KCT0001271已完成未知
Safety and efficacy of administration of EBV specific cytotoxic T lymphocytes in chemotherapy responding EBV positive NK/T cell lymphoma patients.
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 11
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 14(Year) 至 74(Year)(—)
- 性别
- All
入选标准
- •Patients matching all of the following were included:
- •1)Histologically verified extranodal NK/T-cell lymphoma, nasal type, according to the World Health Organization (WHO) classification
- •2)Achieved complete response (CR) following induction or salvage therapy.
- •3)Patients who are at least 14 years old up to 74 years old
- •4) Eastern Cooperative Oncology Group (ECOG) performance rating of 0, 1, 2
- •5) Patients with adequate kidney function (serum creatinine less than 1.5 times the normal upper limit)
- •6) Patients with adequate liver function (bilirubin less than 1.5 times the normal upper limit in the serum)
- •7) Patients with adequate heart function (there should be no specific electrocardiographic findings according to the principal investigator's judgment)
- •8) No evidence of secondary tumor, heart failure, infection chronic lung disease ultimately according to the principal investigator's judgment.
- •9) Voluntarily signed the informed patient consent
排除标准
- •Patients with any of the following were excluded from the study:
- •1) Pregnancy, lactation or potential of pregnancy
- •2) Bacterial or fungal infection of unknown cause or patients with fever (=38?) or active infection in progress
- •3) Patients under 14 years old or over 75 years old
- •4) Eastern Cooperative Oncology Group (ECOG) performance rating of 3, 4
- •5) Previously demonstrated human immunodeficiency virus (HIV) infection, hypertension (diastolic blood pressure >115mmHg), unstable angina, congestive heart failure (NY class II or higher), severe diabetes that is not well controlled, coronary angioplasty within the last 6 months, patients with acute myocardial infarction or non-malignant diseases including atrial ventricular arrhythima within the past six months
- •6)Patients with a mental disorder or substance abuse that is considered to affect the results of the research
- •7) Patients participating in another clinical trial
- •8) Patients with other serious medical conditions.
- •9) Patients who did not achieve complete response following inital therapy, including chemotherapy and/or radiotherapy, salvage therapy, or high-dose therapy and stem cell transplantation.
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