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Updated: Aug 18, 2026

Refined Murine Model of Idiopathic Pulmonary Fibrosis
Published on: June 17, 2025
Azacitidine-induced interstitial and alveolar fibrosis in a patient with myelodysplastic syndrome
Christopher D Adams1, Paul M Szumita, Steven A Baroletti
1Department of Pharmacy, Brigham and Women's Hospital, Boston, MA 02115, USA. cdadams@partners.org
Abstract:
A 71-year-old Caucasian man diagnosed with myelodysplastic syndrome developed interstitial and alveolar fibrosis after receiving a 7-day course of azacitidine therapy. The patient's pulmonary function began to deteriorate immediately after the administration of his chemotherapy regimen. Other potential causes of pulmonary toxicity were ruled out such as viral, fungal, and bacterial pathogens, as well as other concomitant drugs. To our knowledge, this is the first case report documenting biopsy-proven interstitial and alveolar fibrosis associated with azacitidine. The frequency of this adverse drug reaction is unknown but may become more evident with increasing exposure of the population to azacitidine.