NL-OMON53651撤回不适用
Improving Standard of Care lifestyle support for stage III NSCLC cancer patients - PERCUSSIO
适应症
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 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
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Pathological diagnosis of adequately staged (according to standard practice
- •using chest-CT, FDG-PET, brain imaging MRI/CT) NSCLC
- •Participant is willing and able to give informed consent for participation in
- •Aged 18 years or above
- •Scheduled to receive one of the following two therapeutic strategies:
- •o Concurrent chemotherapy and radiotherapy with photons (60 Gy in 30 fractions
- •of 2 Gy) followed by durvalumab in patients with stage III NSCLC
- •o Concurrent chemotherapy and radiotherapy with protons (60 Gy in 30 fractions
- •of 2 Gy) followed by durvalumab in patients with stage III NSCLC
- •Is able and willing to comply with all trial requirements
排除标准
- •- Mixed non-small cell lung cancer with other histology such as small cell lung
- •- Not able to comply with the study protocol
- •- Less than 18 years* old
- •- Pregnancy or not able to comply with adequate contraception in women with
- •child baring potential
- •- Previous radiotherapy to the chest for benign or malignant conditions,
- •including radiation for breast cancer
- •- Previous malignancies treated within 2 years before inclusion in the present
- •study, except for any in situ cancer or non-melanoma skin cancer when radically
研究者
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