Kris Mark G, Mitsudomi Tetsuya, Peters Solange
Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Faculty of Medicine, Kindai University, Osaka-Sayama, Japan.
Transl Lung Cancer Res. 2023 Apr 28;12(4):824-836. doi: 10.21037/tlcr-22-723. Epub 2023 Apr 7.
Surgical resection followed by adjuvant cisplatin-based chemotherapy is the recommended treatment for patients with completely resected stage IB-IIIA non-small cell lung cancer (NSCLC). Even with the best management, recurrence is common and increases with disease stage (stage I: 26-45%; stage II: 42-62%; stage III: 70-77%). For patients with metastatic lung cancer and tumours that harbour epidermal growth factor receptor (EGFR) mutations, EGFR-tyrosine kinase inhibitors (TKIs) have improved survival. Their effectiveness in advanced stages of NSCLC raises the possibility that these agents may improve outcomes for patients with resectable EGFR-mutated lung cancer. In the ADAURA study, adjuvant osimertinib provided a significant improvement in disease-free survival (DFS) and reduced central nervous system (CNS) disease recurrence in patients with resected stage IB-IIIA EGFR-mutated NSCLC, with or without prior adjuvant chemotherapy. To reap the maximum benefits of EGFR-TKIs for patients with lung cancer, the early and rapid identification of EGFR mutations [and other oncogenic drivers, such as programmed cell death-ligand 1 (PD-L1), with matched targeted therapies] in diagnostic pathologic specimens has become essential. To ensure patients receive the most appropriate treatment, routine, comprehensive histological, immunohistochemical, and molecular analyses (with multiplex next generation sequencing) should be undertaken at the time of diagnosis. The potential for personalised treatments to cure more patients with early-stage lung cancer can only be realised if all therapies are considered when the care plan is formulated, by the multi-specialty experts managing patients. In this review, we discuss the progress and prospects for adjuvant treatments as part of a comprehensive plan of care for patients with resected stages I-III EGFR-mutated lung cancer, and explore how the field could go beyond DFS and overall survival to make cure a more frequent outcome of treatment in patients with resected EGFR-mutated lung cancer.
对于完全切除的ⅠB-ⅢA期非小细胞肺癌(NSCLC)患者,推荐的治疗方法是手术切除后进行以顺铂为基础的辅助化疗。即使采用最佳治疗方案,复发仍很常见,且随着疾病分期增加(Ⅰ期:26%-45%;Ⅱ期:42%-62%;Ⅲ期:70%-77%)。对于转移性肺癌和携带表皮生长因子受体(EGFR)突变的肿瘤患者,EGFR酪氨酸激酶抑制剂(TKIs)可提高生存率。它们在NSCLC晚期的有效性增加了这些药物可能改善可切除EGFR突变肺癌患者预后的可能性。在ADAURA研究中,辅助使用奥希替尼可显著改善切除的ⅠB-ⅢA期EGFR突变NSCLC患者的无病生存期(DFS),并减少中枢神经系统(CNS)疾病复发,无论患者是否接受过辅助化疗。为了使肺癌患者从EGFR-TKIs中获得最大益处,在诊断病理标本中早期快速鉴定EGFR突变[以及其他致癌驱动因素,如程序性细胞死亡配体1(PD-L1),并匹配靶向治疗]变得至关重要。为确保患者接受最合适的治疗,应在诊断时进行常规、全面的组织学、免疫组织化学和分子分析(采用多重下一代测序)。只有在制定护理计划时,由管理患者的多专科专家考虑所有治疗方法,个性化治疗治愈更多早期肺癌患者的潜力才能实现。在本综述中,我们讨论了辅助治疗作为切除的Ⅰ-Ⅲ期EGFR突变肺癌患者综合护理计划一部分的进展和前景,并探讨该领域如何超越DFS和总生存期,使切除的EGFR突变肺癌患者的治疗更频繁地实现治愈。