AKI in Patients Receiving Chimeric Antigen Receptor T Cells: Risk Factors and Characteristics

Background: Chimeric antigen receptor T-cell (CAR-T) therapy is a breakthrough in hematologic malignancies treatment but carries risks, including acute kidney injury (AKI). This study is intended to report the incidence and characteristics of AKI and potential associated factors in patients receiving CAR-T therapy. Methods: We analyzed 186 patients treated with CAR-T therapy in an academic institution, assessing AKI incidence, timing, severity, and associated risk factors within 100 days post-infusion of CAR-T product. AKI and Chronic Kidney Disease (CKD) were defined per KDIGO criteria and recorded from the day of infusion. Cytokine Release Syndrome (CRS) was graded based on the criteria of the American Society of Transplantation and Cellular Therapy. Chi-square test and Fischer's exact test were used for categorical values. T-Tests done where appropriate. Results: Among 186 patients (103 with multiple myeloma (MM), 75 with non-Hodgkin Lymphoma (NHL), and 8 with leukemia), 34% developed AKI (95% CI: 27%-40.7%) with similar incidence by cancer type. Most cases (77.8%) occurred within three weeks post-infusion. AKI was more common among African American individuals (57.7%, P = 0.015) and with older age compared to those without AKI (mean 67 vs. 62.3 years, P = 0.007). Patients with CKD were more likely to have AKI compared to those without (50.8% vs. 25.6%, P < 0.001). Overall CRS incidence was 82.8% (95% CI: 77.3% to 88.1%), and 35.1% had AKI although no statistical significance found when compared to those without CRS. Higher grades of CRS had higher incidence of AKI (grade 1 = 33.6%; Grade 2 = 36.7%, Grade 3 = 42.9%, P= 0.9). Most AKI episodes were Grade I (68.3%) and reversible; 74.6% recovered baseline kidney function, while 25.8% did not, two died within 100 days, 1 required dialysis. AKI post-infusion was common among patients with prior AKI (50.8%) (P < 0.001). Conclusion: AKI is a frequent and early complication of CAR-T therapy, particularly among African American patients, older individuals, those with CKD and prior history of AKI. While most cases are mild and reversible, further studies are needed to implement measures to potentially mitigate and lower the incidence of AKI in these individuals.

Authors

Institutions

Publication Details

Journal
Journal of the American Society of Nephrology
Published
2025-10-01
DOI
https://doi.org/10.1681/asn.2025gxgre87j
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

AKI in Patients Receiving Chimeric Antigen Receptor T Cells: Risk Factors and Characteristics

J. Curran Henson, Grant M. Spears, Toshali Pandey, Sruthi Vellanki et al.
Journal of the American Society of Nephrology
CAR-T cell therapy research
article

AKI in Patients Receiving Chimeric Antigen Receptor T Cells: Risk Factors and Characteristics

J. Curran Henson, Grant M. Spears, Toshali Pandey, Sruthi Vellanki, Nishank Jain, Bhavesh Mohan Lal, Anup Kumar Trikannad Ashwini Kumar, Zelalem Mekuria, Rahaf Omaish, Lean Alkhatib, Abedalrahman Almashayekh
article en

Abstract

Background: Chimeric antigen receptor T-cell (CAR-T) therapy is a breakthrough in hematologic malignancies treatment but carries risks, including acute kidney injury (AKI). This study is intended to report the incidence and characteristics of AKI and potential associated factors in patients receiving CAR-T therapy. Methods: We analyzed 186 patients treated with CAR-T therapy in an academic institution, assessing AKI incidence, timing, severity, and associated risk factors within 100 days post-infusion of CAR-T product. AKI and Chronic Kidney Disease (CKD) were defined per KDIGO criteria and recorded from the day of infusion. Cytokine Release Syndrome (CRS) was graded based on the criteria of the American Society of Transplantation and Cellular Therapy. Chi-square test and Fischer's exact test were used for categorical values. T-Tests done where appropriate. Results: Among 186 patients (103 with multiple myeloma (MM), 75 with non-Hodgkin Lymphoma (NHL), and 8 with leukemia), 34% developed AKI (95% CI: 27%-40.7%) with similar incidence by cancer type. Most cases (77.8%) occurred within three weeks post-infusion. AKI was more common among African American individuals (57.7%, P = 0.015) and with older age compared to those without AKI (mean 67 vs. 62.3 years, P = 0.007). Patients with CKD were more likely to have AKI compared to those without (50.8% vs. 25.6%, P < 0.001). Overall CRS incidence was 82.8% (95% CI: 77.3% to 88.1%), and 35.1% had AKI although no statistical significance found when compared to those without CRS. Higher grades of CRS had higher incidence of AKI (grade 1 = 33.6%; Grade 2 = 36.7%, Grade 3 = 42.9%, P= 0.9). Most AKI episodes were Grade I (68.3%) and reversible; 74.6% recovered baseline kidney function, while 25.8% did not, two died within 100 days, 1 required dialysis. AKI post-infusion was common among patients with prior AKI (50.8%) (P < 0.001). Conclusion: AKI is a frequent and early complication of CAR-T therapy, particularly among African American patients, older individuals, those with CKD and prior history of AKI. While most cases are mild and reversible, further studies are needed to implement measures to potentially mitigate and lower the incidence of AKI in these individuals.

Journal of the American Society of NephrologyVol. 36(10S)
University of Arkansas for Medical Sciences (US)
Openalex Percentile: Top 48%
CAR-T cell therapy research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.