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CAR-T 细胞治疗中枢神经系统淋巴瘤的疗效与安全性:符合 PRISMA 的单臂荟萃分析

英文原题:Efficacy and safety of chimeric antigen receptor T-cells treatment in central nervous system lymphoma: a PRISMA-compliant single-arm meta-analysis.

查看英文原题

Efficacy and safety of chimeric antigen receptor T-cells treatment in central nervous system lymphoma: a PRISMA-compliant single-arm meta-analysis.

PubMed 2022/07/07(内容时间) Cancer Immunol Immunother Q1 · IF 5.8(JCR 2025)

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研究概要

由于短期缓解率高且副作用可控,CAR-T 细胞治疗是治疗中枢神经系统淋巴瘤的有前景的选择。

中文摘要

嵌合抗原受体(CAR)T细胞用于治疗难治或复发B细胞淋巴瘤。静脉给药后,可在脑脊液中检测到CAR-T 细胞,因此其可能用于治疗中枢神经系统淋巴瘤(CNSL)。本荟萃分析旨在阐明CAR-T 治疗CNSL的疗效和安全性。

纳入接受CAR-T 治疗且报告总应答(OR)、完全应答(CR)和部分应答(PR)的CNSL研究。采用双反正弦转换后的随机效应或固定效应模型进行合并分析,并为所有结局计算95%置信区间(CI)。

共纳入8项研究、63名患者。CAR-T 治疗后合并OR率和CR率分别为69%(95% CI 56%–81%)和51%(95% CI 37%–64%)。缓解后疾病进展的合并率为38%(95% CI 21%–55%)。3级或以上神经毒性合并发生率为12%(95% CI 3%–24%;I²=0.00%,P=0.53),未报告治疗相关死亡。

CAR-T 因短期缓解率高、副作用可控制,是治疗CNSL的有前景选择。但缓解后复发率较高,仍需解决。还需要大样本长期随访数据更好评估CAR-T 疗效和安全性。注册信息:PROSPERO,CRD42022301332。

展开英文摘要原文

Chimeric antigen receptor (CAR) T cells are used to treat refractory and recurrent B-cell lymphoma. When administered intravenously, CAR T cells can be detected in cerebrospinal fluid, and thus represent a promising method for the treatment of central nervous system lymphoma (CNSL). This meta-analysis aimed to clarify the effectiveness and safety of CAR T-cell therapy in the treatment of CNSL.

Studies involving patients with CNSL who received CAR T-cell therapy that reported overall response (OR), complete response (CR), and partial response (PR) were included. A random-effects or fixed-effects model with double arcsine transformation was used for the pooled analysis and 95% confidence intervals (CI) were determined for all outcomes.

Eight studies, comprising 63 patients, were identified and were included in the meta-analysis. The pooled OR and CR rates after treatment with CAR T cells were 69% (95% CI, 56-81%) and 51% (95% CI, 37-64%), respectively. The pooled rate of progressive disease after remission was 38% (95% CI, 21-55%). The pooled rate for neurotoxicity grade 3 or above was 12% (95% CI, 3-24%, I 2 = 0.00%, p = 0.53). No treatment-related deaths were reported.

CAR T-cell therapy is a promising option for the treatment of CNSL owing to a high short-term remission rate and controllable side effects. However, the high recurrence rate after remission must be addressed. Long-term follow-up data with large sample sizes are also needed to better assess the effectiveness and safety of CAR T-cell therapy. REGISTRATION: This meta-analysis was registered in the international prospective register of systematic reviews (PROSPERO) (CRD42022301332).

论文信息

作者
Lv L、Wu Y、Shi H、Sun X、Deng Z、Huo H、Li R、Liu Y
第一作者单位
Department of Hematology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.China
通讯作者单位
Department of Hematology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China. yuanbol@ccmu.edu.cn.China
文献类型
荟萃分析
期刊
Cancer immunology, immunotherapy : CII2023 Jan
原文标识
PubMed 35796863 · DOI 10.1007/s00262-022-03246-w