Rapid response in relapsed follicular lymphoma to novel anti-CD19 CAR-T therapy with pseudo-progression and cytomegalovirus infection: A case report

医学 滤泡性淋巴瘤 淋巴瘤 内科学 耐火材料(行星科学) CD19 嵌合抗原受体 免疫学 肿瘤科 胃肠病学 抗原 T细胞 生物 免疫系统 天体生物学
作者
Nan Zhong,Qihong Ma,Shiting Gong,Yuanyuan Shi,Lijun Zhao,Danyu Wang,Huanhuan Zhou,Ning Liu,Ye Yuan,Jianxun Wang,Liqiong Liu,Zhi Guo
出处
期刊:International Immunopharmacology [Elsevier BV]
卷期号:134: 112174-112174 被引量:3
标识
DOI:10.1016/j.intimp.2024.112174
摘要

CD19-directed chimeric antigen receptor (CAR) T cell therapy has been shown to achieve a considerably durable response in patients with refractory or relapsed B cell non-Hodgkin lymphomas. Most of these CARs were generated by lentivirus. With the exception of Yescarta and Tecartus, few patients with relapsed-/refractory- lymphoma have been treated clinically with a CARs using retroviral vector (RV). Here, we reported a relapsed/refractory grade 2 follicular lymphoma patient with multiple chemotherapy failures, and was treated with a novel CD19 CAR-T cell manufactured from a RV. After tumor burden was reduced with Obinutuzumab and Duvelisib, the patient was infused novel CD19 CAR-T cells at a dose of 3 × 106 cells/ kg. Then he experienced a rapid response and achieved almost complete remission by day 26. Only grade 2 CRS, bilateral submaxillary lymph node enlargement and cytomegalovirus (CMV) infection occurred without neurotoxicity, and the patient's condition improved after a series of symptomatic treatments. In addition, CAR copy number peaked at 532,350 copies/μg on day 15 and continued to expand for 5 months. This may be the first case report of RV preparation of novel CD19 CAR-T cells for direct treatment of recurrent follicular lymphoma. We will observe its long-term efficacy and conduct trials in more patients in the future.

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