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CD19靶向CAR-T细胞自体回输治疗儿童复发/难治性B细胞急性淋巴细胞白血病/淋巴瘤

英文原题:CD19-targeted CAR T Cell Autotransfusion for the Treatment of Recurrent/Refractory B-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma in Children With CD19+

ClinicalTrials.gov 2024/04/09(首次登记) 注册临床试验(分期未标注) · 招募中

⚠ 该试验的登记信息已有 30 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。

简要介绍

这是一项分期未标注的注册临床试验,评估 CAR-T 细胞治疗白血病、淋巴瘤的安全性、可行性及初步疗效。当前状态:招募中。计划入组 60 例。试验地点:中国 · 天津(共 2 个中心,其中中国 2 个)。登记号:NCT06355739。

入组条件决定能不能参加

不限性别 · ≥ 3 Years 且 ≤ 18 Years

纳入标准:年龄3-18岁(含),男女不限;临床诊断复发/难治性B细胞急性淋巴细胞白血病/淋巴母细胞淋巴瘤,且至少符合以下一项:标准诱导化疗方案至少2个疗程后未达到完全骨髓缓解(MRD>1%);治疗前特异性分子标志物及免疫表型提示疾病,但治疗后未转阴;化疗期间复发、停药后早期复发(<12个月)或完全缓解后晚期复发(≥12个月),且1个标准诱导治疗疗程后仍未完全缓解(MRD>1%);骨髓移植后复发;单纯骨髓、单纯髓外(睾丸白血病、中枢神经系统白血病)或两者联合复发;Lansky评分≥60;治疗相关抗原检测阳性(CD19/CD20/CD22);签署知情同意书时预期生存期>3个月;血红蛋白≥70 g/L(可输血);肝肾及心肺功能符合:肌酐≤正常值上限1.5倍,LVEF≥50%,血氧饱和度>90%,总胆红素≤正常值上限1.5倍,ALT和AST≤2.5倍。排除标准:严重心功能不全、LVEF<50%;严重肺功能损害史;合并其他晚期恶性肿瘤;严重且无法有效控制的感染;严重自身免疫病或先天性免疫缺陷;活动性肝炎(HBV DNA或HCV RNA阳性);HIV感染或已知AIDS、梅毒感染;对生物制品(包括抗生素)有严重过敏史;异体造血干细胞移植后停用免疫抑制剂1个月仍有急性GVHD;其他可能增加参加风险、干扰研究结果或被研究者判定不适合参加的严重身心疾病或实验室异常。
核对登记原文(英文)
Inclusion Criteria:

1, age 3-18 years old (including boundary value), male and female;

2\. The patient was clinically diagnosed as relapsed/refractory B acute lymphoblastic leukemia/lymphoblastic lymphoblastic

Patients with tumors who meet one of the following conditions:

• Complete marrow response (MRD\>1%) or not achieved after at least 2 courses of standardized induction regimen chemotherapy

Complete response at the molecular level and immunology (characterized by specific molecular markers and immunophenotypes prior to treatment)

Patients, did not turn negative after treatment);

* Recurrence during chemotherapy, early recurrence after drug withdrawal (\<12 months) or late recurrence after complete remission (≥

  12 months) and did not achieve complete remission after 1 course of standard induction regimen (MRD\>1%);
* Recurrence after bone marrow transplantation;
* Simple bone marrow, simple extramedullary (testicular leukemia, central nervous system leukemia) or combined

recrudescence

3\. Lansky score ≥60;

4, the treatment related antigen test result is positive (CD19/CD20/CD22);

5\. The expected survival period from the signing date of the informed consent is more than 3 months;

6, HGB≥70g/L (blood transfusion);

7, liver and kidney function, cardiopulmonary function meet the following requirements:

1. Creatinine ≤1.5×ULN;
2. Left ventricular ejection fraction ≥50%;
3. Blood oxygen saturation \>90%;
4. Total bilirubin ≤1.5×ULN; ALT and AST≤2.5 x ULN.-

   Exclusion Criteria:
   * 1, severe cardiac insufficiency, left ventricular ejection fraction \<50%;

     2, have a history of severe lung function impairment;

     3\. Combined with other advanced malignant tumors;

     4, combined with serious infection and can not be effectively controlled;

     5, combined with serious autoimmune disease or congenital immune deficiency;

     6, active hepatitis (hepatitis B virus deoxyribonucleic acid \[HBVDNA\] or hepatitis C virus ribonucleic acid \[HCVRNA\] positive);

     7, human immunodeficiency virus (HIV) infection or known acquired immunodeficiency syndrome (AIDS), or syphilis infection;

     8\. Have a history of severe allergy to biological products (including antibiotics);

     9\. Patients with allogeneic hematopoietic stem cell transplantation still had acute graft-versus-host response (GvHD) one month after immunosuppressant discontinuation;

     10, the presence of other serious physical or mental illnesses or abnormalities in laboratory tests that may increase the risk of participating in the study or interfere with the study results, as well as patients deemed unsuitable for participation in the study by the investigator.

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

  • 主要终点总生存期及无事件生存期CAR-T细胞输注后24个月。
  • 次要终点总缓解率
  • 次要终点不良事件
核对登记原文(英文)

主要终点:Overall survival and event-free survival · The prognosis of ALL children who underwent CAR-T cell therapy · 24 months post CAR-T cell infusion
次要终点:Overall remission rate;Adverse events

研究设计怎么做的

研究类型
干预性研究
入组人数
60 人(预计)
分组方式
不适用(单臂)
  • 儿童B细胞急性淋巴细胞白血病CD19自体细胞回输其他
核对分组登记原文(英文)
  • CD19 autotransfusion for B-cell acute lymphoblastic leukemia in children · OTHER

关键日期

开始日期
2024-02-01
主要完成日期
2026-12-01
全部完成日期
2027-01-15
登记状态核实于
2024-04

联系与责任方

主要研究者
Zhu Xiaofan
申办方
Zhu Xiaofan

登记简述

评估BIC-19GG、BIC-2019和BIC-2219治疗儿童复发/难治性B细胞急性淋巴细胞白血病/淋巴母细胞淋巴瘤的安全性和疗效。

核对登记原文(英文)

To evaluate the safety and efficacy of BIC-19GG, BIC-2019, BIC-2219 in the treatment of relapsed/refractory B acute lymphoblastic leukemia/lymphoblastic lymphoma in children

登记原文与核验信息

试验登记号
NCT06355739
试验期别
NA
试验状态
招募中
中国试验中心(2 个)
Department of Pediatrics, Institute of Hematology and Blood Disease Hospital, Chinese Academy of Medical Sciences · 天津 · 中国 | InstituteHBDH · 天津 · 中国
适应症(原文)
B Lymphocytic Leukemia; B Lymphoblastic Lymphoma
干预方式(原文)
CAR T cell injection