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Patients with uncommon EGFR mutations also benefit from first-line osimertinib
Nature Reviews Clinical Oncology ( IF 78.8 ) Pub Date : 2023-12-06 , DOI: 10.1038/s41571-023-00847-x
Diana Romero

Around one-third of non-small-cell lung cancers (NSCLCs) are driven by mutations in EGFR. The most common of these alterations (in ~85% of patients) are exon 19 deletions and exon 21 L858R; the remaining alterations are referred to as uncommon. Osimertinib is the standard-of-care first-line therapy for patients with metastatic EGFR-mutated NSCLC, although limited evidence is available on efficacy in those with uncommon mutations. Now, data from the single-arm phase II UNICORN trial reveal that first-line osimertinib has promising activity in this patient population.



中文翻译:

具有罕见 EGFR 突变的患者也可从一线奥希替尼中受益

大约三分之一的非小细胞肺癌 (NSCLC) 是由EGFR突变引起的。这些改变中最常见的(约 85% 的患者)是外显子 19 缺失和外显子 21 L858R;其余的改变被认为是不常见的。奥希替尼是转移性EGFR突变 NSCLC患者的标准一线治疗,尽管关于罕见突变患者疗效的证据有限。现在,单臂 II 期 UNICORN 试验的数据表明,一线奥西替尼在该患者群体中具有良好的活性。

更新日期:2023-12-07
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