Pulmonary sarcoid‐like granulomatosis induced by nivolumab

H Montaudié, J Pradelli, T Passeron… - British Journal of …, 2017 - academic.oup.com
H Montaudié, J Pradelli, T Passeron, JP Lacour, S Leroy
British Journal of Dermatology, 2017academic.oup.com
The use of antibodies against programmed death (PD) 1, such as nivolumab and
pembrolizumab, has dramatically improved the prognosis of patients with advanced
melanoma. Nivolumab is also approved in advanced squamous cell nonsmall‐cell lung
cancer. These immunotherapies are associated with a unique set of toxicities termed
immune‐related adverse events, which are different from toxicities observed with
conventional cytotoxic chemotherapy. We report the case of a 56‐year‐old man who was …
Summary
The use of antibodies against programmed death (PD)1, such as nivolumab and pembrolizumab, has dramatically improved the prognosis of patients with advanced melanoma. Nivolumab is also approved in advanced squamous cell nonsmall‐cell lung cancer. These immunotherapies are associated with a unique set of toxicities termed immune‐related adverse events, which are different from toxicities observed with conventional cytotoxic chemotherapy. We report the case of a 56‐year‐old man who was diagnosed with metastatic melanoma and who received nivolumab. One week after the second infusion, he developed pulmonary symptoms, dry eye syndrome and a bilateral swelling of the parotid glands. Investigations were negative for infection. The bronchoalveolar lavage differential cell count showed 32% lymphocytes with an increased CD4 : CD8 ratio, and bronchial biopsies revealed noncaseating epithelioid granulomas, without malignant cells. The clinical and radiological courses were rapidly favourable with oral corticosteroid. This case illustrates that sarcoidosis can be induced by nivolumab treatment. With the increasing use of anti‐PD1 inhibitors in patients with advanced melanoma and squamous cell nonsmall‐cell lung cancer, clinicians should be aware of this potential associated immune‐related adverse event.
Oxford University Press