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细胞因子诱导的杀伤细胞用于癌症免疫治疗的国际注册十年更新。

Ten-year update of the international registry on cytokine-induced killer cells in cancer immunotherapy.

机构信息

Department of Integrated Oncology, Center for Integrated Oncology (CIO), University Hospital Bonn, Bonn, Germany.

出版信息

J Cell Physiol. 2020 Dec;235(12):9291-9303. doi: 10.1002/jcp.29827. Epub 2020 Jun 2.

DOI:10.1002/jcp.29827
PMID:32484595
Abstract

Cytokine-induced killer (CIK) cells represent an exceptional T-cell population uniting a T cell and natural killer cell-like phenotype in their terminally differentiated CD3 CD56 subset, which features non-MHC-restricted tumor-killing activity. CIK cells have provided encouraging results in initial clinical studies and revealed synergistic antitumor effects when combined with standard therapeutic procedures. We established the international registry on CIK cells (IRCC) to collect and evaluate clinical trials for the treatment of cancer patients in 2010. Moreover, our registry set new standards on the reporting of results from clinical trials using CIK cells. In the present update, a total of 106 clinical trials including 10,225 patients were enrolled in IRCC, of which 4,889 patients in over 30 distinct tumor entities were treated with CIK cells alone or in combination with conventional or novel therapies. Significantly improved median progression-free survival and overall survival were shown in 27 trials, and 9 trials reported a significantly increased 5-year survival rate. Mild adverse effects and graft-versus-host diseases were also observed in the studies. Recently, more efforts have been put into the improvement of antitumoral efficacy by CIK cells including the administration of immune checkpoint inhibitors and modification with chimeric antigen receptorc. The minimal toxicity and multiple improvements on their tumor-killing activity both make CIK cells a favorable therapeutic tool in the clinical practice of cancer immunotherapy.

摘要

细胞因子诱导的杀伤(CIK)细胞代表了一种特殊的 T 细胞群体,在其终末分化的 CD3 CD56 亚群中融合了 T 细胞和自然杀伤细胞样表型,具有非 MHC 限制的肿瘤杀伤活性。CIK 细胞在初步的临床研究中取得了令人鼓舞的结果,并与标准治疗程序联合使用时显示出协同的抗肿瘤作用。我们于 2010 年建立了 CIK 细胞国际注册中心(IRCC),以收集和评估治疗癌症患者的临床试验。此外,我们的注册中心为使用 CIK 细胞的临床试验结果报告制定了新标准。在本次更新中,IRCC 共纳入了 106 项临床试验,共 10225 例患者,其中 4889 例患者在 30 多种不同的肿瘤实体中单独或联合常规或新型疗法接受了 CIK 细胞治疗。27 项试验显示中位无进展生存期和总生存期显著改善,9 项试验报告 5 年生存率显著提高。研究中还观察到轻微的不良反应和移植物抗宿主病。最近,人们更加努力地通过 CIK 细胞来提高抗肿瘤疗效,包括免疫检查点抑制剂的给药和嵌合抗原受体的修饰。CIK 细胞的最小毒性和对其肿瘤杀伤活性的多种改善使其成为癌症免疫治疗临床实践中的一种有利治疗工具。

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