Effect of Tyrosine Kinase Inhibitor Therapy on Estimated Glomerular Filtration Rate in Patients with Chronic Myeloid Leukemia

被引:2
作者
Sonmez, Oezge [1 ]
Yurttas, Nurguel Ozguer [2 ]
Ihtiyaroglu, Ilker [1 ]
Cakir, Halil Mete [3 ]
Atli, Zeynep [4 ]
Elverdi, Tugrul [2 ]
Salihoglu, Ayse [2 ]
Seyahi, Nurhan [5 ]
Ar, Muhlis Cem [2 ]
Ongoeren, Seniz [2 ]
Baslar, Zafer [2 ]
Soysal, Teoman [2 ]
Eskazan, Ahmet Emre [2 ]
机构
[1] Istanbul Univ Cerrahpas, Cerrahpasa Fac Med, Dept Internal Med, Istanbul, Turkiye
[2] Istanbul Univ Cerrahpasa, Cerrahpasa Fac Med, Dept Internal Med, Div Hematol, Istanbul, Turkiye
[3] Istanbul Univ Cerrahpasa, Cerrahpasa Fac Med, Istanbul, Turkiye
[4] Sinop Univ, Fac Sci & Letters, Dept Stat, Sinop, Turkiye
[5] Istanbul Univ Cerrahpasa, Cerrahpas Fac Med, Dept Internal Med, Div Rheumatol, Istanbul, Turkiye
关键词
Chronic kidney disease; Chronic myeloid leukemia; CML; Glomerular filtration rate; Imatinib; CHRONIC MYELOGENOUS LEUKEMIA; TUBULAR REGENERATION; IMATINIB MESYLATE;
D O I
10.1016/j.clml.2023.12.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this study, we evaluated the possible kidney toxicity of tyrosine kinase inhibitors (TKIs) in patients with chronic myeloid leukemia (CML). We examined 195 patients with CML and 138 patients with chronic kidney disease (CKD). We found a downward trend in the glomerular filtration rate under TKI treatment during follow up which was comparable to that of CKD patients. Introduction: The advent of tyrosine kinase inhibitors (TKIs) was revolutionary in the management of chronic myeloid leukemia (CML). Although TKIs were generally considered to be safe, they can be associated with renal injury. We evaluated the effect of TKIs on renal functions in a cohort of patients with long-term follow-up. Material and Methods: We retrospectively examined patients with chronic phase CML treated with TKIs. We analyzed the estimated glomerular filtration rate (eGFR) of patients from the initiation of TKI to the last follow-up. eGFR values of CML patients were compared to those of patients with stage 1 or 2 chronic kidney disease (CKD). Results: A total of 195 patients with CML and 138 patients with CKD were examined. eGFR decline was 1.556 ml/min/1.73m 2 /year for patients with CML ( P = .221). Patients receiving second-generation TKIs (2GTKI) were estimated to have 0.583 ml/min/1.73m 2 higher eGFR value than that of the imatinib group, but it was not significant ( P = .871). eGFR of patients who had used bosutinib had a downward trend. Duration of TKI therapy, age, and hypertension were found to be significant factors in eGFR decline for CML patients. Lower baseline GFR was associated with an increased risk of CKD development. Conclusion: Imatinib could result in a decline in eGFR which was clinically similar to early-stage CKD patients. We did not observe significant kidney function deterioration in patients receiving 2GTKIs including dasatinib and nilotinib. We recommend close renal function monitoring in patients receiving imatinib, especially for elderly patients with lower baseline eGFR and hypertension.
引用
收藏
页码:232 / 239
页数:8
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