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:Evolving Magnetic Resonance Imaging (MRI) Findings in Immune Effector Cell-Associated Neurotoxicity Syndrome.
Evolving Magnetic Resonance Imaging (MRI) Findings in Immune Effector Cell-Associated Neurotoxicity Syndrome.
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免疫效应细胞相关神经毒性综合征(ICANS)是一种可能危及生命的并发症,常见于接受CAR-T 细胞疗法等免疫治疗的患者。本病例报告基于对患者病史、 primary team 的体格检查、实验室检查、影像学发现以及患者住院和后续就诊的出院小结的病历回顾。
我们报告一例中年多发性骨髓瘤男性患者,在接受两个周期 talquetamab(Talvey)治疗后出现 ICANS。患者最初的症状包括发热和精神状态改变。磁共振成像(MRI)显示多处病灶,包括下丘脑和尾状核头部的 T1 强化、尾状核和室管膜下区的液体衰减反转恢复(FLAIR)高信号、豆状核的磁敏感伪影,以及胼胝体的弥散受限。精神状态改变、发热和脑脊液蛋白升高引起了对可能神经毒性的担忧,患者接受了类固醇和托珠单抗治疗。24 天后进行的随访 MRI 显示尾状核信号异常进展,以及双侧尾状核头部新出现的磁敏感边缘。在原始 MRI 后 99 天进行了第三次 MRI,追踪到弥散受限和 FLAIR 异常的消退,但注意到磁敏感伪影进一步增加,以及双侧尾状核头部新出现的周边强化病灶。在初始 MRI 后 250 天进行的最后一次 MRI 追踪到尾状核病灶的消退,磁敏感伪影稳定。本病例凸显了ICANS的演变特性,并强调了系列MRI在追踪神经毒性进展、指导治疗及改善免疫治疗相关并发症预后中的作用。
Immune effector cell-associated neurotoxicity syndrome (ICANS) is a potentially life-threatening complication often observed in patients receiving immunotherapies like chimeric antigen receptor T-cell (CAR-T) therapy. This case report is based on a chart review of the history, physical examination of the primary team, laboratory tests, imaging findings, and discharge summary of the patient's hospital admission and subsequent encounters.
We present the case of a middle-aged man with multiple myeloma who developed ICANS following two cycles of talquetamab (Talvey) therapy. The patient's initial symptoms included fever and altered mental status. Magnetic resonance imaging (MRI) revealed a multitude of foci, including T1 enhancement of the hypothalamus and caudate heads, fluid-attenuated inversion recovery (FLAIR) hyperintensities of the caudate nuclei and subependymal regions, susceptibility artifacts in the lentiform nuclei, and diffusion restriction in the corpus callosum. Altered mental status, fever, and elevations in cerebrospinal protein raised concern for possible neurotoxicity, and the patient was treated with steroids and tocilizumab.
A follow-up MRI taken 24 days later demonstrated a progression of signal abnormalities in the caudate nuclei and a new rim of susceptibility in the bilateral caudate heads. A third MRI was performed 99 days after the original MRI, which tracked the resolution of the diffusion restriction and FLAIR abnormalities, but noted further increased susceptibility artifacts and new peripherally enhancing lesions in the bilateral caudate heads.
A final MRI taken 250 days after the initial MRI tracked the resolution of the caudate lesions, with stable susceptibility artifacts. This case highlights the evolving nature of ICANS and underscores the role of serial MRI in tracking neurotoxicity progression, guiding treatment, and improving outcomes in immunotherapy-related complications.
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