Effects of Bosutinib Treatment on Renal Function in Patients With Philadelphia Chromosome-Positive Leukemias

被引:45
作者
Cortes, Jorge E. [1 ]
Gambacorti-Passerini, Carlo [2 ]
Kim, Dong-Wook [3 ]
Kantarjian, Hagop M. [1 ]
Lipton, Jeff H. [4 ]
Lahoti, Amit [1 ]
Talpaz, Moshe [5 ]
Matczak, Ewa [6 ]
Barry, Elly [7 ]
Leip, Eric [7 ]
Bruemmendorf, Tim H. [8 ,9 ]
Khoury, H. Jean [10 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[2] Univ Milano Bicocca, Monza, Italy
[3] Seoul St Marys Hosp, Seoul, South Korea
[4] Princess Margaret Canc Ctr, 610 Univ Ave, Toronto, ON, Canada
[5] Univ Michigan, Comprehens Canc Ctr, Ann Arbor, MI 48109 USA
[6] Pfizer Inc, New York, NY USA
[7] Pfizer Inc, Cambridge, MA USA
[8] Univ Klinikum RWTH Aachen, Aachen, Germany
[9] Hubertus Wald Tumorzentrum Univ, Canc Ctr Hamburg, Dept Internal Med 2, Hamburg, Germany
[10] Emory Univ, Winship Canc Inst, Atlanta, GA 30322 USA
关键词
Adverse events; Chronic myeloid leukemia; Renal toxicity; Tyrosine kinase inhibitors; CHRONIC MYELOID-LEUKEMIA; GLOMERULAR-FILTRATION-RATE; TUMOR LYSIS SYNDROME; TYROSINE KINASE; HEART-FAILURE; IMATINIB; DASATINIB; NILOTINIB; INHIBITORS; SAFETY;
D O I
10.1016/j.clml.2017.06.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We evaluated the incidence of renal adverse events and estimated glomerular filtration rate in patients with Philadelphia chromosome-positive leukemias receiving first-line bosutinib (n = 248) or imatinib (n = 251), or second-line or later bosutinib (n = 570). Results show that long-term bosutinib treatment is associated with an apparently reversible decline in renal function with frequency and characteristics similar to those observed with long-term imatinib. Background: The purpose of the study was 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 III trial), or second-line or later bosutinib (phase I/II trial; n = 570). Adverse events (AEs) and changes from baseline in estimated glomerular filtration rate (eGFR) and serum creatinine were assessed. Results: Time from the last patient's first dose to data cutoff was >= 48 months. Renal AEs were reported in 73/570 patients (13%) receiving second-line or later bosutinib, and in 22/248 (9%) and 16/251 (6%) receiving first-line bosutinib and imatinib, respectively. eGFR in patients receiving bosutinib declined over time with more patients developing Grade >= 3b eGFR (< 45 mL/min/1.73m(2) according to the Modification of Diet in Renal Disease method) with second-line or later bosutinib (139/570, 24%) compared with first-line bosutinib (26/248, 10%) and imatinib (25/251, 10%); time to Grade >= 3b eGFR was shortest with second-line or later bosutinib. Similar proportions of patients receiving second-line or later bosutinib (74/139, 53%), first-line bosutinib (15/26, 58%), and first-line imatinib (15/25, 60%) improved to >= 45 mL/min/1.73m(2) eGFR as of the last follow-up. In a regression analysis, first-line treatment with bosutinib versus imatinib was not a significant predictor of Grade >= 3b eGFR. Conclusion: Long-term bosutinib treatment is associated with an apparently reversible decline in renal function with frequency and characteristics similar to renal decline observed with long-term imatinib treatment. Patients with risk factors for Grade >= 3b eGFR should be monitored closely. (C) 2017 The Authors. Published by Elsevier Inc.
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收藏
页码:684 / +
页数:18
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