| Literature DB >> 34263927 |
Melissa R Hines1, Camille Keenan2, Gabriela Maron Alfaro3, Cheng Cheng4, Yinmei Zhou4, Akshay Sharma5, Caitlin Hurley1,5, Kim E Nichols6, Stephen Gottschalk5, Brandon M Triplett5, Aimee C Talleur5.
Abstract
Chimeric antigen receptor T-cell (CAR T-cell) therapy is associated with significant toxicities secondary to immune activation, including a rare but increasingly recognised severe toxicity resembling haemophagocytic lymphohistiocytosis (carHLH). We report the development of carHLH in 14·8% of paediatric patients and young adults treated with CD19-specific CAR T-cell therapy with carHLH, occurring most commonly in those with high disease burden. The diagnosis and treatment of carHLH required a high index of suspicion and included multidrug immunomodulation with variable response to therapies. Compared to patients without carHLH, patients with carHLH had both reduced response to CAR T-cell therapy (P-value = 0·018) and overall survival (P-value = < 0·0001).Entities:
Keywords: chimeric antigen receptor T-cell therapy; cytokine release syndrome; haemophagocytic lymphohistiocytosis; refractory acute B-cell lymphoblastic leukaemia
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Year: 2021 PMID: 34263927 PMCID: PMC8756350 DOI: 10.1111/bjh.17662
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998