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临床试验/JPRN-UMIN000010721
JPRN-UMIN000010721招募中2 期

Assessment of efficacy and safety of continouation maintenance therapy with gemcitabine after cisplatin-gemcitabine induction chemotherapy in advanced squamous cell lung cancer (KTORG1302) - Assessment of efficacy and safety of CDDP+GEM followed by GEM in advanced squamous cell lung cancer

Kyoto Thoracic Oncology Research Group (KTORG)0 个研究点目标入组 60 人开始时间: 2013年5月15日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
60

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
20years-old 至 75years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Patients with histologically proven non-squamous cell lung cancer 2) Recognized ILD or pulmonary fibrosis on X-rays 3) Pleural effusion, peritoneal fluid and pericardial fluid that need treatment 4) Superior vena cava syndrome 5) Symptomatic brain metastasis 6) Active concomitant malignancy 7) Prior therapy with gemcitabine 8) Diabetes and hypertension that cannot be controlled 9) Liver cirrhosis 10) Symptomatic or asymptomatic but treated heart disease 11) Severe infectious disease 12) Pregnant women, possibly pregnant women, wishing to become pregnant 13) Serious drug hypersensitivity or a history of drug allergy 14) Refusal of supportive care such as blood transfusion 15) Bleeding tendency 16) Other conditions not suitable for this study

研究者

发起方
Kyoto Thoracic Oncology Research Group (KTORG)

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