Departments of Medicine; Microbiology, Immunology & Infectious Disease; Community Health Sciences, University of Calgary , Calgary, AB, Canada.
Snyder Institute for Chronic Diseases , Calgary, AB, Canada.
Expert Opin Investig Drugs. 2020 Oct;29(10):1107-1124. doi: 10.1080/13543784.2020.1805733. Epub 2020 Oct 10.
Cystic fibrosis (CF) is a genetic disease affecting multiple organ systems. Research and innovations in novel therapeutic agents and health care delivery have resulted in dramatic improvements in quality of life and survival for people with CF. Despite this, significant disease burden persists for many and this is compounded by disparities in treatment access and care which globally necessitates further work to improve outcomes. Because of the advent of numerous therapies which include gene-targeted modulators in parallel with specialized care delivery models, innovative efforts continue.
In this review, we discuss the available data on investigational agents in clinical development and currently available treatments for CF. We also evaluate approaches to care delivery, consider treatment gaps, and propose future directions for advancement.
Since the discovery of the CF gene, CFTR modulators have provided a hallmark of success, even though it was thought not previously possible. This has led to reinvigorated efforts and innovations in treatment approaches and care delivery. Numerous challenges remain because of genetic and phenotypic heterogeneity, access issues, and therapeutic costs, but the collaborative approach between stakeholders for continued innovation fuels optimism. CF cystic fibrosis; CFF Cystic Fibrosis Foundation (USA); CFTR cystic fibrosis transmembrane regulator; CRISPR clustered regularly interspaced short palindromic repeats; COX cyclo oxygenase; FDA US Food and Drug Administration; FEV1% forced expiratory volume in one second % predicted; F508del deletion of phenylalanine (F) in the 508th position (most common mutation); G551D substitution of the amino acid glycine by aspartate at position 551 in the nucleotide binding domain-1 of the CFTR gene; LMIC low- and middle-income country; LTB4 leukotriene B4; MDT multi-disciplinary care team; NO nitric oxide; NSAIDs non-steroidal anti-inflammatory drugs; SLPI secretory leukocyte protease inhibitor.
囊性纤维化(CF)是一种影响多个器官系统的遗传性疾病。新型治疗药物和医疗保健提供方式的研究和创新,使 CF 患者的生活质量和存活率得到了显著提高。尽管如此,许多人仍然面临着巨大的疾病负担,而在治疗机会和护理方面的差异在全球范围内更是加剧了这一问题,因此需要进一步努力来改善治疗效果。由于众多治疗方法的出现,包括与专门护理提供模式并行的靶向基因调节剂,创新工作仍在继续。
在这篇综述中,我们讨论了临床开发中具有研究性的药物和 CF 目前可用的治疗方法的现有数据。我们还评估了护理提供方式,考虑了治疗差距,并提出了未来的发展方向。
自 CF 基因发现以来,CFTR 调节剂已经取得了显著的成功,尽管此前人们认为这是不可能的。这激发了治疗方法和护理提供方式的重新努力和创新。由于遗传和表型异质性、获取问题和治疗费用等诸多挑战仍然存在,但利益相关者之间的合作创新方法激发了乐观情绪。CF 囊性纤维化;CFF 囊性纤维化基金会(美国);CFTR 囊性纤维化跨膜转导调节因子;CRISPR 成簇规律间隔短回文重复序列;COX 环氧化酶;FDA 美国食品和药物管理局;FEV1% 一秒用力呼气量占预计值的百分比;F508del 第 508 位苯丙氨酸缺失(最常见的突变);G551D 在 CFTR 基因核苷酸结合域 1 中第 551 位的甘氨酸被天冬氨酸取代;LMIC 低收入和中等收入国家;LTB4 白三烯 B4;MDT 多学科护理团队;NO 一氧化氮;NSAIDs 非甾体抗炎药;SLPI 分泌白细胞蛋白酶抑制剂。