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临床试验/NCT02488850
NCT02488850已完成不适用

Determination of Peripheral Immune Cell Activity During Treatment With Either Surgery or Radiotherapy in Patients With Early Stage Non-small Cell Lung Cancer HAMLET Study

Erasmus Medical Center4 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2012年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
32
试验地点
4
主要终点
Number of IFN-gamma/ Granzyme B producing CD8 T cells

研究概览

简要总结

Rationale: An anatomical surgical resection is considered to be the standard of care in fit patients who present with early stage non-small cell lung cancer (NSCLC). However, surgery is less frequently performed in both elderly patients (aged ≥75 years), who represent the fastest-growing group of patients with stage I/II NSCLC, and in patients who have significant co-morbidity. Following the introduction of stereotactic ablative radiotherapy (SABR), an outpatient treatment that is typically delivered in between 3-8 fractions, the median survival of all elderly patients undergoing radiotherapy in The Netherlands increased by 9.3 months. Randomized trials comparing SABR and surgery have yet to be completed and results of the ongoing ACOSOG Z4032 studies will not be available in the within 5 years. A recent data retrospective study comparing both modalities has raised interesting questions about the impact of local therapy on recurrence patterns. It was found that a better loco-regional disease control rate was achieved with SABR.

Objective: To study the effect of surgery and SABR on both immunostimulatory (with primary endpoint CD8 positive cells) and immunosuppressive cells in peripheral blood in patients with early stage non-small cell lung cancer who are treated with either modality.

Study population: 40 patients with cT1-2aN0M0 either cytologically or histologically proven NSCLC.

Main study parameters/endpoints: To determine whether an increase in CD8 activity can be established after SABR in patients with early stage lung cancer and to compare this increase with that in patients undergoing a surgical intervention. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Only risks in participation are the risks with drawing blood. Subjects will not have any benefits. This pilot study will be used to generate information concerning both treatments useful for the decision to plan a future study in a larger series of patients.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Basic Science
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

入选标准

  • Cytologically or histologically proven cT1-2aN0M0 NSCLC
  • Patients ≥ 18 years old
  • Patients should be fit to undergo both treatments in accordance with institutional protocols

排除标准

  • Patients with any signs of any co-existing infectious disease or immunosuppressive treatment (inhalation steroids are permitted)
  • Mentally incapacitated subjects

结局指标

主要结局

Number of IFN-gamma/ Granzyme B producing CD8 T cells

时间窗: Week 6

Number and activation status of peripheral CD8+ T cells

次要结局

  • CD4/CD8 ratio in peripheral blood(Week 6)
  • number of regulatory T cells(Week 6)
  • Activation marker expression on T cells(Week 6)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Joachim Aerts, MD PhD

Prof. dr.

Erasmus Medical Center

研究点 (4)

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