ArticleThe American journal of case reports2025
Pancreatic Inflammation Induced by Immune Checkpoint Inhibitors in Melanoma Treatment: A Case Report.
Article in The American journal of case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
BACKGROUND Immunotherapy has seen an exponential increase recently, as has the study of its associated adverse effects. Although a wide range of reactions to immunotherapy has been described, reports of immune-mediated focal pancreatitis remain rare. Autoimmune pancreatitis related to immune checkpoint inhibitors occurs because of the hyperactivation of T lymphocytes, which act against pancreatic cells, causing inflammation. CASE REPORT This case report describes a previously healthy 41-year-old man with a diagnosis of metastatic melanoma with inguinal lymph node metastasis. The patient underwent 1 year of adjuvant treatment with nivolumab and had excellent tolerance. After a 1-year suspension of this treatment, nodal and peritoneal recurrence occurred, leading to the initiation of combined therapy with ipilimumab and nivolumab, followed by maintenance nivolumab, resulting in a complete response. After 10 cycles of nivolumab, PET-CT and MRI identified a lesion in the head of the pancreas, which was suspected to be a primary neoplasm. The patient was asymptomatic, with normal tumor markers and elevated amylase and lipase levels. An endoscopic ultrasound-guided biopsy was performed to rule out primary pancreatic cancer, revealing moderately active chronic inflammation associated with immunotherapy. Nivolumab treatment was interrupted for 2 weeks, during which pancreatic enzyme levels improved. Treatment was resumed thereafter. The patient continued with monthly nivolumab applications, maintaining a complete response. without changes in imaging or laboratory test results. CONCLUSIONS This case is atypical for autoimmune pancreatitis owing to the absence of corticosteroid intervention, self-limiting nature of inflammation, and lack of inflammatory recurrence despite the continued use of immunotherapy.
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