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Delayed Autoimmune Toxicity Occurring Several Months After Cessation of Anti-PD-1 Therapy
Sagun Parakh1,2,3, Jonathan Cebon1,2,3, Oliver Klein4,2
1Medical Oncology Unit, Austin Health, Melbourne, Victoria, Australia.
Abstract:
Treatment with anti-programmed cell death protein 1 (PD-1) antibodies has demonstrated clinical efficacy in a whole range of malignancies including advanced melanoma, renal cell cancer, bladder cancer, and non-small cell lung cancer. Immune-related adverse events are a unique side effect of checkpoint regulator therapy including anti-PD-1 antibodies. Treatment-related autoimmunity can occur in any organ system, with the median onset usually within 5-15 weeks from the commencement of therapy, depending on the organ system involved. This study describes for the first time a case of delayed autoimmunity occurring 8 months after discontinuing treatment with the anti-PD-1 antibody nivolumab in a patient with metastatic melanoma. The case highlights the need for ongoing surveillance of patients treated with immune checkpoint inhibitors even after cessation of therapy, especially as patients increasingly stop treatment after achieving durable responses.
Insights
Anti-programmed cell death protein 1 (PD-1) antibodies effectively treat cancers but can cause immune-related adverse events. This case shows delayed autoimmunity 8 months after stopping nivolumab, emphasizing the need for continued patient surveillance.
Area of Science:
- Immunology
- Oncology
- Clinical Medicine
Background:
- Anti-programmed cell death protein 1 (PD-1) antibodies are effective cancer treatments.
- Immune-related adverse events (irAEs) are known side effects of these therapies.
- irAEs typically manifest within weeks of treatment initiation.
Observation:
- A patient with metastatic melanoma developed delayed autoimmunity 8 months after discontinuing nivolumab.
- This represents a novel presentation of irAEs associated with anti-PD-1 therapy.
Findings:
- Delayed-onset autoimmunity can occur long after anti-PD-1 therapy cessation.
- The specific organ system involved influences the onset of irAEs.
Implications:
- Ongoing surveillance for irAEs is crucial even after anti-PD-1 treatment discontinuation.
- This finding is particularly relevant as patients achieve durable responses and stop therapy.
- Further research is needed to understand the mechanisms of delayed irAEs.
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