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临床试验/NCT03011255
NCT03011255Unknown2 期

Phase II Study of Radiation Therapy With Peptide Specific CTL Therapy in Treating Patients With Unresectable, Advanced or Recurrent Esophageal Cancer

Shixiu Wu1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2016年12月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
发起方
入组人数
20
试验地点
1
主要终点
Local control

研究概览

简要总结

Immunotherapy is now considered to be one of promising approaches for treating cancer. Radiation therapy has been to be a cornerstone treatment for unresectable advanced esophageal cancer. Radiation-induced mutation genes were identified as new sources of tumor associated antigens using exon sequencing and peptide microarray technologies. Epitope peptides for these targets are able to induce peptide specific cytotoxic T lymphocytes (CTL). In this clinical trial, investigators evaluate the efficacy and safety of peptide specific CTL therapy in combination with radiation therapy in treating patients with unresectable, advanced or recurrent esophageal cancer.

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 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients must have unresectable, locally advanced, recurrent disease of esophageal cancer. Histologically confirmed cancer of the esophagus.
  • measurable disease by CT scan
  • ECOG performance status of 0 to 2
  • Expected survival of at least 3months
  • Laboratory values as follow:
  • Absolute neutrophil count (ANC) ≥ 1.5×109
  • White blood cell count ≥ 3×109/L
  • Platelets ≥ 100×109/L
  • Haemoglobin (Hb) ≥ 10g/dL (patients'Hb should be corrected to >10g/dL before treatment)
  • Adequate liver function (within 1 week prior to randomization)
  • Serum bilirubin ≤ 1.5× ULN
  • Alanine aminotransferase/aspartate transaminase (ALT / AST) ≤ 2.5× ULN
  • Alkaline phosphatase (ALP) ≤ 3× ULN
  • Able and willing to give valid written informed consent

排除标准

  • Pregnancy (women of childbearing potential:Refusal or inability to use effective means of contraception)
  • Breastfeeding
  • Active or uncontrolled infection
  • Prior chemotherapy, radiation therapy or immunotherapy
  • Concurrent treatment with steroid or immunosuppressing agent
  • Patient with peptic ulcer disease
  • Other malignancy within 5 years prior to entry into the study, expect for treated non-melanoma skin cancer and cervical carcinoma in situ
  • Disease to the central nervous system
  • Decision of unsuitableness by principal investigator or physician-in-charge

研究组 & 干预措施

peptide specific CTL arm

Experimental

peptide specific CTL, radiation

干预措施: peptide specific CTL (Biological)

结局指标

主要结局

Local control

时间窗: two years after enrollment

occurrence of local or regional progression

次要结局

  • Overall survival(1 year)
  • Objective response rate as assessed by RECIST criteria(3 months)
  • Time to progression(1 year)
  • Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability](3 months)

研究者

发起方
Shixiu Wu
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Shixiu Wu

director of the hospital

Hangzhou Cancer Hospital

研究点 (1)

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