2023
DOI: 10.3390/jcm12051985
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Hemophagocytic Lymphohistiocytosis Associated with Immunological Checkpoint Inhibitors: A Pharmacovigilance Study

Abstract: Background: Acquired hemophagocytic lymphohistiocytosis (HLH) is a rare but potentially fatal condition characterized by hyperactivation of macrophages and cytotoxic lymphocytes, combining a series of non-specific clinical symptoms and laboratory disorders. Etiologies are multiple: infectious (mainly viral) but also oncologic, autoimmune or drug-induced. Immune checkpoint inhibitors (ICI) are recent anti-tumor agents associated with a novel profile of adverse events triggered by immune system over-activation. … Show more

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Cited by 15 publications
(10 citation statements)
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“…According to the HLH-2004 and Hscore diagnostic criteria, common symptoms in patients with HLH include fever and splenomegaly ( 123 , 124 ). Typical laboratory findings include 2 or 3 lineages of peripheral blood cytopenias, hypertriglyceridemia, hypofibrinogenemia, elevated serum ferritin, and sCD25 ( 125 ). The biopsy can reveal hemophagocytosis in the bone marrow, spleen, or lymph nodes ( 126 ).…”
Section: Etiology Of Fever Of Unknown Origin Induced By Icismentioning
confidence: 99%
“…According to the HLH-2004 and Hscore diagnostic criteria, common symptoms in patients with HLH include fever and splenomegaly ( 123 , 124 ). Typical laboratory findings include 2 or 3 lineages of peripheral blood cytopenias, hypertriglyceridemia, hypofibrinogenemia, elevated serum ferritin, and sCD25 ( 125 ). The biopsy can reveal hemophagocytosis in the bone marrow, spleen, or lymph nodes ( 126 ).…”
Section: Etiology Of Fever Of Unknown Origin Induced By Icismentioning
confidence: 99%
“…Patients typically present with fever, organomegaly, pancytopenia, significantly elevated ferritin and low fibrinogen. Features of haemophagocytosis may be evident on bone marrow aspiration, but not universally [ 62 , 63 ]. The diagnosis of HLH is often delayed due to lack of clinician awareness of the condition as well as overlapping differential diagnoses with similar symptoms and laboratory abnormalities.…”
Section: Haematological Toxicitymentioning
confidence: 99%
“…Hemophagocytic lymphohistiocytosis (HLH) is less common and, in contrast to other hematological irAEs, is more frequently linked to anti-CTLA4 treatment [139,142,145]. HLH also differs from other hematological toxicities due to the high mortality rate despite immunosuppressive treatment [139].…”
Section: Hematological Iraesmentioning
confidence: 99%