CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Frontal Intermittent Rhythmic Delta Activity Is a Useful Diagnostic Tool of Neurotoxicity After CAR T-Cell Infusion.
Frontal Intermittent Rhythmic Delta Activity Is a Useful Diagnostic Tool of Neurotoxicity After CAR T-Cell Infusion.
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FIRDA 是 ICANS 的可靠诊断工具,灵敏度为 88%,阴性预测值为 100%。
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。
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.
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