NL-OMON47175已完成不适用
Obtaining and analyzing plasmasamples from patients with non small cell lung cancer, referred for radiation treatment and/or chemotherapy - ICD
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 20
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 64（—）
入选标准
- •Participant is willing and able to give informed consent for participation in the trial.
- •Male or female, aged 18 years or above.
- •Diagnosed with non-small cell lung cancer
- •Scheduled to receive one of the following two therapeutic strategies:
- •- Concurrent cisplatin-doublet chemotherapy and radiotherapy (minimal dose of 60 Gy in fractionated non-ablative doses) in patients with stage III NSCLC
- •- SBRT for stage I NSCLC: 54Gy in 3 fractions, 48 Gy in 4 fractions or 60 Gy in 8 or 5 fractions
- •Is able and willing to comply with all trial requirements.
排除标准
- •- Chronic use of corticosteroids, except when used as anti-emetics for chemotherapy or inhalers
- •- NSAIDs taken until 5 days before radiotherapy or during radiation (low dose Aspirin at a maximum of 160 mg/day, is allowed)
- •- Active auto-immune diseases
- •- Immunosuppressive medication
研究者
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