Theik Nyein Wint Yee, De Armas Suset Almuinas, Rosas Daniel, Kiamos Amy, Thaw Dar Nyein Nyein, Shoreibah Ahmed, Hussein Atif, Raez Luis E
Memorial Healthcare System, Internal Medicine Residency Program, Pembroke Pines, FL 33028, USA.
Memorial Cancer Institute, Memorial Healthcare System, Hematology-Oncology Fellowship Program, Pembroke Pines, FL 33028, USA.
Int J Mol Sci. 2025 Apr 17;26(8):3802. doi: 10.3390/ijms26083802.
Non-small cell lung cancer (NSCLC) is operated commonly by diverse genetic alterations, and oncogenic fusions represent a significant therapeutic role. Common fusions include ALK, ROS1, RET, and NTRK, signaling pathways in tumorigenesis. Recent advances in investigating tumor molecular biology include underlying fusions, including chromosomal rearrangements, highlighting their role as oncogenic drivers. The development of targeted therapies, such as tyrosine kinase inhibitors (TKIs), has impacted most patients' NSCLC treatment. Despite the greater profiles, such as remarkable efficiency and tolerable side effects compared to traditional chemotherapy, challenges, such as acquired mutations, lead to more ongoing research-optimized future NSCLC therapies.
非小细胞肺癌(NSCLC)通常由多种基因改变驱动,致癌融合在其中发挥着重要的治疗作用。常见的融合包括ALK、ROS1、RET和NTRK,它们在肿瘤发生过程中涉及信号通路。肿瘤分子生物学研究的最新进展包括对潜在融合的研究,其中包括染色体重排,突出了它们作为致癌驱动因素的作用。靶向治疗的发展,如酪氨酸激酶抑制剂(TKIs),已经影响了大多数非小细胞肺癌患者的治疗。尽管这些治疗有诸多优势,比如与传统化疗相比疗效显著且副作用可耐受,但仍面临一些挑战,如获得性突变,这促使更多持续的研究以优化未来的非小细胞肺癌治疗。