1. Efficacy of Megestrol Acetate (Megace) in the Treatment of Patients With Early Endometrial Adenocarcinoma: Our Experiences With 21 Patients
- Author
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Hadi Shojaei, Zahra Eftekhar, Zahra Rezaei, Þ Fariba Yarandi, Narges Izadi-Mood, and Saeedeh Mohagheghi
- Subjects
Adult ,medicine.medical_specialty ,Antineoplastic Agents, Hormonal ,medicine.medical_treatment ,Adenocarcinoma ,Young Adult ,medicine ,Carcinoma ,Humans ,Prospective Studies ,Young adult ,Prospective cohort study ,Pregnancy ,Hysterectomy ,medicine.diagnostic_test ,business.industry ,Megestrol Acetate ,Obstetrics and Gynecology ,Middle Aged ,medicine.disease ,Curettage ,Endometrial Neoplasms ,Surgery ,Fertility ,Oncology ,Hysteroscopy ,Megestrol acetate ,Female ,business ,Infertility, Female ,medicine.drug - Abstract
Background:There are therapeutic dilemmas regarding fertility-preserving treatment among young women with well-differentiated endometrial carcinoma.Materials and Methods:Twenty-one patients with stage IA well-differentiated endometrial adenocarcinoma were enrolled in a prospective study. The treatment initiated with 160 mg/d of megestrol acetate. The patients underwent dilatation and curettage and hysteroscopy after 3 months, and in cases of normal pathology, the therapy continued for another 3-month period. In patients who did not respond to treatment, the dosage of the drug was doubled (320 mg/d), and the therapy continued for another 3 months. At the second time, patients who did not respond to treatment were recommended for hysterectomy, and in patients who responded to treatment, an additional 3 months of treatment with megestrol acetate (320 mg/d) was administered.Results:Our results showed a response rate of 85.71% (18 patients), and 3 patients underwent hysterectomy. The mean (SD) treatment duration was 8.85 (2.00) months (range, 6-12 months). The response to therapy was observed in 5 patients (27.78%) with a dosage of 160 mg/d, and the remaining patients with 320 mg/d. Pregnancy occurred in 5 patients (27.78%). Recurrence happened in 3 (16.67%) of 18 patients who responded to treatment who did not give a permit to undergo hysterectomy and received medication again. Two (66.67%) of these patients experienced remission again, whereas the other one was candidate for hysterectomy.Conclusions:The results of this study show that, when an initial response is not achieved or when disease recurs, use of 320 mg/d seems to be associated with a better therapeutic response. Furthermore, serious complications were not observed with this dosage.
- Published
- 2009
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