跳至主要内容
临床试验/JPRN-UMIN000012450
JPRN-UMIN000012450已完成2 期

Phase II study of continuation maintenance by use of nab-Paclitaxel and Bevacizumab after induction chemotherapy of Carboplatin and nab-Paclitaxel pulse bevacizumab in chemotherapy-naïve patients with Stage IIIB / IV non-squamous and non-small cell lung cancer. - Phase II of Carboplatin (CBDCA) and nab-Paclitaxel (nab-PTX) pulse bevacizumab (BEV) followed by nab-Paclitaxel and bevacizumab

Department of Respiratory Medicine National Center for Global health and Medicine-Hospital0 个研究点目标入组 42 人开始时间: 2013年12月2日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
42

研究概览

简要总结

Because of slow accrual, this study will not be capable of completion. The study committee decided termination of this study.

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)Patients with squamous cell lung cancer. 2)History of allergic reaction for agents of present treatment 3)Severe myelosupperssion, renal dysfunction or hepatic dysfunction 4)Active concomitant malignancy except carcinoma in situ, intra-mucosal carcinoma or cancer with more than 5 year disease free 5)Active infection more than and equal to grade 2 6)Massive pleural effusion, peritoneal effusion or cardiac effusion required for tube drainage 7)Patients required for continuing more than and equal to 10 mg/day of steroid therapy 8)A history of significant hemoptysis (> 2.5 mL red blood per episode) within 3 months before enrolment 9)History of thromboembolic events 10)Any history of cerebral, myocardial, and pulmonary infarction 11)Bleeding tendency, blood coagulation disorder 12)Other ineligible for bevacizumab 13)Pregnant status or lactation 14)Uncontrolled psychiatric disease 15)Other ineligible status judged by medical oncologist.

研究者

发起方
Department of Respiratory Medicine National Center for Global health and Medicine-Hospital

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