Westhoff Julia, Naehrlich Lutz
Department of Pediatrics, Pediatric Pulmonology, Justus-Liebig-University, Giessen, Germany.
Curr Opin Pulm Med. 2024 Nov 1;30(6):633-639. doi: 10.1097/MCP.0000000000001115. Epub 2024 Aug 22.
Advanced cystic fibrosis lung disease remains the main cause of death in people with cystic fibrosis (pwCF). Cystic fibrosis transmembrane regulator (CFTR) modulators have changed the disease burden for eligible pwCF with access to this therapy.
Real-world data show that there are no safety concerns for patients with advanced cystic fibrosis lung disease treated with highly effective triple CFTR modulator therapy. The improvements are comparable to those in other people with cystic fibrosis and in part even better. Mortality and rates of lung transplantation have decreased since the approval of CFTR modulator therapy and, especially, highly effective triple CFTR modulator therapy. Nevertheless, at least 10% of people with cystic fibrosis are not eligible for highly effective CFTR modulator therapy, and the development of alternative treatments remains important.
The approval of highly effective CFTR modulator therapies has been a breakthrough in treatment for most people with cystic fibrosis, especially those with advanced lung disease, improving survival and reducing the burden of the disease.
晚期囊性纤维化肺病仍是囊性纤维化患者(pwCF)的主要死因。囊性纤维化跨膜传导调节因子(CFTR)调节剂改变了有机会接受该疗法的合格pwCF的疾病负担。
真实世界数据表明,接受高效三联CFTR调节剂治疗的晚期囊性纤维化肺病患者不存在安全性问题。改善情况与其他囊性纤维化患者相当,部分甚至更好。自CFTR调节剂疗法获批以来,尤其是高效三联CFTR调节剂疗法获批以来,死亡率和肺移植率有所下降。然而,至少10%的囊性纤维化患者不符合高效CFTR调节剂疗法的条件,因此开发替代疗法仍然很重要。
高效CFTR调节剂疗法的获批对大多数囊性纤维化患者,尤其是那些患有晚期肺病的患者来说是治疗上的突破,提高了生存率并减轻了疾病负担。