Journal of Gynecologic Oncology · 2019 · 35 citations · 15 references
MedicineOncologyPharmacotherapyEndocrine PharmacotherapyReproductive EndocrinologyReproductive MedicineEndometrial CancerFertility PreservationGynecologic Cancer PharmacotherapyGynecologic EndocrinologyHormonal Cancer TherapyHormonal TherapyFertility-sparing AlternativesFertility-sparing PharmacotherapyGnrh AgonistsGnrh AnaloguesGonadotropin-releasing Hormone Agonist TherapyLive Birth Outcome AssessmentObesity-associated Endometrial CancerPregnancy Rate Assessment
OBJECTIVE: This study aims to evaluate the effects and pregnancy outcomes of gonadotropin-releasing hormone agonist (GnRH agonist) combined with aromatase inhibitor (AI) in preserving the fertility of obese women with grade 1 endometrial cancer (EC). METHODS: This study recruited obese EC patients who wished to preserve their fertility. The treatment regimen consisted of intramuscular GnRH agonist 3.75 mg every 4 weeks and oral AI 2.5 mg daily. The maintenance regimen was the same as the initial treatment regimen. Primary outcomes included response rate, time to complete response (CR), and time to recurrence; pregnancy outcomes included the time to pregnancy, pregnancy rate and live birth rate. RESULTS: Six obese patients with EC were included in this study, with the age (mean±standard deviation [SD]) of 30.5±3.3 years and body mass index (mean±SD) of 35.0±1.4 kg/m². CR rate was 100%, and time to CR was 3-6 months. None of the patients had recurrence after a median follow-up of 4.0 years (range, 1.3-7.0 years). The most common side effects were menopause-like symptoms. Among these patients, no weight gain was observed during treatment. The pregnancy rate and live birth rate was 50.0% and 75.0%, respectively, with a median time to pregnancy of 2.4 years (range, 1.0-5.5 years). CONCLUSION: The combination of GnRH agonist and AI demonstrated promising long-term effect in young obese EC patients who wished to preserve their fertility. No weight gain side effects were observed. Further studies with a larger sample size are needed to fully evaluate this novel treatment regimen.
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Medicine, Gynecology, Obstetrics +15