首页> 美国卫生研究院文献>Case Reports in Oncology >Successful Treatment with Lorlatinib after the Development of Alectinib-Induced Liver Damage in ALK-Positive Non-Small-Cell Lung Cancer: A Case Report
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Successful Treatment with Lorlatinib after the Development of Alectinib-Induced Liver Damage in ALK-Positive Non-Small-Cell Lung Cancer: A Case Report

机译:在邻吲哚菌诱导的肝脏损伤的肺阳性非小细胞肺癌中造成后的成功治疗:案例报告

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摘要

Alectinib is a key drug for treating anaplastic lymphoma kinase (ALK)-positive non-small-cell lung cancer (NSCLC). Alectinib-induced hepatotoxicity is less common than that through other ALK inhibitors, such as crizotinib or ceritinib. Herein, we describe a case of ALK-positive adenocarcinoma successfully treated with lorlatinib after developing alectinib-induced hepatotoxicity. A 57-year-old Japanese man received alectinib as first-line therapy for ALK-positive NSCLC. After 79 days, alectinib was discontinued because of hepatotoxicity and later restarted at 150 mg/day, inducing hepatotoxicity again after 64 days. Switching to lorlatinib treatment (continued for >4 months) caused no severe adverse effects. Hence, lorlatinib may be useful for patients experiencing alectinib-induced hepatotoxicity.
机译:alectinib是一种用于治疗促进淋巴瘤激酶(ALK)阳性非小细胞肺癌(NSCLC)的关键药物。抗渗润诱导的肝毒性不如通过其他ALK抑制剂的常见,例如克里齐替尼或Ceritinib。在此,我们描述了在发育邻接肺诱导的肝毒性后用洛拉替尼成功处理的ALK阳性腺癌的情况。一名57岁的日本人接受了Alectinib作为ALK阳性NSCLC的一线治疗。 79天后,由于肝毒性,后来停止了莱切韦,后来在150毫克/天重新开始,64天后再次诱导肝毒性。切换到洛拉替尼治疗(持续> 4个月)造成严重不利影响。因此,Lorlatinib可能对经历邻接肺诱导的肝毒性的患者有用。

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