Huang Qing, Li Yuanxiang, Huang Yingdan, Wu Jingyi, Bao Wendai, Xue Chang, Li Xiaoyu, Dong Shuang, Dong Zhiqiang, Hu Sheng
Department of Medical Oncology, Huazhong University of Science and Technology, Tongji Medical College, Hubei Cancer Hospital, Wuhan, 430079, Hubei, China.
Center for Neurological Disease Research, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, Hubei, China.
Signal Transduct Target Ther. 2025 Jun 15;10(1):186. doi: 10.1038/s41392-025-02243-6.
Over the past two decades, non-small cell lung cancer (NSCLC) has witnessed encouraging advancements in basic and clinical research. However, substantial unmet needs remain for patients worldwide, as drug resistance persists as an inevitable reality. Meanwhile, the journey towards amplifying the breadth and depth of the therapeutic effect requires comprehending and integrating diverse and profound progress. In this review, therefore, we aim to comprehensively present such progress that spans the various aspects of molecular pathology, encompassing elucidations of metastatic mechanisms, identification of therapeutic targets, and dissection of spatial omics. Additionally, we also highlight the numerous small molecule and antibody drugs, encompassing their application alone or in combination, across later-line, frontline, neoadjuvant or adjuvant settings. Then, we elaborate on drug resistance mechanisms, mainly involving targeted therapies and immunotherapies, revealed by our proposed theoretical models to clarify interactions between cancer cells and a variety of non-malignant cells, as well as almost all the biological regulatory pathways. Finally, we outline mechanistic perspectives to pursue innovative treatments of NSCLC, through leveraging artificial intelligence to incorporate the latest insights into the design of finely-tuned, biomarker-driven combination strategies. This review not only provides an overview of the various strategies of how to reshape available armamentarium, but also illustrates an example of clinical translation of how to develop novel targeted drugs, to revolutionize therapeutic landscape for NSCLC.
在过去二十年中,非小细胞肺癌(NSCLC)在基础和临床研究方面取得了令人鼓舞的进展。然而,由于耐药性仍是不可避免的现实,全球患者仍有大量未满足的需求。与此同时,要扩大治疗效果的广度和深度,就需要理解和整合多样而深刻的进展。因此,在本综述中,我们旨在全面介绍涵盖分子病理学各个方面的此类进展,包括转移机制的阐明、治疗靶点的识别以及空间组学的剖析。此外,我们还重点介绍了众多小分子和抗体药物,包括它们在晚期、一线、新辅助或辅助治疗中的单独应用或联合应用。然后,我们详细阐述了耐药机制,主要涉及靶向治疗和免疫治疗,这些机制是我们提出的理论模型所揭示的,以阐明癌细胞与各种非恶性细胞之间的相互作用,以及几乎所有的生物调节途径。最后,我们概述了通过利用人工智能将最新见解纳入精准的、生物标志物驱动的联合策略设计中,以寻求NSCLC创新治疗方法的机制观点。本综述不仅概述了如何重塑现有治疗手段的各种策略,还举例说明了如何开发新型靶向药物进行临床转化,以彻底改变NSCLC的治疗格局。