Department of Pediatrics, Faculty of Medicine, University of Thessaly, Larisa, Greece.
Aretaieion University Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Front Endocrinol (Lausanne). 2024 Apr 2;15:1366970. doi: 10.3389/fendo.2024.1366970. eCollection 2024.
The first phase of the GAIL study ("Girls treated with an Aromatase Inhibitor and Leuprorelin," ISRCTN11469487) has shown that the combination of anastrozole and leuprorelin for 24 months is safe and effective in improving the predicted adult height (PAH) in girls with early puberty and compromised growth prediction by +1.21 standard deviation score (SDS; +7.51 cm) compared to inhibition of puberty alone, +0.31 SDS (+1.92 cm).
In the second phase of the GAIL study, we assessed the adult height (AH)/near-adult height (NAH) at the end of the first phase and, in addition, the efficacy of anastrozole monotherapy thereafter in further improving NAH.
We measured the AH (age 16.5 years)/NAH [bone age (BA), 15 years] of the 40 girls included, divided into two matched groups: group A (20 girls on anastrozole + leuprorelin) and group B (20 girls on leuprorelin alone). Group A was further randomized into two subgroups: A1 and A2. Group A1 ( = 10), after completion of the combined therapy, received anastrozole 1 mg/day as monotherapy until BA 14 years, with a 6-month follow-up. Group A2 ( = 10) and group B ( = 20), who received only the combined treatment and leuprorelin alone, respectively, were recalled for evaluation of AH/NAH.
AH or NAH exceeded the PAH at the completion of the 2-year initial phase of the GAIL study in all groups, but the results were statistically significant only in group A1: NAH-PAH group A1, +3.85 cm (+0.62 SDS, = 0.01); group A2, +1.6 cm (+0.26 SDS, = 0.26); and group B, +1.7 cm (+0.3 SDS, = 0.08). The gain in group A1 was significantly greater than that in group A2 ( = 0.04) and in group B ( = 0.03). Anastrozole was determined to be safe even as monotherapy in Group A1.
In early-maturing girls with compromised growth potential, the combined treatment with leuprorelin and anastrozole for 2 years or until the age of 11 years resulted in a total gain in height of +9.7 cm when continuing anastrozole monotherapy until the attainment of NAH, as opposed to +7.4 cm if they do not continue with the anastrozole monotherapy and +3.6 cm when treated with leuprorelin alone. Thus, the combined intervention ends at the shortest distance from the target height if continued with anastrozole monotherapy until BA 14 years.
GAIL 研究的第一阶段(“接受芳香化酶抑制剂和亮丙瑞林治疗的女孩”,ISRCTN86203625)表明,与单独抑制青春期相比,使用阿那曲唑联合亮丙瑞林治疗 24 个月可安全有效地改善预测成年身高(PAH),24 个月后成年身高(PAH)预测值增加 1.21 个标准差评分(+7.51cm)。
在 GAIL 研究的第二阶段,我们评估了第一阶段结束时的成年身高(AH)/接近成年身高(NAH),此外,还评估了阿那曲唑单药治疗在此后进一步改善 NAH 的疗效。
我们测量了 40 名入组女孩的 AH(16.5 岁)/NAH[骨龄(BA),15 岁],将她们分为两组:A 组(20 名接受阿那曲唑+亮丙瑞林治疗的女孩)和 B 组(20 名仅接受亮丙瑞林治疗的女孩)。A 组进一步随机分为两个亚组:A1 和 A2。A1 组(n=10)在完成联合治疗后接受阿那曲唑 1mg/天单药治疗,直至 BA 为 14 岁,随访 6 个月。A2 组(n=10)和 B 组(n=20)分别仅接受联合治疗和亮丙瑞林单药治疗,然后评估 AH/NAH。
在 GAIL 研究的初始 2 年阶段结束时,所有组的 AH 或 NAH 均超过了 PAH,但仅在 A1 组的结果具有统计学意义:NAH-PAH A1 组,+3.85cm(+0.62 SDS, = 0.01);A2 组,+1.6cm(+0.26 SDS, = 0.26);B 组,+1.7cm(+0.3 SDS, = 0.08)。A1 组的增益明显大于 A2 组( = 0.04)和 B 组( = 0.03)。A1 组的阿那曲唑即使作为单药治疗也是安全的。
在生长潜力受损的早期性成熟女孩中,使用亮丙瑞林和阿那曲唑联合治疗 2 年或直至 11 岁,然后继续阿那曲唑单药治疗直至达到 NAH,总身高增加 9.7cm,而如果不继续使用阿那曲唑单药治疗,身高增加 7.4cm,如果仅用亮丙瑞林治疗,身高增加 3.6cm。因此,如果继续阿那曲唑单药治疗直至 BA 为 14 岁,联合干预可以在最短的距离内达到目标身高。