2019
DOI: 10.1007/s10147-019-01490-2
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Immune checkpoint inhibitor-induced sarcoidosis-like granulomas

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Cited by 42 publications
(30 citation statements)
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“…Functional lung tests performed in some cases showed either a moderate restrictive pattern and reduced carbon monoxide diffusing capacity [93] or were normal [101,102]. Patients developing ICI-induced sarcoid-like reactions were usually asymptomatic and the majority did not mandate permanent ICI discontinuation or systemic treatment [81,94,103], although ICI discontinuation and/or additional steroid treatment became necessary for resolution of granulomatous reactions in some cases. For cutaneous granulomatosis, topical steroids have been proven effective.…”
Section: Sarcoidosis and Sarcoid-like Reactionsmentioning
confidence: 99%
“…Functional lung tests performed in some cases showed either a moderate restrictive pattern and reduced carbon monoxide diffusing capacity [93] or were normal [101,102]. Patients developing ICI-induced sarcoid-like reactions were usually asymptomatic and the majority did not mandate permanent ICI discontinuation or systemic treatment [81,94,103], although ICI discontinuation and/or additional steroid treatment became necessary for resolution of granulomatous reactions in some cases. For cutaneous granulomatosis, topical steroids have been proven effective.…”
Section: Sarcoidosis and Sarcoid-like Reactionsmentioning
confidence: 99%
“…The development of sarcoid‐like granulomas with checkpoint inhibition may mimic disease progression and pose a clinical conundrum which may impact treatment decisions. The most common sites of involvement are the mediastinal and hilar lymph nodes (71% of cases), lung parenchyma (60% of cases), and skin (54.5% of cases) .…”
Section: Discussionmentioning
confidence: 99%
“…Sarcoidosis is a granulomatous disease characterized by the formation of non‐caseating granulomas in multiple organ systems . Sarcoid‐like granulomatous inflammation is an uncommon irAE that has been associated with inhibition of cytotoxic T lymphocyte antigen‐4 (CTLA‐4) with ipilimumab, programmed death‐1 (PD‐1) with nivolumab and pembrolizumab, and PD‐L1 with atezolizumab and avelumab . We report a case of sarcoid‐like granulomatous lymphadenopathy associated with durvalumab, an anti‐PD‐L1 selective human immunoglobulin G1 (IgG1) monoclonal antibody in a woman with lung adenocarcinoma.…”
Section: Introductionmentioning
confidence: 99%
“…Sarcoidosis presenting with hilar and mediastinal lymphadenopathy was reported in a lung cancer patient who received carboplatin/pemetrexed and pembrolizumab . T helper‐1 and T helper‐17 cells may play a role in the development of sarcoidosis . It is important to take a biopsy to differentiate sarcoidosis and disease progression.…”
Section: Toxicity Profilementioning
confidence: 99%
“…14 T helper-1 and T helper-17 cells may play a role in the development of sarcoidosis. 15 It is important to take a biopsy to differentiate sarcoidosis and disease progression. Most patients required discontinuation of therapy completely for a short period of time as well as immunosuppressant treatment.…”
Section: Toxicity Profilementioning
confidence: 99%