine, 2006
- Use of a gonadotropin‐releasing hormone analog for protection against premature ovarian failure during cyclophosphamide therapy in women with severe lupusArthritis & Rheumatism, 2005
- Ovarian failure in systemic lupus erythematosus patients treated with pulsed intravenous cyclophosphamideLupus, 2004
- Low-dose intravenous cyclophosphamide in systemic sclerosis: a preliminary safety studyClinical Rheumatology, 2003
- In vitro maturation and fertilization of oocytes from unstimulated ovaries: Predicting the number of immature oocytes retrieved by early follicular phase ultrasonographyAmerican Journal of Obstetrics and Gynecology, 2002
- Role of intravenous cyclophosphamide in the treatment of severe neuropsychiatric systemic lupus erythematosusThe American Journal of Medicine, 1995
- Therapy of Lupus NephritisNew England Journal of Medicine, 1986
- Wegener's Granulomatosis: Prospective Clinical and Therapeutic Experience With 85 Patients for 21 YearsAnnals of Internal Medicine, 1983