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:Laryngeal edema as a symptom of local cytokine release syndrome after BCMA-targeting CAR-T therapy for relapsed and refractory multiple myeloma.
Laryngeal edema as a symptom of local cytokine release syndrome after BCMA-targeting CAR-T therapy for relapsed and refractory multiple myeloma.
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细胞因子释放综合征(CRS)可能是CAR-T 细胞治疗的主要副作用,并且在高肿瘤负荷或体能状态差等因素的患者中,偶尔可能危及生命。在靶向B细胞成熟抗原(BCMA)的CAR-T 治疗中观察到的众多CRS事件中,由于局部症状(也称为局部CRS)发生率低,人们对其了解甚少。
在此,我们报告一例54岁难治性多发性骨髓瘤女性患者,表现为喉水肿作为局部CRS。在接受CAR-T 治疗前,她因左侧甲状腺肿块被诊断为疾病进展。在局部放疗后,她接受了靶向BCMA的CAR-T 药物idecabtagene vicleucel(ide-cel)。第2天,患者发生CRS,经tocilizumab治疗后缓解。
然而,第4天,喉水肿加重,被判断为局部CRS。静脉注射dexamethasone迅速减轻了水肿。总之,喉水肿作为局部CRS很少发生,据我们所知,从未有ide-cel输注后发生此情况的报道。Dexamethasone对于减轻在tocilizumab治疗全身症状后持续存在的局部反应有效。
Cytokine release syndrome (CRS) can be a major side effect of chimeric antigen receptor T-cell (CAR-T) therapy, and may occasionally become life-threatening in patients with factors such as high tumor burden or poor performance status. Among the many CRS events observed in B-cell maturation antigen (BCMA)-targeting CAR-T therapy, local symptoms (also called local CRS) are poorly understood due to their low frequency.
Here, we present the case of a 54-year-old woman with refractory multiple myeloma exhibiting laryngeal edema as a local CRS. Before CAR-T therapy, she was diagnosed with progressive disease indicated by a left thyroid mass. After local irradiation, she received the BCMA-targeting CAR-T agent idecabtagene vicleucel (ide-cel). On day 2, the patient developed CRS, which resolved on treatment with tocilizumab.
However, on day 4, laryngeal edema worsened, and was judged to be a local CRS. Intravenous dexamethasone rapidly reduced this edema.
In conclusion, laryngeal edema rarely occurs as a local CRS, and to the best of our knowledge, has never been reported after ide-cel infusion. Dexamethasone was effective for reducing the local reaction that persisted after treatment of systemic symptoms with tocilizumab.
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