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:Efficacy and safety of chimeric antigen receptor T-cells treatment in central nervous system lymphoma: a PRISMA-compliant single-arm meta-analysis.
Efficacy and safety of chimeric antigen receptor T-cells treatment in central nervous system lymphoma: a PRISMA-compliant single-arm meta-analysis.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
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。
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。
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).
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