Table 1

Clinical and demographic characteristics of our multicentre cohort of patients with SSc-ILD

Clinical and demographic characteristics90 patients
Female, n (%)65 (72)
Age (years), mean±SD57.6±13.4
Disease duration (years), mean±SD8.8±7.6
Smokers, n (%) (active or former)18 (20)
Cutaneous subset
 Diffuse, n (%)40 (44.0)
 Limited, n (%)41 (45)
 Sine scleroderma, n (%)9 (10)
Autoantibodies
 Anti-topoisomerase I Ab, n (%)67 (74)
 Anti-RNA polymerase III Ab, n (%)2 (2)
 Anti-centromere Ab, n (%)5 (5)
 Anti-U1-RNP Ab, n (%)6 (7)
 Anti-Th/T0, n (%)2 (2)
Organ involvement
 GI involvement83 (92)
 Myositis9 (10)
 Myocarditis10 (11)
 Scleroderma renal crisis0 (0)
 Digital ulcer11 (12)
 Pulmonary arterial hypertension1 (1)
Previous therapies84 patients
 Mycophenolate mofetil, n (%)65 (77)
 Methotrexate, n (%)8 (9)
 Cyclophosphamide, n (%)31 (37)
 Azathioprine, n (%)14 (17)
 Tocilizumab, n (%)6 (7)
 Rituximab, n (%)26 (31)
Concurrent therapies77 patients
 Corticosteroids, n (%)71 (92)
 Mycophenolate mofetil, n (%)63 (81)
 Methotrexate, n (%)2 (3)
 Cyclophosphamide, n (%)0 (0)
 Azathioprine, n (%)2 (3)
 Tocilizumab, n (%)5 (6)
 Rituximab, n (%)18 (23)
Baseline HRCT89 patients
 NSIP, n (%)61 (69)
 UIP, n (%)28 (31)
  • Ab, antibodies; GI, gastrointestinal; HRCT, high-resolution CT; ILD, interstitial lung disease; n, number; NSIP, non-specific interstitial pneumonia; SSc, systemic sclerosis; UIP, usual interstitial pneumonia.