Background

Nivolumab, a programmed cell death protein 1 (PD-1) antibody, and ipilimumab, a cytotoxic T-lymphocyte antigen 4 (CTLA-4) antibody, are immune checkpoint inhibitors (ICI) which have emerged as first- and second-line therapy of stage IV melanoma [1, 2]. However, they can induce immune-related adverse events (irAEs) involving a range of organs similar to auto-immune diseases [1, 3, 4]. The endocrine system is often affected [1, 3, 4], with disturbances of the thyroid and the pituitary gland being the most common endocrinopathies [1]. Inflammation of the thyroid gland can often lead to an initial hyperthyroidism and subsequent hypothyroidism. Inflammation of the pituitary gland can lead to insufficiencies of the thyroid, adrenal and gonadal axis. Also, rarer endocrinopathies such as adrenalitis have been described, but the course of such inflammations and also the pathomechanisms are less well-known.

Case report

Here, we report on a 53-year old patient with stage IV melanoma who was admitted to the hospital after he presented with generalized paresthesia, stiffness in both hands, a feeling of obstruction in his throat and mild dizziness. He had metastases in the liver, spleen, lung and bones but not in the brain (Fig. 1a). Treatment of his melanoma with nivolumab 1 mg/kg and ipilimumab 3 mg/kg was started 4 weeks earlier and two doses had been given before the time point of presentation. He reported a significant worsening of symptoms over the past few days. His medical history included arterial hypertension treated with valsartan and bisoprolol and intermittent stomach complaints treated with pantoprazole. He had no known auto-immune disorders before the treatment with nivolumab and ipilimumab was started. Serologies for hepatitis B and C virus were negative before the start and serum levels of TSH and free T4 were within the normal limits. At presentation, his vital signs showed no abnormalities. Physical examination was unremarkable with negative Chovestek’s and Trousseau’s signs. ECG showed a prolonged corrected QT interval (493 ms). Laboratory testing revealed hypocalcemia (calcium 1,35 mmol/l [normal range 2.10–2.65], albumin 38 g/l [normal range 35–52], ionized calcium 0,7 mmol/l [normal range 1,15-1,3]), marginal hypomagnesemia (0,69 mmol/l [normal range 0,70-1,00]) and hyperphosphatemia (1,75 mmol/l [normal range 0,8-1,5]. Intact parathyroid hormone (iPTH) level was inadequately low (7,2 pg/ml [normal range 15–65]), 25-hydroxy vitamin D₃ level was just above normal range (121 nmol/l [normal range 13.2–118]), venous blood gas showed normal pH of 7.418. There was no clinical sign of other auto-immune endocrinopathies, thyroid hormone and cortisol levels were normal.

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Fig. 1

Clinical response to nivolumab and ipilimumab. a, Lung lesion before the treatment with anti-CTLA-4 and anti-PD-1 antibodies and after 8 weeks. There was a marked regression with 8 weeks of the treatement. b, After 16 weeks of treatment, a complete metabolic response was observed in the ¹⁸FDG-PET/CT scan

The patient was diagnosed with acute symptomatic hypocalcemia most likely due to immune-mediated hypoparathyroidism and hospitalized for further treatment. He was given a total of 4 g calcium gluconate in divided doses and 3 g of magnesium sulfate (corresponding 12,15 mmol) intravenously. Oral calcitriol and calcium carbonate was started in parallel. Intact parathyroid hormone remained low even after normalization of magnesium. Symptoms subsided after elevation of calcium levels and the patient was discharged on oral treatment. However, two weeks later, he was readmitted with symptoms of hypocalcemia which was triggered by acute vomiting and severe diarrhea (7–8 stools per day, grade 3). No stool pathogens were identified. Colon biopsies revealed regenerative changes of crypt epithelia and focal surface epithelial defects suggestive of an immune-mediated colitis under PD-1 and CTLA-4 blockade. Thus, the patient was treated with prednisone at 2 mg/kg intravenously and upon persistence of symptoms switched to treatment with infliximab (5 mg/kg), which led to a rapid reduction of stool frequency and eventually resolution of the diarrhea. The steroid therapy was tapered slowly over the course of 4 weeks. The infliximab treatment was repeated once after 2 weeks. No further episode of diarrhea occurred. We interpreted the colitis most likely as a consequence of CTLA-4 blockade and therefore decided to continue the PD-1 blocking antibody nivolumab alone. The hypocalcemia was corrected by substitution therapy.

¹⁸F-FDG PET/CT at 5 months after initiation of checkpoint inhibitor therapy showed a complete metabolic remission and an almost complete regression of pulmonary, lymphogenic, splenic and hepatic lesions (Fig. 1b). No enlargement or hypermetabolism was detectable in the typical location of the parathyroid glands. Interestingly, the PTH was increasing during intensified immune suppression with infliximab, but the levels were sinking again during tapering of steroids (Fig. 2). The patient had to be constantly substituted with calcium and in addition, was treated with calcitriol. In order to investigate the reason for the hypoparathyroidism, we analyzed antibodies against the calcium sensing receptor (CaSR). We found detectable levels of auto-antibodies against CaSR in this patient. However, when we analyzed control patients that had also undergone immunotherapy with nivolumab and ipilimumab for melanoma, similar levels of auto-antibodies against CaSR were found, suggesting that the detected antibody concentrations were probably not pathogenic and the test for such low concentrations is most likely unspecific. During the course of the treatment, the patient developed 8 months after start of the immunotherapy an inflammatory oligoarthritis with affection of the right knee and the right ankle. The oligoarthritis was well manageable with local steroid injections. Since a complete response was achieved, we decided at this point to stop the PD-1 blockade. After stopping nivolumab, the calcium substitution could be reduced.

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Fig. 2

Blood levels of calcium, magnesium, phosphate, intact PTH and 25-OH-vitamin D over the time course of the therapy