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A new strategy for immunotherapy of microsatellite-stable (MSS)-type advanced colorectal cancer: Multi-pathway combination therapy with PD-1/PD-L1 inhibitors.
- Source :
-
Immunology [Immunology] 2024 Oct; Vol. 173 (2), pp. 209-226. Date of Electronic Publication: 2024 Mar 22. - Publication Year :
- 2024
-
Abstract
- Colorectal cancer (CRC) is a frequent gastrointestinal malignancy with high rates of morbidity and mortality; 85% of these tumours are proficient mismatch repair (pMMR)-microsatellite instability-low (MSI-L)/microsatellite stable (MSS) CRC known as 'cold' tumours that are resistant to immunosuppressive drugs. Monotherapy with programmed death 1 (PD-1)/programmed death ligand 1 (PD-L1) inhibitors is ineffective for treating MSS CRC, making immunotherapy for MSS CRC a bottleneck. Recent studies have found that the multi-pathway regimens combined with PD-1/PD-L1 inhibitors can enhance the efficacy of anti-PD-1/PD-L1 in MSS CRC by increasing the number of CD8+ T cells, upregulating PD-L1 expression and improving the tumour microenvironment. This paper reviews the research progress of PD-1/PD-L1 inhibitors in combination with cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) inhibitors, oncolytic virus, intestinal flora, antiangiogenic agents, chemotherapy, radiotherapy and epigenetic drugs for the treatment of pMMR-MSI-L/MSS CRC.<br /> (© 2024 John Wiley & Sons Ltd.)
- Subjects :
- Humans
Tumor Microenvironment immunology
Animals
Combined Modality Therapy
Colorectal Neoplasms immunology
Colorectal Neoplasms therapy
Colorectal Neoplasms drug therapy
Colorectal Neoplasms genetics
Immune Checkpoint Inhibitors therapeutic use
Immune Checkpoint Inhibitors pharmacology
Microsatellite Instability
Programmed Cell Death 1 Receptor antagonists & inhibitors
Programmed Cell Death 1 Receptor immunology
Programmed Cell Death 1 Receptor metabolism
Immunotherapy methods
B7-H1 Antigen antagonists & inhibitors
B7-H1 Antigen metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1365-2567
- Volume :
- 173
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Immunology
- Publication Type :
- Academic Journal
- Accession number :
- 38517066
- Full Text :
- https://doi.org/10.1111/imm.13785