Ogliari Francesca R, Huijs Jarno W J, Jongbloed Mandy, Willmann Jonas, Hendriks Lizza E L, De Ruysscher Dirk K M
Università Vita-Salute San Raffaele, Milan, Italy.
Department of Medical Oncology, IRCCS Ospedale San Raffaele, Milan, Italy.
Transl Lung Cancer Res. 2025 Aug 31;14(8):3142-3152. doi: 10.21037/tlcr-2025-144. Epub 2025 Aug 12.
The role of post-operative radiotherapy (PORT) in radically resected non-small-cell lung cancer (NSCLC) remains a topic of debate, particularly in pN2 disease. While phase III trials like PORT-C and LungART have demonstrated a significant reduction in mediastinal recurrence, they have failed to show improvements in disease-free survival (DFS) or overall survival (OS), raising concerns about increased cardiopulmonary toxicity. The rapid integration of chemo-immunotherapy and targeted therapies into peri-operative treatment has reshaped the NSCLC landscape, lowering the risk of distant failure and overall mortality while leaving local recurrence rates largely unchanged. Striking results from trials on immune checkpoint inhibitors and tyrosine kinase inhibitors in early-stage NSCLC highlight the potential for improved outcomes, yet the role of PORT in this evolving framework remains uncertain. Preclinical evidence suggests that PORT could enhance loco-regional control when combined with systemic treatments, but the lack of prospective trials exploring this synergy along with unanswered questions about additive toxicity hinders its clinical implementation. There is a critical need for tailored clinical trials that integrate advanced radiation techniques and systemic therapies to further optimize patients' outcome, both in terms of survival and quality of life. Such studies should focus on balancing the risks of mediastinal relapse, systemic progression and treatment-related toxicities, particularly for PORT-related grade 3 and 4 cardiac or pulmonary events. As treatment strategies continue to evolve, a multidisciplinary and personalized approach will be key to refining the management of resected NSCLC.
术后放疗(PORT)在根治性切除的非小细胞肺癌(NSCLC)中的作用仍是一个有争议的话题,尤其是在pN2期疾病中。虽然PORT-C和LungART等III期试验已证明纵隔复发显著减少,但它们未能显示无病生存期(DFS)或总生存期(OS)有所改善,这引发了对心肺毒性增加的担忧。化疗免疫疗法和靶向疗法迅速纳入围手术期治疗,重塑了NSCLC的格局,降低了远处转移失败风险和总体死亡率,而局部复发率基本保持不变。早期NSCLC中免疫检查点抑制剂和酪氨酸激酶抑制剂试验的显著结果突出了改善预后的潜力,但PORT在这一不断演变的框架中的作用仍不确定。临床前证据表明,PORT与全身治疗联合使用时可增强局部区域控制,但缺乏探索这种协同作用的前瞻性试验,以及关于附加毒性的未解决问题,阻碍了其临床应用。迫切需要开展量身定制的临床试验,将先进的放疗技术和全身治疗相结合,以进一步优化患者的生存和生活质量结局。此类研究应侧重于平衡纵隔复发、全身进展和治疗相关毒性的风险,特别是与PORT相关的3级和4级心脏或肺部事件。随着治疗策略不断发展,多学科和个性化方法将是优化切除的NSCLC管理的关键。