Petrella Francesco, Cara Andrea, Cassina Enrico Mario, Degiovanni Sara, Libretti Lidia, Lo Torto Sara, Pirondini Emanuele, Raveglia Federico, Spinelli Francesca, Tuoro Antonio, Rizzo Stefania
Department of Thoracic Surgery, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.
Department of Thoracic Surgery, Tor Vergata University Polyclinic, 00133 Roma, Italy.
Cancers (Basel). 2025 May 31;17(11):1844. doi: 10.3390/cancers17111844.
Lung cancer is the leading cause of cancer-related death worldwide, ranking first among men and second among women for both incidence and mortality. Surgery remains the primary treatment for early-stage, resectable non-small cell lung cancer (NSCLC), encompassing stages I and selected cases of stage IIIB. For patients with stage II to III disease, as well as some stage IB tumors, neoadjuvant or adjuvant systemic therapies are recommended. It is well recognized that specific driver gene mutations play a critical role in tumor progression and aggressiveness, and patients with these genetic alterations may benefit from targeted treatment approaches. These alterations are referred to as "druggable", "targetable", or "actionable", representing specific targets for personalized treatments. Tyrosine kinase inhibitors (TKIs) are now the preferred first-line treatment for patients harboring mutations in EGFR, ALK, ROS1, and BRAF. Additionally, targeted therapies exist for patients with alterations in RET, ERBB2, KRAS, MET, and NTRK, either for those who have received prior treatments or as part of ongoing clinical trials. The success of targeted therapies is reshaping treatment approaches for NSCLC with targetable driver gene alterations, both in early-stage and locally advanced settings. This review focuses on current therapeutic strategies that combine targeted therapies with surgical resection in patients with resectable non-small cell lung cancer (NSCLC) harboring actionable driver gene alterations.
肺癌是全球癌症相关死亡的主要原因,在男性和女性的发病率和死亡率中均排名第一和第二。手术仍然是早期、可切除的非小细胞肺癌(NSCLC)的主要治疗方法,包括I期和部分IIIB期病例。对于II至III期疾病的患者以及一些IB期肿瘤患者,建议进行新辅助或辅助全身治疗。众所周知,特定的驱动基因突变在肿瘤进展和侵袭性中起关键作用,具有这些基因改变的患者可能从靶向治疗方法中获益。这些改变被称为“可药物治疗的”、“可靶向的”或“可采取行动的”,代表个性化治疗的特定靶点。酪氨酸激酶抑制剂(TKIs)现在是携带EGFR、ALK、ROS1和BRAF突变患者的首选一线治疗药物。此外,对于RET、ERBB2、KRAS、MET和NTRK发生改变的患者,无论是接受过先前治疗的患者还是作为正在进行的临床试验的一部分,都有靶向治疗方法。靶向治疗的成功正在重塑具有可靶向驱动基因改变的NSCLC的治疗方法,无论是在早期还是局部晚期情况下。本综述重点关注在具有可采取行动的驱动基因改变的可切除非小细胞肺癌(NSCLC)患者中,将靶向治疗与手术切除相结合的当前治疗策略。