Table 2.

Clinical characteristics of patients with MA-ILD who responded to or failed conventional treatment (n = 54). Values are n unless otherwise specified.

Clinical CharacteristicsResponders, n = 31Nonresponders, n = 23p
Age at onset of myositis, yrs46.842.20.34
Sex
  Male6100.055
  Female2513
Race
  Black14120.12
  White139
  Asian40
  Hispanic02
Smoking history
  Never20180.068
  Former102
  Active13
Myositis
  Polymyositis20100.013
  Dermatomyositis713
  CADM40
Baseline CK, U/l2588.93431.00.20
Baseline aldolase29.634.40.29
Serologic data
  ANA16160.18
  Anti-Jo11890.17
  SSA1390.84
  Mi-2120.39
  PL-7010.43
  SRP110.68
  Ku010.43
PFT, %
  FVC62.560.40.39
  TLC68.868.30.46
  DLCO58.357.30.62
CT chest
  Honeycombing absent21170.62
  Honeycombing present106
Lung histopathology
  COP320.60
  UIP12
  NSIP03
  Others*12
Conventional DMARD
  AZA19160.53
  MTX890.30
  MMF650.55
  • * COP with NSIP, COP with hypersensitivity pneumonitis, and COP with diffuse alveolar damage. MA-ILD: myositis-associated interstitial lung disease; CADM: clinically amyopathic dermatomyositis; CK: creatine kinase; ANA: antinuclear antibody; SRP: signal recognition particle; PFT: pulmonary function test; FVC: forced vital capacity; TLC: total lung capacity; CT: computed tomography; COP: cryptogenic organizing pneumonia; UIP: usual interstitial pneumonia; NSIP: nonspecific interstitial pneumonia; DMARD: disease-modifying antirheumatic drugs; AZA: azathioprine; MTX: methotrexate; MMF: mycophenolate mofetil.