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Hyperinflammatory syndrome resembling haemophagocytic lymphohistiocytosis following axicabtagene ciloleucel and brexucabtagene autoleucel.

Authors :
Porter TJ
Lazarevic A
Ziggas JE
Fuchs E
Kim K
Byrnes H
Luznik L
Bolaños-Meade J
Ali SA
Shah NN
Wagner-Johnston N
Jain T
Source :
British journal of haematology [Br J Haematol] 2022 Dec; Vol. 199 (5), pp. 720-727. Date of Electronic Publication: 2022 Sep 16.
Publication Year :
2022

Abstract

Haemophagocytic lymphohistiocytosis-like toxicity following chimeric antigen receptor T cells (CAR-HLH) is being increasingly recognized, while published data are limited and criteria for recognition are elusive. We describe three patients who developed CAR-HLH after infusion of brexucabtagene autoleucel (n = 2) or axicabtagene ciloleucel (n = 1). All three patients presented following cytokine release syndrome, with fever, recurrent or worsening cytopenias, hyperferritinaemia, elevated soluble interleukin (IL)-2 receptor, hypofibrinogenaemia, hypertriglyceridaemia, elevated liver transaminases, and decreasing C-reactive protein and IL-6. Clinical improvement following treatment with anakinra (n = 2) and ruxolitinib (n = 1) was observed. Our report offers an opportunity for prompt recognition and initiation of potentially life-saving treatment for CAR-HLH.<br /> (© 2022 British Society for Haematology and John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-2141
Volume :
199
Issue :
5
Database :
MEDLINE
Journal :
British journal of haematology
Publication Type :
Academic Journal
Accession number :
36111395
Full Text :
https://doi.org/10.1111/bjh.18454