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Toxicity management of immunotherapy for patients with metastatic melanoma
Helena Linardou1, Helen Gogas2
1First Department of Medical Oncology, Metropolitan Hospital, Athens, Greece ;
Abstract:
Checkpoint inhibitors have revolutionized the treatment of patients with metastatic melanoma offering improved responses and significant survival benefit. These agents are now approved for the treatment of metastatic melanoma, squamous and non-squamous non-small cell lung cancer (NSCLC) and kidney cancer, while they are now being investigated in a range of other malignancies. In addition, another anti-PD-L1 monoclonal antibody (atezolizumab) was recently approved for urothelial cancer. Ipilimumab, an anti-cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) antibody and the anti-PD-1 agents nivolumab and pembrolizumab have followed large clinical development programs, therefore, information regarding their safety and toxicity profile is readily available. Unique toxicities have been observed, which stem from and relate to the immune activation by these agents and are thus termed as immune-related adverse events (irAEs). Clinicians and patients should be aware of this different toxicity profile, so as to promptly recognize, identify and manage symptoms related to irAEs. Indeed, clinical experience has shown that these immune events, when they are early recognized and timely managed, are mostly reversible otherwise they can evoke severe or even life-threatening situations. Several recommendations and guidelines have been developed for the management of irAEs and algorithms have been published based primarily on our knowledge from the ipilimumab trials.
Insights
Checkpoint inhibitors, like anti-CTLA-4 and anti-PD-1 antibodies, offer survival benefits in cancers. Awareness and prompt management of unique immune-related adverse events (irAEs) are crucial for patient safety.
Area of Science:
- Oncology
- Immunology
Background:
- Checkpoint inhibitors have transformed cancer therapy, notably in metastatic melanoma, lung cancer, and kidney cancer.
- Approved agents include ipilimumab (anti-CTLA-4) and anti-PD-1 antibodies (nivolumab, pembrolizumab), with atezolizumab (anti-PD-L1) approved for urothelial cancer.
Purpose of the Study:
- To highlight the unique toxicity profile of immune-activating checkpoint inhibitors.
- To emphasize the importance of recognizing and managing immune-related adverse events (irAEs).
Main Methods:
- Review of clinical development programs and safety data for approved checkpoint inhibitors.
- Analysis of observed toxicities related to immune activation.
Main Results:
- Checkpoint inhibitors demonstrate significant survival benefits across various malignancies.
- Unique toxicities, termed immune-related adverse events (irAEs), arise from immune activation.
Conclusions:
- Early recognition and timely management of irAEs are critical for reversibility and preventing severe outcomes.
- Clinical guidelines and algorithms are available for managing irAEs, largely based on ipilimumab trial data.
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