University of Washington School of Medicine, Department of Pediatrics, Division of Pulmonology, 4800 Sand Point Way NE, Seattle, WA 98105, USA; Seattle Children's Research Institute, Cystic Fibrosis Foundation Therapeutics Development Network Coordinating Center, PO Box 5371, Seattle, WA 98145, USA.
University of Washington School of Medicine, Department of Family Medicine, 4311 11th Ave. NE, Seattle, WA 98105, USA; University of Washington School of Medicine, Department of Obstetrics and Gynecology, 4311 11th Ave. NE, Seattle, WA 98105, USA.
J Cyst Fibros. 2017 Nov;16(6):687-694. doi: 10.1016/j.jcf.2017.01.008. Epub 2017 Feb 10.
Little is known about how new therapies that partially correct the basic cystic fibrosis (CF) defect (ivacaftor and lumacaftor) might alter hormonal contraceptive effectiveness, impact pregnancy outcomes, or affect pregnancy timing. Examination of pregnancy rates among CF women during periods of CFTR modulator therapy initiation will provide foundation for further research in this area.
The Cystic Fibrosis Foundation Patient Registry was used to examine pregnancy rates and outcomes by genotype class before, during, and after the introduction of CFTR modulator therapies between 2005 and 2014.
Among women with CF, ages 15-44years, there was a slight downward trend in annual pregnancy rates from 2005 to 2014 (2% reduction per year, p=0.041). Among women with G551D, pregnancy rates during phase 3 ivacaftor trial years was 14.4/1000 women-years compared to 34.0/1000 prior to the trial period (relative risk [RR]=0.65; 95% CI=0.43-0.96; p=0.011) and 38.4/1000 after drug approval in June 2012 (RR=1.52 post-approval compared to trial period; 95% CI=1.26, 1.83; p<0.001). Pregnancy outcomes did not significantly change between 2005 and 2014 for any genotype class.
Evidence of significantly increased numbers of pregnancies among women taking approved CFTR modulators is important because of the unknown risk to pregnancy and fetal outcomes. Increases may be temporary following pregnancy prevention during controlled clinical trials, or from altered perceptions about maternal survival with new approved treatments. As more women with CF become eligible to receive modulators, the CF community must study their effect on contraceptive efficacy and safety during pregnancy. With increased health and survival due to modulation, family planning topics will become more common in CF.
对于部分纠正囊性纤维化(CF)基本缺陷的新型疗法(依伐卡托和卢美卡托)如何改变激素避孕效果、影响妊娠结局或影响妊娠时机,目前知之甚少。检查 CF 调节剂治疗开始期间 CF 女性的妊娠率将为该领域的进一步研究提供基础。
利用囊性纤维化基金会患者登记处,检查了 2005 年至 2014 年 CFTR 调节剂治疗引入前后,不同基因型类别中 CF 女性的妊娠率和结局。
在 15-44 岁的 CF 女性中,2005 年至 2014 年期间,每年的妊娠率呈轻微下降趋势(每年减少 2%,p=0.041)。在 G551D 女性中,在第 3 期依伐卡托试验年的妊娠率为 14.4/1000 名女性年,而在试验前为 34.0/1000 名女性年(相对风险[RR]=0.65;95%CI=0.43-0.96;p=0.011),在 2012 年 6 月药物批准后为 38.4/1000 名女性年(RR=1.52 批准后比试验期;95%CI=1.26,1.83;p<0.001)。在任何基因型类别中,2005 年至 2014 年期间,妊娠结局均无显著变化。
服用已批准的 CFTR 调节剂的女性妊娠数量显著增加的证据很重要,因为这对妊娠和胎儿结局的风险未知。在受控临床试验期间进行妊娠预防后,或者由于对新批准的治疗方法提高母体生存率的看法发生变化,这种增加可能是暂时的。随着越来越多的 CF 女性有资格接受调节剂治疗,CF 社区必须研究其对妊娠期间避孕效果和安全性的影响。由于调节作用,健康和生存状况得到改善,计划生育问题将在 CF 中变得更加普遍。