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临床试验/NL-OMON33139
NL-OMON33139撤回不适用

Etude de phase 1 évaluant le RAD001 en association avec la radiothérapie dans les cancers bronchiques non à petites cellules - RAD001-RT

ederlands Kanker Instituut0 个研究点目标入组 5 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
发起方
入组人数
5

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 99(—)

入选标准

  • 1) Unresectable non-small cell lung cancer, stage IIIA/B, or stage IV for which the primary tumor is symptomatic (cough, dyspnea, pain) without extra-thoracic lesions rapidly evolving
  • 2) Measurable lesion, documented histologically, potentially accessible during fiberoptic bronchoscopy.
  • 3) Age > 18 years, WHO 0-1,
  • 4) Neutrophil count > 1500 /mm3, Hemoglobin > 9 g/dL, Platelet count > 100,000/mm3
  • 5) Bilirubin < 1.5 mg/dL, Transaminases < 3 N, albumin >30 g / L, PT > 70%
  • 6) Creatinine < 120 µM/L
  • 7) Patient information and informed consent form signed.
  • 8) No previous treatment for lung cancer (surgery, radiotherapy, chemotherapy).

排除标准

  • 1) Patients previously treated with RAD001 (everolimus) or any other mTOR inhibitor
  • 2) Stage IV for which the primary tumor is not symptomatic with extra-thoracic lesions rapidly evolving requiring systemic treatment
  • 3) Previous radiotherapy,
  • 4) Venous or arterial thrombosis, pulmonary embolism during the previous six months
  • 5) Concomitant treatment with phenytoin, phenobarbital or any other antiepileptic agent, history of epilepsy
  • 6) Concomitant treatment with medicinal products that inhibit, induce or are substrates for CYP3A4

研究者

发起方
ederlands Kanker Instituut

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