Advances and challenges of first-line immunotherapy for non-small cell lung cancer: A review
Open Access
- 19 January 2024
- journal article
- research article
- Published by Wolters Kluwer Health in Medicine
- Vol. 103 (3) , e36861
Abstract
The current use of immune checkpoint inhibitors (ICIs) for the treatment of lung cancer has dramatically changed the clinical strategy for metastatic non-small cell lung cancer (mNSCLC). As a result of great achievements in clinical trials, 6 programmed death-1 inhibitors (sintilimab, camrelizumab, tislelizumab, pembrolizumab, cemiplimab, and nivolumab), 2 programmed death-ligand 1 inhibitors (sugemalimab and atezolizumab), and 1 cytotoxic T lymphocyte-associated antigen-4 inhibitor (ipilimumab) have been approved as first-line treatment for mNSCLC by the US Food and Drug Administration. Recently, research on ICIs has shifted from a large number of second-line to first-line settings in clinical trials. Results from first-line trials have shown that almost all driver-negative mNSCLC are treated with ICIs and significantly prolong patient survival; however, the low response rate and adverse reactions to immunotherapy remain to be addressed. Here, we summarize the use of ICIs, including monotherapy and combination therapy, in the first-line treatment of mNSCLC in recent years and discuss the low response rate and adverse reactions of ICIs as well as the challenges and expectations for the first-line treatment of mNSCLC in the future.Keywords
This publication has 104 references indexed in Scilit:
- Amphiregulin Confers Regulatory T Cell Suppressive Function and Tumor Invasion via the EGFR/GSK-3β/Foxp3 AxisJournal of Biological Chemistry, 2016
- CTLA-4 controls follicular helper T-cell differentiation by regulating the strength of CD28 engagementProceedings of the National Academy of Sciences, 2014
- Anti-programmed-death-receptor-1 treatment with pembrolizumab in ipilimumab-refractory advanced melanoma: a randomised dose-comparison cohort of a phase 1 trialThe Lancet, 2014
- Eradication of metastatic mouse cancers resistant to immune checkpoint blockade by suppression of myeloid-derived cellsProceedings of the National Academy of Sciences, 2014
- Improved Survival with T Cell Clonotype Stability After Anti–CTLA-4 Treatment in Cancer PatientsScience Translational Medicine, 2014
- Phase I/II trial of a biweekly combination of S-1 plus docetaxel in patients with previously treated non-small cell lung cancer (KRSG-0601)British Journal of Cancer, 2012
- The blockade of immune checkpoints in cancer immunotherapyNature Reviews Cancer, 2012
- T cell exhaustionNature Immunology, 2011
- Yeast β-Glucan Amplifies Phagocyte Killing of iC3b-Opsonized Tumor Cells via Complement Receptor 3-Syk-Phosphatidylinositol 3-Kinase PathwayThe Journal of Immunology, 2006
- Genomic Organization of the MammalianMhcAnnual Review of Immunology, 2003