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临床试验/NCT02551211
NCT02551211终止不适用

Association Between Circulating Immune Cells and the Tumor Immune Contexture in Resectable Non-small Cell Lung Cancer

University Hospital, Rouen1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2016年12月14日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
发起方
入组人数
22
试验地点
1
主要终点
Level of expression of the T regulator over total lymphocytes count ratio in the blood

研究概览

简要总结

With the recent approval of Nivolumab for second-line treatment of stage IIIb/IV non-small cell lung cancer (NSCLC), immune checkpoint inhibitors are entering the standard of care for lung cancer. Other immune checkpoint inhibitors are under evaluation, both in resectable and non-resectable NSCLC. In order to refine our use of these molecules, comprehensive data on the immune contexture of NSCLC are needed. Moreover,a blood marker of this contexture would allow physicians to monitor the immune status of their patient's tumor and though to evaluate the rightful place of immunotherapy in the multimodal treatment of NSCLC. No such blood marker has been validated so far. The LYMPHOLUNG study investigate the concordance between blood and intratumoral counts of immune cells in resectable stage I to IIIA NSCLC. By the use of 30-marker cytometry, a precise immune profile of NSCLC will be depicted. The prognostic value of the circulating and intra-tumoral T regulator over total lymphocytes ratio for 2-year recurrence-free survival will also be addressed.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
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

  • •Men and women over 18 years of age
  • •Histologically- or cytologically- confirmed non-small cell lung cancer diagnostic
  • •Stage I, II or IIIA NSCLC (according to version 7 of the International Association for the Study of Lung Cancer Staging Manual in Thoracic Oncology). Staging must have included an abdominal and thoracic CTscan, a CTscan or MRI of the brain and a 18FDG PETscan
  • •Subjects for whom a surgical resection is indicated
  • •Signed written informed consent

排除标准

  • •- previous, ongoing or planned neo-adjuvant treatment (chemotherapy, targeted therapy, immunotherapy or radiotherapy)
  • •contraindications to general anesthesia
  • •contraindication to the planned surgical resection
  • •history of immunosuppressive disorder
  • •known history of testing positive for human immunodeficiency virus
  • •subjects with a condition requiring systemic treatment with either corticosteroids or other immunosuppressive medications within 30 days of randomization.
  • •clinical suspicion of active infection (either acute or chronic)
  • •severe (hemoglobin < 8.0 g/dL) or symptomatic anemia
  • •women of childbearing potential must have a negative urine pregnancy test
  • •women must not be breastfeeding
  • •prisoners or subjects who are involuntarily incarcerated
  • •subjects under guardianship

研究组 & 干预措施

Patients with resectable non-small cell lung cancer

Experimental

干预措施: surgical resection of cancer (Procedure)

Patients with resectable non-small cell lung cancer

Experimental

干预措施: blood drawn (Procedure)

结局指标

主要结局

Level of expression of the T regulator over total lymphocytes count ratio in the blood

时间窗: Day 1

Level of expression of the T regulator over total lymphocytes count ratio into the tumor

时间窗: Day 1

次要结局

  • Number of patient alive 2 years after resection(2 years)
  • Number of cell population counts as blood markers for the corresponding population in the tumor(Day 1)

研究者

发起方
University Hospital, Rouen
申办方类型
Other
责任方
Sponsor

研究点 (1)

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