Department of Obstetrics and Gynecology, Haseki Training and Research Hospital, Istanbul, Turkey.
Department of Obstetrics and Gynecology, Memorial Atasehir Hospital, Istanbul, Turkey.
Arch Gynecol Obstet. 2022 Oct;306(4):1313-1319. doi: 10.1007/s00404-022-06676-0. Epub 2022 Jul 14.
To evaluate the effects of adjuvant letrozole administration on outcomes of gonadotropin-releasing hormone (GnRH) antagonist cycles with intra-cytoplasmic sperm injection in POSEIDON groups 3 and 4 expected poor responder women.
This study was conducted by retrospective analysis of patients with expected poor ovarian response (POSEIDON groups 3 and 4) that underwent GnRH antagonist cycles with intra-cytoplasmic sperm injection between 2010 and 2020. A total of 488 patients with letrozole co-administration and 2564 patients without any adjuvant treatment that underwent GnRH antagonist cycles within the selected period of time were included in the study.
Implantation rates, clinical pregnancy rates and live birth delivery rates were significantly higher in letrozole administered patients in comparison to controls among POSEIDON group 3 women (0.39 ± 0.46 vs 0.27 ± 0.40, p = 0.01; 46.1% vs 33%, p = 0.014; 42.7% vs 31.5%, p = 0.034, respectively). Mean total doses of gonadotropins required per cycle were significantly lower in letrozole administered patients among both POSEIDON groups 3 and 4 women (2864.65 ± 878.47 IU vs 3757.27 ± 1088.89 IU, p < 0.001; 3286.06 ± 770.16 IU vs 3666.48 ± 959.66 IU, p < 0.001, respectively).
Adjuvant letrozole co-administration in intra-cytoplasmic sperm injection cycles following GnRH antagonist protocol appears to improve implantation, clinical pregnancy and live birth delivery rates in women with POSEIDON group 3 expected poor ovarian response.
评估在 GnRH 拮抗剂周期中添加来曲唑对 POSEIDON 分组 3 和 4 中预计卵巢反应不良的患者行卵胞浆内单精子注射结局的影响。
本研究通过回顾性分析 2010 年至 2020 年间接受 GnRH 拮抗剂周期和卵胞浆内单精子注射的预计卵巢反应不良(POSEIDON 分组 3 和 4)患者。在选定的时间段内,共有 488 例接受来曲唑辅助治疗的患者和 2564 例未接受任何辅助治疗的患者纳入研究。
POSEIDON 分组 3 患者中,来曲唑组的胚胎着床率、临床妊娠率和活产分娩率显著高于对照组(0.39±0.46 比 0.27±0.40,p=0.01;46.1%比 33%,p=0.014;42.7%比 31.5%,p=0.034)。POSEIDON 分组 3 和 4 患者中,来曲唑组的每个周期所需的促性腺激素总剂量均显著低于对照组(2864.65±878.47 IU 比 3757.27±1088.89 IU,p<0.001;3286.06±770.16 IU 比 3666.48±959.66 IU,p<0.001)。
在 GnRH 拮抗剂方案后,在卵胞浆内单精子注射周期中添加来曲唑似乎可以提高 POSEIDON 分组 3 中预计卵巢反应不良患者的胚胎着床、临床妊娠和活产分娩率。