Hyperinflammatory syndrome resembling haemophagocytic lymphohistiocytosis following axicabtagene ciloleucel and brexucabtagene autoleucel

Timothy J. Porter, Ana Lazarevic, Jamie E. Ziggas, Ephraim Fuchs, Kiryoung Kim, Helen Byrnes, Leo Luznik, Javier Bolaños-Meade, Syed Abbas Ali, Nirali N. Shah, Nina Wagner-Johnston, Tania Jain

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish (US)
Pages (from-to)720-727
Number of pages8
JournalBritish journal of haematology
Volume199
Issue number5
DOIs
StatePublished - Dec 2022

Keywords

  • CAR T cells
  • HLH-like syndrome
  • delayed hyperinflammatory syndrome

ASJC Scopus subject areas

  • Hematology

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