JPRN-jRCTs031180403进行中（未招募）2 期
A phase II trial of induction CDDP plus TS-1 with concurrent radiotherapy followed by surgical resection in patients with pathologically confirmed stage IIIA-N2 squamous-cell non-small cell lung cancer.
适应症
试验速览
- 阶段
- 2 期
- 状态
- 进行中（未招募）
- 发起方
- Suzuki Kenji
- 入组人数
- 45
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
- >= 20age old 至 <= 75age old（—）
- 性别
- All
入选标准
- •(1) Histologically or cytologically proven squamous cel carcinoma of the lung, diagnosed using specimen material
- •(2) Stage IIIA- pathologically proven N2 disease
- •(3) Without previously treatment for lung cancer
- •(4) 20 years or more , 75 years or less
- •(5) ECOG PS 0-1
- •(6) Expected FEV 1.0 > 800ml after lung resection , SpO2 (Room air) >95%
- •(7) Adequate organ function
- •(8) Written informed consent
排除标准
- •(1) Uncontrollable systemic disease (hyper tension, diabetes mellitus etc.)
- •(2) Under administration of flucytosine
- •(3) History of active infection
- •(4) Hepatitis Bs antigen positive
- •(5) History of severe heart disease
- •(6) Traumatic fracture of un recovery
- •(7) Severe diarrhea
- •(8) Severe drug allergy
- •(9) Investigational new drug or the unapproved drug is administered
- •(10) Interstitial pneumonia or pulmonary fibrosis detectable on chest CT
- •(11) History of active double cancer
- •(12) History of pregnancy or lactation
- •(13) Any other medical condition that makes the patient unsuitable for inclusion in the study according to the opinion of the investigator
研究者
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