Foffano Lorenzo, Bertoli Elisa, Bortolot Martina, Torresan Sara, De Carlo Elisa, Stanzione Brigida, Del Conte Alessandro, Puglisi Fabio, Spina Michele, Bearz Alessandra
Department of Medical Oncology, CRO di Aviano, National Cancer Institute, IRCCS, 33081 Aviano, Italy.
Department of Medicine, University of Udine, 33100 Udine, Italy.
Int J Mol Sci. 2025 Jan 11;26(2):583. doi: 10.3390/ijms26020583.
Non-small cell lung cancer (NSCLC) remains a leading cause of cancer-related mortality worldwide. The discovery of specific driver mutations has revolutionized the treatment landscape of oncogene-addicted NSCLC through targeted therapies, significantly improving patient outcomes. However, immune checkpoint inhibitors (ICIs) have demonstrated limited effectiveness in this context. Emerging evidence, though, reveals significant heterogeneity among different driver mutation subgroups, suggesting that certain patient subsets may benefit from ICIs, particularly when combined with other therapeutic modalities. In this review, we comprehensively examine the current evidence on the efficacy of immunotherapy in oncogene-addicted NSCLC. By analyzing recent clinical trials and preclinical studies, along with an overview of mechanisms that may reduce immunotherapy efficacy, we explored potential strategies to address these challenges, to provide insights that could optimize immunotherapy approaches and integrate them effectively into the treatment algorithm for oncogene-addicted NSCLC.
非小细胞肺癌(NSCLC)仍然是全球癌症相关死亡的主要原因。特定驱动基因突变的发现通过靶向治疗彻底改变了对癌基因成瘾性NSCLC的治疗格局,显著改善了患者的预后。然而,在这种情况下,免疫检查点抑制剂(ICI)的有效性有限。不过,新出现的证据揭示了不同驱动基因突变亚组之间存在显著异质性,这表明某些患者亚组可能从ICI中获益,特别是与其他治疗方式联合使用时。在这篇综述中,我们全面审视了目前关于免疫治疗在癌基因成瘾性NSCLC中疗效的证据。通过分析近期的临床试验和临床前研究,以及对可能降低免疫治疗疗效的机制进行概述,我们探索了解决这些挑战的潜在策略,以提供可优化免疫治疗方法并将其有效整合到癌基因成瘾性NSCLC治疗方案中的见解。