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嵌合抗原受体 T 细胞靶向 CD19 治疗 B 细胞恶性肿瘤的过继免疫疗法:疗效和安全性的系统评价。

Adoptive Immunotherapy for B-cell Malignancies Using CD19- Targeted Chimeric Antigen Receptor T-Cells: A Systematic Review of Efficacy and Safety.

机构信息

Shenzhen Geno-Immune Medical Institute, Shenzhen 518057, China.

Institute of Cancer Stem Cells, Dalian Medical University, Dalian 116044, China.

出版信息

Curr Med Chem. 2019;26(17):3068-3079. doi: 10.2174/0929867324666170801101842.

Abstract

BACKGROUND

Adoptive infusion of chimeric antigen receptor transduced T- cells (CAR-T) is a powerful tool of immunotherapy for hematological malignancies, as evidenced by recently published and unpublished clinical results.

OBJECTIVE

In this report, we performed a meta-analysis to evaluate the efficacy and side effects of CAR-T on refractory and/or relapsed B-cell malignancies, including leukemia and lymphoma.

METHODS

Clinical studies investigating efficacy and safety of CAR-T in acute and chronic lymphocytic leukemia and lymphoma were identified by searching PubMed and EMBASE. Outcomes of efficacy subjected to analysis were the rates of complete remission (CR) and partial remission (PR). The safety parameters were the prevalence of adverse effects including fever, hypotension, and acute renal failure. Meta analyses were performed using R software. Weighted hazard ratio (HR) with 95% confidence intervals was calculated for each outcome. Fixed or random-effects models were employed depending on the heterogeneity across the included studies.

RESULTS

Nineteen published clinical studies with a total of 391 patients were included for the meta-analysis. The pooled rate of complete remission was 55% (95% CI 41%-69%); the pooled rate of partial remission was 25% (95% CI: 19%-33%). The prevalence of fever was 62% (95% CI: 41%-79%), the hypotension was 22% (95% CI: 15%-31%), and the acute renal failure was 24% (95% CI: 16%-34%). All adverse effects were manageable and no death was reported due to toxicity.

CONCLUSION

CD19-targeted CAR-T is an effective modality in treating refractory B-cell malignancies including leukemia and lymphoma. However, there is still a need to develop strategies to improve the safety in its clinical use.

摘要

背景

嵌合抗原受体修饰 T 细胞(CAR-T)过继输注是血液系统恶性肿瘤免疫治疗的有力工具,最近发表和未发表的临床结果证明了这一点。

目的

本报告通过检索 PubMed 和 EMBASE,进行荟萃分析评估 CAR-T 治疗复发/难治性 B 细胞恶性肿瘤(包括白血病和淋巴瘤)的疗效和不良反应。

方法

通过检索 PubMed 和 EMBASE,确定了评估 CAR-T 在急性和慢性淋巴细胞白血病和淋巴瘤中的疗效和安全性的临床研究。分析的疗效结果为完全缓解(CR)和部分缓解(PR)的比例。安全性参数为发热、低血压和急性肾衰竭等不良反应的发生率。使用 R 软件进行荟萃分析。计算每个结局的加权风险比(HR)及其 95%置信区间。根据纳入研究之间的异质性,采用固定或随机效应模型。

结果

共纳入 19 项发表的临床研究,共 391 例患者进行荟萃分析。完全缓解率为 55%(95%CI 41%-69%);部分缓解率为 25%(95%CI:19%-33%)。发热的发生率为 62%(95%CI:41%-79%),低血压的发生率为 22%(95%CI:15%-31%),急性肾衰竭的发生率为 24%(95%CI:16%-34%)。所有不良反应均可控制,无因毒性导致的死亡报告。

结论

CD19 靶向 CAR-T 是治疗复发/难治性 B 细胞恶性肿瘤(包括白血病和淋巴瘤)的有效方法。然而,在其临床应用中仍需要开发提高安全性的策略。

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