Spotlight on Furmonertinib (Alflutinib, AST2818). The Swiss Army Knife (del19, L858R, T790M, Exon 20 Insertions, "uncommon-G719X, S768I, L861Q") Among the Third-Generation EGFR TKIs?

IF 5.1 Q1 ONCOLOGY
Lung Cancer: Targets and Therapy Pub Date : 2022-10-25 eCollection Date: 2022-01-01 DOI:10.2147/LCTT.S385437
Shannon S Zhang, Sai-Hong Ignatius Ou
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引用次数: 2

Abstract

Osimertinib, a third-generation (3G) epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) is now considered the standard of care for the first-line (1L) treatment of advanced EGFR+ NSCLC due to statistically significant improved progression-free survival (PFS) and overall survival (OS) compared with first-generation (1G) treatment from the FLAURA trial. Recently two other 3G EGFR TKIs (aumolertinib and furmonertinib) have been approved in China for treatment of EGFR T790M+ NSCLC. Randomized Phase 3 trials of these two 3G EGFR TKIs have also demonstrated PFS over gefitinib respectively. Among these two Chinese home-grown, 3G EGFR TKIs, furmonertinib seems to most closely resemble osimertinib in terms of dosing regimen, efficacy and adverse events profile. In this article, we reviewed the clinical activity and adverse events of furmonertinib at 80 mg daily (approved dose), potential usage of 160 mg daily for CNS metastasis in EGFR+ NSCLC, and usage of 160 mg or 240 mg daily in EGFR exon20 insertion positive (EGFRex20ins+) NSCLC patients.

Abstract Image

Abstract Image

聚焦于Furmonertinib (Alflutinib, AST2818)第三代EGFR TKIs中的瑞士军刀(del19, L858R, T790M,外显子20插入,“不常见的g719x, S768I, L861Q”)?
奥西替尼是一种第三代(3G)表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKI),目前被认为是晚期EGFR+ NSCLC一线(1L)治疗的标准治疗方案,因为与FLAURA试验的第一代(1G)治疗相比,奥西替尼的无进展生存期(PFS)和总生存期(OS)有统计学显著改善。最近,另外两种3G EGFR TKIs (aumolertinib和furmonertinib)在中国被批准用于治疗EGFR t7.9 m + NSCLC。这两种3G EGFR TKIs的随机3期试验也分别显示了吉非替尼对PFS的影响。在这两种中国自主研发的3G EGFR TKIs中,福莫那替尼在给药方案、疗效和不良事件方面似乎与奥西替尼最相似。在本文中,我们回顾了furmonertinib的临床活性和不良事件,每日80 mg(批准剂量),每日160 mg用于EGFR+ NSCLC的中枢神经系统转移,以及每日160 mg或240 mg用于EGFR exon20插入阳性(EGFRex20ins+) NSCLC患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.10
自引率
0.00%
发文量
10
审稿时长
16 weeks
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