Attili Ilaria, Corvaja Carla, Spitaleri Gianluca, Del Signore Ester, Trillo Aliaga Pamela, Passaro Antonio, de Marinis Filippo
Division of Thoracic Oncology, European Institute of Oncology IRCCS, Via G. Ripamonti 435, 20141 Milan, Italy.
Cancers (Basel). 2023 Oct 20;15(20):5079. doi: 10.3390/cancers15205079.
Tyrosine kinase inhibitors (TKIs) revolutionized the treatment of patients with advanced or metastatic non-small cell lung cancer (NSCLC) harboring most driver gene alterations. Starting from the first generation, research rapidly moved to the development of newer, more selective generations of TKIs, obtaining improved results in terms of disease control and survival. However, the use of novel generations of TKIs is not without limitations. We reviewed the main results obtained, as well as the ongoing clinical trials with TKIs in oncogene-addicted NSCLC, together with the biology underlying their potential strengths and limitations. Across driver gene alterations, novel generations of TKIs allowed delayed resistance, prolonged survival, and improved brain penetration compared to previous generations, although with different toxicity profiles, that generally moved their use from further lines to the front-line treatment. However, the anticipated positioning of novel generation TKIs leads to abolishing the possibility of TKI treatment sequencing and any role of previous generations. In addition, under the selective pressure of such more potent drugs, resistant clones emerge harboring more complex and hard-to-target resistance mechanisms. Deeper knowledge of tumor biology and drug properties will help identify new strategies, including combinatorial treatments, to continue improving results in patients with oncogene-addicted NSCLC.
酪氨酸激酶抑制剂(TKIs)彻底改变了对大多数驱动基因发生改变的晚期或转移性非小细胞肺癌(NSCLC)患者的治疗方式。从第一代开始,研究迅速转向开发更新的、更具选择性的几代TKIs,在疾病控制和生存方面取得了更好的结果。然而,新一代TKIs的使用并非没有局限性。我们回顾了所取得的主要成果,以及正在进行的针对致癌基因成瘾性NSCLC的TKIs临床试验,以及其潜在优势和局限性背后的生物学原理。在各种驱动基因改变中,与前几代相比,新一代TKIs能够延迟耐药、延长生存期并改善脑内渗透,尽管毒性特征不同,这通常使它们的使用从后续治疗线转移到一线治疗。然而,新一代TKIs的预期定位导致取消了TKIs治疗排序的可能性以及前几代的任何作用。此外,在这种更有效药物的选择压力下,会出现携带更复杂且难以靶向的耐药机制的耐药克隆。对肿瘤生物学和药物特性的更深入了解将有助于确定新的策略,包括联合治疗,以继续改善致癌基因成瘾性NSCLC患者的治疗效果。