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奥莫替尼:非小细胞肺癌的综述。

Aumolertinib: A Review in Non-Small Cell Lung Cancer.

机构信息

Springer Nature, Mairangi Bay, Private Bag 65901, Auckland, 0754, New Zealand.

出版信息

Drugs. 2022 Apr;82(5):577-584. doi: 10.1007/s40265-022-01695-2. Epub 2022 Mar 19.

Abstract

Aumolertinib (formerly almonertinib; Ameile) is an oral, third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (EGFR-TKI) that is selective for mutant EGFR over wild-type EGFR. It has been developed for the treatment of advanced EGFR mutation-positive non-small cell lung cancer (NSCLC). In the phase 3 AENEAS trial conducted in Chinese patients, aumolertinib as first-line treatment significantly prolonged progression-free survival (PFS) and duration of response (DoR) compared with gefitinib in patients with advanced EGFR mutation-positive NSCLC; overall survival (OS) data from this study are immature. In the phase 1/2 APOLLO trial, aumolertinib showed good clinical activity (based on objective response rate, PFS, DoR and OS) in Chinese patients with locally advanced or metastatic EGFR T790M mutation-positive NSCLC who had progressed on or after prior EGFR-TKI therapy. Aumolertinib has a generally manageable tolerability profile; adverse events associated with wild-type EGFR inhibition (e.g. rash and diarrhoea) were less frequent with aumolertinib than gefitinib in AENEAS. Thus, aumolertinib is a promising new option for both first-line and second-line treatment in patients with advanced EGFR mutation-positive NSCLC.

摘要

奥莫替尼(前身为阿美替尼;艾美)是一种口服的第三代表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(EGFR-TKI),对突变型 EGFR 具有选择性,而对野生型 EGFR 则无活性。它是为治疗晚期 EGFR 突变阳性非小细胞肺癌(NSCLC)而开发的。在中国患者中进行的 III 期 AENEAS 试验中,与吉非替尼相比,奥莫替尼作为一线治疗药物,显著延长了晚期 EGFR 突变阳性 NSCLC 患者的无进展生存期(PFS)和缓解持续时间(DoR);该研究的总生存期(OS)数据尚不成熟。在 I/II 期 APOLLO 试验中,奥莫替尼在中国局部晚期或转移性 EGFR T790M 突变阳性 NSCLC 患者中显示出良好的临床活性(基于客观缓解率、PFS、DoR 和 OS),这些患者在先前的 EGFR-TKI 治疗后进展。奥莫替尼的耐受性总体上易于管理;与 AENEAS 中的吉非替尼相比,奥莫替尼与野生型 EGFR 抑制相关的不良反应(如皮疹和腹泻)发生频率较低。因此,奥莫替尼是晚期 EGFR 突变阳性 NSCLC 患者一线和二线治疗的一个有前途的新选择。

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