2017
DOI: 10.1093/annonc/mdx113
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Pembrolizumab associated hemophagocytic lymphohistiocytosis

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Cited by 46 publications
(22 citation statements)
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“…HLH, an uncommon but previously described and potentially fatal hematologic disorder , was also reported in 26 cases. HLH can be triggered by underlying malignancy but has also been described as complicating ICIs.…”
Section: Resultsmentioning
confidence: 98%
“…HLH, an uncommon but previously described and potentially fatal hematologic disorder , was also reported in 26 cases. HLH can be triggered by underlying malignancy but has also been described as complicating ICIs.…”
Section: Resultsmentioning
confidence: 98%
“…On literature review, the case reports discussing immunotherapy-induced HLH have described a wide range of underlying malignancies including Squamous Cell Carcinoma of the Lung, Urothelial Carcinoma, Thymic Carcinoma, Merkel Cell Carcinoma, Breast Cancer, and Melanoma however to our knowledge this is the first report of immunotherapy-induced HLH in a HNSCC patient [3][4][5][6][7][8][9][10][11]. The time to HLH onset after starting immunotherapy has been shown to be highly variable, ranging from less than a month after receiving either pembrolizumab, nivolumab, or combination ipilimumab/nivolumab to over a year in a patient treated with pembrolizumab [3,4,7].…”
Section: Discussionmentioning
confidence: 95%
“…To our knowledge, there have only been three previous reports on ICI-related HLH. Two of them involved melanoma and bladder cancer (12,13). The other one referred to a lung cancer patient on pembrolizumab without rheumatologic conditions (14).…”
Section: Discussionmentioning
confidence: 99%