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临床试验/NCT02579564
NCT02579564Unknown3 期

Systemic Chemotherapy Combined With Thoracic Cavity Perfusion of Recombinant Human Adenovirus Type 5 and Endostatin Injections Versus Cisplatin for Treatment Malignant Hydrothorax in Non Small Cell Lung Cancer (NSCLC) Patients: A Multi-center, Randomized, Controlled Clinical Trial

Xinqiao Hospital of Chongqing0 个研究点目标入组 134 人开始时间: 2016年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
发起方
入组人数
134
主要终点
Objective response rate (ORR) of malignant pleural effusions

研究概览

简要总结

The purpose of this multi-center clinical trial is to verify more effective on local control of malignant pleural effusions in NSCLC patients by thoracic cavity perfusion of recombinant human adenovirus type 5 injection and recombinant human Endostatin injection (Endostar) compared with cisplatin perfusion, with acceptable side effects.

详细描述

Malignant pleural effusion, which can malfunction of circulatory and respiratory systems, is a common complication in advanced NSCLC, finally decreases the quality of life and lifespan. Nowadays, it is still a challenge to effectively control malignant pleural effusion. In this multi-center randomized and controlled clinical trial, 134 NSCLC patients diagnosed as malignant pleural effusion in the first time will enroll. Based on systemic chemotherapy and pleural cavity perfusion, all eligible patients are randomly assigned into treatment group (recombinant human adenovirus type 5 and Endostatin injections) and control group (cisplatin) with ratio 1:1. Local control rate and side effects are record respectively. The anticipation is that treatment group obtains faster and longer control of pleural effusion.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age 18-75 yrs;
  • Kamofsky score (KPS) ≥70, and a predicted lifespan >3 months;
  • Enough function of vital organs, such as heart, liver and kidney;
  • Advanced NSCLC diagnosed by cytology or pathology
  • Unilateral or bilateral of malignant pleural effusion in the first time;
  • Patients who are considered as malignant pleural effusion by cytology or biomarkers (CEA, CA199, CA125) in pleural effusion;
  • Without systemic infection or high fever;
  • Without active EGFR mutation or unwilling to targeted molecular therapy;
  • NO Anti tumor Radiotherapy chemotherapy and molecular targeted therapy,or Received Anti tumor Radiotherapy chemotherapy and molecular and clinical remission more than three months and in the past month ,disease progress with pleural cavity effusion but haven't use systemic or local anti tumor treatment.
  • No pleural cavity injection of antineoplastic drugs.

排除标准

  • Non-malignant pleural effusion;
  • Pleural effusion cause by other malignant tumors;
  • Allergic to Recombinant human adenovirus type 5 injection or Endostar;
  • Pregnant or lactation women;
  • Previously using Medicine for treating NSCLC with pleural cavity effusion by Systemic or pleural cavity perfusion treatment one month prior to enrollment;
  • Previously using the diuretics, albumin and anti-angiogenesis drugs, or dexamethasone one month prior to enrollment.

研究组 & 干预措施

chemotherapy with Oncorine and Endostar

Experimental

Systemic chemotherapy with standard schemes, such as GP (Gemcitabine/Cisplatin), NP (Vinorelbine/Cisplatin), TP (Paclitaxel/Cisplatin) or PP (Pemetrexed/Cisplatin). Thoracic cavity perfusion of recombinant human adenovirus type 5 injection 1.5ml and Endostar 30mg each time, twice a week for four times.

干预措施: Gemcitabine (Drug)

chemotherapy with Oncorine and Endostar

Experimental

Systemic chemotherapy with standard schemes, such as GP (Gemcitabine/Cisplatin), NP (Vinorelbine/Cisplatin), TP (Paclitaxel/Cisplatin) or PP (Pemetrexed/Cisplatin). Thoracic cavity perfusion of recombinant human adenovirus type 5 injection 1.5ml and Endostar 30mg each time, twice a week for four times.

干预措施: Vinorelbine (Drug)

chemotherapy with Oncorine and Endostar

Experimental

Systemic chemotherapy with standard schemes, such as GP (Gemcitabine/Cisplatin), NP (Vinorelbine/Cisplatin), TP (Paclitaxel/Cisplatin) or PP (Pemetrexed/Cisplatin). Thoracic cavity perfusion of recombinant human adenovirus type 5 injection 1.5ml and Endostar 30mg each time, twice a week for four times.

干预措施: Paclitaxel (Drug)

chemotherapy with Oncorine and Endostar

Experimental

Systemic chemotherapy with standard schemes, such as GP (Gemcitabine/Cisplatin), NP (Vinorelbine/Cisplatin), TP (Paclitaxel/Cisplatin) or PP (Pemetrexed/Cisplatin). Thoracic cavity perfusion of recombinant human adenovirus type 5 injection 1.5ml and Endostar 30mg each time, twice a week for four times.

干预措施: Pemetrexed (Drug)

chemotherapy with Oncorine and Endostar

Experimental

Systemic chemotherapy with standard schemes, such as GP (Gemcitabine/Cisplatin), NP (Vinorelbine/Cisplatin), TP (Paclitaxel/Cisplatin) or PP (Pemetrexed/Cisplatin). Thoracic cavity perfusion of recombinant human adenovirus type 5 injection 1.5ml and Endostar 30mg each time, twice a week for four times.

干预措施: Oncorine (Drug)

chemotherapy with Oncorine and Endostar

Experimental

Systemic chemotherapy with standard schemes, such as GP (Gemcitabine/Cisplatin), NP (Vinorelbine/Cisplatin), TP (Paclitaxel/Cisplatin) or PP (Pemetrexed/Cisplatin). Thoracic cavity perfusion of recombinant human adenovirus type 5 injection 1.5ml and Endostar 30mg each time, twice a week for four times.

干预措施: Endostar (Drug)

chemotherapy with Oncorine and Endostar

Experimental

Systemic chemotherapy with standard schemes, such as GP (Gemcitabine/Cisplatin), NP (Vinorelbine/Cisplatin), TP (Paclitaxel/Cisplatin) or PP (Pemetrexed/Cisplatin). Thoracic cavity perfusion of recombinant human adenovirus type 5 injection 1.5ml and Endostar 30mg each time, twice a week for four times.

干预措施: Cisplatin (Drug)

chemotherapy with cisplatin

Active Comparator

Systemic chemotherapy with standard schemes without cisplatin, such as Gemcitabine, Vinorelbine, Paclitaxel or Pemetrexed. Thoracic cavity perfusion of cisplatin 30mg/m2 each time, twice a week for four times.

干预措施: Gemcitabine (Drug)

chemotherapy with cisplatin

Active Comparator

Systemic chemotherapy with standard schemes without cisplatin, such as Gemcitabine, Vinorelbine, Paclitaxel or Pemetrexed. Thoracic cavity perfusion of cisplatin 30mg/m2 each time, twice a week for four times.

干预措施: Vinorelbine (Drug)

chemotherapy with cisplatin

Active Comparator

Systemic chemotherapy with standard schemes without cisplatin, such as Gemcitabine, Vinorelbine, Paclitaxel or Pemetrexed. Thoracic cavity perfusion of cisplatin 30mg/m2 each time, twice a week for four times.

干预措施: Paclitaxel (Drug)

chemotherapy with cisplatin

Active Comparator

Systemic chemotherapy with standard schemes without cisplatin, such as Gemcitabine, Vinorelbine, Paclitaxel or Pemetrexed. Thoracic cavity perfusion of cisplatin 30mg/m2 each time, twice a week for four times.

干预措施: Pemetrexed (Drug)

chemotherapy with cisplatin

Active Comparator

Systemic chemotherapy with standard schemes without cisplatin, such as Gemcitabine, Vinorelbine, Paclitaxel or Pemetrexed. Thoracic cavity perfusion of cisplatin 30mg/m2 each time, twice a week for four times.

干预措施: Cisplatin (Drug)

结局指标

主要结局

Objective response rate (ORR) of malignant pleural effusions

时间窗: up to 3 years

Assessed by WHO Cancerous effusion scoring system

次要结局

  • progression-free survival(up to 3 years)

研究者

发起方
Xinqiao Hospital of Chongqing
申办方类型
Other
责任方
Principal Investigator
主要研究者

Zhengtang Chen

Chief Physician

Xinqiao Hospital of Chongqing

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