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临床试验/KCT0001271
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.

The Catholic University of Korea, Seoul St. Mary's Hospital0 个研究点目标入组 11 人开始时间: 待定最近更新:
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.

研究者

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