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Interstitial Lung Disease: How Should Therapeutics Be Implemented?
Cosimo Bruni1, Corrado Campochiaro2, Jeska K de Vries-Bouwstra3
1Department of Rheumatology, University Hospital Zurich, University of Zurich, Schmelzbergstrasse 24, Zurich 8006, Switzerland; Division of Rheumatology, Department of Experimental Medicine, Careggi University Hospital - University of Florence, Florence, Italy.
Systemic sclerosis-interstitial lung disease (SSc-ILD) presents significant challenges in clinical practice. This review summarizes current evidence on SSc-ILD monitoring and treatment, highlighting areas needing further research.
Area of Science:
- Rheumatology
- Pulmonology
- Internal Medicine
Background:
- Systemic sclerosis-interstitial lung disease (SSc-ILD) is a severe complication of systemic sclerosis (SSc), leading to significant morbidity and mortality.
- Current treatment options for SSc-ILD include cyclophosphamide, mycophenolate mofetil, tocilizumab, and nintedanib, with proven efficacy.
- The unpredictable disease course, challenges in progression assessment, and varied treatment strategies complicate clinical management.
Purpose of the Study:
- To review and synthesize current evidence regarding the monitoring and treatment of SSc-ILD.
- To identify and discuss areas where further research is critically needed for improved SSc-ILD management.
Main Methods:
- Comprehensive literature search of existing evidence on SSc-ILD monitoring and treatment.
- Synthesis and critical appraisal of the collected data.
Main Results:
- Established efficacy of certain treatments like tocilizumab and nintedanib in SSc-ILD.
- Identification of complexities in predicting and managing SSc-ILD progression.
- Summary of current monitoring strategies and treatment guidelines.
Conclusions:
- Effective management of SSc-ILD requires a thorough understanding of current evidence and ongoing research.
- Further research is essential to address the complexities in SSc-ILD monitoring, prediction, and treatment optimization.
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