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异体 NK 细胞多次鞘内注射治疗难治/复发性脑肿瘤患儿的安全性与可行性

英文原题:The safety and feasibility of multiple intrathecal injections of allogenic NK cells in pediatrics with refractory/recurrent brain tumors.

查看英文原题

The safety and feasibility of multiple intrathecal injections of allogenic NK cells in pediatrics with refractory/recurrent brain tumors.

PubMed 2025/05/27(内容时间) BMC Cancer Q2 · IF 4.1(JCR 2025)

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研究概要

多次鞘内注射异体 NK 细胞在复发/难治性胶质瘤儿童患者中安全可行。

中文摘要

儿童胶质瘤较为罕见,但复发率高,可导致显著死亡和发病。本研究是一项I期非随机临床试验,旨在评估多次鞘内(IT)注射异基因NK细胞治疗难治/复发性儿童胶质瘤的安全性、可行性和潜在疗效。

从随机健康无关供者中通过CD56+细胞阳性分选分离异基因NK细胞。根据纳入标准选出9例患者,每周接受给药,最多10次,每次注射5×10⁷个NK细胞。依据不良事件通用术语标准(CTCAE)检查表进行不良事件分级。疗效组成指标包括肿瘤大小、脊髓播散程度和18个月随访期间复发间隔。此外,回顾性选取6例接受常规治疗的患者。

儿童胶质瘤多次鞘内注射异基因NK细胞是安全的,未发生严重不良事件(SAE)。最常见不良事件为头痛[29%(17%为1级,13%为2级)]、发热和寒战[21%(17%为1级,4%为2级)]、呕吐[13%,均为2级]和背痛[12%(4%为1级,8%为2级)]。18个月随访时,在干预组仍存活的5例患者(截至2024年8月7日)中,3例疾病稳定(SD),1例疾病进展(PD),1例部分缓解(PR),肿瘤体积缩小。4例死亡患者中,2例死于肿瘤进展,2例死于感染。回顾性对照组中,6例有5例出现PD和软脑膜播散(LMS),其中4例死亡;1例患者影像学显示完全缓解(CR)。脑脊液(CSF)分析显示NK和T细胞比例升高,IFN-γ和TNF-α水平显著降低。

对难治/复发性儿童胶质瘤患者多次鞘内注射异基因NK细胞安全且可行。尽管我们观察到复发事件减少和总生存期延长,仍需延长随访并设置适当对照组,以评估NK细胞疗法疗效。试验注册:伊朗临床试验注册中心IRCT20170122032121N6,注册日期2021年11月19日。

展开英文摘要原文

Pediatric glioma is a rare condition that can lead to significant mortality and morbidity due to its high recurrence rate. This study is a phase I nonrandomized clinical trial that was conducted to assess the safety, feasibility, and potential efficacy of the intrathecal (IT) injection of multiple doses of allogenic NK cells in pediatric patients with refractory/recurrent gliomas.

Allogeneic NK cells were isolated from random healthy unrelated donors via positive selection of CD56 + cells. Nine patients were selected according to the inclusion criteria and received weekly doses of up to 10 doses of 5 10 7 NK cells/injection. Adverse events grading was done based on Common Terminology Criteria for Adverse Events (CTCAE) Check lists. The size of the tumor, degree of spinal spreading and duration of relapse during 18 month followup were considered components of efficacy. Additionally, six patients who received conventional treatment were selected retrospectively.

Multiple intrathecal injections of allogeneic NK cells in pediatric gliomas were safe, without any serious adverse events (SAEs). The most prevalent AEs were headache [29% (17% grade 1 and 13% grade 2)], fever and chills [21% (17% grade 1 and 4% grade 2)], vomiting [13% grade 2], and back pain [12% (4% grade 1 and 8% grade 2)]. 18 months of follow-up, among the five patients in the intervention group who were still alive (August 7, 2024), three exhibited stable disease (SD), one had progressive disease (PD), and one experienced a partial response (PR) with a reduction in tumor size. Among the four deceased patients, two died due to tumor progression, and two died due to infections. In the retrospective control group, five out of six patients developed PD and leptomeningeal spread (LMS), four of whom died, and one patient showed radiological evidence of a complete response (CR). Cerebrospinal fluid (CSF) analysis revealed increases in the percentages of NK and T cells and significant reductions in the levels of IFN- and TNF- .

Multiple intrathecal injections of allogeneic NK cells are safe and feasible in pediatric patients with refractory/recurrent gliomas. Although we reported a reduction in recurrence episodes and an increase in overall survival, further studies with extended follow-up periods and appropriate control groups are necessary to assess the efficacy of NK cell therapy in these patients. TRIAL REGISTRATION: The trial was registered on the Iranian Registry of Clinical Trials (IRCT20170122032121N6), Date 2021-11-19.

论文信息

作者
Mahdizadeh H、Izadpanah A、Nouri Y、Shams P、Daneshjou D、Ahari AA、Tabibkhooei A、Haghighatkhah H
第一作者单位
Department of Research and Development, Kian Immune Cell Co., Tehran, Iran.Iran
通讯作者单位
Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran. m.ebrahimi@royan-rc.ac.ir.Iran
文献类型
I 期临床试验
期刊
BMC cancer2025 May 27
原文标识
PubMed 40426086 · DOI 10.1186/s12885-025-14314-6