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厄洛替尼致肝损害
引用本文:白帆,刘阳,冯雷.厄洛替尼致肝损害[J].药物不良反应杂志,2013(4):228-229.
作者姓名:白帆  刘阳  冯雷
作者单位:中国医学科学院北京协和医学院北京协和医院药剂科,100730
摘    要:1例表皮生长因子受体阳性的初诊78岁男性肺癌患者接受厄洛替尼150mg,1次/d口服化疗。化疗前丙氨酸转氨酶(ALT)12U/L,天冬氨酸转氨酶(AST)16U/L,总胆红素(TBil)22.0μmol/L,直接胆红素(DBil)7.6μmol/L。化疗2周复查:ALT30U/L,AST33U/L,TBil20.0μmol/L,DBil6.3μmol/L。化疗2个月患者出现尿色加深,全身皮肤及巩膜黄染。化疗约75d实验窄检查:ALT368U/L,TBil182.1μmol/L,DBil155.2μmol/L。停用厄洛替尼,予保肝治疗。停药第4天,ALT171U/L,AST177U/L,TBil322.0μmol/L,DBil278.2μmol/L。停药第6天,加用甲泼尼尼。停约第12火,AUF132U/L,AST141U/L,TBil172.6μmol/L,DBil135.4μmol/L。停用厄洛替尼2个月,ALT12U/L,AST30U/L,TBil19.8μmol/L,DBil13.5μnol/L。随后换用吉西他滨联合尼妥珠单抗继续化疗6个疗程,未再出现肝功能异常。

关 键 词:厄洛替尼  肝损害

Liver damage due to erlotinib
BAI Fan,LIU Yang,FENG Lei.Liver damage due to erlotinib[J].Adverse Drug Reactions Journal,2013(4):228-229.
Authors:BAI Fan  LIU Yang  FENG Lei
Institution:( Department of Pharmacy, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China)
Abstract:A 78-year-old man, who was newly diagnosed with epidermal growth factor receptor- received treatment with oral erlotinib 150 mg once daily. Laboratory test before the chemotherapy showed the following values : alanine aminotransferase ( ALT ) 12 U/L, asp'mate aminotransferase (AST) 16 U/L, total bilirubin (TBil) 22.0μmol/L, direct bilirubin (DBil) 7.6μmol/L. Two weeks after chemotherapy treatment, re-examination revealed the following values: ALT 30 U/L, AST 33 U/L, TBil 20.0μmol/L, DBil 6.3μmol/L. Two months after chemotherapy, the patient presented with dark urine and yellowish whole skin and sclera. Seventy-five days after the chemotherapy, laboratory test showed the following values: ALT 368 U/L, TBil 182. 1μmol/L, DBil 155. 2 μmol/L. Erlotinib was discontinued and liver-protective treatment was given. On day 4 after erlotinib discontinuation, the levels of ALT, AST, TBil, and DBil were 171 U/L, 177 U/L, 322.0μmol/L, and 278.2μmol/L, respectively. On day 6 after erlotinib discontinuation, methylprednisolone was added to his regimen. On day 12 after erlotinib discontinuation, the levels of ALT, AST, TBil, and DBil were 132 U/L, 141 U/L, 172.6μmoL/L, 135.4 p, mol/l,, respectively. Two months after erlotinib discontinuation, the levels of ALT, AST, TBil, and DBil were 12 U/L, 30 U/L, 19. 8μmol/L, and 13.5 μmol/L, respectively. Then chemotherapy was switched to 6 cycles of gemcitabine and nimotuzumab and abnormal liver function did not recur.
Keywords:Erlotinib  Liver damage
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