Disease staging and sub setting of interstitial lung disease associated with systemic sclerosis: impact on therapy

Expert Rev Clin Immunol. 2018 Feb;14(2):127-135. doi: 10.1080/1744666X.2018.1427064. Epub 2018 Jan 20.

Abstract

Interstitial lung disease (ILD) is the most serious complication of systemic sclerosis (SSc). There is no accepted guidance as to which clinical, radiological or physiological thresholds should prompt initiation or changes in treatment. Furthermore, some patients with extensive disease remain stable without the need for intervention whilst others with limited disease at the outset, experience a precipitous decline. Areas covered: In this article, evidence for the integration of a number of disease-specific and patient-related domains are discussed and proposed. Introduction and maintenance of therapy requires a nuanced understanding of these factors and is crucial when weighing up the risks and benefits of immunomodulation. The evidence for the existing treatment modalities is discussed and the future directions for management of patients with SSc-ILD, which may include antifibrotic or biologic therapy, are explored. Expert commentary: In the management of SSc-ILD, a multidisciplinary team approach which integrates physiology and radiology with the patient at the centre of the process is crucial for effective management and provision of the best outcomes.

Keywords: SLS; Systemic sclerosis; azathioprine; cyclophosphamide; interstitial lung disease; mycophenolate mofetil; nintedanib; pirfenidone; scleroderma; staging; treatment pulmonary fibrosis.

MeSH terms

  • Evidence-Based Medicine
  • Humans
  • Immunosuppressive Agents / therapeutic use*
  • Immunotherapy / methods*
  • Indoles / therapeutic use*
  • Lung Diseases, Interstitial / diagnosis*
  • Lung Diseases, Interstitial / therapy
  • Phenotype
  • Pyridones / therapeutic use
  • Risk Assessment
  • Scleroderma, Systemic / diagnosis*
  • Scleroderma, Systemic / therapy

Substances

  • Immunosuppressive Agents
  • Indoles
  • Pyridones
  • pirfenidone
  • nintedanib