Adverse and unconventional reactions related to immune checkpoint inhibitor therapy for cancer
[Display omitted] •The blockade of immune checkpoint inhibitors (ICIs) was an effective immunotherapy for cancer treatment.•Immune related adverse events commonly occurred during treatment with ICIs.•Pseudoprogression and hyperprogression were unconventional responses to ICI treatment. Immunotherapy...
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Published in | International immunopharmacology Vol. 108; p. 108803 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.07.2022
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Subjects | |
Online Access | Get full text |
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Summary: | [Display omitted]
•The blockade of immune checkpoint inhibitors (ICIs) was an effective immunotherapy for cancer treatment.•Immune related adverse events commonly occurred during treatment with ICIs.•Pseudoprogression and hyperprogression were unconventional responses to ICI treatment.
Immunotherapy is an emerging method for the treatment of cancer. Immune checkpoint inhibitors (ICIs) are monoclonal antibodies that block immune checkpoint pathways and release the body’s anti-tumor immunity. They consist mainly of antibodies against cytotoxic T lymphocyte associated antigen-4 (CTLA-4), programmed death receptor 1 (PD-1), and programmed death ligand 1 (PD-L1). Although ICI therapy has been shown to be effective at treating cancer, it can also destroy immune tolerance and lead to organ toxicity. These unwanted side effects are known as immune related adverse events (irAEs). ICI treatment can also cause unconventional reactions such as pseudoprogression and hyperprogression. Pseudoprogression looks like an increase in the tumor parenchyma but is actually a temporary inflammation in the tumor; hyperprogression refers to the acceleration of tumor growth after the start of immunotherapy. Understanding the mechanisms of these two phenomena and distinguishing their differences are necessary for the effective prevention and treatment of unconventional reactions. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 1567-5769 1878-1705 |
DOI: | 10.1016/j.intimp.2022.108803 |