wt -1特异性CD8+ t细胞治疗复发性间变性少突胶质细胞瘤的长期缓解:1例报告。

Ho-Shin Gwak, Beom Kyu Choi, Young Joo Lee, Na Young Han, Kook Hee Yang
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引用次数: 0

摘要

我们报告了一例间变性少突胶质细胞瘤在使用自体Wilms肿瘤1 (WT-1)特异性CD8+ T细胞进行过继细胞治疗(ACT)后完全缓解的病例。一名40岁女性复发性间变性少突胶质细胞瘤后转至我院进行辅助化疗,最初表现为左额部肿瘤,通过癫痫发作诊断,次全切除证实少突胶质细胞瘤(WHO 2级)。放疗治疗残余肿瘤,达到部分缓解,直到2.5年后复发,第二次开颅后发生恶性转化为间变性少突胶质细胞瘤(WHO分级3级)。经丙卡嗪、洛莫司汀、长春新碱化疗3个周期后,残余肿瘤稳定3年。然而,后续的MRI发现了一个新的增强病变,促使第三次开颅手术。复发性间变性少突胶质细胞瘤确诊,并开始辅助质子束治疗和替莫唑胺化疗。两年后,在相邻的内侧额叶出现了另一个增强性病变。在多学科回顾之后,我们引入了wt -1特异性ACT。虽然在治疗后1个月观察到短暂的肿胀,但肿瘤在3-9个月内表现出反应。持续消退导致完全缓解-在15个月的随访中通过MRI证实,持续4.7年。患者外周血单核细胞谱和免疫相关细胞因子分析显示WT-1致敏后t细胞活化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-Term Remission of Recurrent Anaplastic Oligodendroglioma With WT-1-Specific CD8+ T-Cell Therapy: A Case Report.

We report a case of complete remission in anaplastic oligodendroglioma following adoptive cell therapy (ACT) with autologous Wilms tumor 1 (WT-1)-specific CD8+ T cells. A 40-year-old woman referred to our hospital for adjuvant chemotherapy after recurrent anaplastic oligodendroglioma initially presented with a left frontal tumor, diagnosed through seizure onset, and subtotal resection confirmed oligodendroglioma (WHO grade 2). Radiation therapy treated the residual tumor, achieving partial remission until recurrence 2.5 years later when malignant transformation to anaplastic oligodendroglioma (WHO grade 3) occurred following a second craniotomy. After three cycles of procarbazine, lomustine, and vincristine chemotherapy, the residual tumor stabilized for 3 years. However, follow-up MRI identified a new enhancing lesion, prompting a third craniotomy. Recurrent anaplastic oligodendroglioma was confirmed, and adjuvant proton beam therapy and temozolomide chemotherapy were initiated. Two years later, another enhancing lesion appeared on the adjacent medial frontal lobe. Following multidisciplinary review, we introduced WT-1-specific ACT. Although transient swelling was observed 1 month post-therapy, the tumor demonstrated a response within 3-9 months. Continued regression led to complete remission-confirmed via MRI at the 15-month follow-up and sustained for 4.7 years. The patient's peripheral blood monocyte profiles and immune-associated cytokine analysis indicated T-cell activation following WT-1 sensitization.

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