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Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography
Published on: February 17, 2022
The life-threatening eruptions of immune checkpoint inhibitor therapy
Emily L Coleman1, Brianna Olamiju1, Jonathan S Leventhal1
1Department of Dermatology, Yale University School of Medicine, New Haven, Connecticut, USA.
Abstract:
Immune checkpoint inhibitors (ICPi) have emerged as a new frontier of cancer therapy. Although monoclonal antibodies to cytotoxic T-lymphocyte associated protein 4 (CTLA-4), programmed cell death 1 (PD-1), and programmed cell death ligand 1 (PD-L1) have revolutionized oncologic management, these agents may result in a spectrum of immune-related adverse events (irAE) of which dermatologic toxicities are among the most frequent. Prompt recognition and management of irAE is essential for dermatologists caring for the expanding population of cancer patients exposed to these drugs. Cutaneous toxicities range from mild cases to severe and life-threatening presentations that may cause significant morbidity and mortality. This review provides an overview of severe cutaneous adverse reactions (SCARs) that may develop during ICPi therapy, including Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalized exanthematous pustulosis (AGEP). In addition, immunobullous disorders, erythroderma, neutrophilic dermatoses, and cutaneous eruptions associated with systemic manifestations are discussed.
Insights
Immune checkpoint inhibitors (ICPi) can cause frequent skin toxicities. This review details severe cutaneous adverse reactions (SCARs) like SJS, TEN, DRESS, and AGEP, crucial for dermatologists to manage.
Area of Science:
- Oncology
- Dermatology
- Immunology
Background:
- Immune checkpoint inhibitors (ICPi) targeting CTLA-4, PD-1, and PD-L1 are revolutionizing cancer therapy.
- Dermatologic toxicities are frequent immune-related adverse events (irAE) associated with ICPi.
- Effective management of irAE is critical for patients receiving ICPi therapy.
Purpose of the Study:
- To provide an overview of severe cutaneous adverse reactions (SCARs) associated with ICPi therapy.
- To discuss the recognition and management of various dermatologic toxicities.
- To highlight the importance of dermatologists in managing ICPi-induced skin reactions.
Main Methods:
- Review of literature on ICPi-related dermatologic toxicities.
- Categorization and description of severe cutaneous adverse reactions (SCARs).
- Discussion of immunobullous disorders, erythroderma, and neutrophilic dermatoses.
Main Results:
- ICPi can lead to a spectrum of cutaneous toxicities, ranging from mild to life-threatening.
- Severe reactions include Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), DRESS, and AGEP.
- Other discussed reactions include immunobullous disorders, erythroderma, and neutrophilic dermatoses.
Conclusions:
- Prompt recognition and management of ICPi-induced dermatologic toxicities are essential.
- Dermatologists play a key role in managing these immune-related adverse events.
- Understanding SCARs is vital for optimizing cancer patient care during ICPi treatment.
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