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:Case Report: CAR-T therapy for relapsed diffuse large B-cell lymphoma in a patient with pre-existing Parkinson's disease-unfolding clinical challenges.
Case Report: CAR-T therapy for relapsed diffuse large B-cell lymphoma in a patient with pre-existing Parkinson's disease-unfolding clinical challenges.
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CAR-T 细胞疗法已改变了复发/难治性弥漫性大B细胞淋巴瘤(DLBCL)的结局。然而,免疫效应细胞相关神经毒性综合征(ICANS)仍是一个令人担忧的问题。既存神经系统疾病,如帕金森病(PD),由于存在不可预测并发症的风险,带来了额外的、研究不足的挑战。
我们报告一例62岁男性复发DLBCL患者,既往患有PD,接受lisocabtagene maraleucel治疗。神经科、物理治疗和言语-语言团队的基线评估使得能够进行量身定制的监测,包括使用改良的免疫效应细胞相关脑病(ICE)评分。其多巴胺能药物方案在治疗前已优化。在淋巴细胞清除和CAR-T 输注后,他出现了1级细胞因子释放综合征,经tocilizumab和病房内支持治疗得以缓解。尽管在1个月和3个月时的PET-CT扫描观察到稳定的部分缓解,但截至最近一次随访(第+86天)未出现ICANS或PD恶化,这表明在采用量身定制策略的情况下,包括多学科方法、改良的神经毒性监测以及谨慎选择CAR-T 构建体,CAR-T 疗法可安全用于既存PD的患者。需要进一步的研究和更长时间的随访来阐明该人群的长期安全性。
Chimeric antigen receptor T-cell (CAR-T) therapy has transformed the outcomes for relapsed/refractory diffuse large B-cell lymphoma (DLBCL).
However, immune effector cell-associated neurotoxicity syndrome (ICANS) remains a concern. Pre-existing neurological disorders such as Parkinson's disease (PD) introduce additional, poorly studied challenges due to the risk of unpredictable complications.
We report a 62-year-old man with relapsed DLBCL and pre-existing PD who was treated with lisocabtagene maraleucel. Baseline assessments by neurology, physiotherapy, and speech-language teams enabled tailored monitoring, including use of a modified Immune Effector Cell-Associated Encephalopathy (ICE) score. His dopaminergic regimen was optimised prior to therapy. Following lymphodepletion and CAR-T infusion, he experienced grade 1 cytokine release syndrome, which resolved with tocilizumab and ward-based supportive care.
Although a stable partial response was observed on PET-CT scan at 1 and 3 months, the absence of ICANS or PD worsening up to his most recent follow-up on Day +86 suggests that CAR-T therapy can be safely delivered in patients with pre-existing PD when tailored strategies are applied, including a multidisciplinary approach, modified neurotoxicity monitoring, and careful selection of the CAR-T construct.
Further studies and longer follow-up are needed to clarify long-term safety in this population.
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