A pilot study of intermittent intravenous cyclophosphamide for the treatment of systemic sclerosis associated lung disease

György Várai, Linda Earle, Sergio A. Jimenez, Robert M. Steiner, John Varga*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

76 Scopus citations


Objective. Pulmonary fibrosis, a frequent manifestation of systemic sclerosis (SSc), is considered incurable. Our aim was to assess the effect of therapy with intravenous (iv) cyclophosphamide on the course of pulmonary fibrosis in patients with SSc. Methods. Five patients with SSc and clinical, laboratory, or radiographic findings of interstitial lung disease were treated with cyclophosphamide (1 g) administered iv monthly for 48 weeks. The dyspnea score, pulmonary function tests, arterial blood oxygen content, radiologic abnormalities, and bronchoalveolar lavage (BAL) fluid cellularity were determined before and after therapy. Results. The dyspnea score decreased by 42% after 48 weeks of therapy. Forced vital capacity (FVC, percentage of predicted) increased by 7%, and carbon monoxide diffusing capacity (DLCO) decreased by 12%, but these changes were not statistically significant. Arterial blood oxygenation remained unchanged. At baseline, high resolution computed tomography of the lungs showed honey-combing, reticulonodular, or ground glass patterns in each patient examined. These radiologic abnormalities did not improve during treatment. A marked decrease in BAL fluid cell number, but not in the percentage of neutrophils, was observed after therapy. Nausea and leukopenia were frequent but mild side effects. One patient developed hemorrhagic cystitis. Conclusion. The results suggest that intermittent treatment with iv cyclophosphamide reduces the severity of dyspnea, but fails to improve FVC or DLCO, or cause resolution of radiologic abnormalities, in patients with SSc.

Original languageEnglish (US)
Pages (from-to)1325-1329
Number of pages5
JournalJournal of Rheumatology
Issue number7
StatePublished - Jul 1998


  • Cyclophosphamide
  • Interstitial lung disease
  • Systemic sclerosis

ASJC Scopus subject areas

  • Rheumatology
  • Immunology and Allergy
  • Immunology

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