» Articles » PMID: 29925736

Immune Checkpoint Inhibitors (ICIs) in Non-Small Cell Lung Cancer (NSCLC)

Overview
Journal J UOEH
Date 2018 Jun 22
PMID 29925736
Citations 37
Authors
Affiliations
Soon will be listed here.
Abstract

Cancer immunotherapy with immune checkpoint inhibitors (ICIs) has become a "game changer" in the treatment of advanced non-small cell lung cancer (NSCLC). Its most clinically important advantage over traditional chemotherapy using cytotoxic agents are its long-term survival benefits, and some advanced NSCLC patients treated with an antibody against programmed cell death 1 (PD-1) have survived for 5 years or longer. Immune checkpoint inhibitors (ICIs) are also potentially useful for earlier-stage NSCLC when used in combination with surgery or radiotherapy. A recent clinical trial has shown that consolidation treatment with an antibody against a ligand of PD-1 (PD-L1) following chemo-radiotherapy significantly improves progression-free survival for patients with locally advanced NSCLC. However, current single-agent treatment with an anti-PD-1/PD-L1 antibody may provide significant survival benefits only in a small subset of patients. PD-L1 expression status on tumor cells is an approved biomarker to predict response to ICIs, but is not enough for optimal patient selection. To improve the therapeutic outcomes, development of novel biomarkers other than PD-L1 expression status is essential. Combination treatment strategies based on blockade of PD-1/PD-L1 may also be promising, and a variety of combinations, such as ICIs plus chemotherapy, are being examined in ongoing clinical trials. Here we review and discuss the current status and future perspectives of immunotherapy with ICIs.

Citing Articles

The Between Lung Cancer and Interstitial Lung Diseases: A Focus on Acute Exacerbation.

Zanini U, Faverio P, Bonfanti V, Falzone M, Cortinovis D, Arcangeli S J Clin Med. 2024; 13(23).

PMID: 39685543 PMC: 11641964. DOI: 10.3390/jcm13237085.


The Prevalence of Programmed Death Ligand-1 (PD-L1) Expression in Non-Small Cell Lung Cancer: An Experience From Tertiary Care Hospital.

Mehta A, Priya V P L, Teja L, Pillai K Cureus. 2024; 16(10):e72291.

PMID: 39583517 PMC: 11585287. DOI: 10.7759/cureus.72291.


Bojungikki-Tang Augments Pembrolizumab Efficacy in Human PBMC-Injected H460 Tumor-Bearing Mice.

Na S, Yi J, Yeo H, Park S, Jeong M, Chun J Life (Basel). 2024; 14(10).

PMID: 39459546 PMC: 11508561. DOI: 10.3390/life14101246.


Pathogenesis, pathological characteristics and individualized therapy for immune-related adverse effects.

Miao K, Zhang L Chin Med J Pulm Crit Care Med. 2024; 1(4):215-222.

PMID: 39171279 PMC: 11332905. DOI: 10.1016/j.pccm.2023.08.002.


Dynamic Changes in Circulating Tumor Fraction as a Predictor of Real-World Clinical Outcomes in Solid Tumor Malignancy Patients Treated with Immunotherapy.

Gentzler R, Guittar J, Mitra A, Iams W, Driessen T, Schwind R Oncol Ther. 2024; 12(3):509-524.

PMID: 39037536 PMC: 11333675. DOI: 10.1007/s40487-024-00287-2.