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Delayed-Onset Immune-Mediated Hepatitis Following Pembrolizumab Discontinuation: A Case Report
Connor Barry1, Jialing Huang2, Chukwunonso B Ubanatu1
1Internal Medicine, Geisinger Health System, Wilkes Barre, USA.
Immune checkpoint inhibitors (ICIs) such as pembrolizumab (Keytruda) have transformed the treatment landscape for various malignancies, yet they are associated with immune-related adverse events (irAEs), including hepatotoxicity. While most cases of ICI-induced hepatitis occur within weeks of initiating therapy, delayed-onset presentations are increasingly recognized. We report a case of severe transaminase elevation developing three months after cessation of pembrolizumab in a patient with a history of gallbladder carcinoma. Her chemotherapy was placed on hold after a recent stroke led to a worsening functional status, with the initial intent to resume pembrolizumab once her functional status normalized. Workup excluded infectious, metabolic, and autoimmune causes. Liver biopsy revealed immune-mediated hepatitis with histologic evidence of only mild cholestasis. The patient responded to corticosteroid therapy, supporting the diagnosis of ICI-induced hepatotoxicity. This case underscores the importance of maintaining a high index of suspicion for immune-mediated liver injury well beyond the period of active immunotherapy and highlights the diagnostic value of liver biopsy in complex presentations.
Immune checkpoint inhibitors (ICIs) such as pembrolizumab (Keytruda) have transformed the treatment landscape for various malignancies, yet they are associated with immune-related adverse events (irAEs), including hepatotoxicity. While most cases of ICI-induced hepatitis occur within weeks of initiating therapy, delayed-onset presentations are increasingly recognized. We report a case of severe transaminase elevation developing three months after cessation of pembrolizumab in a patient with a history of gallbladder carcinoma. Her chemotherapy was placed on hold after a recent stroke led to a worsening functional status, with the initial intent to resume pembrolizumab once her functional status normalized. Workup excluded infectious, metabolic, and autoimmune causes. Liver biopsy revealed immune-mediated hepatitis with histologic evidence of only mild cholestasis. The patient responded to corticosteroid therapy, supporting the diagnosis of ICI-induced hepatotoxicity. This case underscores the importance of maintaining a high index of suspicion for immune-mediated liver injury well beyond the period of active immunotherapy and highlights the diagnostic value of liver biopsy in complex presentations.
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