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血液系统恶性肿瘤患者 CAR-T 细胞治疗后一过性急性肾损伤

英文原题:Transient acute kidney injury after chimeric antigen receptor T-cell therapy in patients with hematological malignancies.

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Transient acute kidney injury after chimeric antigen receptor T-cell therapy in patients with hematological malignancies.

PubMed 2024/02/20(内容时间) Clin Kidney J Q1 · IF 5.3(JCR 2025)

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研究概要

我们的结果表明,AKI 是一种常见但轻微的不良事件,多数患者恢复迅速。

研究思路结论见上方概要

30%接受嵌合抗原受体(CAR)T细胞输注的患者会发生急性肾损伤(AKI)。本研究旨在识别接受CAR-T 细胞治疗患者发生AKI后的危险因素和长期结局。

收集了2018年7月至2021年5月期间在Vall d'Hebron大学医院接受CD19靶向CAR-T 细胞治疗的115例R/R血液系统恶性肿瘤成年患者的医疗记录。收集了基线人口统计学数据,包括年龄、性别、种族、体重指数(BMI)和合并症,以及血液系统肿瘤类型和既往治疗线数。回顾性审查了包括血清肌酐和全血血红蛋白在内的实验室参数,并收集了输注后第+1、+7、+14、+21和+28天的数值。

共有24/115(21%)例患者发生与CAR-T 细胞治疗相关的AKI;6/24例为慢性肾脏病(CKD)基础上的AKI。2例患者在淋巴细胞清除(LD)化疗背景下发生AKI,其余22例发生在CAR-T 细胞输注后,3例从第+1天开始,13例从第+7天开始,1例从第+14天开始,2例从第+21天开始,3例从第+28天开始。19/24(79%)例患者在输注后第一个月内肾功能恢复。男性、CKD、细胞因子释放综合征(CRS)和免疫效应细胞相关神经毒性综合征(ICANS)与AKI相关。多变量分析中,男性、CKD、ICANS 3级和CRS 2级被确定为AKI的独立危险因素。就最常见的CAR-T 细胞相关并发症而言,95例(82%)患者观察到CRS,33例(29%)患者观察到ICANS。34例(30%)患者需要使用类固醇,37例(32%)患者需要使用tocilizumab。6例(5%)患者入住重症监护病房(1例为感染性休克,4例为CRS 2级合并ICANS 2级,1例为CRS 3级)。共有5例(4.4%)患者在CAR-T 细胞输注后前30天内因疾病进展以外的原因死亡,包括4例感染性并发症和1例心力衰竭。

展开英文摘要原文

Acute kidney injury (AKI) occurs in 30% of patients infused with chimeric antigen receptor (CAR) T-cells. The purpose of this study was to identify risk factors and long-term outcomes after AKI in patients who received CAR T-cell therapy.

Medical records of 115 adult patients with R/R hematological malignancies treated with CD19-targeted CAR T-cells at Vall d'Hebron University Hospital between July 2018 and May 2021. Baseline demographic data including age, gender, ethnicity, body mass index (BMI), and co-morbidities, as well as the type of hematological neoplasia and prior lines of therapy were collected. Laboratory parameters including serum creatinine and whole blood hemoglobin were retrospectively reviewed and values were gathered for days +1, +7, +14, +21, and +28 post-infusion.

A total of 24/115 (21%) patients developed AKI related to CAR T-cell therapy; 6/24 with AKI over chronic kidney disease (CKD). Two patients had AKI in the context of lymphodepleting (LD) chemotherapy and the other 22 after CAR T-cell infusion, starting at day+1 in 3 patients, day+7 in 13 patients, day +14 in 1 patient, day+21 in 2 patients, and day+28 in 3 patients. Renal function was recovered in 19/24 (79%) patients within the first month after infusion. Male gender, CKD, cytokine release syndrome (CRS), and immune effector cell-associated neurotoxicity syndrome (ICANS) were associated with AKI. Male gender, CKD, ICANS grade 3 and CRS grade 2 were identified as independent risk factors for AKI on multivariable analysis. In terms of the most frequent CAR T-cell related complications, CRS was observed in 95 (82%) patients and ICANS in 33 (29%) patients. Steroids were required in 34 (30%) patients and tocilizumab in 37 (32%) patients. Six (5%) patients were admitted to the intensive care unit (1 for septic shock, 4 for CRS grade 2 associated to ICANS grade 2, and 1 for CRS grade 3). A total of 5 (4.4%) patients died in the first 30 days after CAR T-cell infusion for reasons other than disease progression, including 4 cases of infectious complications and 1 of heart failure.

Our results suggest that AKI is a frequent but mild adverse event, with fast recovery in most patients.

论文信息

作者
León-Román J、Iacoboni G、Bermejo S、Carpio C、Bolufer M、García-Carro C、Sánchez-Salinas M、Alonso-Martínez C
第一作者单位
Nephrology Department, Vall d'Hebron University Hospital, Vall d'Hebron Institute of Research, CSUR National Unit of Expertise for Complex Glomerular Diseases of Spain, Barcelona, Spain.Spain
通讯作者单位
N ephrology Department, Vall d'Hebron University Hospital, Vall d'Hebron Institute of Research, CSUR National Unit of Expertise for Complex Glomerular Diseases of Spain, Barcelona, Spain.Spain
期刊
Clinical kidney journal2024 Mar
原文标识
PubMed 38500492 · DOI 10.1093/ckj/sfae027