Phase I Study of Donor Derived,Gene Modified, Multi-virus-specific, Cytotoxic T-Lymphocytes Redirected to GD2 for Relapsed/Refractory Neuroblastoma Post-allo Stem Cell Transplantation With Submyeloblative Conditioning
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 5
- 试验地点
- 2
- 主要终点
- Number of Participants With Immediate and Short Term Toxicity of Infusion Over 8 Weeks
研究概览
简要总结
This is a single-center, investigator-initiated, single-arm, pilot study of post-allogeneic transplant, adoptive immunotherapy for the treatment of patients with relapsed/refractory neuroblastoma expressing the mesenchymal tumor marker GD2. Three patients will be treated. The study will focus on the safety and efficacy of allogeneic, donor derived viral specific cytotoxic T-lymphocytes, retrovirally transduced to express a chimeric antigen receptor specific for disialoganglioside, GD2, expressed on neuroblastoma.
详细描述
Neuroblastoma (NB) is the most common extracranial tumor of childhood and prognosis for patients with relapsed or refractory disease is < 10% and there is no standard therapy for these patients. Research toward immunotherapeutic agents has intensified as monoclonal antibody targeting GD2, when incorporated into upfront NB therapy, prolongs survival. Allogeneic Hematopoietic stem cell transplantation (HSCT) has been utilized in patients with NB with evidence of a graft versus tumor (GVT) effect but transplant related mortality (TRM) has nullified the survival benefit. In an effort to harness the GVT effect of allogeneic transplant and lower TRM, harvested viral specific cytotoxic T-cells from the donor will be infused early post-HSCT to the HSCT recipient to shorten the recovery of immunity toward the most significant viral infections. The investigators will also retrovirally transduce the viral specific CTL with a chimeric antigen receptor (CAR) gene complex such that the tV-CTL can expand, via their native T-cell receptors in response to viral infections post-HSCT and carry the capability of killing tumor cells through their transduced receptor which, on the extracellular component of the CAR, has specificity for GD2 expressed on the surface of NB. In essence, the investigators intend to take the specificity of the monoclonal antibody to GD2, already utilized in therapy for NB, and combine this specificity with the cytotoxicity of T-cells to target NB. The investigators hypothesize that the infusion will be safe and viral specificity of the tV-CTL will provide long term immunity to both viral infections and the investigators will see anti-tumor effects.
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 Months 至 17 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Allogeneic transduced tV-CTLs with >15% expression of 14g2a.zeta chimeric antigen receptor
- •Patient or responsible person must be able to understand and sign a permission/assent or consent form for infusion
- •Age 18 months through 17 years at time of relapse/progression
- •Life expectancy >8weeks
- •Karnofsky score 60% or greater if 10 yrs old or older. Lansky score 60% or greater if under 10 yrs old
- •Patient must be HIV negative
- •ANC >500
- •Pulse ox>90% on room air
- •AST/ALT/direct bili <5x upper limit of normal
- •Recovered from toxic effects of all prior chemotherapy
- •Absence of human/anti-mouse antibody (HAMA) (patients who have received prior therapy with murine antibodies)
- •>50% donor engraftment
排除标准
- •Patient pregnant or lactating or refuses birth control methods
- •HIV positive
- •Uncontrolled intercurrent infection
- •Renal failure (creatinine clearance <40ml/min/1.73m2)
- •Active hepatitis or cirrhosis with bilirubin, AST, ALT >5xnormal
- •Rapidly progressive disease
- •Currently receiving any investigational drugs
- •Tumor potentially causing airway obstruction
- •Cardiomegaly or bilateral pulmonary infiltrates on CXR
- •Receiving >0.25mg/kg/day methylprednisolone or equivalent systemic steroid. Topical steroid therapy is acceptable
- •Receiving more than one lymphocyte inhibiting agent (ex. Tacrolimus/CSA and MMF or other similar agent
- •Patients relapsing or progressing before the age of 18 months from Stage I/II disease, and/or those who, in the opinion of their oncologist, may benefit from further conventional therapy
- •Donor lymphocyte infusion in last 28 days
- •Evidence of GvHD greater than or equal to grade 2
研究组 & 干预措施
GD2 CAR modified Tri-virus CTL infusion
A single infusion of 2x10e6 cells per meter squared was performed 30 to 120 days following allogeneic stem cell transplant.
干预措施: GD2 CAR modified Tri-virus specific cytotoxic t-cells (Biological)
结局指标
主要结局
Number of Participants With Immediate and Short Term Toxicity of Infusion Over 8 Weeks
时间窗: Post infusion week 8
Immediate: Patients were monitored following infusion to assess for toxicity related to infusion. Potential toxicities related to cellular therapy infusions, such as allergic reaction to the cellular product or cryopreservation media, hemolytic reactions, volume overload, and hemodynamic instability, were monitored. Short Term: Patients were monitored for 8 weeks for short term toxicity related to infusion. Such adverse reactions monitored were acute graft versus host disease and cytokine release syndrome.
Peak Transgene Copy Number Per 1000ng PBMC DNA
时间窗: 1 year
Peak Transgene Copy Number per 1000ng PBMC DNA from peripheral blood samples measured during study participation.
Death Within 8 Weeks of Infusion
时间窗: 8 weeks
次要结局
- Peak Viral Specific SFU/2x10e5 Mononuclear Cells Per Well(up to 1 year)
- Maximum Tumor Response (RECIST 1.1)(1 year)
研究者
Doug Myers
Principal Investigator
Children's Mercy Hospital Kansas City