Department of Pediatric Pulmonology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Department of Pulmonology, Haga Teaching Hospital, The Hague, the Netherlands.
J Cyst Fibros. 2021 Sep;20(5):e63-e66. doi: 10.1016/j.jcf.2021.06.001. Epub 2021 Jun 24.
Substantial progress has been made in the treatment of Cystic fibrosis due to introduction of CFTR modulators. However, little is known about the long term side effects of treatment with these drugs. We here present a 7 year old girl with CF who presented with breast development as a rare dose dependent side effect of treatment with ivacaftor and we report data on the correlation between drug plasma concentration and clinical effect, bodyweight, and BSA in 16 patients. Higher plasma concentrations did not correlate with clinical effect, as change in FEV1 and sweat chloride concentration. Patients with low bodyweight or BSA tended to have higher plasma concentrations. This might indicate that the current recommended dose of ivacaftor is at the top of the dose-response curve and that some patients can be treated with lower doses of ivacaftor with similar clinical effect.
由于 CFTR 调节剂的引入,囊性纤维化的治疗取得了重大进展。然而,对于这些药物治疗的长期副作用知之甚少。我们在此介绍一例 7 岁女孩,她因服用 ivacaftor 而出现乳房发育,这是一种罕见的剂量依赖性副作用,并报告了 16 例患者中药物血浆浓度与临床疗效、体重和 BSA 之间相关性的数据。较高的血浆浓度与 FEV1 和汗液氯化物浓度的临床疗效无关。体重或 BSA 较低的患者血浆浓度往往较高。这可能表明当前推荐的 ivacaftor 剂量已处于剂量反应曲线的顶端,并且一些患者可以用较低剂量的 ivacaftor 进行治疗,而临床疗效相似。