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额区间歇节律性 δ 活动是 CAR-T 细胞输注后神经毒性的有用诊断工具

英文原题:Frontal Intermittent Rhythmic Delta Activity Is a Useful Diagnostic Tool of Neurotoxicity After CAR T-Cell Infusion.

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Frontal Intermittent Rhythmic Delta Activity Is a Useful Diagnostic Tool of Neurotoxicity After CAR T-Cell Infusion.

PubMed 2023/04/14(内容时间) Neurol Neuroimmunol Neuroinflamm Q1 · IF 8(JCR 2025)

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研究概要

FIRDA 是 ICANS 的可靠诊断工具,灵敏度为 88%,阴性预测值为 100%。

中文摘要

CAR-T 显著改善复发/难治性血液恶性肿瘤预后,但CRS及ICANS发生率可分别高达100%和50%。本研究评估脑电图(EEG)模式能否用于ICANS诊断。

前瞻性纳入2020年9月至2021年7月在蒙彼利埃大学医院接受CAR-T 者。输注后14天每日监测神经症状及实验室指标;输注后第6至8天进行EEG和脑MRI,若ICANS在其他时间发生,则于发作日复查EEG。比较有无ICANS患者资料。

连续纳入38人(14名女性,中位年龄65岁)。17人(44%)发生ICANS,中位发生时间为输注后6天,中位等级2级。ICANS与第4天CRP峰值较高(146 mg/L,p=0.004)、第5天血钠较低(131 mmol/L,p=0.005),以及第6至8天EEG额部间歇性节律性δ活动(FIRDA,p<0.001)相关。FIRDA仅见于ICANS患者(17例中15例,敏感度88%),且通常在激素治疗后随ICANS缓解而消失。除低钠血症外,无其他毒性或代谢指标与FIRDA相关;输注第7天抗利尿激素替代指标copeptin在ICANS者更高。讨论:FIRDA是可靠ICANS诊断工具,敏感度88%、阴性预测值100%,也可能用于监测神经毒性。研究提示CRP升高、继而低钠血症,最终出现ICANS和FIRDA的潜在病理链条,仍需更多研究验证。证据等级:III级,支持点测EEG的FIRDA可准确区分CAR-T 后有无ICANS者。

展开英文摘要原文

Patients who received CAR T-cell therapy at Montpellier University Hospital between September 2020 and July 2021 were prospectively enrolled. Neurologic signs/symptoms and laboratory parameters were monitored daily for 14 days after CAR T-cell infusion. EEG and brain MRI were performed between day 6 and 8 after CAR T-cell infusion. EEG was performed again on the day of ICANS occurrence, if outside this time window. All collected data were compared between patients with and without ICANS.

Thirty-eight consecutive patients were enrolled (14 women; median age: 65 years, interquartile range: [55-74]). ICANS was observed in 17 of 38 patients (44%) after a median time of 6 days after CAR T-cell infusion (4-8). The median ICANS grade was 2 (1-3). Higher C-reactive protein peak (146 mg/L [86-256], p = 0.004) at day 4 (3-6), lower natremia (131 mmol/L [129-132], p = 0.005) at day 5 (3-6), and frontal intermittent rhythmic delta activity (FIRDA, p < 0.001) on EEG between days 6 and 8 after infusion were correlated with ICANS occurrence. FIRDA was only observed in patients with ICANS (N = 15/17, sensitivity of 88%) and disappeared after ICANS resolution, usually after steroid therapy. Except for hyponatremia, no other toxic/metabolic marker was associated with FIRDA ( p = 0.002). The plasma concentration of copeptin, a surrogate marker of antidiuretic hormone secretion, assessed at day 7 after infusion, was significantly higher in patients with (N = 8) than without (N = 6) ICANS ( p = 0.043). DISCUSSION: FIRDA is a reliable diagnostic tool for ICANS, with a sensitivity of 88% and a negative predictive value of 100%. Moreover, as this EEG pattern disappeared concomitantly with ICANS resolution, FIRDA could be used to monitor neurotoxicity. Finally, our study suggests a pathogenic pathway that starts with increased C-reactive protein, followed by hyponatremia and eventually ICANS and FIRDA. More studies are required to confirm our results. CLASSIFICATION OF EVIDENCE: This study provides Class III evidence that FIRDA on spot EEG accurately distinguishes patients with ICANS compared with those without after CAR T-cell therapy for hematologic malignancy.

论文信息

作者
Huby S、Gelisse P、Tudesq JJ、Labauge P、Duflos C、Cartron G、Gallerand MA、Platon L
单位
From the Department of Neurology (S.H., P.G., P.L., M.-A.G., X.A., G.T.), CHU Montpellier; Clinical Research and Epidemiology Unit (C.D.), CHU Montpellier; Department of Hematology (J.-J.T., G.C., S.L.), CHU Montpellier; Department of Intensive Care (L.P.), CHU Montpellier; Department of Biochemistry and Hormonology (S.B.), CHU Montpellier; Department of Neuroradiology (N.M.C.), CHU Montpellier, University of Montpellier; University of Montpellier (X.A.), INSERM (INM), Department of Neurology, Montpellier University Hospital; and University of Montpellier (G.T.), CNRS (IGF), Department of Neurology, Montpellier University Hospital, France. sophie.huby27@gmail.com.France
文献类型
非美国政府资助研究
期刊
Neurology(R) neuroimmunology & neuroinflammation2023 Jul
原文标识
PubMed 37059470 · DOI 10.1212/NXI.0000000000200111