Home » Health » Upadacitinib Beats Mycophenolate for SSc-ILD: New Study

Upadacitinib Beats Mycophenolate for SSc-ILD: New Study


Upadacitinib Shows Promise in Treating Systemic Sclerosis-Associated Interstitial Lung Disease

A recent clinical trial has revealed that the JAK inhibitor upadacitinib demonstrates effectiveness in treating systemic sclerosis-associated interstitial lung disease (SSc-ILD). The study, presented at the European Alliance of Associations for Rheumatology (EULAR) 2024 annual Meeting, indicates that upadacitinib reduces the rate of decline in forced vital capacity (FVC) in patients with SSc-ILD, compared to the current standard treatment, mycophenolate mofetil.

Upadacitinib Outperforms Standard Treatment in Lung Function preservation

The research, led by Dr. Manal Hassanien from Assiut University, Egypt, showed that after one year, the difference in the annual rate of decline in FVC between the upadacitinib and mycophenolate groups was 20.9 mL/year, favoring upadacitinib (P = .05).This suggests a meaningful benefit in preserving lung function for patients treated with upadacitinib.

Did You Know? Forced vital capacity (FVC) is the maximum amount of air a person can exhale after a maximum inhalation. It’s a key indicator of lung function.

The double-blinded, randomized study involved 57 patients with SSc, with disease onset of more than 3 years. All participants had an FVC less than 75% of the predicted normal value and evidence of lung fibrosis. Patients were administered either 15 mg of upadacitinib daily or 2000 mg of mycophenolate daily.

Detailed Study Results: FVC and DLCO Improvements

After 52 weeks, a decline of ≥ 5% in FVC from baseline was observed in 20.6% of the upadacitinib group, compared to 37.5% in the mycophenolate group. Furthermore,a 10% drop in FVC from baseline at 1 year was more common in patients taking mycophenolate (17.9%) than in those taking upadacitinib (6.8%).

Changes in diffusing capacity of the lungs for carbon monoxide (DLCO) at 52 weeks were also more favorable in the upadacitinib group (-62.7 mL) compared to the mycophenolate group (-93.3 mL). DLCO measures how well the lungs transfer gas from inhaled air to the bloodstream, providing another critical measure of lung health according to the american Thoracic Society.

Pro tip: Monitoring FVC and DLCO regularly can definitely help track the progression of SSc-ILD and assess the effectiveness of treatments.

Expert Commentary and Future Considerations

Dr. Iulia Szabo, a rheumatologist at “Iuliu Haţieganu” University of Medicine and Pharmacy, Romania, commented on the study, calling the results “really promising.” she noted that previous studies have shown encouraging evidence using other JAK inhibitors in SSc-ILD treatment, although the data were mostly experimental.

Szabo also cautioned that the younger age of participants in the study may mean that older patients could experience a higher risk of adverse events associated with JAK inhibitors.”The problem we might have will be with older patients as we certainly know all the adverse effects that JAK inhibitors have, and probably we should be a bit more cautious,” she said.

Current Treatment Landscape and Upadacitinib’s Potential Role

Currently, upadacitinib is FDA-approved for various conditions, including rheumatoid arthritis, psoriatic arthritis, and Crohn’s disease. However,for SSc-ILD,nintedanib and tocilizumab remain the only FDA-approved treatments. The findings from this study suggest that upadacitinib could potentially become another valuable option for managing this challenging condition.

Key metrics: Upadacitinib vs. Mycophenolate in SSc-ILD Treatment
Metric Upadacitinib Mycophenolate
Annual FVC decline Difference Favored Upadacitinib (20.9 mL/year)
≥ 5% FVC Decline at 52 Weeks 20.6% 37.5%
10% FVC Drop at 1 Year 6.8% 17.9%
DLCO Change at 52 Weeks -62.7 mL -93.3 mL

What are your thoughts on the potential of upadacitinib for treating SSc-ILD?

How might these findings impact treatment strategies for patients with systemic sclerosis?

Evergreen Insights on Systemic Sclerosis-Associated Interstitial Lung Disease

Systemic sclerosis (SSc), also known as scleroderma, is a chronic autoimmune disease characterized by hardening and tightening of the skin and connective tissues. Interstitial lung disease (ILD) is a common and serious complication of SSc, affecting a significant proportion of patients. SSc-ILD can lead to progressive scarring of the lungs, resulting in shortness of breath, reduced exercise capacity, and ultimately, respiratory failure.

The management of SSc-ILD typically involves immunosuppressive medications aimed at reducing inflammation and slowing the progression of lung damage.however, current treatments have limitations, and new therapeutic options are needed to improve outcomes for patients with this debilitating condition. The emergence of JAK inhibitors like upadacitinib offers a promising avenue for future treatment strategies.

Frequently Asked Questions About Upadacitinib and SSc-ILD

Is upadacitinib a cure for systemic sclerosis-associated interstitial lung disease?
No, upadacitinib is not a cure for SSc-ILD. However, it may help to slow the progression of the disease and improve lung function.
How long does it take to see results with upadacitinib for SSc-ILD?
The clinical trial showed improvements in lung function within 52 weeks of treatment. Individual results may vary.
Are there any side effects associated with upadacitinib?
Yes,like all medications,upadacitinib can cause side effects. Common side effects may include infections, nausea, and headache. It is indeed critically important to discuss potential side effects with your healthcare provider.
Can upadacitinib be used in combination with other treatments for SSc-ILD?
The safety and efficacy of upadacitinib in combination with other treatments for SSc-ILD have not been fully established. Your healthcare provider can determine the best treatment approach for your individual situation.
Where can I find more information about systemic sclerosis-associated interstitial lung disease?
You can find more information about SSc-ILD from reputable sources such as the Scleroderma Foundation and the American Lung Association.

Disclaimer: This article provides information for general knowledge and awareness only. It does not constitute medical advice and should not be substituted for professional consultation with a qualified healthcare provider.

Share this article and join the conversation! What other advancements in autoimmune disease treatments are you excited about?

You may also like

Leave a Comment

This site uses Akismet to reduce spam. Learn how your comment data is processed.