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Feasibility and efficacy of gonadotropin-releasing hormone agonists for the prevention of chemotherapy-induced ovarian insufficiency in patients with malignant ovarian germ cell tumours (KGOG 3048R)

Authors
Choi M.C.Chung Y.S.Lee J.-W.Kwon B.S.Park B.K.Kim S.I.Shim S.-H.Lee K.-B.Seong S.J.Lee S.J.Lee S.H.Yoo H.-J.Song T.Kim M.K.Baek M.-H.Kang S.Kim Y.-M.
Issue Date
Jul-2020
Publisher
Elsevier Ltd
Keywords
Chemotherapy; Gonadotropin releasing hormone agonist; Ovarian germ cell cancer; Ovarian insufficiency
Citation
European Journal of Cancer, v.133, pp.56 - 65
Journal Title
European Journal of Cancer
Volume
133
Start Page
56
End Page
65
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/61759
DOI
10.1016/j.ejca.2020.03.030
ISSN
0959-8049
Abstract
Background: This study assessed the effects of gonadotropin-releasing hormone agonists (GnRHa) on the prevention of chemotherapy-induced ovarian insufficiency among young patients with malignant ovarian germ cell tumour (MOGCT) receiving chemotherapy. Methods: This multicentre, retrospective study was conducted at 15 sites affiliated with the Korean Gynecologic Oncology Group and enrolled 354 patients between January 1995 and September 2018. Among them, 227 patients were included in this study and divided into two groups according to the use of GnRHa during chemotherapy (GnRHa versus no GnRHa groups). The primary objective was to compare the rates of menstrual resumption between the two groups. We also assessed the clinical determinants affecting menstrual resumption among the study groups. Results: There were no significant differences between the GnRHa (n = 63) and no GnRHa (n = 164) groups regarding age at diagnosis, parity, ethnicity, age at menarche, body mass index, International Federation of Gynecology and Obstetrics stage, mode of surgery and surgery type. The rate of menstrual resumption after chemotherapy was 100% (63 of 63) in the GnRHa group and 90.9% (149 of 164) in the no GnRHa group (p = 0.013). The mean periods from last chemotherapy to menstrual resumption were 7.4 and 7.3 months in the GnRHa and no GnRHa groups, respectively. GnRHa co-administration during chemotherapy reduced the likelihood of amenorrhoea after chemotherapy, although statistical significance was not confirmed in the univariate analysis (odds ratio: 0.276; 95% confidence interval, 0.004–1.317; p = 0.077). Conclusion: Temporary ovarian suppression with GnRHa during chemotherapy does not significantly increase the chances of menstrual resumption in young patients with MOGCT. © 2020 Elsevier Ltd
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