| Literature DB >> 23877149 |
Se-Il Go1, Won Sup Lee, Gyeong-Won Lee, Jung Hun Kang, Myung Hee Kang, Jeong-Hee Lee, Hoon-Gu Kim.
Abstract
Nilotinib is a second-generation tyrosine kinase inhibitor active in patients with chronic myeloid leukemia (CML) resistant to imatinib, and has been recently approved for newly diagnosed patients. We present a case of nilotinib-induced interstitial lung disease (ILD). A 67-year-old female patient was initially treated with imatinib for chronic-phase Philadelphia chromosome-positive (Ph(+)) CML. Imatinib was replaced by nilotinib because of hematological toxicity. The patient had received nilotinib for about 3 years without significant adverse effects. She visited the clinic due to chronic cough; chest X-ray revealed consolidations in both lung fields. Nilotinib-induced ILD was diagnosed based on intensive workup, including lung biopsy. She responded dramatically to corticosteroid therapy. To our knowledge, this is the first reported case of nilotinib-induced ILD in a patient with Ph(+) CML. We emphasize that if unexplained lung abnormalities progress in patients receiving nilotinib, physicians should consider this potentially fatal complication in their differential diagnoses.Entities:
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Year: 2013 PMID: 23877149 DOI: 10.1007/s12185-013-1398-5
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490