Additional points to consider before incorporating the Food and Drug Administration-approved therapies for systemic sclerosis-associated interstitial lung disease.
Markus BredemeierPublished in: Arthritis & rheumatology (Hoboken, N.J.) (2021)
We congratulate the authors for the excellent review, not only restricted to recently approved therapies, on the treatment of systemic sclerosis-associated interstitial lung disease (SSc-ILD) (1). However, it is our opinion that some aspects that currently affect our medical practice merit further commentary. The pandemic of COVID-19 has generated unique challenges in the therapy of SSc-ILD, especially impacting the decision to start treatment. While there is no evidence suggesting that cyclophosphamide or rituximab can reduce mortality in SSc-ILD (2), these drugs have been associated with higher incidence of serious outcomes and mortality in COVID-19 patients (3, 4).
Keyphrases
- interstitial lung disease
- systemic sclerosis
- drug administration
- sars cov
- rheumatoid arthritis
- coronavirus disease
- idiopathic pulmonary fibrosis
- healthcare
- risk factors
- primary care
- cardiovascular events
- diffuse large b cell lymphoma
- type diabetes
- stem cells
- mesenchymal stem cells
- coronary artery disease
- bone marrow
- weight loss
- cell therapy
- smoking cessation