Effect of leuprolide acetate on ovarian function after cyclophosphamide–doxorubicin-based chemotherapy in premenopausal patients with breast cancer: results from a phase II randomized trial

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• 作者：Guiping Song (1)
  Hui Gao (2)
  Zhixiang Yuan (3)
  
• 关键词：Leuprolide acetate ; Ovarian function ; Chemotherapy
• 刊名：Medical Oncology
• 出版年：2013
• 出版时间：September 2013
• 年：2013
• 卷：30
• 期：3
• 全文大小：263KB
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• 作者单位：Guiping Song (1)
  Hui Gao (2)
  Zhixiang Yuan (3)
  
  1. Department of Pharmacy, Jiangyin Hospital Affiliated to Nanjing University of Traditional Chinese Medicine, No. 130 Renmingzhong Road, Jiangyin, 214400, Jiangsu, China
  2. Medical College, Qingdao University, Qingdao, Shandong, 266021, China
  3. Sichuan Academy of Chinese Medicine Sciences, Chengdu, 610041, Sichuan, China
  

文摘

Previous studies provided inconclusive evidence for the effectiveness of gonadotropin-releasing hormone analogue on ovarian function protection against chemotherapy-induced genotoxicity in premenopausal patients. This study was designed to examine the efficacy of leuprolide acetate on ovarian function preservation in patients with breast cancer. A total of 220 patients were recruited in this prospective clinical trial and were assigned randomly to receive cyclophosphamide–doxorubicin-based chemotherapy only or chemotherapy plus leuprolide acetate. Resumption of menses or premenopausal levels of both follicle-stimulating hormone (FSH) and estradiol (E 2) within 12?months after the end of chemotherapy were considered as effective ovarian preservation. A total of 183 patients were considered evaluable (94 in chemotherapy-only group and 89 in chemotherapy plus leuprolide acetate group). At the end of follow-up, 27 patients in chemotherapy group and 15 in chemotherapy plus leuprolide acetate group resumed menses; seven patients in chemotherapy group and 14 in chemotherapy plus leuprolide acetate group restored premenopausal levels of FSH and E 2. The median time to resume menses was 9.2?months for patients in chemotherapy plus leuprolide acetate group and was not reached in chemotherapy-only group. In addition, our results demonstrated that age and chemotherapy doses made no significant difference in the occurrence of premature menopause. The leuprolide acetate treatment simultaneously with cyclophosphamide–doxorubicin-based chemotherapy reduced the risk of developing premature menopause in premenopausal patients with breast cancer.