Cited by 190Cancer Immunotherapy and BiomarkersLung Cancer Treatments and MutationsFerroptosis and cancer prognosis

The DOI matches its Crossref record; 180 of the 184 references it cites were found in a registry or an index.

Immune Checkpoint Inhibitors in EGFR-Mutated NSCLC: Dusk or Dawn?

Open access

Abstract

Although immune checkpoint inhibitors (ICIs) that target programmed cell death protein-1/programmed cell death ligand-1 axis have significantly shifted the treatment paradigm in advanced NSCLC, clinical benefits of these agents are limited in patients with EGFR-mutated NSCLC. Several predictive biomarkers (e.g., programmed cell death ligand-1 expression, tumor mutation burden), which have been validated in EGFR-wild type NSCLC, however, are not efficacious in EGFR-mutated tumors, suggesting the unique characteristics of tumor microenvironment of EGFR-mutated NSCLC. Here, we first summarized the clinical evidence on the efficacy of ICIs in patients with EGFR-mutated NSCLC. Then, the cancer immunogram features of EGFR-mutated NSCLC was depicted to visualize the state of cancer-immune system interactions, including tumor foreignness, tumor sensitivity to immune effectors, metabolism, general immune status, immune cell infiltration, cytokines, and soluble molecules. We further discussed the potential subpopulations with EGFR mutations that could benefit from ICI treatment. Lastly, we put forward future strategies to adequately maximize the efficacy of ICI treatment in patients with EGFR-mutated NSCLC in the upcoming era of combination immunotherapies.

Overview

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Crossref · 10.1016/j.jtho.2021.04.003

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Show all 184 references

4 of the 184 references couldn’t be matched to a known paper.

Research works printed but not linked: 3

  1. Garon, 2015, Prior TKI therapy in NSCLC EGFR mutant patients associates with lack of response to anti-PD-1 treatment, J Thorac Oncol, 10
  2. Qiao, 2021, MA13.06 Deciphering the characteristics of tumor microenvironment in EGFR-mutated non-small cell lung cancer, J Thorac Oncol, 16
  3. Le, 2019, Abstract 5028: Characterization of the tumor immune microenvironment in treatment-nave EGFR-mutant NSCLC uncovers a low IFN-gamma suppressive immune phenotype, Proceedings: AACR Annual Meeting

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Items 101–190 of 190

Metadata

Authors
Qiao, M., Jiang, T., Liu, X., Mao, S., Zhou, F., Li, X., Zhao, C., Chen, X., Su, C., Ren, S., & Zhou, C.
Affiliations
Tongji University (CN)
Corresponding author
Zhou, Caicun
Venue
Journal of Thoracic Oncology
Publisher
Elsevier BV
Published
2021-08
Volume
16
Issue
8
Pages
1267-1288
ISSN
1556-0864 (ISSN-L)
OpenAlex
W3159640891
Cited by
186
References
184
Citations by year
2026: 24 · 2025: 39 · 2024: 39 · 2023: 35 · 2022: 35 · 2021: 14
FWCI
3.85
Type
journal article
Language
en
Open access
Locations
  • Journal of Thoracic Oncology (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Natural Science Foundation of China (81871865, 81972167)
Topics
  • Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Treatments and Mutations
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Ferroptosis and cancer prognosis
Keywords
immune checkpoint inhibitors, EGFR-mutant non-small cell lung cancer, PD-1/PD-L1 axis, predictive biomarkers, tumor mutational burden, PD-L1 expression, tumor microenvironment, immune cell infiltration, cytokines, combination immunotherapy, treatment response
MeSH terms
Immune Checkpoint Inhibitors, Carcinoma, Non-Small-Cell Lung, Humans, Lung Neoplasms, Mutation, Biomarkers, Tumor, Tumor Microenvironment, B7-H1 Antigen, ErbB Receptors

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