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Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
New therapeutic strategies for systemic sclerosis--a critical analysis of the literature
Gisele Zandman-Goddard1, Nurit Tweezer-Zaks, Yehuda Shoenfeld
1Department of Medicine B and Center for Autoimmune Diseases, Sheba Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Israel.
Abstract:
Systemic sclerosis (SSc) is a multi-system disease characterized by skin fibrosis and visceral disease. Therapy is organ and pathogenesis targeted. In this review, we describe novel strategies in the treatment of SSc. Utilizing the MEDLINE and the COCHRANE REGISTRY, we identified open trials, controlled trials, for treatment of SSc from 1999 to April 2005. We used the terms scleroderma, systemic sclerosis, Raynaud's phenomenon, pulmonary hypertension, methotrexate, cyclosporin, tacrolimus, relaxin, low-dose penicillamine, IVIg, calcium channel blockers, losartan, prazocin, iloprost, N-acetylcysteine, bosentan, cyclophosphamide, lung transplantation, ACE inhibitors, anti-thymocyte globulin, and stem cell transplantation. Anecdotal reports were omitted. Methotrexate, cyclosporin, tacrolimus, relaxin, low-dose penicillamine, and IVIg may be beneficial in improving the skin tightness in SSc. Calcium channel blockers, the angiotensin II receptor type 1 antagonist losartan, prazocin, the prostacyclin analogue iloprost, N-acetylcysteine and the dual endothelin-receptor antagonist bosentan may be beneficial for Raynaud's phenomenon. Epoprostenol and bosentan are approved for therapy of pulmonary hypertension (PAH). Other options under investigation include intravenous or aerolized iloprost. Cyclophosphamide (CYC) pulse therapy is effective in suppressing active alveolitis. Stem cell and lung transplantation is a viable option for carefully selected patients. Renal crisis can be effectively managed when hypertension is aggressively controlled with angiotensin converting enzyme (ACE) inhibitors. Patients should continue taking ACE inhibitors even after beginning dialysis in hope of discontinuing dialysis. Antithymocyte globulin and mycophenolate mofetil appear safe in SSc. The improvement in skin score and the apparent stability of systemic disease during the treatment period suggest that controlled studies of these agents are justified. Stem cell transplantation is under investigation for severe disease. Novel therapies are currently being tested in the treatment of SSc and have the potential of modifying the disease process and overall clinical outcome. The evaluation of these studies is still a difficult process.
Insights
Novel treatments for Systemic Sclerosis (SSc) show promise for skin fibrosis and organ complications. Research highlights emerging therapies targeting SSc pathogenesis, offering hope for improved patient outcomes.
Area of Science:
- Rheumatology
- Immunology
- Pharmacology
Background:
- Systemic sclerosis (SSc) is a complex multi-system autoimmune disease.
- Characterized by widespread fibrosis affecting skin and internal organs.
- Current therapies are often organ-specific and pathogenesis-targeted.
Purpose of the Study:
- To review novel treatment strategies for Systemic Sclerosis.
- To identify emerging therapies based on recent clinical trials.
- To assess the potential of new treatments for SSc manifestations.
Main Methods:
- Literature search of MEDLINE and Cochrane Registry for SSc treatment trials (1999-2005).
- Inclusion of controlled and open trials, excluding anecdotal reports.
- Keywords included SSc, specific drug names, and affected organ systems.
Main Results:
- Methotrexate, cyclosporine, tacrolimus, relaxin, penicillamine, and IVIg show potential for skin fibrosis.
- Treatments like calcium channel blockers, losartan, iloprost, N-acetylcysteine, and bosentan may benefit Raynaud's phenomenon.
- Cyclophosphamide is effective for alveolitis; ACE inhibitors manage renal crisis; stem cell and lung transplantation are options for severe cases.
Conclusions:
- Novel therapies are under investigation for Systemic Sclerosis.
- Emerging treatments offer potential to modify disease progression and improve clinical outcomes.
- Further controlled studies are warranted to validate the efficacy of these agents.