Kong Jee Hyun, Yoo Seung-Hyun, Lee Kyoung Eun, Nam Seung Hyun, Kwon Jung Mi, Lee Sang Min, Chang Hye Jung, Choi Moon Young, Cho Min Sun, Mun Yeung-Chul, Nam Eunmi, Lee Soon Nam, Seong Chu-Myong
Division of Hematology-Oncology, Department of Internal Medicine, School of Medicine, Ewha Womans University, Seoul, Korea.
Acta Haematol. 2007;118(4):205-8. doi: 10.1159/000111092. Epub 2007 Nov 15.
Imatinib mesylate is the first molecule of targeted therapy in chronic myelogenous leukaemia inhibiting constitutively activated BCR-ABL kinase. There are no long-term follow-up studies of large sample sizes to assess the toxicity of the use of imatinib mesylate over 10 years. Several cases of hepatotoxicity, including fatal liver failure, have been associated with the long-term use of imatinib mesylate. We report here on a patient who experienced immediate dominant cholestatic damage of the liver and mild hepatocyte damage during imatinib mesylate therapy. This differs from most reports showing dominantly acute hepatitis with necrosis associated with the use of imatinib mesylate.
甲磺酸伊马替尼是慢性粒细胞白血病靶向治疗的首个分子,可抑制组成型激活的BCR-ABL激酶。目前尚无大样本的长期随访研究来评估使用甲磺酸伊马替尼超过10年的毒性。几例肝毒性病例,包括致命的肝衰竭,都与长期使用甲磺酸伊马替尼有关。我们在此报告1例患者,在甲磺酸伊马替尼治疗期间出现了即时性的、以肝内胆汁淤积性损害为主及轻度肝细胞损害。这与大多数显示使用甲磺酸伊马替尼后以急性肝炎伴坏死为主的报告不同。