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Review
. 2024 Sep 18;25(18):10046.
doi: 10.3390/ijms251810046.

Emerging Targets in Non-Small Cell Lung Cancer

Affiliations
Review

Emerging Targets in Non-Small Cell Lung Cancer

Louisa Liu et al. Int J Mol Sci. .

Abstract

Lung cancer is responsible for a high burden of disease globally. Over the last two decades, the discovery of targetable oncogenic genomic alterations has revolutionized the treatment landscape for early-stage and advanced non-small cell lung cancer (NSCLC). New molecular drivers continue to emerge as promising therapeutic targets, including KRAS non-G12C, RAF/MEK, HER3, Nectin-4, folate receptor alpha, ITGB6, and PRMT5. In this review, we summarize the emerging molecular targets with a potential clinical impact in advanced NSCLC, elaborating on their clinical characteristics and specific mechanisms and molecular pathways for which targeted treatments are currently available. Additionally, we present an aggregate of ongoing clinical trials investigating the available treatment options targeting such alterations, in addition to their current recruitment status and preliminary efficacy data. These advancements may guide further research endeavors and inform future treatment strategies to improve the management of and transform outcomes for patients with advanced NSCLC.

Keywords: non-small cell lung cancer; novel combinatorial approaches; oncogene driver; targeted therapies.

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Conflict of interest statement

L.L. and J.S. have no conflicts of interest to disclose. K.S.: Research funding to institution: Genentech; Black Diamond; Lilly; Harpoon Therapeutics; Merck. K.R.: Consultant with honoraria to self: Amgen; AstraZeneca; Blueprint; Daiichi Sankyo; Genentech; GlaxoSmithKline; Janssen; Lilly; Mirati; Novartis; Novocure. Research funding to institution: Genentech; Blueprint; Daiichi Sankyo; Elevation Oncology; Janssen.

Figures

Figure 1
Figure 1
Depiction of the interplay of the major pathways to be discussed in this review (KRAS, BRAF/MEK, and HER3).

References

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