Clinical Impact of Cytokine Release Syndrome on Prolonged Hematotoxicity after Chimeric Antigen Receptor T Cell Therapy: KyoTox A-Score, a Novel Prediction Model

被引:6
|
作者
Nakamura, Naokazu [1 ]
Jo, Tomoyasu [1 ,2 ]
Arai, Yasuyuki [1 ,2 ]
Kitawaki, Toshio [1 ]
Nishikori, Momoko [1 ,3 ]
Mizumoto, Chisaki [1 ]
Kanda, Junya [1 ]
Yamashita, Kouhei [1 ]
Nagao, Miki [2 ]
Takaori-Kondo, Akifumi [1 ,2 ]
机构
[1] Kyoto Univ Hosp, Dept Hematol & Oncol, Kyoto, Japan
[2] Kyoto Univ Hosp, Ctr Res & Applicat Cellular Therapy, 54 Shogoin Kawahara Cho,Sakyo Ku, Kyoto 6068507, Japan
[3] Kyoto Univ, Grad Sch Med, Dept Human Hlth Sci, Kyoto, Japan
来源
TRANSPLANTATION AND CELLULAR THERAPY | 2024年 / 30卷 / 04期
关键词
Chimeric antigen receptor T cell therapy; Prolonged hematotoxicity; Cytokine release syndrome; Inflammation; LYMPHOMA;
D O I
10.1016/j.jtct.2024.01.073
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Prolonged hematotoxicity is the most common long-term adverse event in chimeric antigen receptor T cell therapy (CAR-T). To evaluate the impact on prolonged cytopenia of inflammatory status after CAR T infusion, we performed a single-center retrospective study and analyzed patients with B cell lymphomas after CAR-T. Among 90 patients analyzed at 90 days after infusion, the cumulative incidence was 57.5% for prolonged neutropenia, 36.7% for anemia, and 49.8% for thrombocytopenia. Patients who experienced cytokine release syndrome (CRS) had significantly higher incidence and longer duration of prolonged cytopenia. In addition, we found that among patients with grade 1 CRS, those with a longer duration of CRS-related symptoms (>5 days; grade 1b in modified CRS grading [m-CRS]) had a significantly higher incidence and longer duration of prolonged cytopenia than those whose CRS-related symptoms resolved within 5 days (grade 1a m-CRS). Multivariate analysis revealed that a higher m-CRS grade (grade 1b or 2; hazard ratio [HR], 2.42), higher peak CRP (>= 10 mg/dL; HR, 1.66), longer duration of elevated CRP (>= 10 days; HR, 1.83), and a decrease in serum inorganic phosphorus concentration (>= 30% from baseline; HR, 1.95) were associated with significantly higher cumulative incidence of prolonged neutropenia, as well as anemia and thrombocytopenia. Using these factors, we developed a new predictive scoring model for prolonged hematotoxicity, the KyoTox a-score, which can successfully stratify the incidence and duration of cytopenia independent of the existing model, CAR-HEMATOTOX, which is based on laboratory data at lymphodepletion. Thus, this newly developed post-CAR-T inflammation-dependent score is accurate and useful for predicting prolonged hematotoxicity. (c) 2024 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
引用
收藏
页码:404 / 414
页数:11
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