Back to Search
Start Over
Acute kidney injury after CAR-T cell therapy: exploring clinical patterns, management, and outcomes.
- Source :
-
Clinical kidney journal [Clin Kidney J] 2024 May 30; Vol. 17 (6), pp. sfae123. Date of Electronic Publication: 2024 May 30 (Print Publication: 2024). - Publication Year :
- 2024
-
Abstract
- Background: Acute kidney injury (AKI) has been reported after CAR-T cells, but available data are limited. We sought to describe the incidence of AKI in a cohort of patients hospitalized in the intensive care unit (ICU) following CAR-T cell reinjection, identify the primary factors linked to the onset of AKI, and ascertain the key determinants associated with kidney outcomes and mortality.<br />Methods: We retrospectively analyzed 119 patients hospitalized in ICU after CAR-T cell therapy between 2017 and 2023. Factors associated with AKI, mortality, and kidney sequelae were identified using multivariate analyses.<br />Results: Of the 119 patients, 41 patients fulfilled diagnostic criteria of AKI (34%). By multivariate analysis, grade ≥3 cytokine release syndrome (CRS) [OR = 1.20 CI95% (1.01-1.43)] and elevated lactate dehydrogenase (LDH) levels at admission [OR = 1.44 CI95% (1.04-1.99)] were significantly associated with the occurrence of AKI during ICU stay. AKI KDIGO ≥2 was an independent risk factor for hospital mortality [OR = 1.50 (1.22-1.85), P  < 0.001]. Nine out of 12 (75%) and 6/9 (67%) patients who had experienced AKI and survived had chronic kidney disease (CKD) at 6 months and 1 year, respectively. We did not identify any specific factor associated with kidney recovery.<br />Conclusion: AKI may occur in ICU patients receiving CAR-T cell therapy, especially those who experience CRS and exhibit elevated LDH levels. Early recognition of AKI is of utmost importance as it substantially compromises survival in these patients. Future studies should aim to elucidate the underlying pathophysiological mechanisms of AKI in this context and pinpoint predictive factors for long-term risks of CKD.<br />Competing Interests: S.V. reports non-financial support from Pfizer, personal fees from Gilead-Kite, and personal fees from Sanofi. C.T. reports non-financial support from BMS-Celgene, Janssen, Gilead, personal fees from Gilead, Kite, Takeda, Novartis, BMS-Celgene, Astrazeneca, Janssen, Sanofiu, and Roche. F.R. reports personal fees from Kite, Gilead, and Jazz Pharmaceuticals. L.Z. reports receiving fees for lectures for MSD and Sanofi and a research grant from Jazz Pharmaceuticals. Other authors declare that they have no competing interests.<br /> (© The Author(s) 2024. Published by Oxford University Press on behalf of the ERA.)
Details
- Language :
- English
- ISSN :
- 2048-8505
- Volume :
- 17
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Clinical kidney journal
- Publication Type :
- Academic Journal
- Accession number :
- 38915438
- Full Text :
- https://doi.org/10.1093/ckj/sfae123