CRP and ferritin in addition to the EASIX score predict CAR-T–related toxicity

医学 内科学 铁蛋白 细胞因子释放综合征 毒性 胃肠病学 乳酸脱氢酶 累积发病率 免疫学 移植 T细胞 免疫系统 生物 嵌合抗原受体 生物化学
作者
Uri Greenbaum,Paolo Strati,Rima M. Saliba,Janet Rodríguez‐Torres,Gabriela Rondón,Yago Nieto,Chitra Hosing,Samer A. Srour,Jason R. Westin,Luis Fayad,Hun Ju Lee,Swaminathan P. Iyer,Ranjit Nair,Loretta J. Nastoupil,Simrit Parmar,Maria Alma Rodriguez,Felipe Samaniego,Raphaël Steiner,Michael Wang,Chelsea C. Pinnix,Christopher R. Flowers,Sudhakar Tummala,Jeremy Ramdial,Fevzi Fırat Yalniz,Misha Hawkins,Katayoun Rezvani,Richard E. Champlin,Elizabeth J. Shpall,Sattva S. Neelapu,Partow Kebriaei,Sairah Ahmed
出处
期刊:Blood Advances [Elsevier BV]
卷期号:5 (14): 2799-2806 被引量:69
标识
DOI:10.1182/bloodadvances.2021004575
摘要

The Endothelial Activation and Stress Index (EASIX) score, defined as [(creatinine × lactate dehydrogenase [LDH])/platelets], is a marker of endothelial activation that has been validated in the allogeneic hematopoietic stem cell transplant setting. Endothelial activation is one of the mechanisms driving immune-mediated toxicities in patients treated with chimeric antigen receptor-T (CAR-T)-cell therapy. This study's objective was to evaluate the association between EASIX and other laboratory parameters collected before lymphodepletion and the subsequent onset of cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) those patients. Toxicity data were collected prospectively on 171 patients treated with axicabtagene ciloleucel (axi-cel) for large B-cell lymphoma (LBCL). CRS grades 2 to 4 were diagnosed in 81 (47%) patients and ICANS grades 2 to 4 in 84 (49%). EASIX combined with ferritin (EASIX-F) identified 3 risk groups with CRS grades 2 to 4 cumulative incidence of 74% (hazards ratio [HR], 4.8; 95% confidence interval [CI], 2.1-11; P < .001), 49% (HR, 2.3; 95% CI, 1.02-5; P = .04), and 23% (reference), respectively. EASIX combined with CRP and ferritin (EASIX-FC) identified 3 risk groups with an ICANS grade 2 to 4 cumulative incidence of 74% (HR, 3.6; 95% CI, 1.9-6.9; P < .001), 51% (HR, 2.1; 95% CI, 1.1-3.9; P = .025), and 29% (reference). Our results indicate that common laboratory parameters before lymphodepletion correlate with CAR-T-related toxicities and can help support clinical decisions, such as preemptive toxicity management, hospitalization length, and proper setting for CAR-T administration.

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