AACE Clinical Case Reports (Jan 2017)

Nivolumab-Induced Isolated Adrenal Insufficiency: A Case Report

  • Rebecca Neril, MD,
  • Julie Lorton, MD,
  • Joel Zonszein, MD, CDE, FACE, FACP

DOI
https://doi.org/10.4158/ep161491.cr
Journal volume & issue
Vol. 3, no. 3
pp. e210 – e212

Abstract

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ABSTRACT: Objective: Novel autoimmune therapies such as nivolumab, an antibody that blocks the programmed death-1 receptor (PD-1), have revolutionized management of patients with cancer. Autoimmune therapies, however, can be associated with immune-related adverse effects. Cases of pituitary and thyroid dysfunction have been previously reported. We describe a case of isolated adrenocorticotropic hormone (ACTH) deficiency associated with the immune checkpoint inhibitor nivolumab in a patient with non-small cell adenocarcinoma.Methods: The clinical presentation, laboratory data, and imaging studies for the acute episode of adrenal insufficiency are described, as well as literature review.Results: An 84-year-old male with stage IV non-small cell lung cancer (NSCLC) was hospitalized for hypotension, malaise, and confusion while undergoing chemotherapy with nivolumab. Endocrine evaluation showed a morning serum cortisol level of 1.1 μg/dL (reference range, 5 to 25 μg/dL), with an ACTH level of 9 pg/mL (reference range, 6 to 50 pg/mL). A 6-hour ACTH stimulation test showed a basal serum cortisol of 0.7 μg/dL that increased to 14.7 μg/dL. Further evaluation revealed normal anterior pituitary function and normal contrast-enhanced magnetic resonance imaging. Treatment with steroid hormone replacement showed clinical improvement.Conclusion: This case highlights a unique presentation of isolated ACTH deficiency in a patient with NSCLC treated with the PD-1 inhibitor nivolumab. It is critical to recognize side effects that immunotherapy may have in the endocrine system and treat appropriately.Abbreviations:ACTH = adrenocorticotropic hormoneCTLA-4 = cytotoxic T-lymphocyte-associated protein 4IRAEs = immune-related adverse effectsPD-1 = programmed death-1 receptorTSH = thyroid-stimulating hormone