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Effects of bosutinib treatment on renal function in patients with Philadelphia chromosome-positive leukemias

Abstract Purpose To assess renal function in patients with Philadelphia chromosome-positive leukemias receiving bosutinib or imatinib. Patients and Methods Patients received first-line bosutinib (n=248) or imatinib (n=251; phase 3 trial), or second-line or later bosutinib (phase 1/2 trial; N=570).Ad...

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Published in:Clinical lymphoma, myeloma and leukemia myeloma and leukemia, 2017-10, Vol.17 (10), p.684-695.e6
Main Authors: Cortes, Jorge E., MD, Gambacorti-Passerini, Carlo, MD, Kim, Dong-Wook, MD, PhD, Kantarjian, Hagop M., MD, Lipton, Jeff H., MD, PhD, FRCPC, Lahoti, Amit, MD, Talpaz, Moshe, MD, Matczak, Ewa, MD, Barry, Elly, MD, Leip, Eric, PhD, Brümmendorf, Tim H., MD, Khoury, H. Jean, MD, FACP
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Language:English
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Summary:Abstract Purpose To assess renal function in patients with Philadelphia chromosome-positive leukemias receiving bosutinib or imatinib. Patients and Methods Patients received first-line bosutinib (n=248) or imatinib (n=251; phase 3 trial), or second-line or later bosutinib (phase 1/2 trial; N=570).Adverse events (AEs) and changes from baseline in estimated glomerular filtration rate (eGFR) and serum creatinine were assessed. Results Time from last patient’s first dose to data cutoff was ≥48 months. Renal AEs were reported in 13% of patients receiving second-line or later bosutinib, and in 9% and 6% receiving first-line bosutinib and imatinib, respectively. eGFR in patients receiving bosutinib declined over time with more patients developing grade ≥3b eGFR (
ISSN:2152-2650
2152-2669
DOI:10.1016/j.clml.2017.06.001