Kunimasa Kei, Yoshioka Hiroshige, Iwasaku Masahiro, Nishiyama Akihiro, Korogi Yohei, Masuda Gen, Takaiwa Takuya, Ishida Tadashi
Department of Respiratory Medicine, Kurashiki Central Hospital, Japan.
Intern Med. 2012;51(4):431-4. doi: 10.2169/internalmedicine.51.6285. Epub 2012 Feb 15.
Gefitinib and erlotinib are first-generation small molecular inhibitors of EGFR tyrosine kinase activity. To the best of our knowledge, to date, two reports have stated that patients with NSCLC who develop severe hepatotoxicity secondary to gefitinib treatment can be safely switched to erlotinib. However, the reverse situation has not been reported. Here, we present the first case with non-small cell lung cancer harboring EGFR mutation who developed grade 3/4 hepatotoxicity after initiation of erlotinib, which resolved when therapy was changed to gefitinib. As far as we know, this is the first report showing the efficacy of gefitinib for a non-small cell lung cancer patient who developed severe hepatotoxicity while under erlotinib therapy.
吉非替尼和厄洛替尼是第一代表皮生长因子受体(EGFR)酪氨酸激酶活性小分子抑制剂。据我们所知,迄今为止,有两份报告指出,非小细胞肺癌(NSCLC)患者在接受吉非替尼治疗继发严重肝毒性后可安全换用厄洛替尼。然而,相反的情况尚未见报道。在此,我们报告首例携带EGFR突变的非小细胞肺癌患者,在开始使用厄洛替尼后出现3/4级肝毒性,在改用吉非替尼治疗后肝毒性得到缓解。据我们所知,这是第一份显示吉非替尼对一名在接受厄洛替尼治疗时出现严重肝毒性的非小细胞肺癌患者有效的报告。