Abstract

Objective: Interstitial lung disease (ILD) frequently complicates systemic sclerosis (SSc). Cyclophosphamide (CYC) is a promising immunosuppressive therapy for SSc-related ILD. Our objective was to investigate the effectiveness of an intravenous CYC (iv CYC) pulse regime in SSc-related ILD during treatment and thereafter.Methods:In a prospective observational study ten consecutive patients with SSc-related ILD were treated with iv CYC in a pulse regime lasting from 6 to 24 months. Clinical status, pulmonary functional testing (PFT) and high resolution computed tomography (HRCT) of the chest were evaluated at enrolment and 6, 12 and 24 months thereafter. After treatment withdrawal, patients were followed up every 6 months with PFT and chest HRCT to monitor lung disease.Results:Clinical improvement was apparent in 8 out of 10 patients. The median values of forced vital capacity (FVC), forced expiratory volume in the first second (FEV1) and diffusion lung capacity for carbon monoxide (DLCO) as well as ground-glass pattern on HRCT did not change significantly after 6, 12 and 24 months of therapy. The follow-up continued in 8 out of 10 patients after treatment withdrawal for a median of 26.5 months (range: 12-48 months). The final median FVC was 54.5% of predicted value (interquartile range, IQR= 31.6%-94%). Only one patient suffered a FVC deterioration greater than 10%, even though less than 160 ml. The final median DLCO was 68% of predicted value (IQR=38.3-83.6%). Only 2 patients who developed pulmonary arterial hypertension deteriorated their DLCO values of more than 15%.Conclusions:An iv CYC pulse regimen over 24 months may stabilize pulmonary activity in patients with SSc-related ILD during the course of treatment and for a median of 26.5 months thereafter.

Highlights

  • The incidence of pulmonary fibrosis in systemic sclerosis (SSc) varies from 25% to 90%, depending on the method used to identify the interstitial lung disease (ILD) [1]

  • Pulmonary fibrosis is the major cause of morbidity and mortality in SSc patients [2,3,4,5,6]

  • Disease extent is mainly assessed by pulmonary function testing (PFT) and high resolution computed tomography (HRCT) [7]

Read more

Summary

Introduction

The incidence of pulmonary fibrosis in systemic sclerosis (SSc) varies from 25% to 90%, depending on the method used to identify the interstitial lung disease (ILD) [1]. Pulmonary fibrosis is the major cause of morbidity and mortality in SSc patients [2,3,4,5,6]. Disease extent is mainly assessed by pulmonary function testing (PFT) and high resolution computed tomography (HRCT) [7]. While HRCT is the most sensitive and specific tool to identify pulmonary fibrosis in SSc patients, it is not necessarily indicative of the severity of lung impairment [7]. PFT is the only widely available means able to identify whether the disease is sufficiently severe to justify immediate therapeutic intervention

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call