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:Intravenous Immunoglobulin (IVIG) for Patients with Severe Neurotoxicity Associated with Chimeric Antigen Receptor T-Cell (CAR-T) Therapy.
Intravenous Immunoglobulin (IVIG) for Patients with Severe Neurotoxicity Associated with Chimeric Antigen Receptor T-Cell (CAR-T) Therapy.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
接受阿基仑赛(axi-cel)治疗的大B细胞淋巴瘤(LBCL)患者中,约30%会发生重度免疫效应细胞相关神经毒性综合征(ICANS)。除标准糖皮质激素治疗外,目前可用治疗策略有限,因此亟需寻找其他重度ICANS管理方法。
我们回顾性研究了2015年5月至2019年2月接受axi-cel治疗的LBCL患者神经系统结局。纳入发生重度ICANS并接受糖皮质激素后静脉注射免疫球蛋白(IVIG,n=9)或单用糖皮质激素治疗(n=10)的患者。两组重度ICANS缓解时间(TTR)无统计学显著差异;不过,IVIG组患者基线体能状态较差,且ICANS分级更重。IVIG组和单用糖皮质激素组累积使用激素天数分别为11.2天和13.5天。axi-cel治疗后,重度ICANS患者使用IVIG具有良好的耐受性和安全性;对于低丙种球蛋白血症患者,CAR-T 治疗中通常建议使用IVIG。未来可通过前瞻性研究进一步探索将IVIG作为重度ICANS的潜在治疗手段。
Severe immune effector cell-associated neurotoxicity syndrome (ICANS) occurs in about 30% of all patients with large B-cell lymphoma (LBCL) who are treated with axicabtagene ciloleucel (axi-cel). There are currently limited treatment strategies other than the standard corticosteroids, and it is essential to find additional therapies to manage severe ICANS.
We conducted a retrospective study of neurologic outcomes among patients who received axi-cel for LBCL from May 2015 to February 2019.
We identified patients who developed severe ICANS and were treated with glucocorticoids followed by intravenous immunoglobulin (IVIG) (n = 9) or glucocorticoids alone (n = 10). There was no statistically significant difference in the time to resolution (TTR) of severe ICANS between groups; however, patients in the IVIG had more severe grades of ICANS with a lower performance status at baseline.
The cumulative steroid days were 11. 2 in the IVIG arm and 13. 5 in the glucocorticoids-only arm. The use of IVIG for severe ICANS after axi-cel therapy was tolerable and safe and is generally recommended in the CAR-T setting in patients with hypogammaglobinemia. The use of IVIG as a potential therapeutic agent for severe ICANS can be further explored in future prospective studies.
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