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Review
. 2022 Jun 22:14:2079-2090.
doi: 10.2147/CMAR.S366738. eCollection 2022.

Immunotherapy in Advanced Non-Small Cell Lung Cancers: Current Status and Updates

Affiliations
Review

Immunotherapy in Advanced Non-Small Cell Lung Cancers: Current Status and Updates

Ratoe Suraya et al. Cancer Manag Res. .

Abstract

Non-small-cell lung cancer (NSCLC) is a major health burden, and novel therapeutic options are needed to help solve this problem. One such option is immunotherapy, which targets immune checkpoint molecules that inhibit cancer cells, decreasing immune system activation, for example, immunotherapies target PD-1, its ligand PD-L1, and CTLA-4. There have been major advances in the development of agents that inhibit these molecules, called immune checkpoint inhibitors, and several of them are already approved for usage in NSCLC patients, especially in advanced stages. In this review, the reasons why immune checkpoint inhibitors could be beneficial and the clinical results of studies using these drugs for advanced or recurrent NSCLC patients are discussed, as is the safety profile of the drugs.

Keywords: CTLA-4; PD-1; PD-L1; immune checkpoint inhibitors; non-small cell lung cancer.

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Conflict of interest statement

Dr. Motoko Tachihara reports grants and personal fees from AstraZeneca K.K; personal fees from Eli Lilly Japan K.K., Chugai Pharmaceutical Co. Ltd., Ono Pharmaceutical Co. Ltd., MSD K.K., Nippon Boehringer Ingelheim Co. Ltd., Bristol-Myers Squibb Co. Ltd., and Novartis pharmaceuticals K.K, outside the submitted work. Prof. Dr. Yoshihiro Nishimura reports personal fees from AstraZeneca and grants from Chugai Pharmaceutical Co., Ltd., outside the submitted work. The authors report no other conflicts of interest in this work.

Figures

Figure 1
Figure 1
Schematic overview of immune checkpoints in NSCLC and ICI agents targeting specific immune checkpoint molecules. APC, antigen-presenting cell; TCR, T cell receptor; MHC, major histocompatibility complex; PD-1, programmed cell death protein-1; PD-L1, programmed cell death protein ligand 1; CTLA-4, cytotoxic T lymphocyte-associated protein 4.

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