2017
DOI: 10.1016/j.ejca.2017.05.017
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Immune-related eosinophilia induced by anti-programmed death 1 or death-ligand 1 antibodies

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Cited by 58 publications
(61 citation statements)
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“…7 Given our stringent inclusion criteria, our objective here was to describe the patients with the most severe ICI-induced AEs; according to Bernard-Teissier et al these patients may account for up to 1-2% of people treated with ICIs. 6 We found that a high proportion of these patients developed Eo-irAEs (57%)suggesting that although blood eosinophilia is highly unusual, 6 it should not be neglected by attending physicians because severe eosinophil-related organ dysfunction is likely to occur. In the present study, we chose to include patients (n = 7) with an AEC >0.5 G/L at baseline (i.e.…”
Section: Discussionmentioning
confidence: 92%
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“…7 Given our stringent inclusion criteria, our objective here was to describe the patients with the most severe ICI-induced AEs; according to Bernard-Teissier et al these patients may account for up to 1-2% of people treated with ICIs. 6 We found that a high proportion of these patients developed Eo-irAEs (57%)suggesting that although blood eosinophilia is highly unusual, 6 it should not be neglected by attending physicians because severe eosinophil-related organ dysfunction is likely to occur. In the present study, we chose to include patients (n = 7) with an AEC >0.5 G/L at baseline (i.e.…”
Section: Discussionmentioning
confidence: 92%
“…Moreover, this time to onset was shorter in our study than in Berrnard-Teissier et al's retrospective observational study of 26 cases with a normal AEC at baseline and an AEC >0.5G/L 3 [0.6─31.3] months after ICI initiation. 6 Although the time course of eosinophilia onset has yet to be characterized, one can reasonably hypothesize that moderate-to-severe eosinophilia may have an early onset. Similarly, the median time to the AEC peak observed in our study (3.4 Figure 1.…”
Section: Discussionmentioning
confidence: 99%
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“…Most of the hema‐AEs manifested as monolineage cytopenia, or bilineage cytopenia such as thrombocytopenia with neutropenia, and even pancytopenia such as aplastic anemia. Other rare AEs include acquired hemophilia A, eosinophilia, large granular lymphocytosis (LGL), even life‐threatening diseases such as hemophagocytic lymphohistiocytosis., This article aims to provide a comprehensive description of hematological irAEs in cancer patients treated with ICIs and suggest preliminary treatment recommendations.…”
Section: Introductionmentioning
confidence: 99%