A Study of CMV-TCR-T Cells in the Treatment of Refractory CMV Viremia After HSCT
试验速览
- 阶段
- 1 期
- 发起方
- 入组人数
- 12
- 试验地点
- 1
- 主要终点
- Adverse events
研究概览
简要总结
This is a single centre, single arm, open-label, phase I study to evaluate the safety and effectiveness of CMV-TCR-T cell immunotherapy in treating refractory CMV infection after HSCT.
详细描述
CMV infection is a major and potentially life-threatening complication after allogenic hematopoietic stem cell transplantation (allo-SCT). Pharmacotherapy with ganciclovir and foscarnet remains the mainstay of treatment and has significantly improve clinical results, however, it is unsatisfactory owing to toxicity, limited efficacy and risk of developing resistance.
In recent years, adoptive T cell therapy has been proposed as an alternative option for CMV infection after allo-SCT. However, patients with transplants from CMV-negative donors are at highest risk, and an adoptive therapy is missing because CMV-specific T cells are not available.
CMV TCR-transduced donor-derived T Cells (CMV-TCR-T cells) is an attractive strategy to specifically redirect T-cell immunity toward CMV. In this prospective clinical phase I trial, we propose to evaluate the safety and efficacy of stem cell donor-derived CMV-TCR-T cells for patients with refractory CMV infection after allo-SCT. Donor derived CMV-TCR-T(HLA-A*1101\0201\2402) cells will be intravenously infused with a escalated dose of 0.3-1×10E7CMV-TCR-T cells. The CMV DNA copies and CMV-TCR-T cell proliferation will be monitored in the scheduled time (day 0, day 4, day 7, day 10, day 14, day 28).
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with acute leukemia (AL) or myelodysplastic syndrome (MDS) who receive haploid allogeneic hematopoietic stem cell transplantation, pre-transplantation assessment ≤CR2;
- •Age 18-60, including boundary value, gender unlimited;
- •Refractory CMV infection occurred in the early stage of transplantation : After 2 weeks of standard antiviral treatment, the CMV DNA copy number continued to be ≥1000 copies/mL, and the CMV DNA copy number at the beginning of the treatment decreased by <log10 ；
- •The transplant donor's HLA-A matching is one of 2402, 0201 or 1101, and the physical examination is qualified;
- •ECOG ≤ 3, estimated life expectancy> 3 months;
- •Patients who voluntarily sign informed consent and are willing to comply with treatment plans, visit arrangements, laboratory tests and other research procedures.
排除标准
- •Patients with active aGVHD III-IV and / or mild and severe cGVHD;
- •Have received cell therapy such as DLI, CTL, CAR-T, NK or participated in any other clinical research on drugs and medical devices;
- •Patients who have developed CMV disease;
- •patients with organ failure:
- •Heart: NYHA heart function grade IV;
- •Liver: Grade C that achieves Child-Turcotte liver function grading;
- •Kidney: kidney failure and uremia;
- •Lung: symptoms of respiratory failure;
- •Brain: a person with a disability;
- •Pregnant or lactating women;
- •The researchers found that it was unsuitable for the recipients to be enrolled.
结局指标
主要结局
Adverse events
时间窗: 3 months
Percentage of participants with adverse events
次要结局
- CMV-specific immunity reconstitution(3 months)
- Changes of CMV-DNA copies(3 months)
研究者
Xiao-Jun Huang
Director
Peking University People's Hospital