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临床试验/JPRN-UMIN000017010
JPRN-UMIN000017010已完成2 期

Weekly nab-PTX in Combination with Gemcitabine in Patients with Non-Small-Cell Lung Cancer Previously Treated with Platinum based Chemotherapy - Weekly nab-PTX in Combination with Gemcitabine in Lung Cancer patient Previously Treated with Platinum based Chemotherapy

Division of Respiratory Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine0 个研究点目标入组 28 人开始时间: 2015年4月1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
28

研究概览

简要总结

The overall response rate was 17.9%. The disease control rate was 67.9%. The median progression-free survival was 3.1 months. Adverse events were generally tolerable except grade 3 interstitial pneumonia with in 4 patients.

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)interstitial pneumonia or pulmonary fibrosis detectable on CT scan 2)history of drug induced interstitial pneumonia 3)history of severe drug allergy 4)patients previously treated with paclitaxel, gembcitabine, nab-paclitaxel. 5)history of active infection or other serious disease condition 6)history of poorly controlled pleural effusion,pericardial effusion and ascites 7)history of severe heart disease(uncontrollable arrythmia,uncontrollable angina pectoris,heart failure, etc.) 8)uncontrollable diabetes mellitus 9)curative radiotherapy pretreated to the chest. 10)current neuropathy >Grade2 11)history of active double cancer 12)history of active psychological disease 13)history of pregnancy or lactation 14)any other medical condition that makes the patient unsuitable for inclusion in the study according to the opinion of the investigator.

研究者

发起方
Division of Respiratory Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine

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