Multi-center Phase I/II Study of NY-ESO-1 T Cell Receptor Gene Transferred T Lymphocytes in Patients with Synovial Sarcoma
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 8
- 试验地点
- 5
- 主要终点
- (Phase I) Adverse event, mortality, severe adverse event, discontinuation due to adverse event, laboratory test values
研究概览
简要总结
The purpose of this study is to evaluate the safety and the efficacy of TBI-1301 for NY-ESO-1 expressing synovial sarcoma when administered following cyclophosphamide pre-treatment.
详细描述
Following pre-treatment with cyclophosphamide, NY-ESO-1-specific T cell receptor (TCR) gene transduced T lymphocytes are transferred to human leukocyte antigen (HLA)-A*02:01 or HLA-A*02:06 positive patients with synovial sarcoma expressing NY-ESO-1, which are surgically unresectable and refractory to anthracycline therapy. The primary objective is to evaluate the safety in the phase 1 and the efficacy in the phase 2.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Sequential
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Histologically confirmed synovial sarcoma
- •Surgically unresectable tumor
- •Progressing or recurrent synovial sarcoma which has been treated with 1-4 regimens of systemic chemotherapies including anthracycline
- •HLA-A*02:01 or HLA-A*02:06 positive
- •Tumor that express NY-ESO-1 by immunohistochemistry
- •≥ 18 years of age
- •Measurable lesions that are evaluable by the RECIST ver1.1
- •ECOG Performance Status of 0, 1 or 2
- •No treatment such as chemotherapy and be expected to recover fully from the previous treatment at the time of the lymphocytes collection for manufacturing
- •Life expectancy ≥ 16 weeks after consent
- •No severe damage on the major organs (bone marrow, heart, lung, liver, kidney, etc) and meet the following lab value criteria; Total bilirubin ≤ 1.5 x upper limit of normal (ULN); AST(GOT), ALT(GPT) < 3.0 x ULN; Creatinine < 1.5 x ULN; 2,500/μL < WBC ≤ULN; Hemoglobin ≥ 8.0g/dL; Platelets ≥ 75,000/μL
- •Patients must be able to understand the study contents and to give a written consent at his/her free will. Additionally, if patients are below 20 years of age, proxies must be able to give a written consent.
排除标准
- •Patients with the following conditions are excluded from the study; Unstable angina, cardiac infarction, or heart failure; Uncontrolled diabetes or hypertension; Active infection; Obvious interstitial pneumonia or lung fibrosis by chest X-ray; Active autoimmune disease requiring steroids or immunosuppressive therapy.
- •Active metastatic tumor cell invasion into CNS
- •Active multiple cancer
- •Positive for HBs antigen or HBV-DNA observed in serum
- •Positive for HCV antibody and HCV-RNA observed in serum
- •Positive for antibodies against HIV or HTLV-1
- •Left Ventricular Ejection Fraction (LVEF) ≤ 50%
- •History of serious hypersensitivity reactions to bovine or murine derived substances.
- •History of hypersensitivity reaction to ingredients or excipients of investigational drugs used in this study
- •History of hypersensitivity reaction to antibiotics used in manufacturing for the investigational drug used in this study.
- •Pregnant females, lactating females (except when they cease and do not resume lactation) or female and male patients who cannot agree to practice the adequate birth control from the consent to 6 months after infusion of the investigational drug.
- •Clinically significant systemic illness that in the judgment of the PI or sub-investigator would compromise the patient's ability to tolerate protocol therapy or significantly increase the risk of complications.
研究组 & 干预措施
Split dose of 5x10^9 TBI-1301
Split dose of 5x10^9 TBI-1301 will be administered intravenously for 2 days following cyclophosphamide pre-treatment 750 mg/m2/d for 2 days.
干预措施: TBI-1301 (Biological)
Split dose of 5x10^9 TBI-1301
Split dose of 5x10^9 TBI-1301 will be administered intravenously for 2 days following cyclophosphamide pre-treatment 750 mg/m2/d for 2 days.
干预措施: Cyclophosphamide (Drug)
结局指标
主要结局
(Phase I) Adverse event, mortality, severe adverse event, discontinuation due to adverse event, laboratory test values
时间窗: 52 weeks
Confirm the toxicity profile, which is measured by the degree of grade and seriousness, duration, causality, classification, etc. of the adverse events.
(Phase I) Appearance of replication competent retrovirus (RCR) by PCR
时间窗: 52 weeks
Confirm that no replication competent retrovirus observed.
(Phase I) Blood kinetics of TBI-1301 by realtime-PCR
时间窗: 52 weeks
Evaluate persistence and expansion of transferred TBI-1301.
(Phase II) Overall response rate
时间窗: 52 weeks
Evaluate response rate by measuring response using RECIST v1.1 and irRECIST
(Phase I) Appearance of clonality by linear amplification mediated (LAM)-PCR
时间窗: 52 weeks
Confirm that no clonality is observed.
次要结局
- (Phase I) Objective response rate(52 weeks)
- (Phase I/II) Progression free rate(12 weeks)
- (Phase I/II) Progression free survival(52 weeks)
- (Phase I/II) Overall survival(52 weeks)
- (Phase II) Adverse event, mortality, severe adverse event, discontinuation due to adverse event, laboratory test values(52 weeks)
- (Phase II) Appearance of RCR(52 weeks)
- (Phase II) Appearance of clonality (LAM-PCR)(52 weeks)
- (Phase II) Blood kinetics of TBI-1301 by realtime-PCR(52 weeks)