简要介绍
这是一项 II 期注册临床试验,评估细胞治疗用于胶质母细胞瘤、胶质瘤的安全性、可行性及初步疗效。当前状态:招募中。计划入组 40 例。试验地点:其他 · 德黑兰(共 1 个中心)。登记号:NCT06687681。
入组条件决定能不能参加
不限性别 · ≥ 3 Years 且 ≤ 70 Years
纳入标准:根据WHO分类新诊断的3或4级脑肿瘤,且属于以下类型之一:IDH突变型星形细胞瘤;IDH突变型少突胶质细胞瘤;IDH野生型胶质母细胞瘤;弥漫性中线胶质瘤;弥漫性半球胶质瘤;IDH野生型弥漫性儿童型高级别胶质瘤;年龄3-60岁,性别不限;Lansky/Karnofsky体能状态评分>60;患者、父母或儿童患者法定监护人知情同意;血红蛋白>10 g/dL;绝对粒细胞计数>500/μL;血小板>50000/μL;INR<2且PTT<正常值上限1.5倍;血浆胆红素<正常值上限1.5倍;ALT和AST<正常值上限3倍;血浆肌酐<正常值上限1.5倍。排除标准:MRI或磁共振波谱(MRS)显示放射性坏死;因急症无法耐受新治疗;其他恶性肿瘤史;免疫缺陷病或免疫功能受损状况史;脑脊液分流装置破裂或无法进行腰椎穿刺;妊娠;未控制慢性疾病史,如糖尿病、充血性心力衰竭、肝硬化、慢性肾病等。
核对登记原文(英文)
Inclusion Criteria: New diagnosed patients with grade 3 or 4 brain tumor, based on WHO classification, which are included in the one of the following conditions: • Astrocytoma, IDHmutant • Oligodendroglioma, IDH-mutant • Glioblastoma, IDH-wild type • Diffuse midline glioma • Diffuse hemispheric glioma • Diffuse pediatric-type high-grade glioma, IDH-wild type Age range of 3 to 60 years old both sex Lansky/Karnofsky performance score above 60 Obtained informed consent of patients or parents or legal attendance in cases of pediatrics Hemoglobin above 10 gr/dL of blood Absolute granulocyte count (AGC) above 500 per microliter of blood Platelet count above 50000 per microliter of blood INR below 2 and PTT less than 1.5 times of maximum normal value Plasma bilirubin level less than 1.5 times of maximum normal value Plasma hepatic transaminases (ALT and AST) level less than 3 times of maximum normal value Plasma creatinine level less than 1.5 times of maximum normal value -
Exclusion Criteria: Evidence of radio necrosis in MRI or MRS Intolerance of new treatment due to emergency condition History of other malignancies History of any immunodeficiency diseases or any immune compromising conditions Rupture of cerebral shunt or unable to perform a lumbar puncture Pregnancy History of uncontrolled chronic diseases such as: Diabetes, CHF, liver cirrhosis, CKD, etc
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以上为辅助阅读译文。是否适合入组须由主治医生判断,最终以登记平台与研究者确认为准。
研究终点衡量什么算有效
- 主要终点鞘内NK细胞输注后的肿瘤反应从入组至治疗结束,最长12个月。
- 次要终点不良事件(AE)
核对登记原文(英文)
主要终点:To measure tumor response after infusion of intrathecal NK cells · Imaging and Immunotherapy Response Assessment in Neuro-oncology (iRANO) guidelines · From enrollment to the end of treatment at 12 months
次要终点:Adverse Events (AEs)
研究设计怎么做的
- 研究类型
- 干预性研究
- 入组人数
- 40 人(预计)
- 分组方式
- 随机分组
核对分组登记原文(英文)
- Test group · EXPERIMENTAL · patients will recieve 3 cources of 2\* 10 8 intrathecal infusion of NK cells every 3 weeks
- Control group · NO_INTERVENTION · patients will recieve only conventional treatment
关键日期
- 开始日期
- 2024-11-25
- 主要完成日期
- 2025-11-25
- 全部完成日期
- 2027-11-25
- 登记状态核实于
- 2025-04
联系与责任方
- 主要研究者
- Marzieh Ebrahimi
- 申办方
- Marzieh Ebrahimi
- 联系邮箱
- mebrahimi@royan-rc.ac.ir
- 联系电话
- +98 21 235 62516
登记简述
胶质瘤是最常见的恶性脑肿瘤,常见高级别肿瘤,儿童和成人患者预后较差、生存率较低。手术切除是主要治疗方式,也可采用全脑放疗,但后者有显著副作用,且研究显示对改善生存的作用有限。靶向治疗及近期研究的新方法可使部分肿瘤缩小,但多数患者初始缩小后仍复发,因此延长生存的效果有限。过去20年,免疫治疗,尤其是特异性免疫细胞治疗,已成为一种新方法,可识别并清除癌细胞,特别适用于传统疗法效果有限的肿瘤。自然杀伤(NK)细胞是有前景的免疫治疗方法之一。研究团队目前已在胶质瘤患者中开展I期临床试验。
核对登记原文(英文)
Gliomas are the most common malignant brain tumors, which are often associated with high-grade tumors characterized by an inferior prognosis and low patient survival rates in both children and adults. Surgical removal and tumor resection are the primary treatment approaches for gliomas. In such cases, whole-brain radiation therapy is also employed as a therapeutic option, which itself has significant side effects, and studies have shown limited impact on improving patient survival. Targeted therapy and recently investigated approaches such as targeted therapy have shown some tumor regression, but in most cases, tumor recurrence has been observed after initial regression. Therefore, they have a limited impact on prolonging patient survival. Immunotherapy, particularly immunotherapy with specific immune cells, can effectively identify and eliminate cancer cells and has been utilized as a new approach in the past two decades, especially in cancers where conventional methods have limited success. Among the effective immunotherapy methods, using natural killer cells (NK cells) can be one of the promising approaches. Currently, phase I clinical trials have been conducted by our research group in patients with gliomas.