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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Neuralgic Amyotrophy Following B-Cell Maturation Antigen-Directed CAR-T Therapy.
Neuralgic Amyotrophy Following B-Cell Maturation Antigen-Directed CAR-T Therapy.
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神经痛性肌萎缩可能是 BCMA 靶向 CAR-T 治疗一种认识不足的并发症。发病时间一致、双侧受累以及对皮质类固醇有反应,均支持炎症机制。临床医生应保持对该并发症的警惕,因为及时识别和治疗可能减轻长期神经系统的病残。
我们描述了在单个三级医疗中心接受B细胞成熟抗原(BCMA)靶向CAR-T 治疗后发生神经痛性肌萎缩的临床、电生理和影像学特征。
我们识别出4例在接受靶向BCMA的CAR-T 治疗后发生神经痛性肌萎缩的患者,占当时接受治疗患者总数的1.5%。患者在CAR-T 输注后8-12天出现急性双侧肩痛,随后出现无力。表现为翼状肩胛和手臂无力,肌电图显示失神经支配,最明显位于胸长神经和肩胛上神经支配的肌肉。使用糖皮质激素似乎与症状改善相关,但多数患者仍存在残余无力。3例患者因将症状错误归因于其他病因导致诊断延迟。
We characterize the clinical, electrophysiologic, and imaging features of neuralgic amyotrophy after B-cell maturation antigen (BCMA)-directed CAR-T therapy at a single tertiary care center.
We identified four patients with neuralgic amyotrophy following BCMA-directed CAR-T therapy, corresponding to 1.5% of total patients treated in that time. Patients developed acute bilateral shoulder pain followed by weakness 8-12 days after CAR-T infusion. Manifestations included scapular winging and arm weakness, with electromyography showing denervation most prominently in the muscles supplied by the long thoracic and suprascapular nerves. Corticosteroid use appeared to be associated with symptomatic improvement, although residual weakness persisted in most. Diagnosis was delayed in three patients due to misattribution of symptoms to other causes. DISCUSSION: Neuralgic amyotrophy may represent an underrecognized complication of BCMA-directed CAR-T therapy. The consistent timing of onset, bilateral involvement, and responsiveness to corticosteroids support an inflammatory mechanism. Clinicians should maintain vigilance for this complication, as prompt recognition and treatment may mitigate long-term neurological morbidity.
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