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奥希替尼治疗表皮生长因子受体突变的非小细胞肺癌早期和局部晚期:当前证据与未来展望

Osimertinib in the Treatment of Epidermal Growth Factor Receptor-Mutant Early and Locally Advanced Stages of Non-Small-Cell Lung Cancer: Current Evidence and Future Perspectives.

作者信息

Veccia Antonello, Dipasquale Mariachiara, Lorenzi Martina, Monteverdi Sara, Kinspergher Stefania, Zambotti Elena, Caffo Orazio

机构信息

Medical Oncology, Santa Chiara Hospital, Largo Medaglie d'Oro 1, 38122 Trento, Italy.

出版信息

Cancers (Basel). 2025 Feb 16;17(4):668. doi: 10.3390/cancers17040668.

Abstract

The treatment of epidermal growth factor receptor (EGFR)-mutant non-small-cell lung cancer (NSCLC) patients was dramatically revolutionized by the introduction of EGFR tyrosine kinase inhibitors in clinical practice, both in advanced and locally advanced/early stages. The present work focuses on osimertinib use in locally advanced and early NSCLC stages. Phase 3 clinical trials have supported the use of osimertinib as the new standard of care, both in the adjuvant setting and in locally advanced disease. The ADAURA study reported an overall survival (OS) advantage for adjuvant osimertinib in completely resected stage II-IIIA EGFR-mutant tumors, while the LAURA study proved a statistically significant benefit in progression-free survival (PFS) and a delay of central nervous system metastasis development in EGFR-mutant patients treated with osimertinib maintenance after concurrent chemoradiotherapy for locally advanced disease. In the neoadjuvant setting, data on osimertinib's efficacy are conflicting; therefore, the Neo-ADAURA study is evaluating the efficacy and safety of neoadjuvant osimertinib alone or in combination with chemotherapy in patients with stage II-IIIB NSCLC and common EGFR mutations. We discuss several issues that need to be clarified, such as the efficacy of the drug on uncommon mutations, the long-term impact on survival, and the management of resistance mechanisms. Moreover, we report the studies that are trying to identify potential biomarkers of response, such as the circulating tumor DNA (ctDNA), with the aim of selecting patients who will benefit most from osimertinib.

摘要

表皮生长因子受体(EGFR)突变的非小细胞肺癌(NSCLC)患者的治疗因表皮生长因子受体酪氨酸激酶抑制剂引入临床实践而发生了巨大变革,无论是在晚期还是局部晚期/早期阶段。目前的工作聚焦于奥希替尼在局部晚期和早期NSCLC阶段的应用。3期临床试验支持将奥希替尼用作辅助治疗和局部晚期疾病的新护理标准。ADAURA研究报告了辅助使用奥希替尼治疗完全切除的II-IIIA期EGFR突变肿瘤患者的总生存期(OS)优势,而LAURA研究证明,对于局部晚期疾病同步放化疗后接受奥希替尼维持治疗的EGFR突变患者,其无进展生存期(PFS)有统计学意义的获益,且中枢神经系统转移的发生有所延迟。在新辅助治疗方面,关于奥希替尼疗效的数据存在冲突;因此,Neo-ADAURA研究正在评估新辅助使用奥希替尼单药或联合化疗在II-IIIB期NSCLC且有常见EGFR突变患者中的疗效和安全性。我们讨论了几个需要阐明的问题,例如该药物对罕见突变的疗效、对生存的长期影响以及耐药机制的处理。此外,我们报告了一些旨在识别潜在反应生物标志物的研究,如循环肿瘤DNA(ctDNA),目的是选择能从奥希替尼中获益最大的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e6b/11853037/1892c1afca54/cancers-17-00668-g001.jpg

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