Use of Hormonal Protection for Chemotherapy-induced Gonadotoxicity

被引:63
作者
Kim, S. Samuel [1 ]
Lee, Jung Ryeol [3 ]
Jee, Byung Chul [3 ,4 ]
Suh, Chang Suk [3 ,4 ]
Kim, Seok Hyun [4 ]
Ting, Alison [5 ]
Petroff, Brian [2 ]
机构
[1] Univ Kansas, Sch Med, Dept Obstet & Gynecol, Kansas City, KS 66103 USA
[2] Univ Kansas, Sch Med, Dept Internal Med, Kansas City, KS USA
[3] Seoul Natl Univ, Bundang Hosp, Dept Obstet & Gynecol, Seoul 151, South Korea
[4] Seoul Natl Univ, Coll Med, Dept Obstet & Gynecol, Seoul 151, South Korea
[5] Oregon Natl Primate Res Ctr, Dept Reprod Sci, Portland, OR USA
关键词
fertility preservation; GnRH agonist; gonadotoxicity; tamoxifen; cancer; chemotherapy; PREMATURE OVARIAN FAILURE; HODGKIN-LYMPHOMA; GNRH ANTAGONIST; CANCER-PATIENTS; BREAST-CANCER; FERTILITY PRESERVATION; RHESUS-MONKEYS; HIGH-RISK; CYCLOPHOSPHAMIDE; TAMOXIFEN;
D O I
10.1097/GRF.0b013e3181f96cb1
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
It is still controversial that GnRH agonist (GnRHa) protects ovarian function from chemotherapy-induced gonadotoxicity. Indeed, the results of many studies related to this issue are neither consistent nor convincing because of the weak study design and the inadequate sample size. We identified 11 prospective controlled studies (8 nonrandomized and 3 randomized) for the systemic review and meta-analysis. The meta-analysis showed that GnRHa cotreatment during chemotherapy can protect ovarian function. However, it is worthy to note that the result of this meta-analysis is influenced by nonrandomized studies. The protective effect of GnRHa will remain elusive until the currently ongoing large, prospective, randomized studies are completed. In addition, tamoxifen, a selective estrogen receptor modulator, may have the protective effect against loss of follicles and ovarian function, which was caused by chemotherapy.
引用
收藏
页码:740 / 752
页数:13
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