Department of Pediatrics and Adolescent Medicine, Ulm University Medical Center, Ulm University, Eythstr 24, 89075, Ulm, Germany.
Department of Otorhinolaryngology, Head and Neck Surgery, Ulm University Medical Center, Ulm, Germany.
Eur Arch Otorhinolaryngol. 2023 Jul;280(7):3271-3277. doi: 10.1007/s00405-023-07859-4. Epub 2023 Feb 4.
Sinunasal symptoms and chronic rhinusinutitis are common in patients with cystic fibrosis. Cystic fibrosis transmembrane regulator (CFTR) modulators have led to dramatic improvements of respiratory symptoms and quality of life in patients with cystic fibrosis. This study aims to evaluate subjective and objective sinunasal symptoms after start of CFTR-modulator triple therapy.
43 patients (n = 6 < 18 years), treated with highly effective CFTR-modulator therapy with elexacaftor-tezacaftor-ivacaftor (ELX/TEZ/IVA) were included, as were 20 controls with cystic fibrosis but without CFTR-modulator therapy (n = 6 < 18 years). All assessed their sinunasal symptoms retrospectively and the intervention group at a mean of 9.3 (2-16) months after start of ELX/TEZ/IVA.
Improvements in SNOT-22 overall score from m = 32.7 to m = 15.7 points (p < 0.0001) as well in the nasal, emotional, otologic, and sleep subdomains could be demonstrated in the intervention group. No changes were found in the control group. Children showed lower SNOT-22 scores than adults and a reduction of SNOT-22 total score from m = 9.4 to m = 2.2 (p = 0.25) was found. 8 patients were evaluated by an otorhinolaryngologist before and after start of ELX/TEZ/IVA and showed pronounced objective clinical improvement.
Highly effective CFTR-modulator therapy has a significant positive impact on both subjective and objective sinunasal symptoms in patients with CF and some improvement could be demonstrated in children < 18 years as well.
鼻窦症状和慢性鼻鼻窦炎在囊性纤维化患者中很常见。囊性纤维化跨膜转导调节因子(CFTR)调节剂已显著改善囊性纤维化患者的呼吸道症状和生活质量。本研究旨在评估 CFTR 调节剂三联疗法开始后主观和客观的鼻窦症状。
纳入 43 名(n = 6 < 18 岁)接受高效 CFTR 调节剂治疗(依伐卡托/泰比卡托/艾美拉唑)的患者,以及 20 名未接受 CFTR 调节剂治疗(n = 6 < 18 岁)的囊性纤维化对照患者。所有患者均回顾性评估其鼻窦症状,干预组在开始依伐卡托/泰比卡托/艾美拉唑治疗后平均 9.3 个月(2-16 个月)进行评估。
干预组 SNOT-22 总分从 m = 32.7 分改善至 m = 15.7 分(p < 0.0001),鼻部、情绪、耳科和睡眠亚域也有改善。对照组无变化。儿童的 SNOT-22 评分低于成人,SNOT-22 总分从 m = 9.4 分降至 m = 2.2 分(p = 0.25)。8 名患者在开始依伐卡托/泰比卡托/艾美拉唑治疗前后接受了耳鼻喉科评估,显示出明显的客观临床改善。
高效 CFTR 调节剂治疗对 CF 患者的主观和客观鼻窦症状均有显著的积极影响,< 18 岁的儿童也有一定程度的改善。