决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Treatment of CD19 Chimeric Antigen Receptor T Cells for Pediatric Patients With CD19-positive B-cell Acute Lymphoblastic Leukemia Who Are Indicated for Hematopoietic Stem Cell Transplantation
⚠ 该试验的登记信息已有 32 个月未更新, 页面上显示的「招募中」可能已经失效。联系研究中心之前,建议先到 ClinicalTrials.gov 核对登记原文的最新状态与联系方式。
这是一项 II 期注册临床试验,评估 CD19CAR-T 细胞治疗急性淋巴细胞白血病的安全性、可行性及初步疗效。当前状态:招募中。计划入组 50 例。试验地点:韩国 · 首尔(共 1 个中心)。登记号:NCT06247501。
不限性别 · ≤ 25 Years
纳入标准:接受SNUH-CD19-CAR-T治疗时年龄<25岁;由首诊医生确认初诊为B细胞急性淋巴细胞白血病;初诊时免疫表型分析确认白血病细胞表达CD19,血液学复发患者须在确认复发时再次确认CD19表达;一线或二线化疗(首次挽救治疗)后达到血液学完全缓解(骨髓原始细胞<5%);符合造血干细胞移植适应症,至少满足一项:存在t(9;22)(q34;q11)易位导致费城染色体阳性;低二倍体(染色体<44条);t(17;19)易位导致E2A-HLF融合基因;巩固及维持治疗后通过二代测序检测MRD≥0.01%;一线治疗失败;或研究者判定适合接受移植。排除标准:既往接受造血干细胞移植;无法获得或缺乏足以制备SNUH-CD19-CAR-T的合格白细胞单采产品;已知HIV感染;研究者判定的未控制活动性感染(若已接受适当治疗且入组时无进展迹象,可视为已控制;无其他症状的持续发热不视为感染进展);妊娠或哺乳;研究者根据临床判断认为不适合参加试验。
Inclusion Criteria: * Subject eligibility criteria include individuals who are under the age of 25 at the time of SNUH-CD19-CAR-T administration. Confirmation of B-cell acute lymphoblastic leukemia diagnosed at the initial assessment by a treating physician for the first diagnosis is required. Immunophenotypic analysis of CD19 expression on leukemia cells must be confirmed through immune profiling at the time of the initial diagnosis of B-cell acute lymphoblastic leukemia. In patients experiencing hematologic relapse of B-cell acute lymphoblastic leukemia, CD19 expression should also be confirmed at the time of relapse confirmation. Patients must achieve hematologic complete remission defined as less than 5% blasts in the bone marrow after the first-line or second-line chemotherapy (first salvage therapy). Eligible patients for hematopoietic stem cell transplantation, defined by indications for transplantation, include those meeting at least one of the following criteria: 1. Philadelphia chromosome-positive due to t(9;22)(q34;q11) translocation. 2. Hypodiploidy defined by fewer than 44 chromosomes. 3. E2A-HLF gene fusion due to t(17;19) translocation. 4. Detection of minimal residual disease (MRD) positive at 0.01% or higher by next-generation sequencing confirmed after consolidation therapy and maintenance therapy. 5. Failure of the first-line therapy. 6. Cases not meeting any of the above criteria but deemed eligible for hematopoietic stem cell transplantation based on the investigator's judgment. Exclusion Criteria: * Patients who have undergone hematopoietic stem cell transplantation. * Individuals for whom an adequate or sufficient leukapheresis product suitable for the production of SNUH-CD19-CAR-T cannot be obtained or is unavailable. * Those known to be infected with the human immunodeficiency virus (HIV). * Presence of uncontrolled active infections, determined by the investigator's assessment. If appropriate treatment has been administered for the infection, and there are no signs of progression at the time of enrollment, it is considered controlled. Persistent fever without other symptoms is not interpreted as progressive infection. * Women who are pregnant or breastfeeding. * Individuals deemed clinically inappropriate for participation in the clinical trial based on the investigator's clinical judgment.
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。
主要终点:Event free survival · above 3 year
次要终点:Overall survival
II期临床试验,研究对象为确诊CD19阳性B细胞急性淋巴细胞白血病、被视为极高危的儿童及青少年患者。对符合造血干细胞移植条件的患者,本研究拟使用CD19 CAR-T治疗作为造血干细胞移植的替代方案。患者年龄≤25岁。
This is a phase 2 clinical trial targeting pediatric and adolescent patients diagnosed with CD19-positive B-ALL, considered very high-risk group. The study aims to administer CD19 CAR-T therapy as an alternative to hematopoietic stem cell transplantation in patients eligible for such transplantation. The trial includes patients aged 25 or younger.
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