The future of cystic fibrosis care: a global perspective

Abstract

The past six decades have seen remarkable improvements in health outcomes for people with cystic fibrosis, which was once a fatal disease of infants and young children. However, although life expectancy for people with cystic fibrosis has increased substantially, the disease continues to limit survival and quality of life, and results in a large burden of care for people with cystic fibrosis and their families. Furthermore, epidemiological studies in the past two decades have shown that cystic fibrosis occurs and is more frequent than was previously thought in populations of non-European descent, and the disease is now recognised in many regions of the world. The Lancet Respiratory Medicine Commission on the future of cystic fibrosis care was established at a time of great change in the clinical care of people with the disease, with a growing population of adult patients, widespread genetic testing supporting the diagnosis of cystic fibrosis, and the development of therapies targeting defects in the cystic fibrosis transmembrane conductance regulator (CFTR), which are likely to affect the natural trajectory of the disease. The aim of the Commission was to bring to the attention of patients, health-care professionals, researchers, funders, service providers, and policy makers the various challenges associated with the changing landscape of cystic fibrosis care and the opportunities available for progress, providing a blueprint for the future of cystic fibrosis care. The discovery of the CFTR gene in the late 1980s triggered a surge of basic research that enhanced understanding of the pathophysiology and the genotype-phenotype relationships of this clinically variable disease. Until recently, available treatments could only control symptoms and restrict the complications of cystic fibrosis, but advances in CFTR modulator therapies to address the basic defect of cystic fibrosis have been remarkable and the field is evolving rapidly. However, CFTR modulators approved for use to date are highly expensive, which has prompted questions about the affordability of new treatments and served to emphasise the considerable gap in health outcomes for patients with cystic fibrosis between high-income countries, and low-income and middle-income countries (LMICs). Advances in clinical care have been multifaceted and include earlier diagnosis through the implementation of newborn screening programmes, formalised airway clearance therapy, and reduced malnutrition through the use of effective pancreatic enzyme replacement and a high-energy, high-protein diet. Centre-based care has become the norm in high-income countries, allowing patients to benefit from the skills of expert members of multidisciplinary teams. Pharmacological interventions to address respiratory manifestations now include drugs that target airway mucus and airway surface liquid hydration, and antimicrobial therapies such as antibiotic eradication treatment in early-stage infections and protocols for maintenance therapy of chronic infections. Despite the recent breakthrough with CFTR modulators for cystic fibrosis, the development of novel mucolytic, anti-inflammatory, and anti-infective therapies is likely to remain important, especially for patients with more advanced stages of lung disease. As the median age of patients with cystic fibrosis increases, with a rapid increase in the population of adults living with the disease, complications of cystic fibrosis are becoming increasingly common. Steps need to be taken to ensure that enough highly qualified professionals are present in cystic fibrosis centres to meet the needs of ageing patients, and new technologies need to be adopted to support communication between patients and health-care providers. In considering the future of cystic fibrosis care, the Commission focused on five key areas, which are discussed in this report: the changing epidemiology of cystic fibrosis (section 1); future challenges of clinical care and its delivery (section 2); the building of cystic fibrosis care globally (section 3); novel therapeutics (section 4); and patient engagement (section 5). In panel 1, we summarise key messages of the Commission. The challenges faced by all stakeholders in building and developing cystic fibrosis care globally are substantial, but many opportunities exist for improved care and health outcomes for patients in countries with established cystic fibrosis care programmes, and in LMICs where integrated multidisciplinary care is not available and resources are lacking at present. A concerted effort is needed to ensure that all patients with cystic fibrosis have access to high-quality health care in the future.

Copyright © 2020 Elsevier Ltd. All rights reserved.

Figures

Figure 1. Pathophysiology of Cystic Fibrosis

A-D, Role of CFTR in healthy airways and molecular mechanisms causing CFTR dysfunction in cystic fibrosis (CF). A, In healthy airways, CFTR is expressed at the apical surface of airway epithelial cells together with the epithelial sodium channel (ENaC). Coordinated regulation of CFTR and ENaC enables proper airway surface hydration and effective mucociliary clearance. B-D, In CF, different mutations in CFTR cause CFTR dysfunction via different molecular mechanisms. B, CFTR nonsense or splicing mutations abrogate CFTR production. C, Many missense mutations, including the common F508del mutation, impair proper folding of CFTR and lead to retention in the endoplasmic reticulum and degradation by the proteasome. D, Some missense and splicing mutations produce CFTR chloride channels that reach the cell surface but are not fully functional. CFTR = cystic fibrosis transmembrane conductance regulator; ENaC = epithelial sodium channel. Reproduced from Gentzsch and Mall, CHEST 2018; 154(2):383–393 by permission of Elsevier Ltd Copyright 2018 American College of Chest Physicians.

Figure 2. Classes of CFTR Mutations.

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene can be divided into six classes. Class I mutations result in no protein production. Class II mutations (including the most prevalent, Phe508del) cause retention of a misfolded protein at the endoplasmic reticulum, and subsequent degradation in the proteasome. Class III mutations affect channel regulation, impairing channel opening (eg, Gly551Asp). Class IV mutants show reduced conduction—ie, decreased flow of ions (eg, Arg117His). Class V mutations cause substantial reduction in mRNA or protein, or both, Class VI mutations cause substantial plasma membrane instability and include Phe508del when rescued by most correctors (rPhe508del). Reproduced with permission Boyle MP, De Boeck K. A new era in the treatment of cystic fibrosis: correction of the underlying CFTR defect. Lancet Respir Med 2013; 1: 158–63.

Figure 3. Median FEV1 % predicted for people with Cystic Fibrosis in the United States by Age (1998 to 2018).

Cystic fibrosis patients under care at CF Foundation-accredited care center in the United States, who consented to have their data entered. Reproduced with permission of the US Cystic Fibrosis Foundation, Bethesda Maryland. Cystic Fibrosis Foundation Patient Registry Bethesda, Maryland ©2019 Cystic Fibrosis Foundation.

Figure 4. The Number of Children and Adults with Cystic Fibrosis (USA),1987–2017

Cystic fibrosis patients under care at CF Foundation-accredited care centers in the United States, who consented to have their data entered. Reproduced with permission of the US Cystic Fibrosis Foundation, Bethesda Maryland. 2017 Annual Data Report Bethesda, Maryland ©2018 Cystic Fibrosis Foundation.

Figure 5. Maps of Countries with Cystic Fibrosis Registries and their Population Size

Countries with a cystic fibrosis registry Reproduced with permission of the US Cystic Fibrosis Foundation, Bethesda Maryland.

Figure 6. CFTR Function and Clinical Phenotype

CBAVD – congenital bilateral absence of toe vas deferens.

Figure 7. Cystic fibrosis Standards of Care

Green – comprehensive, Blue – partial, Orange – limited, Red – minimal or unknown.

Figure 8. Schematic of approach to CFTR restoration with small molecules, by mutation class.

Adapted from Sloane PA, Rowe SM. Cystic fibrosis transmembrane conductance regulator protein repair as a therapeutic strategy in cystic fibrosis. Current Opinion in Pulmonary Medicine 2010;16(6):591–597. Schematic of approach to CFTR restoration with small molecules, by mutation class. Therapeutic approaches with definitive studies in solid boxes; those under investigation with dotted boxes.

Figure 9. Cystic fibrosis drug development pipeline of the US Cystic Fibrosis Foundation

Reproduced with permission of the US Cystic Fibrosis Foundation, Bethesda Maryland.

Figure 10. CFTR Modulators – countries where approval and funded

Panel A Countries with significant population of European Origin Panel B Ivacaftor (inset Europe) Panel C Lumacaftor/Ivacaftor (inset Europe) Panel D Tezacaftor/Ivacaftor (inset Europe) Phase III triple combination therapy studies (Vertex Pharmaceuticals Inc) have been completed but as yet approval applications have not been submitted to Regulatory Authorities.

Figure 10. CFTR Modulators – countries where approval and funded

Panel A Countries with significant population of European Origin Panel B Ivacaftor (inset Europe) Panel C Lumacaftor/Ivacaftor (inset Europe) Panel D Tezacaftor/Ivacaftor (inset Europe) Phase III triple combination therapy studies (Vertex Pharmaceuticals Inc) have been completed but as yet approval applications have not been submitted to Regulatory Authorities.

Figure 10. CFTR Modulators – countries where approval and funded

Panel A Countries with significant population of European Origin Panel B Ivacaftor (inset Europe) Panel C Lumacaftor/Ivacaftor (inset Europe) Panel D Tezacaftor/Ivacaftor (inset Europe) Phase III triple combination therapy studies (Vertex Pharmaceuticals Inc) have been completed but as yet approval applications have not been submitted to Regulatory Authorities.