High pretreatment disease burden as a risk factor for infectious complications following CD19 chimeric antigen receptor T-cell therapy for large B-cell lymphoma.


Journal

HemaSphere
ISSN: 2572-9241
Titre abrégé: Hemasphere
Pays: United States
ID NLM: 101740619

Informations de publication

Date de publication:
Jan 2024
Historique:
received: 29 06 2023
accepted: 22 11 2023
medline: 4 3 2024
pubmed: 4 3 2024
entrez: 4 3 2024
Statut: epublish

Résumé

Infection has emerged as the chief cause of non-relapse mortality (NRM) post CD19-targeting chimeric antigen receptor T-cell therapy (CAR-T) therapy. Even though up to 50% of patients may remain infection-free, many suffer multiple severe, life-threatening, or fatal infectious events. The primary aim of this study was to explore severe and life-threatening infections post licensed CAR-T therapy in large B-cell lymphoma, with a focus on the role of disease burden and disease sites in assessing individual risk. We sought to understand the cohort of patients who experience ≥2 infections and those at the highest risk of infectious NRM. Our analysis identifies a higher disease burden after bridging therapy as associated with infection events. Those developing ≥2 infections emerged as a uniquely high-risk cohort, particularly if the second (or beyond) infection occurred during an episode of immune effector cell-associated neurotoxicity syndrome (ICANS) or while on steroids and/or anakinra for ICANS. Herein, we also describe the first reported cases of "CAR-T cold sepsis," a phenomenon characterized by the lack of an appreciable systemic inflammatory response at the time of detection of infection. We propose a risk-based strategy to encourage heightened clinician awareness of cold sepsis, with a view to reducing NRM.

Identifiants

pubmed: 38434533
doi: 10.1002/hem3.29
pii: HEM329
pmc: PMC10878197
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e29

Informations de copyright

© 2024 The Authors. HemaSphere published by John Wiley & Sons Ltd on behalf of European Hematology Association.

Déclaration de conflit d'intérêts

M. O. R.: Honoraria Kite Gilead, Novartis, and Janssen, Advisory boards Kite Gilead and Autolus, conference support Kite Gilead and Novartis. S. M. C.: Employee of AstraZeneca Ltd. N. S.: Speaker fees Kite Gilead, Pfizer and Shionogi, research grant Kite Gilead. K. P. L. C.: Honoraria Kite Gilead. A. K.: Kite Gilead conference support, honoraria, advisory board, Novartis: honoraria, research funding, Advisory board: Roche, Abbvie, BMS. C. R.: Advisory boards and speakers fees Novartis, Kite Gilead, BMS, Amgen, Autolus. R. S.: Kite Gilead speakers bureau, honoraria, conference travel, Novartis speakers bureau, honoraria, conference travel. The other authors declare no conflict of interest.

Auteurs

Maeve A O'Reilly (MA)

Department of Haematology University College London Hospital London UK.
University College London Cancer Institute London UK.

Lorna Neill (L)

Department of Haematology University College London Hospital London UK.

Simon M Collin (SM)

Bristol Medical School University of Bristol Bristol UK.

Neil Stone (N)

Department of Infectious Diseases University College London Hospital London UK.

Deborah Springell (D)

Department of Haematology University College London Hospital London UK.

Jeremy Mensah (J)

Department of Haematology King's College London Hospital London UK.

Kathleen P L Cheok (KPL)

Department of Haematology University College London Hospital London UK.

Katarzyna Jalowiec (K)

Department of Haematology University College London Hospital London UK.

Reuben Benjamin (R)

Department of Haematology King's College London Hospital London UK.

Andrea Kuhnl (A)

Department of Haematology King's College London Hospital London UK.

Claire Roddie (C)

Department of Haematology University College London Hospital London UK.
University College London Cancer Institute London UK.

Robin Sanderson (R)

Department of Haematology King's College London Hospital London UK.

Classifications MeSH