Decreased renal function predicts severe cytokine release syndrome after <scp>CAR</scp> ‐T‐cell therapy for large B‐cell lymphoma

decrease; 95% confidence interval [CI] 1.015-1.209; p = 0.022), higher ferritin (aHR 1.006 per 100 ng/mL; 95% CI 1.001-1.010; p = 0.016), C-reactive protein (CRP) (aHR 1.142 per mg/dL; 95% CI 1.091-1.195; p < 0.001) and lactate dehydrogenase (LDH) (aHR 1.073 per 100 U/L; 95% CI 1.008-1.142; p = 0.028) independently predicted grade ≥ 2 CRS. We then built a four-factor CRS pre-infusion risk evaluation model, cytokine release syndrome-pre-infusion risk evaluation (CRS-PRE), that stratified grade ≥ 2 CRS risk into low, intermediate and high groups with incidences of 2.8%, 26.0% and 50.0% respectively. Decreased eGFR, a surrogate of host renal reserve, with elevated ferritin, CRP and LDH emerged as predictors of high-grade CRS. The CRS-PRE may facilitate risk-adapted monitoring and intervention in clinical practice.

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Publication Details

Journal
British Journal of Haematology
Published
2026-04-15
DOI
https://doi.org/10.1111/bjh.70488
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00

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article

Decreased renal function predicts severe cytokine release syndrome after CAR ‐T‐cell therapy for large B‐cell lymphoma

Yoshihiro Umezawa, Tatsu Shimoyama, Tomoyasu Jo, Daisuke Kaji et al.
British Journal of Haematology
CAR-T cell therapy research
article

Decreased renal function predicts severe cytokine release syndrome after CAR ‐T‐cell therapy for large B‐cell lymphoma

Yoshihiro Umezawa, Tatsu Shimoyama, Tomoyasu Jo, Daisuke Kaji, Motohiro Kato, Yasuyuki Arai, Haryoon Kim, Shinichi Makita, Toshio Kitawaki, Satoshi Yoshihara, Kazuyuki Shimada, Takayuki Sato, Hideki Goto, Emiko Sakaida, Go Yamamoto, Keisuke Kataoka, Yasuhiro Nakashima, Akiyo Yoshida, Koji Kato, Masatoshi Sakurai, Nobuharu Fujii, Yoshiko Atsuta
article en

Abstract

decrease; 95% confidence interval [CI] 1.015-1.209; p = 0.022), higher ferritin (aHR 1.006 per 100 ng/mL; 95% CI 1.001-1.010; p = 0.016), C-reactive protein (CRP) (aHR 1.142 per mg/dL; 95% CI 1.091-1.195; p < 0.001) and lactate dehydrogenase (LDH) (aHR 1.073 per 100 U/L; 95% CI 1.008-1.142; p = 0.028) independently predicted grade ≥ 2 CRS. We then built a four-factor CRS pre-infusion risk evaluation model, cytokine release syndrome-pre-infusion risk evaluation (CRS-PRE), that stratified grade ≥ 2 CRS risk into low, intermediate and high groups with incidences of 2.8%, 26.0% and 50.0% respectively. Decreased eGFR, a surrogate of host renal reserve, with elevated ferritin, CRP and LDH emerged as predictors of high-grade CRS. The CRS-PRE may facilitate risk-adapted monitoring and intervention in clinical practice.

British Journal of Haematology
Aichi Medical University (JP), Keio University (JP), Kyoto University (JP), Tokyo Metropolitan Komagome Hospital (JP), Kurashiki Central Hospital (JP), Kyushu University Hospital (JP), Chiba University Hospital (JP), Okayama University Hospital (JP), Kanazawa University Hospital (JP), University of Tokyo Hospital (JP), Hokkaido University Hospital (JP), Kyoto University Hospital (JP), The Japanese Data Center for Hematopoietic Cell Transplantation (JP), Tokyo National Hospital (JP), Osaka City University Hospital (JP), Toranomon Hospital (JP), Osaka Metropolitan University (JP), Nagoya University (JP), The University of Tokyo (JP)
Ministry of Education, Culture, Sports, Science and Technology, Japan Society for the Promotion of Science
Openalex Percentile: Top 22%
CAR-T cell therapy research
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