Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2024 Jun 1;47(6):291-303.
doi: 10.1097/COC.0000000000001088. Epub 2024 Feb 20.

Advancements in NSCLC: From Pathophysiological Insights to Targeted Treatments

Affiliations
Review

Advancements in NSCLC: From Pathophysiological Insights to Targeted Treatments

Jianan Xu et al. Am J Clin Oncol. .

Abstract

With the global incidence of non-small cell lung cancer (NSCLC) on the rise, the development of innovative treatment strategies is increasingly vital. This review underscores the pivotal role of precision medicine in transforming NSCLC management, particularly through the integration of genomic and epigenomic insights to enhance treatment outcomes for patients. We focus on the identification of key gene mutations and examine the evolution and impact of targeted therapies. These therapies have shown encouraging results in improving survival rates and quality of life. Despite numerous gene mutations being identified in association with NSCLC, targeted treatments are available for only a select few. This paper offers an exhaustive analysis of the pathogenesis of NSCLC and reviews the latest advancements in targeted therapeutic approaches. It emphasizes the ongoing necessity for research and development in this domain. In addition, we discuss the current challenges faced in the clinical application of these therapies and the potential directions for future research, including the identification of novel targets and the development of new treatment modalities.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

FIGURE 1
FIGURE 1
Molecular targets and therapeutic interventions in non-small cell lung cancer treatment. The depicted schematic provides a concise overview of the key molecular targets in NSCLC and the suite of targeted therapies designed to intervene. It encompasses a spectrum of inhibitors for pathways such as EGFR, ALK, VEGFR, MET, and RET, as well as agents that modulate the KRAS, BRAF, MEK, and the PI3K/AKT/mTOR cascades. Featured as well are the CDK4/6 inhibitors, a novel class of drugs that govern cell cycle progression. Each therapeutic agent is specified by its target, underscoring the targeted approach integral to contemporary NSCLC treatment paradigms.

References

    1. Bozorgmehr F, Muller A, Rawluk J, et al. . Immune checkpoint inhibitors in non-small cell lung cancer—when should we dare to stop treatment? Lung Cancer. 2023;184:107340. - PubMed
    1. Longo V, Catino A, Montrone M, et al. . Controversial role of mast cells in NSCLC tumor progression and angiogenesis. Thorac Cancer. 2022;13:2929–2934. - PMC - PubMed
    1. Li J, Kwok HF. Current strategies for treating NSCLC: from biological mechanisms to clinical treatment. Cancers (Basel). 2020;12:12. - PMC - PubMed
    1. Greenhalgh J, Dwan K, Boland A, et al. . First-line treatment of advanced epidermal growth factor receptor (EGFR) mutation positive non-squamous non-small cell lung cancer. Cochrane Database Syst Rev. 2016;25:CD010383. - PubMed
    1. Memarzia A, Saadat S, Asgharzadeh F, et al. . Therapeutic effects of medicinal plants and their constituents on lung cancer, in vitro, in vivo and clinical evidence. J Cell Mol Med. 2023;27:2841–2863. - PMC - PubMed

MeSH terms