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Acute Kidney Injury after Pembrolizumab-Induced Adrenalitis and Adrenal Insufficiency

Pembrolizumab is an immune checkpoint inhibitor that targets the programmed cell death protein 1 (PD-1) antigen and induces an immune response against tumor tissues. It has been successful in inducing remission in patients with severe metastatic disease, often refractory to other chemotherapeutic ag...

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Autores principales: Hanna, Ramy M., Selamet, Umut, Bui, Patrick, Sun, Shih-Fan, Shenouda, Olivia, Nobakht, Niloofar, Barsoum, Marina, Arman, Farid, Rastogi, Anjay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120420/
https://www.ncbi.nlm.nih.gov/pubmed/30197906
http://dx.doi.org/10.1159/000491631
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author Hanna, Ramy M.
Selamet, Umut
Bui, Patrick
Sun, Shih-Fan
Shenouda, Olivia
Nobakht, Niloofar
Barsoum, Marina
Arman, Farid
Rastogi, Anjay
author_facet Hanna, Ramy M.
Selamet, Umut
Bui, Patrick
Sun, Shih-Fan
Shenouda, Olivia
Nobakht, Niloofar
Barsoum, Marina
Arman, Farid
Rastogi, Anjay
author_sort Hanna, Ramy M.
collection PubMed
description Pembrolizumab is an immune checkpoint inhibitor that targets the programmed cell death protein 1 (PD-1) antigen and induces an immune response against tumor tissues. It has been successful in inducing remission in patients with severe metastatic disease, often refractory to other chemotherapeutic agents. The risk of injury of other organ systems has been noted with reported cases of glomerular disease and endocrine disease. In addition, hypophysitis as well as dermatological and gastroenterological side effects have been reported. Renal injury with immune checkpoint inhibitors like nivolumab and pembrolizumab is usually mediated via interstitial nephritis, though glomerular disease presentations like anti-neutrophil cytoplasmic antibody-associated vasculitis, immune complex disease, and thrombotic microangiopathy have also been reported. We report a 70-year-old Caucasian male who underwent treatment with pembrolizumab for adenocarcinoma of the lung. He developed acute adrenal insufficiency and concomitant severe hypotension upon presentation. He did not require renal replacement therapy, rather his severe acute kidney injury resolved with hydration, normalization of blood pressures with vasopressors, and treatment with high-dose corticosteroids. His urinary indices (fractional excretion of urea, FEUrea) and clinical course were highly suspicious for acute tubular necrosis that resolved quickly after treating his underlying adrenalitis. The urinary sediment, proteinuria, and clinical course were not typical for the usually expected renal lesion of interstitial nephritis in patients treated with immune checkpoint inhibitors.
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spelling pubmed-61204202018-09-07 Acute Kidney Injury after Pembrolizumab-Induced Adrenalitis and Adrenal Insufficiency Hanna, Ramy M. Selamet, Umut Bui, Patrick Sun, Shih-Fan Shenouda, Olivia Nobakht, Niloofar Barsoum, Marina Arman, Farid Rastogi, Anjay Case Rep Nephrol Dial Case Report Pembrolizumab is an immune checkpoint inhibitor that targets the programmed cell death protein 1 (PD-1) antigen and induces an immune response against tumor tissues. It has been successful in inducing remission in patients with severe metastatic disease, often refractory to other chemotherapeutic agents. The risk of injury of other organ systems has been noted with reported cases of glomerular disease and endocrine disease. In addition, hypophysitis as well as dermatological and gastroenterological side effects have been reported. Renal injury with immune checkpoint inhibitors like nivolumab and pembrolizumab is usually mediated via interstitial nephritis, though glomerular disease presentations like anti-neutrophil cytoplasmic antibody-associated vasculitis, immune complex disease, and thrombotic microangiopathy have also been reported. We report a 70-year-old Caucasian male who underwent treatment with pembrolizumab for adenocarcinoma of the lung. He developed acute adrenal insufficiency and concomitant severe hypotension upon presentation. He did not require renal replacement therapy, rather his severe acute kidney injury resolved with hydration, normalization of blood pressures with vasopressors, and treatment with high-dose corticosteroids. His urinary indices (fractional excretion of urea, FEUrea) and clinical course were highly suspicious for acute tubular necrosis that resolved quickly after treating his underlying adrenalitis. The urinary sediment, proteinuria, and clinical course were not typical for the usually expected renal lesion of interstitial nephritis in patients treated with immune checkpoint inhibitors. S. Karger AG 2018-08-10 /pmc/articles/PMC6120420/ /pubmed/30197906 http://dx.doi.org/10.1159/000491631 Text en Copyright © 2018 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Case Report
Hanna, Ramy M.
Selamet, Umut
Bui, Patrick
Sun, Shih-Fan
Shenouda, Olivia
Nobakht, Niloofar
Barsoum, Marina
Arman, Farid
Rastogi, Anjay
Acute Kidney Injury after Pembrolizumab-Induced Adrenalitis and Adrenal Insufficiency
title Acute Kidney Injury after Pembrolizumab-Induced Adrenalitis and Adrenal Insufficiency
title_full Acute Kidney Injury after Pembrolizumab-Induced Adrenalitis and Adrenal Insufficiency
title_fullStr Acute Kidney Injury after Pembrolizumab-Induced Adrenalitis and Adrenal Insufficiency
title_full_unstemmed Acute Kidney Injury after Pembrolizumab-Induced Adrenalitis and Adrenal Insufficiency
title_short Acute Kidney Injury after Pembrolizumab-Induced Adrenalitis and Adrenal Insufficiency
title_sort acute kidney injury after pembrolizumab-induced adrenalitis and adrenal insufficiency
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120420/
https://www.ncbi.nlm.nih.gov/pubmed/30197906
http://dx.doi.org/10.1159/000491631
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