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      New-onset insulin-dependent diabetes due to nivolumab

      research-article
      1 , 2 , 3 , 1
      Endocrinology, Diabetes & Metabolism Case Reports
      Bioscientifica Ltd
      Geriatric, Male, White, United States, Pancreas, Diabetes, Insulin, Diabetes mellitus type 1, Diabetic ketoacidosis, Autoimmune disorders, Metastatic carcinoma, Hyperglycaemia, Metabolic acidosis, Hyperkalaemia, Hyponatraemia, Diabetes mellitus type 1, Diabetic ketoacidosis, Hyperpnoea, Hyperglycaemia, Metabolic acidosis, Dyspnoea, Abdominal pain, Fatigue, Polyuria, Hyponatraemia, Hyperkalaemia, Glucose (blood), X-ray, Ketones (urine), Glucose (blood, fasting), Haemoglobin A1c, C-peptide (blood), CT scan, Red blood cell count, White blood cell count, White blood cell differential count, Platelet count, Sodium, Potassium, Chloride, Bicarbonate, Urea and electrolytes, Albumin, Magnesium, Calcium (serum), Brain natriuretic peptide, Glucose (urine), Urinalysis, Fluid repletion, Nivolumab, Insulin, Insulin Aspart, Insulin glargine, Aspirin, Lisinopril, Tyrosine-kinase inhibitors, Oncology, Unusual effects of medical treatment, March, 2018

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          Summary

          Nivolumab, a monoclonal antibody against programmed cell death-1 receptor, is increasingly used in advanced cancers. While nivolumab use enhances cancer therapy, it is associated with increased immune-related adverse events. We describe an elderly man who presented in ketoacidosis after receiving nivolumab for metastatic renal cell carcinoma. On presentation, he was hyperpneic and laboratory analyses showed hyperglycemia and anion-gapped metabolic acidosis consistent with diabetic ketoacidosis. No other precipitating factors, besides nivolumab, were identified. Pre-nivolumab blood glucose levels were normal. The patient responded to treatment with intravenous fluids, insulin and electrolyte replacement. He was diagnosed with insulin-dependent autoimmune diabetes mellitus secondary to nivolumab. Although nivolumab was stopped, he continued to require multiple insulin injection therapy till his last follow-up 7 months after presentation. Clinicians need to be alerted to the development of diabetes mellitus and diabetic ketoacidosis in patients receiving nivolumab.

          Learning points:
          • Diabetic ketoacidosis should be considered in the differential of patients presenting with metabolic acidosis following treatment with antibodies to programmed cell death-1 receptor (anti-PD-1).

          • Autoimmune islet cell damage is the presumed mechanism for how insulin requiring diabetes mellitus can develop de novo following administration of anti-PD-1.

          • Because anti-PD-1 works by the activation of T-cells and reduction of ‘self-tolerance’, other autoimmune disorders are likely to be increasingly recognized with increased use of these agents.

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          Most cited references39

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          Tumor immunotherapy directed at PD-1.

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            The Programmed Death-1 (PD-1) Pathway Regulates Autoimmune Diabetes in Nonobese Diabetic (NOD) Mice

            Programmed death-1 (PD-1) receptor, an inhibitory costimulatory molecule found on activated T cells, has been demonstrated to play a role in the regulation of immune responses and peripheral tolerance. We investigated the role of this pathway in the development of autoimmune diabetes. PD-1 or PD-L1 but not PD-L2 blockade rapidly precipitated diabetes in prediabetic female nonobese diabetic (NOD) mice regardless of age (from 1 to 10-wk-old), although it was most pronounced in the older mice. By contrast, cytotoxic T lymphocyte–associated antigen 4 (CTLA-4) blockade induced disease only in neonates. Male NOD mice also developed diabetes after PD-1–PD-L1 pathway blockade, but NOR mice, congenic to NOD but resistant to the development of diabetes, did not. Insulitis scores were significantly higher and frequency of interferon γ–producing GAD-reactive splenocytes was increased after PD-1–PD-L1 pathway blockade compared with controls. Interestingly, PD-L1 but not PD-L2 was found to be expressed on inflamed islets of NOD mice. These data demonstrate a central role for PD-1–PD-L1 interaction in the regulation of induction and progression of autoimmune diabetes in the NOD mouse and provide the rationale to develop new therapies to target this costimulatory pathway in this disease.
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              Survival, Durable Response, and Long-Term Safety in Patients With Previously Treated Advanced Renal Cell Carcinoma Receiving Nivolumab.

              Blockade of the programmed death-1 inhibitory cell-surface molecule on immune cells using the fully human immunoglobulin G4 antibody nivolumab mediates tumor regression in a portion of patients with advanced treatment-refractory solid tumors. We report clinical activity, survival, and long-term safety in patients with advanced renal cell carcinoma (RCC) treated with nivolumab in a phase I study with expansion cohorts.

                Author and article information

                Journal
                Endocrinol Diabetes Metab Case Rep
                Endocrinol Diabetes Metab Case Rep
                EDM
                Endocrinology, Diabetes & Metabolism Case Reports
                Bioscientifica Ltd (Bristol )
                2052-0573
                28 March 2018
                2018
                : 2018
                : 17-0174
                Affiliations
                [1 ]Divisions of Pulmonary and Critical Care Medicine , Mayo Clinic, Jacksonville, Florida, USA
                [2 ]Divisions of Endocrinology , Mayo Clinic, Jacksonville, Florida, USA
                [3 ]Divisions of Hematology and Oncology , Mayo Clinic, Jacksonville, Florida, USA
                Author notes
                Correspondence should be addressed to A S Lee Email: lee.augustine@ 123456mayo.edu
                Article
                EDM170174
                10.1530/EDM-17-0174
                5881429
                a24da127-ebfe-4df5-8e94-32e47169b210
                © 2018 The authors

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.

                History
                : 19 February 2018
                : 02 March 2018
                Categories
                Geriatric
                Male
                White
                United States
                Pancreas
                Diabetes
                Insulin
                Diabetes Mellitus Type 1
                Diabetic Ketoacidosis
                Autoimmune Disorders
                Metastatic Carcinoma
                Hyperglycaemia
                Metabolic Acidosis
                Hyperkalaemia
                Hyponatraemia
                Diabetes mellitus type 1
                Diabetic ketoacidosis
                Hyperpnoea
                Hyperglycaemia
                Metabolic acidosis
                Dyspnoea
                Abdominal pain
                Fatigue
                Polyuria
                Hyponatraemia
                Hyperkalaemia
                Glucose (blood)
                X-ray
                Ketones (urine)
                Glucose (blood, fasting)
                Haemoglobin A1c
                C-peptide (blood)
                CT scan
                Red blood cell count
                White blood cell count
                White blood cell differential count
                Platelet count
                Sodium
                Potassium
                Chloride
                Bicarbonate
                Urea and electrolytes
                Albumin
                Magnesium
                Calcium (serum)
                Brain natriuretic peptide
                Glucose (urine)
                Urinalysis
                Fluid repletion
                Nivolumab
                Insulin
                Insulin Aspart
                Insulin glargine
                Aspirin
                Lisinopril
                Tyrosine-kinase inhibitors
                Oncology
                Unusual Effects of Medical Treatment
                Unusual Effects of Medical Treatment

                geriatric,male,white,united states,pancreas,diabetes,insulin,diabetes mellitus type 1,diabetic ketoacidosis,autoimmune disorders,metastatic carcinoma,hyperglycaemia,metabolic acidosis,hyperkalaemia,hyponatraemia,hyperpnoea,dyspnoea,abdominal pain,fatigue,polyuria,glucose (blood),x-ray,ketones (urine),glucose (blood, fasting),haemoglobin a1c,c-peptide (blood),ct scan,red blood cell count,white blood cell count,white blood cell differential count,platelet count,sodium,potassium,chloride,bicarbonate,urea and electrolytes,albumin,magnesium,calcium (serum),brain natriuretic peptide,glucose (urine),urinalysis,fluid repletion,nivolumab,insulin aspart,insulin glargine,aspirin,lisinopril,tyrosine-kinase inhibitors,oncology,unusual effects of medical treatment,march,2018

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